Skip to main content

New treatment options for metastatic renal cell carcinoma with prior anti-angiogenesis therapy


Angiogenesis is a critical process in the progression of advanced renal cell carcinoma. Agents targeting angiogenesis have played a primary role in the treatment of metastatic renal cell carcinoma. However, resistance to anti-angiogenesis therapy almost always occurs, and major progress has been made in understanding its underlying molecular mechanism. Axitinib and everolimus have been used extensively in patients whom have had disease progression after prior anti-angiogenesis therapy. Recently, several new agents have been shown to improve overall survival in comparison with everolimus. This review provides an in-depth summary of drugs employable in the clinical setting, the rationale to their use, and the studies conducted leading to their approval for use and provides perspective on the paradigm shift in the treatment of renal cell carcinoma. Highlighted are the newly approved agents cabozantinib, nivolumab, and lenvatinib for advanced renal cell carcinoma patients treated with prior anti-angiogenesis therapy.


Each year, over 320,000 individuals will be diagnosed with renal cell carcinoma (RCC) accounting for an annual death toll of over 140,000 people. The incidence of RCC has steadily risen over the past 10 years and accounts for 2–3% of all adult malignancies [1]. Upon the diagnosis of RCC, curative surgery is an option for those with early stage localized tumors. However, localized disease may undergo early hematogenous dissemination leading to metastasis. Sites of early metastases include the lungs, lymph nodes, liver, bone, and brain. RCC can also metastasize to the adrenal glands, the contralateral kidney, although less commonly [2]. Individuals with advanced disease face high rates of morbidity and mortality with a median 5-year survival rate of 53% for stage III disease and 8% for metastatic disease [3, 4]. However, death rates from RCC have remained stable or decreased in most countries with advanced healthcare [5]. This steady decline can be attributed to the advent of new biological agents rapidly developed over the past few years that are readily employable in the clinical setting.

RCC is a heterogeneous disease and is subcategorized based on histological and cytogenetic signatures, with 80% characterized as clear cell renal cell carcinoma (ccRCC) and 20% as non-clear cell carcinoma (nccRCC) [6]. Both types can occur either sporadically or due to a hereditary predisposition. However, both forms are associated with gene mutations to the short arm of chromosome 3 and specifically to the VHL tumor suppressor gene [7, 8]. In the natural setting, the VHL gene encodes the substrate recognition module of a ubiquitin ligase that targets hypoxia-inducible factor (HIF) for destruction in the presence of oxygen. However, VHL is mutated or methylated in up to 90% of patients with ccRCC [9]. When the VHL gene is mutated, its tumor suppressor function is lost and HIF accumulates to high levels, leading to the activation of multiple genes including vascular endothelial growth factor (VEGF) and platelet-derived growth factor (PDGF). Ultimately, this cascade of events culminates in unregulated cell growth, uncontrolled angiogenesis, and increased tumor-cell invasion.

Elucidation of this underlying pathway has led to the development of a number of target-based therapies for patients with advanced RCC. Prior to the advances in therapeutics seen over the last decade, the mainstay of treatment for metastatic disease was cytokine-based treatment with high dose interleukin-2 (IL-2) and interferon-alpha (IFN-α) after their FDA approval in the 1990s [10]. Although this therapy regimen produced objective responses, there were significant toxicities, treatment benefit was only seen in 5–15% of patients, and outcome for the majority of patients was poor [11, 12]. Since 2004, the advances in target-based therapy and immunotherapy modalities have created a paradigm shift in the treatment of RCC. These agents have had a remarkable effect on patient outcomes with increased progression-free survival rates; however, virtually all patients eventually develop the progression of disease [7]. The high likelihood of disease progression remains a challenge due to therapeutic resistance. Refractory disease is currently being managed with sequentially changing therapy, but morbidity and mortality remain high. Herein, we review the most up-to-date practices and emerging therapies for the treatment of refractory RCC after anti-angiogenesis therapy and focus on newly approved agents including cabozantinib, nivolumab, and lenvatinib.

The primary role of anti-angiogenesis in first-line therapy for mRCC

The armamentarium of agents approved for the first-line treatment of metastatic RCC (mRCC) has rapidly developed over the years and now includes the small-molecule VEGF tyrosine kinase inhibitor (TKI)-sunitinib and pazopanib, a monoclonal antibody targeting VEGF-bevacizumab in combination with interferon, and an mammalian target of rapamycin (mTOR) inhibitor-temsirolimus, as well as high dose IL-2. In the recent past, the approach to the treatment of patients with mRCC entailed sequential employment of agents targeting VEGF or mTOR pathways. Agents with anti-angiogenesis properties have become the mainstay of initial therapy for advanced RCC due to their preferable efficacy and toxicity profile. The current level 1 recommendation from the National Comprehensive Cancer Network (NCCN) and the European Association or Urology is the use of oral, multi-target, tyrosine kinase inhibitors (TKIs)—specifically sunitinib and pazopanib—in the first-line setting [13, 14].

VEGF-targeted tyrosine kinase inhibitors

Sunitinib is an orally administered multi-target TKI of VEGFR, PDGFR, and c-Kit and is generally well tolerated. Originally, sunitinib demonstrated a progression-free survival (PFS) of 8.3 months in patients who progressed on one line of cytokine-based therapy. This led to a follow-up study on its use as a first-line agent [15]. A pivotal phase III clinical trial involving 750 treatment-naïve patients was conducted to compare sunitinib to IFN-α as first-line treatment for mRCC. The study met its primary endpoint, PFS, and sunitinib demonstrated a superior PFS of 11 months compared to 5 months with IFN-α. Sunitinib also proved superior in overall survival (OS) with 26.4 months as compared to 21.8 months for IFN-α [15]. The side-effect profile has been studied thoroughly, and common adverse effects include hypertension (12%), fatigue (11%), diarrhea (9%), and hand-foot syndrome (9%) [16].

In light of its favorable safety and tolerability profile, a second TKI, pazopanib, was studied in the mRCC population [17]. A phase III, double-blind, placebo-controlled study was designed to evaluate pazopanib in 435 treatment-naïve or cytokine-pretreated patients. Pazopanib was shown to prolong mPFS compared to placebo (11.1 vs. 2.8 months) and to cytokine-pretreatment (7.4 vs. 4.2 months). Sternberg et al. reported a median OS of 22.9 months with pazopanib and 20.5 months with placebo [18]. Common pazopanib toxicities during this trial included diarrhea (52%), hypertension (40%), hair color changes (38%), and nausea (26%) [17].

In order to select the optimal first-line therapy, head-to-head comparison studies were performed for these two TKIs. In 2013, Motzer et al. presented the COMPARZ trial, a global, phase III, randomized, open-label trial comparing sunitinib and pazopanib as first-line agents. Both agents performed similarly, and the mPFS of pazopanib was 10.5 months compared to 10.2 months for sunitinib. OS analysis resulted in 28.4 and 29.3 months for pazopanib and sunitinib, respectively. Overall clinical efficacy was not discernable between the two agents, and pazopanib was concluded to be non-inferior to sunitinib [19]. In addition to the COMPARZ trial, the PISCES study investigated patient-reported outcomes with regard to pazopanib and sunitinib tolerability and patient preference. Stratification of data from this questionnaire-based study revealed a significant number of patients preferred pazopanib over sunitinib. There was a 49% reported difference in preference between the two agents [20]. Interestingly, both agents have uniquely different side-effect profiles despite similar target pathways and mechanisms of action. Pazopanib has a lower incidence of hand-foot syndrome, fatigue, and myelosupression but notable for more frequent hepatic injury. Such a discernable difference in toxicities has been used as a tool to tailor therapy for mRCC patients based on their respective comorbidities [21].

Other TKIs include sorafenib, axitinib, and cabozantinib which were also tested in the first-line setting. Sorafenib was introduced as the first targeted therapy for mRCC in 2004 [22]. An oral, multi-kinase inhibitor of tumor-cell proliferation and tumor angiogenesis, sorafenib, is currently indicated for the treatment of renal, liver, and thyroid cancers. A phase III study, presented as the TARGET trial, enlisted 903 mRCC patients with disease refractory to high dose IL-2 and IFN-α and stratified patients to a placebo or sorafenib treatment group. Sorafenib outperformed placebo in mPFS 5.5 to 2.8 months, respectively [23]. Originally, no significance was found in OS from the study data; however, further analysis censoring placebo patients with crossover demonstrated a survival advantage for sorafenib-treated patients. Moreover, the TARGET trial also provided data suggesting VEGF levels are prognostic for mPFS and OS in mRCC [24]. It must be noted, however, that sorafenib did not improve PFS when compared to IFN-α-2a in the first-line setting [25].

Axitinib, initially approved in the second-line setting, was also studied as a first-line agent in comparison with sorafenib in a randomized, open-label, phase III clinical trial. Although axitinib demonstrated clinical activity with an acceptable safety profile, there was no significant difference in mPFS in patients with treatment-naïve mRCC compared with those treated with sorafenib in the first-line setting [26].

Most recently, the European Society for Medical Oncology announced the results of a phase II multicenter study comparing cabozantinib and sunitinib in the first-line setting. One hundred fifty-seven patients were randomized to receive either agent, and the cabozantinib treatment group showed a 31% reduction in the median rate of progression or death compared to those treated with sunitinib [27]. Although the results are promising, more expansive studies will be needed including phase III studies to solidify the role of cabozantinib in patients with untreated mRCC.

Monoclonal antibody targeting VEGF

Bevacizumab is a humanized recombinant monoclonal antibody against VEGF-A [28]. It was originally evaluated in a randomized phase II trial showing increased time to disease progression in patients who failed high-dose IL-2 [29]. Such promising data culminated in the AVOREN trial, a phase III, randomized, double-blinded study of 641 patients treated with bevacizumab plus IFN-α or placebo with IFN-α. Study results include bevacizumab benefit with mPFS (10.2 vs. 5.4 months), RR (30.6 vs. 12.4%), and a trend towards improved survival [30, 31]. A similar trial studying the viability of bevacizumab in the first-line setting (the CALBG trial) randomized patients to receive bevacizumab with IFN-α or IFN-α alone. In concordance with the AVOREN trial, the CALBG study showed that the patients in the bevacizumab arm had a greater mPFS and RR. These data propelled bevacizumab as a viable first-line agent alongside sunitinib and pazopanib therapies [32]. Bevacizumab has been studied in combination with sunitinib, sorafenib, or temsirolimus, and all encountered significant dose-limiting toxicities [3033]. Currently, bevacizumab in combination with interferon has a category 1 NCCN recommendation for mRCC.

mTOR inhibitors

A serine/threonine kinase and member of the PI3K family, mammalian target of rapamycin (mTOR), is implicated in the activation of a number of growth factors and signaling cascades, therefore having implications in tumorigenesis and angiogenesis [3335]. Interestingly, the role of mTOR signaling in solid cancers was primarily investigated in the RCC model with the ultimate development of targeted agents for systemic therapy in mRCC patients [36, 37]. Over the past few years, experts have supported the growing body of evidence that there is a greater efficacy of VEGFR inhibitors compared to mTOR inhibitors in patients with mRCC [38]. Notwithstanding, temsirolimus and everolimus have had principal roles in mRCC in both the first-line and refractory setting.

Temsirolimus is the only mTOR inhibitor approved for the first-line treatment of mRCC with poor prognosis. In the phase III Global ARCC trial, temsirolimus was studied for first-line use in 626 previously untreated patients with mRCC with poor prognosis features based on MSKCC prognostic model. Participants were considered poor prognosis if three of the following six criteria were met: LDH ≥ 1.5 × ULN, Ca++ of ≥10 mg/dL, diagnosis to treatment initiation of <1 year, KPS 60–70%, ≥2 metastatic sites [39]. Of note, this study was indiscriminant of histological subtype and included both ccRCC and nccRCC subjects. ARCC compared IFN-α or a combination of temsirolimus and IFN-α. Temsirolimus monotherapy demonstrated a superior OS of 10.9 months compared to either IFN-α (7.3 months) or combination therapy (8.4 months). ARCC also reported temsirolimus to have a superior mPFS of 3.8 months over IFN-α (1.9 months) [40]. Temsirolimus is currently recommended by the NCCN for first-line use in patients with mRCC with features of poor prognosis.

While temsirolimus has not been compared directly with either sunitinib or pazopanib in the first-line setting for patients with mRCC, the issue of optimal sequencing between VEGF TKIs and mTOR inhibitors was addressed in the RECORD-3 trial using a different mTOR inhibitor, everolimus. RECORD-3 was a phase II study comparing the mPFS of treatment-naïve mRCC patients treated with sequential first-line everolimus and second-line sunitinib versus first-line sunitinib and second-line everolimus. The use of everolimus followed by sunitinib failed to demonstrate non-inferiority with regard to mPFS. To this end, study outcomes did not support the use of everolimus in first-line setting [41].

Paradigm shift in the treatment of mRCC after anti-angiogenesis therapy

The primary challenge of mRCC is that complete response to treatment with a single agent is rare. Disease progression is expected and tumor resistance is an inevitable reality. mRCC remains incurable in most instances, and mechanisms of tumor-cell resistance to conventional radiotherapy and chemotherapy have been an active area of research. Proposed mechanisms include overexpression of multidrug resistance gene MDR-1, cell survival gene clusterin, PKC-ζ, L2 cell adhesion molecule L1-CAM, P-glycoprotein, various DNA repair proteins, the antiapoptotic gene bcl-2, glutathione S-transferase, decreased expression of DNA topoisomerase, loss of HIF-1α regulation, accumulation of HIF-2α, and suppression of p53 [40, 42]. Targeting these resistance mechanisms is an area of ongoing studies and may play a role in future approaches to the treatment of advanced RCC.

Prior to the approval of everolimus by FDA in 2009 for the second-line use in mRCC, there was no established treatment option for patients who progressed on first-line VEGF-directed therapy. Significant advancement has been made since, and the second-line treatment options now include TKIs—axitinib, cabozantinib, and lenvatinib; an anti-PD1 monoclonal antibody, nivolumab; and an mTOR inhibitor, everolimus. Sequential treatments have emerged as a viable approach to controlling drug resistance and overcoming resistance mechanisms [43], while the optimal sequence of treatment remains to be defined as few studies to date have directly compared drug efficacy [44].


The oral agent mTOR inhibitor, everolimus, was the first drug to be approved for second-line use in mRCC after progression on first-line VEGF TKI treatment. In the RECORD-1 trial, everolimus was compared to placebo in 410 mRCC patients whom had been previously treated for at least 6 months with sunitinib, sorafenib, or both [45]. The study’s primary endpoint was mPFS, and everolimus performed superiorly to placebo with a significant mPFS difference of 4.0 to 1.9 months, respectively. A follow-up trial, RECORD-4, prospectively followed mRCC patients on everolimus after the progression of disease on either sunitinib, additional VEGF TKIs, or cytokine therapy [46] and confirmed the mPFS benefit of everolimus. The role of everolimus has been investigated beyond the second-line setting and investigators proposed that mTOR inhibition may have a role in untreated nccRCC. The ASPEN trial was a multicenter, open-label, randomized phase II trial designed to determine the mPFS of sunitinib and everolimus in a subset of patients with histologically proven nccRCC. Results favored sunitinib over everolimus (8.3 vs. 5.6 months) and reaffirmed the role of everolimus solely as a second-line agent, irrespective of histological subtype [47].

Sorafenib and axitinib

The role of second-line sorafenib has been investigated in the INTORSECT trial, which enrolled patients whom had progressed after sunitinib therapy and randomized them to receive either temsirolimus or sorafenib with a primary endpoint of mPFS and secondary endpoints of safety, ORR and OS. The study concluded there was no difference in mPFS between the two agents; however, sorafenib demonstrated a superior OS of 16.6 months over temsirolimus, 12.3 months. Both agents presented with an acceptable safety profile, and the adverse effects were consistent with the known toxicities of the drugs [48].

Axitinib is an oral, potent, small-molecule TKI that selectively inhibits VEGFR-1, VEGFR-2, and VEGFR-3 [49]. The role of axitinib in the second-line treatment of mRCC has been investigated in the phase III AXIS trial, which randomized 723 patients with mRCC whom had disease progression after first-line systemic therapy [41]. First-line therapy included sunitinib, cytokine therapy, bevacizumab plus IFN-α, or temsirolimus. The trial met its primary endpoint, mPFS, and axitinib was shown to offer a superior mPFS of 6.7 months compared to sorafenib, 4.7 months. There was, however, no difference in the OS between the axitinib-treated group and sorafenib-treated group [50]. Common axitinib toxicities observed in the study included diarrhea (55%), hypertension (40%), and fatigue (39%).


The second-line agents everolimus and axitinib had become the standard of care in refractory disease, but the mPFS was only extended by a mere 3 to 5 months after disease advancement on first-line therapy [41, 48]. Within the past year, two novel VEGFR TKIs, cabozantinib and lenvatinib, have gained FDA approval for use in advanced RCC.

Cabozantinib is an oral, small-molecule TKI-targeting VEGFR that was originally approved for metastatic medullary thyroid cancer. In addition to VEGFR, cabozantinib targets receptor tyrosine kinases implicated in and relevant to mRCC; RET, KIT, AXL, and FLT3 [51]. A landmark study by Zhou et al. provided evidence that MET and AXL are upregulated in chronic sunitinib use and play a role in RCC tumor resistance to TKIs [52]. This data is in concordance with previous studies which suggest poor prognosis when MET/AXL are highly expressed by RCC tumor cells [53]. Cabozantinib was studied in the METEOR trial, which was a randomized, open-label, phase III trial comparing cabozantinib with everolimus in 658 patients with mRCC whom had advanced after TKI therapy. The study’s primary endpoint was mPFS and secondary endpoints were OS and ORR. The rate of disease progression with cabozantinib was 42% lower than with everolimus. The METEOR trial met its primary endpoint, and cabozantinib demonstrated a superior mPFS of 7.4 months compared to 3.8 months with everolimus. An OS advantage was observed with cabozantinib (21.4 compared to 16.5 months), and the ORR significantly favored cabozantinib to everolimus, 21 to 5% (p < 0.001) [38]. Cabozantinib was observed to have a similar safety profile to drugs in its own class (Table 1). The incidence of grade 3 and 4 adverse effects was 68% with cabozantinib. The most common events were hypertension (15%), diarrhea (11%), and fatigue (9%). Dose reductions occurred in 60% of the study patients stratified to cabozantinib treatment. A grade 5 adverse event occurred in one patient [54].

Table 1 Common adverse effects of novel agents approved for mRCC

The METEOR trial was published in November of 2016, and by April 2016, the FDA had approved cabozantinib as second-line treatment for advanced mRCC after anti-angiogenesis therapy. As to the question of where cabozantinib fits in the sequential treatment paradigm, its superiority to everolimus leaves axitinib as a possible comparator for a future study. Similar to the METEOR trial, the AXIS trial investigated disease refractory to sunitinib. Subgroup and post hoc analyses of the AXIS trial revealed that the patients whom had been treated with sunitinib and axitinib sequentially had a mPFS of 4.8 months and an ORR of 11% [41, 55]. Considering the 9.1-month mPFS and ORR of 22% observed in this study, cabozantinib could be a marked advancement in the treatment of mRCC. Moreover, the success of cabozantinib serves as a proof-of-principle that the targets (MET and AXL) that were not affected by previous drugs have an in vivo role in mRCC disease.

Lenvatinib in combination with everolimus

One month after the FDA announcement of approval of cabozantinib for mRCC, lenvatinib was approved for the treatment of patients with advanced mRCC in combination with everolimus following disease resistance to TKIs. Lenvatinib is an oral, multi-target TKI of VEGFR1-3, FGFR1-4, PDGFRα, RET, and KIT [56]. First established as a therapy for differentiated thyroid cancer, lenvatinib has had a favorable antitumor profile with acceptable toxicities in a multitude of solid tumors in both phase I and II trials [57, 58]. The mechanism by which tumors develop VEGF resistance and develop compensatory angiogenesis pathways provides the rationale for studies on drugs with multiple targets [59]. Prior in vivo studies using mouse xenografts of human RCC showed a reduction in tumor volume with a lenvatinib and everolimus combination [60]. Further, in vitro binding studies reveal a highly specific binding site to the receptor kinase domain, suggesting possible limited toxic effects [61]. To this end, lenvatinib had been identified as a candidate for clinical studies in patients with advanced mRCC refractory to first-line agents.

The role of lenvatinib in the treatment of mRCC has been studied in a randomized, phase II, open-label, multicenter trial, which enrolled 153 patients with mRCC that progressed on first-line VEGF-directed therapy [62]. Patients were stratified in a 1:1:1 ratio and received lenvatinib, everolimus, or combination therapy with a primary endpoint of mPFS. Lenvatinib plus everolimus significantly prolonged mPFS compared to everolimus, 14.6 to 5.5 months, but not to single-agent lenvatinib, 7.4 months. Moreover, OS was increased in the group receiving the dual-therapy compared to everolimus alone, although not statistically significant. Single-agent lenvatinib significantly prolonged mPFS compared to everolimus as well. However, the size of the benefit of the combination therapy as compared to the benefit of single-agent lenvatinib suggests that efficacy was most robust with the combination therapy [63]. The design of this three-armed study not only provides objective clinical data but also presents an emerging concept in mRCC therapy that combination drugs targeting multiple pathways (in this case VEGF and mTOR) could simultaneously inhibit two critical independent pathways synergistically and can potentially prevent resistance to single-agent therapy [62].

The toxicity profile of the combination therapy was consistent with the known toxicities of each individual agent (Table 1). Expectedly, the combination therapy exhibited more frequent adverse events than either single therapy. These most common grade 3 and 4 treatment-emergent adverse events from the dual-therapy patient group include constipation (37%), diarrhea (20%), fatigue (14%), and hypertension (14%). The increased likelihood of toxicity is an appreciable concern and should be considered by clinicians when deciding upon second-line therapy.

Immunotherapy with PD-1 and PD-L1 inhibitors

mRCC is highly immunogenic. Neoplastic cells evade immune cell surveillance allowing for uninhibited and unregulated cell growth. The novel principle underlying immunotherapy entails the activation of the endogenous immune system to target cancer at the cellular level and enable checkpoint inhibition [64]. Immunotherapy agents at work in mRCC have a role in two-principle immune signaling mechanisms: (1) cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) and (2) programmed death receptor-1 (PD-1). These two receptors are negative immune regulators imperative to preventing autoimmunity and are endogenous signals for suppression of lymphocytes and natural killer (NK) cells. Although the ability of cancer cells to suppress the immune system is maladaptive, researchers have been able to use this facet of cancer biology as a target for drug development [65].

The targeted therapies reviewed above and immunotherapies have vastly different mechanisms of action; however, both treatment modalities show durable responses in mRCC tumor regression. Interestingly, studies have shown that targeted therapies are able to dramatically enhance immune cell function as well. Together, this creates a paradigm whereby immunotherapy and targeted therapy can be employed concomitantly with a synergistic effect [66]. Herein, we describe the immunotherapies approved by the FDA for mRCC including the newly approved agent nivolumab and highlight the promising data that led to nivolumab’s approval.

PD-1 is a cell surface glycoprotein expressed on T-lymphocytes, B-lymphocytes, macrophages, and NK cells. Ligand binding of the PD-1 receptor inhibits the effector phase of T cell activation and thereby serves as a potent immune checkpoint receptor [6]. The pathogenesis of mRCC cells and their immunomodulatory effect stems from the interface between malignant cells and the PD-1 receptor. The natural ligand to PD-1 is the PD-1 ligand (PD-L1), which is expressed on antigen-presenting cells. Importantly, populations of mRCC cells have also been shown to express PD-L1, and this mimicry can result in not only unregulated tumor cell growth but also apoptosis of antigen-specific T cells [11, 67]. This interplay between malignant cells and immune cells creates a tumor microenvironment with an active yet functionally impaired immune system. Studies have gone on to show that the degree of PD-L1 expression on mRCC cells directly correlates with aggressive pathologic features including advanced TNM staging, tumor size, higher nuclear grade, coagulative necrosis, increased disease progression, cancer-specific death, and overall mortality [68].

Nivolumab is a fully humanized immunoglobulin G4 PD-1 immune checkpoint inhibitor antibody that selectively blocks the receptor activation of PD-L1 and PD-L2. Ultimately, nivolumab enhances T cell function which results in antitumor activity [69]. Nivolumab has changed the landscape for multiple solid and liquid tumors and currently holds FDA approval for the treatment of melanoma, squamous non-small cell lung cancer, and classical Hodgkin’s lymphoma as well as mRCC. The CheckMate016 phase I trial included patients with mRCC and was first presented at ASCO 2015. This study demonstrated that a combination of nivolumab and ipilimumab exhibited a durable antitumor effect with a manageable safety profile [70]. A recently reported 5-year follow-up investigation of the phase I participants revealed a 34% 5-year survival rate for mRCC patients whom failed prior anti-angiogenesis therapy and then placed on maintenance nivolumab [71].

Building on these promising results, investigators recruited 168 patients with histological confirmation of mRCC for a phase II study. The patient had received prior treatment with either a VEGF TKI or VEGF monoclonal antibody and suffered from progression of disease. Patients were stratified to receive varying doses of nivolumab as a single-agent therapy. The study successfully demonstrated nivolumab to prolong mPFS (2.7–4.7 months), ORR (20–22%), and mOS (18.2–25.5). Together, the results of the study suggested promising antitumor activity while exhibiting minimal systemic toxicities [69].

The abovementioned results were encouraging as a proof-of-principle validating immunotherapy as a treatment option for mRCC. CheckMate 025 trial was the first phase III randomized controlled trial examining nivolumab in advanced RCC. Nivolumab was compared to everolimus in disease refractory to VEGFR targeted therapy. Eight hundred twenty-one patients were stratified to receive either nivolumab or everolimus with a primary endpoint of OS. Secondary endpoints included ORR and safety. The results from this study were remarkable and ultimately led to FDA approval of the drug. mOS was 25.0 versus 19.6 months for nivolumab and everolimus, respectively, and met the predetermined criteria for significance. The hazard ratio (HR) for nivolumab met superiority over everolimus (HR 0.73, p < 0.0148). Further significant findings indicating nivolumab superiority included an ORR of 25 versus 5% and an OR of 5.98. There was no difference in mPFS between the two agents. Moreover, the safety and tolerability profiles favored nivolumab over everolimus (Table 1). Nineteen percent of the nivolumab-treated patients reported grade 3 or 4 treatment-related adverse effects compared to 37% of the patients whom had received everolimus. Of note, the durable responses seen by nivolumab were irrespective of MSKCC prognostic score, number of previous anti-angiogenic therapies, and PD-L1 expression [72]. Data extrapolated from the CheckMate 025 trial analyzed the role of nivolumab treatment after progression, an emerging concept in clinical oncology [73]. With regard to the patients in the study treated with nivolumab, 171 of the enrolled patients were treated beyond progression of disease. The patients treated beyond progression experienced a mOS of 28.1 months compared to 15.0 months for the group not treated after progression (p < 0.001) [74]. These data are suggestive that the immune response of nivolumab may be delayed, and further studies are necessary to fully elucidate the timing of the clinical effect of the drug.

A 2016 study building off the results from the CheckMate 025 trial compared health-related quality of life (HRQoL) for patients in the treatment groups of this trial. Nivolumab was associated with an improved HRQoL compared to everolimus in this study population [75]. Although there was no significant difference in the mPFS observed, ad hoc sensitivity analysis of mPFS in the patients whom had not progressed or died within six months of treatment revealed a delay in progression on nivolumab that achieved statistical significance. The landmark CheckMate 025 trial and subsequent studies have resulted in labeling nivolumab as the leading monotherapy for second-line therapy for those who fail VEGFR-targeting therapies [76].

More recent studies have shown that the immunomodulatory effect of nivolumab in the mRCC tumor microenvironment is expansive [77]. In an elegantly designed study, baseline and on-treatment biopsies were obtained from mRCC patients receiving nivolumab therapy (both treatment-naïve and refractory disease patients). Immunohistochemical analysis of these biopsies demonstrated an increased lymphocytic presence in the nivolumab-treated group, reversal of T cell exhaustion within the tumor microenvironment, upregulation of genes that are hallmarks of the Th1 inflammatory response, and increased tumor trafficking or infiltration of T cells. The investigators also report an increase in expression of genes linked to NK cells, suggesting that the immunomodulatory effect of nivolumab may be augmented with NK cell-directed therapies in the future [78].

Treatment selection after anti-angiogenesis therapy

The optimal sequencing of mRCC treatment beyond first-line VEGF TKIs remains controversial, as there are no head-to-head comparisons between currently approved drugs. Everolimus was the first drug approved for second-line treatment of mRCC based on mPFS benefit over placebo; however, objective tumor response was low, and no overall survival benefit had been demonstrated [48]. Nivolumab is arguably the most promising agent with a unique immune mechanism of action and showing an OS benefit over everolimus in the second-line treatment of mRCC. In contrast to previously held belief, there was no significant difference in the median time to progression for nivolumab versus everolimus [72]. Lenvatinib in combination with everolimus, in a phase II trial, demonstrated to offer mPFS benefit over single-agent everolimus, but not over single-agent lenvatinib. Further studies are needed to define the role of lenvatinib, and the cost of combination therapy may be an issue to consider in clinical practice. The OS benefit of both these agents over everolimus is remarkable and solidifies both agents as marked improvements over the therapies previously available for use in clinical practice.

Among TKIs currently approved for second-line use, only axitinib and sorafenib have been compared in a head-to-head fashion. Axitinib is more potent and selective than sorafenib. In the AXIS trial, it demonstrated mPFS benefit over sorafenib, but no overall survival benefit [55]. Cabozantinib has the theoretical benefit of additional inhibition of MET and AXL, which are believed to play a role in the resistance of mRCC to VEGF-directed therapy [57]. Cabozantinib remains the only agent with OS, mPFS, and ORR benefit over everolimus [38]. At the moment, cabozantinib is the preferred TKI in our opinion; however, argument can be made for reserving its use for progression of disease, as cabozantinib was shown to be effective in METEOR trial for patients previously treated with more than one line of VEGF TKIs.

The approach to the decision of drug sequence requires consideration of the drug’s side-effect profile and patient preference. Nivolumab is a biweekly intravenous infusion while cabozantinib is an oral medication that is more convenient but subject to patient compliance. The most common side effect of nivolumab appears to be fatigue, while cabozantinib causes more diarrhea and hand-foot syndrome.

There is no level 1 data to guide the choice between nivolumab and cabozantinib, and the argument can be made in favor of either. A recent study compared the efficacy of nivolumab and cabozantinib through the analysis of data from multiple trials. By extracting survival data from original study data and analyzing the hazard ratio over time, the authors found that the hazard ratio for OS favors cabozantinib in the first few months but then nivolumab afterwards [79]. A conclusion may be drawn that patients with poor prognosis benefit more from cabozantinib while patients with a better prognosis will benefit more from nivolumab. This conclusion is supplemented by the latest update from the METEOR trial, which provides direct evidence supporting the use of cabozantinib in high-risk patients [38]. On the other hand, data from the subgroup analysis of CheckMate 025 trial suggests nivolumab is of benefit across subgroups including high-risk patients.

We have learned from the INTORSECT trial that sorafenib offers superior OS over temsirolimus in the second-line setting and that continued VEGF-directed therapy beyond first-line sunitinib is more efficacious than mTOR inhibitor [43]. In the following years, the large multicenter AXIS, CheckMate, METEOR, and INTORSECT trials introduced a multitude of new promising agents (Table 2). Though these studies have established a role for novel therapies, there is a degree of disconnect between the individual studies and the overall treatment landscape for mRCC.

Table 2 Major clinical trials for the treatment of mRCC after anti-angiogenesis therapy

In our opinion, we recommend choosing either cabozantinib or nivolumab for patients with mRCC who progressed on first-line VEGFR-directed therapy, with cabozantinib preference for patients with high volume disease or symptoms due to its PFS benefit (Fig. 1). Both are acceptable options despite no current level 1 data to support the use of one agent over the other. Lenvatinib with everolimus, too, is a viable option in this setting with its appeal being dual therapy and multiple targets. Drug adverse effects and patient preference consideration should play the deciding role. In practice, we suggest substituting to the alternative agent upon progression of disease before considering everolimus, as both are superior to everolimus in OS. Given the data from the INTORSECT trial, we would consider the use of alternative VEGFR TKIs, e.g., axitinib and sorafenib, prior to the use of everolimus. This recommendation is offered with the caveat that neither has been directly compared to everolimus. Lastly, clinical trial participation is always encouraged during any stage of treatment. The CheckMate214 trial is an ongoing phase II trial comparing nivolumab and ipilimumab versus sunitinib in the first-line setting [80] (Table 3). Such trials assessing immunotherapies are most promising to fully elucidate the survival benefit immunotherapies will have compared to the TKI and monoclonal antibody class agents.

Fig. 1
figure 1

Suggested approach to treatment after anti-angiogenesis therapy. Suggested algorithm for treatment options for mRCC. Sunitnib and pazopanib are recommended in the first-line setting, with the exception of selected patients who may benefit from temsirolimus or IL-2. Upon disease progression, second-line agents can be chosen at the discretion of the clinician. The algorithm provided is based on current clinical data and practice guidelines

Table 3 Active clinical trials investigating future immunotherapies in mRCC


Long-term control of disease in the treatment of mRCC has been a challenge due to drug resistance. We have witnessed the armamentarium of treatment options for mRCC rapidly evolve, including the approval of the novel agents cabozantinib, nivolumab, and lenvatinib. mPFS and OS have been prolonged, toxicities reduced, and treatment options have been extended to the third- and fourth-line settings with the design of targeted and immunotherapies. Additionally, a number of active clinical trials are examining agents for future use in mRCC and will further expand the list of FDA-approved drugs (Table 3). However, the tremendous rate by which novel agents are being designed has created a level of complexity which clinicians must manage; treatment plans for patients have become highly variable with fewer studies assessing optimal sequence or combination of agents [64]. The question of sequencing is not unique to mRCC, as this dilemma is commonly faced when multiple therapeutic agents are developed over a short period of time for any disease process [44]. Thankfully, there are a number of randomized phase II and III trials currently ongoing that are examining both sequencing and combinatorial effects of already employed agents.

Future directions for the management of mRCC are not limited to studies investigating optimal sequence of therapies. There remains ambiguity as to the response of different histological subtypes of RCC to standard treatments [47]. There have been a number of studies in this area; however, the complexity of the various molecular mechanisms behind each subtype requires more expansive research efforts. Histological and pathological variants differ in disease biology, clinical behavior, prognosis, and response to systemic therapy [81]. Characterizing the molecular basis for each subtype will allow for greater precision for future clinical trial design with regard to targeted therapy and choice of agents. Active clinical trials are investigating possible synergism between concomitant targeted therapy and immunotherapy (Table 3). The potential of these studies, together with the advances in genomic medicine, provides a promising outlook for future care of patients with RCC.

In this review, we have highlighted the current landscape for mRCC treatment in the first-line and second-line settings. The anti-angiogenesis agents, sunitinib and pazaopanib, have remained the most utilized first-line agents [82]. After the use of these agents, axitinib and everolimus have been used extensively, but now, new agents including cabozantinib, nivolumab, and lenvatinib in combination with everolimus have provided a paradigm shift for the treatment of patients with prior anti-angiogenesis therapy. These novel therapies have gained traction for use in the second-line setting since their FDA approval. Questions remain as to what is the optimal selection of drugs in this setting. The combination of novel immunotherapies with targeted therapy has potential to dramatically improve the outcome for patients with mRCC.



Clear cell renal cell carcinoma


Cytotoxic T-lymphocyte-associated antigen 4


Health-related quality of life






Median overall survival


Median progression-free survival


Metastatic renal cell carcinoma


Mammalian target of rapamycin


National Comprehensive Cancer Network


Non-clear cell renal cell carcinoma


Natural killer


Objective response rate


Overall survival


Programmed death receptor-1


PD-1 ligand


Platelet-derived growth factor


Progression-free survival


Renal cell carcinoma


Tyrosine kinase inhibitor


Vascular endothelial growth factor


Vascular endothelial growth factor receptor


  1. 1.

    Vitale{Vitale MG, Carteni G. Recent developments in second and third line therapy of metastatic renal cell carcinoma. Expert Rev Anticancer Ther. 2016;16(5):469-71.

  2. 2.

    Capitanio U, Montorsi F. Renal cancer. Lancet. 2016;387(10021):894–906.

    Article  PubMed  Google Scholar 

  3. 3.

    Coppin C, et al. Immunotherapy for advanced renal cell cancer. Cochrane Database Syst Rev. 2005;1:CD001425.

    Google Scholar 

  4. 4.

    Ravaud A, et al. Adjuvant sunitinib in high-risk renal-cell carcinoma after nephrectomy. N Engl J Med. 2016.

  5. 5.

    Kabaria R, Klaassen Z, Terris MK. Renal cell carcinoma: links and risks. Int J Nephrol Renovasc Dis. 2016;9:45–52.

    PubMed  PubMed Central  Google Scholar 

  6. 6.

    Xu KY, Wu S. Update on the treatment of metastatic clear cell and non-clear cell renal cell carcinoma. Biomark Res. 2015;3:5.

    Article  PubMed  PubMed Central  Google Scholar 

  7. 7.

    Srinivasan R, et al. New strategies in renal cell carcinoma: targeting the genetic and metabolic basis of disease. Clin Cancer Res. 2015;21(1):10–7.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  8. 8.

    Latif F, et al. Identification of the von Hippel-Lindau disease tumor suppressor gene. Science. 1993;260(5112):1317–20.

    CAS  Article  PubMed  Google Scholar 

  9. 9.

    Nickerson ML, et al. Improved identification of von Hippel-Lindau gene alterations in clear cell renal tumors. Clin Cancer Res. 2008;14(15):4726–34.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  10. 10.

    Fyfe G, et al. Results of treatment of 255 patients with metastatic renal cell carcinoma who received high-dose recombinant interleukin-2 therapy. J Clin Oncol. 1995;13(3):688–96.

    CAS  PubMed  Google Scholar 

  11. 11.

    Koshkin VS, Rini BI. Emerging therapeutics in refractory renal cell carcinoma. Expert Opin Pharmacother. 2016;17(9):1225–32.

    CAS  Article  PubMed  Google Scholar 

  12. 12.

    Negrier S, et al. Long-term follow-up of patients with metastatic renal cell carcinoma treated with intravenous recombinant interleukin-2 in Europe. Cancer J Sci Am. 2000;6 Suppl 1:S93–8.

    PubMed  Google Scholar 

  13. 13.

    NCCN Clinical Practice Guidelines in Oncology. [Webpage] 2016 2016]; Available from: Accessed 9 Jan 2016.

  14. 14.

    Ljungberg B, et al. EAU guidelines on renal cell carcinoma: 2014 update. Eur Urol. 2015;67(5):913–24.

    Article  PubMed  Google Scholar 

  15. 15.

    Motzer RJ, et al. Sunitinib in patients with metastatic renal cell carcinoma. JAMA. 2006;295(21):2516–24.

    CAS  Article  PubMed  Google Scholar 

  16. 16.

    Motzer RJ, et al. Overall survival and updated results for sunitinib compared with interferon alfa in patients with metastatic renal cell carcinoma. J Clin Oncol. 2009;27(22):3584–90.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  17. 17.

    Sternberg CN, et al. Pazopanib in locally advanced or metastatic renal cell carcinoma: results of a randomized phase III trial. J Clin Oncol. 2010;28(6):1061–8.

    CAS  Article  PubMed  Google Scholar 

  18. 18.

    Sternberg CN, et al. A randomised, double-blind phase III study of pazopanib in patients with advanced and/or metastatic renal cell carcinoma: final overall survival results and safety update. Eur J Cancer. 2013;49(6):1287–96.

    CAS  Article  PubMed  Google Scholar 

  19. 19.

    Motzer RJ, et al. Pazopanib versus sunitinib in metastatic renal-cell carcinoma. N Engl J Med. 2013;369(8):722–31.

    CAS  Article  PubMed  Google Scholar 

  20. 20.

    Trump, D. Commentary on: “Randomized, controlled, double-blind, cross-over trial assessing treatment preference for pazopanib versus sunitinib in patients with metastatic renal cell carcinoma: PISCES study.” Escudier B, Porta C, Bono P, Powles T, Eisen T, Sternberg CN, Gschwend JE, De Giorgi U, Parikh O, Hawkins R, Sevin E, Negrier S, Khan S, Diaz J, Redhu S, Mehmud F, Cella D. Bernard Escudier, Institut Gustave Roussy, Villejuif; Emmanuel Sevin, Centre Francois Baclesse, Caen; Sylvie Negrier, Leon Berard Cancer Center, Lyon, France; Camillo Porta, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico S. Matteo, Pavia; Cora N Sternberg, San Camillo Forlanini Hospital, Rome; Ugo De Giorgi, IRCCS Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori, Meldola, Italy; Petri Bono, Helsinki University Central Hospital, Helsinki, Finland; Thomas Powles, Barts Experimental Cancer Medicine Centre, Barts Cancer Institute, Queen Mary University of London, London; Tim Eisen, Cambridge University Health Partners, Cambridge; Omi Parikh, Royal Preston Hospital, Lancashire; Robert Hawkins, Christie Cancer Research UK, Manchester; Sadya Khan, Jose Diaz, and Faisal Mehmud, GlaxoSmithKline, Uxbridge, United Kingdom; Jurgen E Gschwend, Klinikum Rechts der Isar der Technischen Universitat Munchen, Munich, Germany; Suman Redhu, GlaxoSmithKline, Collegeville, PA; David Cella, Northwestern University Feinberg School of Medicine, Chicago, IL.: J Clin Oncol. 2014 May 10;32(14):1412-1418; doi: 10.1200/JCO.2013.50.8267. [Epub 2014 Mar 31]. Urol Oncol. 2016;34(5):251.

  21. 21.

    Gupta S, Spiess PE. The prospects of pazopanib in advanced renal cell carcinoma. Ther Adv Urol. 2013;5(5):223–32.

    Article  PubMed  PubMed Central  Google Scholar 

  22. 22.

    Ahmad T, Eisen T. Kinase inhibition with BAY 43-9006 in renal cell carcinoma. Clin Cancer Res. 2004;10(18 Pt 2):6388S–92S.

    CAS  Article  PubMed  Google Scholar 

  23. 23.

    Escudier B, et al. Sorafenib in advanced clear-cell renal-cell carcinoma. N Engl J Med. 2007;356(2):125–34.

    CAS  Article  PubMed  Google Scholar 

  24. 24.

    Escudier B, et al. Sorafenib for treatment of renal cell carcinoma: final efficacy and safety results of the phase III treatment approaches in renal cancer global evaluation trial. J Clin Oncol. 2009;27(20):3312–8.

    CAS  Article  PubMed  Google Scholar 

  25. 25.

    Escudier B, et al. Randomized phase II trial of first-line treatment with sorafenib versus interferon Alfa-2a in patients with metastatic renal cell carcinoma. J Clin Oncol. 2009;27(8):1280–9.

    CAS  Article  PubMed  Google Scholar 

  26. 26.

    Hutson TE, et al. Axitinib versus sorafenib as first-line therapy in patients with metastatic renal-cell carcinoma: a randomised open-label phase 3 trial. Lancet Oncol. 2013;14(13):1287–94.

    CAS  Article  PubMed  Google Scholar 

  27. 27.

    Choueiri TK. CABOzantinib versus SUNitinib (CABOSUN) as initial targeted therapy for patients with metastatic renal cell carcinoma (mRCC) of poor and intermediate risk groups: results from ALLIANCE A031203 trial, in ESMO 2016 Congress. Copenhagen; 2016.

  28. 28.

    Agostino NM, Gingrich R, Drabick JJ. Bevacizumab demonstrates prolonged disease stabilization in patients with heavily pretreated metastatic renal cell carcinoma: a case series and review of the literature. Adv Urol. 2010.

  29. 29.

    Yang JC, et al. A randomized trial of bevacizumab, an anti-vascular endothelial growth factor antibody, for metastatic renal cancer. N Engl J Med. 2003;349(5):427–34.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  30. 30.

    Escudier B, et al. Bevacizumab plus interferon alfa-2a for treatment of metastatic renal cell carcinoma: a randomised, double-blind phase III trial. Lancet. 2007;370(9605):2103–11.

    Article  PubMed  Google Scholar 

  31. 31.

    Escudier B, et al. Phase III trial of bevacizumab plus interferon alfa-2a in patients with metastatic renal cell carcinoma (AVOREN): final analysis of overall survival. J Clin Oncol. 2010;28(13):2144–50.

    CAS  Article  PubMed  Google Scholar 

  32. 32.

    Rini BI, et al. Phase III trial of bevacizumab plus interferon alfa versus interferon alfa monotherapy in patients with metastatic renal cell carcinoma: final results of CALGB 90206. J Clin Oncol. 2010;28(13):2137–43.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  33. 33.

    Sawyers CL. Will mTOR inhibitors make it as cancer drugs? Cancer Cell. 2003;4(5):343–8.

    CAS  Article  PubMed  Google Scholar 

  34. 34.

    Yuan R, et al. Targeting tumorigenesis: development and use of mTOR inhibitors in cancer therapy. J Hematol Oncol. 2009;2:45.

    Article  PubMed  PubMed Central  Google Scholar 

  35. 35.

    Akinleye A, et al. Phosphatidylinositol 3-kinase (PI3K) inhibitors as cancer therapeutics. J Hematol Oncol. 2013;6(1):88.

    Article  PubMed  PubMed Central  Google Scholar 

  36. 36.

    Albanell J, et al. mTOR signalling in human cancer. Clin Transl Oncol. 2007;9(8):484–93.

    CAS  Article  PubMed  Google Scholar 

  37. 37.

    Brugarolas J. Renal-cell carcinoma—molecular pathways and therapies. N Engl J Med. 2007;356(2):185–7.

    CAS  Article  PubMed  Google Scholar 

  38. 38.

    Choueiri TK, et al. Cabozantinib versus everolimus in advanced renal cell carcinoma (METEOR): final results from a randomised, open-label, phase 3 trial. Lancet Oncol. 2016;17(7):917–27.

    CAS  Article  PubMed  Google Scholar 

  39. 39.

    Voss MH, Molina AM, Motzer RJ. mTOR inhibitors in advanced renal cell carcinoma. Hematol Oncol Clin North Am. 2011;25(4):835–52.

    Article  PubMed  PubMed Central  Google Scholar 

  40. 40.

    Ge N, et al. Impact of O6-methylguanine-DNA methyltransferase expression on the drug resistance of clear cell renal cell carcinoma. Jpn J Clin Oncol. 2015;45(9):860–6.

    Article  PubMed  Google Scholar 

  41. 41.

    Rini BI, et al. Comparative effectiveness of axitinib versus sorafenib in advanced renal cell carcinoma (AXIS): a randomised phase 3 trial. Lancet. 2011;378(9807):1931–9.

    CAS  Article  PubMed  Google Scholar 

  42. 42.

    Buti S, et al. Chemotherapy in metastatic renal cell carcinoma today? A systematic review. Anticancer Drugs. 2013;24(6):535–54.

    CAS  PubMed  Google Scholar 

  43. 43.

    Burris 3rd HA. Overcoming acquired resistance to anticancer therapy: focus on the PI3K/AKT/mTOR pathway. Cancer Chemother Pharmacol. 2013;71(4):829–42.

    CAS  Article  PubMed  Google Scholar 

  44. 44.

    Fischer S, Gillessen S, Rothermundt C. Sequence of treatment in locally advanced and metastatic renal cell carcinoma. Transl Androl Urol. 2015;4(3):310–25.

    PubMed  PubMed Central  Google Scholar 

  45. 45.

    Motzer RJ, et al. Efficacy of everolimus in advanced renal cell carcinoma: a double-blind, randomised, placebo-controlled phase III trial. Lancet. 2008;372(9637):449–56.

    CAS  Article  PubMed  Google Scholar 

  46. 46.

    Motzer RJ, et al. Phase II trial of second-line everolimus in patients with metastatic renal cell carcinoma (RECORD-4). Ann Oncol. 2016;27(3):441–8.

    CAS  Article  PubMed  Google Scholar 

  47. 47.

    Armstrong AJ, et al. Everolimus versus sunitinib for patients with metastatic non-clear cell renal cell carcinoma (ASPEN): a multicentre, open-label, randomised phase 2 trial. Lancet Oncol. 2016;17(3):378–88.

    CAS  Article  PubMed  Google Scholar 

  48. 48.

    Hutson TE, et al. Randomized phase III trial of temsirolimus versus sorafenib as second-line therapy after sunitinib in patients with metastatic renal cell carcinoma. J Clin Oncol. 2014;32(8):760–7.

    CAS  Article  PubMed  Google Scholar 

  49. 49.

    Escudier B, Gore M. Axitinib for the management of metastatic renal cell carcinoma. Drugs R D. 2011;11(2):113–26.

    Article  PubMed  Google Scholar 

  50. 50.

    Motzer RJ, et al. Axitinib versus sorafenib as second-line treatment for advanced renal cell carcinoma: overall survival analysis and updated results from a randomised phase 3 trial. Lancet Oncol. 2013;14(6):552–62.

    CAS  Article  PubMed  Google Scholar 

  51. 51.

    Vitale MG, Carteni G. Recent developments in second and third line therapy of metastatic renal cell carcinoma. Expert Rev Anticancer Ther. 2016;16(5):469–71.

    CAS  Article  PubMed  Google Scholar 

  52. 52.

    Zhou L, et al. Targeting MET and AXL overcomes resistance to sunitinib therapy in renal cell carcinoma. Oncogene. 2016;35(21):2687–97.

    CAS  Article  PubMed  Google Scholar 

  53. 53.

    Rankin EB, et al. Direct regulation of GAS6/AXL signaling by HIF promotes renal metastasis through SRC and MET. Proc Natl Acad Sci U S A. 2014;111(37):13373–8.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  54. 54.

    Choueiri TK, et al. Cabozantinib versus everolimus in advanced renal-cell carcinoma. N Engl J Med. 2015;373(19):1814–23.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  55. 55.

    Escudier B, et al. Axitinib versus sorafenib in advanced renal cell carcinoma: subanalyses by prior therapy from a randomised phase III trial. Br J Cancer. 2014;110(12):2821–8.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  56. 56.

    Matsui J, et al. E7080, a novel inhibitor that targets multiple kinases, has potent antitumor activities against stem cell factor producing human small cell lung cancer H146, based on angiogenesis inhibition. Int J Cancer. 2008;122(3):664–71.

    CAS  Article  PubMed  Google Scholar 

  57. 57.

    Boss DS, et al. A phase I study of E7080, a multitargeted tyrosine kinase inhibitor, in patients with advanced solid tumours. Br J Cancer. 2012;106(10):1598–604.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  58. 58.

    Schlumberger M, et al. A phase II trial of the multitargeted tyrosine kinase inhibitor lenvatinib (E7080) in advanced medullary thyroid cancer. Clin Cancer Res. 2016;22(1):44–53.

    CAS  Article  PubMed  Google Scholar 

  59. 59.

    Sonpavde G, Willey CD, Sudarshan S. Fibroblast growth factor receptors as therapeutic targets in clear-cell renal cell carcinoma. Expert Opin Investig Drugs. 2014;23(3):305–15.

    CAS  Article  PubMed  Google Scholar 

  60. 60.

    Motzer RJ, et al. Lenvatinib, everolimus, and the combination in patients with metastatic renal cell carcinoma: a randomised, phase 2, open-label, multicentre trial. Lancet Oncol. 2015;16(15):1473–82.

    CAS  Article  PubMed  Google Scholar 

  61. 61.

    Fabian MA, et al. A small molecule-kinase interaction map for clinical kinase inhibitors. Nat Biotechnol. 2005;23(3):329–36.

    CAS  Article  PubMed  Google Scholar 

  62. 62.

    Sosman JA, Puzanov I, Atkins MB. Opportunities and obstacles to combination targeted therapy in renal cell cancer. Clin Cancer Res. 2007;13(2 Pt 2):764s–9s.

    CAS  Article  PubMed  Google Scholar 

  63. 63.

    Molina AM, et al. A phase 1b clinical trial of the multi-targeted tyrosine kinase inhibitor lenvatinib (E7080) in combination with everolimus for treatment of metastatic renal cell carcinoma (RCC). Cancer Chemother Pharmacol. 2014;73(1):181–9.

    CAS  Article  PubMed  Google Scholar 

  64. 64.

    Atkins MB, Larkin J. Immunotherapy combined or sequenced with targeted therapy in the treatment of solid tumors: current perspectives. J Natl Cancer Inst. 2016;108(6):djv414.

    PubMed  Google Scholar 

  65. 65.

    Ma W, et al. Current status and perspectives in translational biomarker research for PD-1/PD-L1 immune checkpoint blockade therapy. J Hematol Oncol. 2016;9(1):47.

    Article  PubMed  PubMed Central  Google Scholar 

  66. 66.

    Kadowaki N. Combination of targeted therapy and immunotherapy for cancer. Gan To Kagaku Ryoho. 2015;42(9):1046–9.

    PubMed  Google Scholar 

  67. 67.

    Dong H, et al. Tumor-associated B7-H1 promotes T-cell apoptosis: a potential mechanism of immune evasion. Nat Med. 2002;8(8):793–800.

    CAS  PubMed  Google Scholar 

  68. 68.

    Thompson RH, Dong H, Kwon ED. Implications of B7-H1 expression in clear cell carcinoma of the kidney for prognostication and therapy. Clin Cancer Res. 2007;13(2 Pt 2):709s–15s.

    CAS  Article  PubMed  Google Scholar 

  69. 69.

    Motzer RJ, et al. Nivolumab for metastatic renal cell carcinoma: results of a randomized phase II trial. J Clin Oncol. 2015;33(13):1430–7.

    CAS  Article  PubMed  Google Scholar 

  70. 70.

    Cancer MRC. Summary from ASCO 2015. Can Urol Assoc J. 2015;9(7-8):S158–61.

    Article  Google Scholar 

  71. 71.

    McDermott DF. Long-term overall survival (OS) with nivolumab in previously treated patients with advanced renal cell carcinoma (aRCC) from phase I and II studies. In 2016 ASCO Annual Meeting. 2016.

  72. 72.

    Motzer RJ, et al. Nivolumab versus everolimus in advanced renal-cell carcinoma. N Engl J Med. 2015;373(19):1803–13.

    CAS  Article  PubMed  Google Scholar 

  73. 73.

    Yerushalmi R, Gelmon K. Treatment beyond progression: is it moving from belief to evidence? Oncologist. 2010;15(8):796–8.

    Article  PubMed  PubMed Central  Google Scholar 

  74. 74.

    George S, et al. Safety and efficacy of nivolumab in patients with metastatic renal cell carcinoma treated beyond progression: a subgroup analysis of a randomized clinical trial. JAMA Oncol. 2016;2(9):1179–86.

    Article  PubMed  Google Scholar 

  75. 75.

    Cella D, et al. Quality of life in patients with advanced renal cell carcinoma given nivolumab versus everolimus in CheckMate 025: a randomised, open-label, phase 3 trial. Lancet Oncol. 2016;17(7):994–1003.

    CAS  Article  PubMed  Google Scholar 

  76. 76.

    Chedgy EC, Black PC. Nivolumab: the new second line treatment for advanced renal-cell carcinoma commentary on: nivolumab versus everolimus in advanced renal-cell carcinoma. Urology. 2016;89:8–9.

    Article  PubMed  Google Scholar 

  77. 77.

    Choueiri TK, et al. Immunomodulatory activity of nivolumab in metastatic renal cell carcinoma. Clin Cancer Res, 2016.

  78. 78.

    Das R, et al. Combination therapy with anti-CTLA-4 and anti-PD-1 leads to distinct immunologic changes in vivo. J Immunol. 2015;194(3):950–9.

    CAS  Article  PubMed  Google Scholar 

  79. 79.

    Wiecek W, Karcher H. Nivolumab versus cabozantinib: comparing overall survival in metastatic renal cell carcinoma. PLoS One. 2016;11(6):e0155389.

    Article  PubMed  PubMed Central  Google Scholar 

  80. 80.

    Rexer H. Therapy of untreated local advanced or metastatic renal cell carcinoma. Phase III, randomized, open-label study of nivolumab combined with ipilimumab versus sunitinib monotherapy in subjects with previously untreated, local advanced or metastatic renal cell carcinoma (CheckMate 214 - AN 36/15 of the AUO). Urologe A. 2015;54(10):1443–5.

    CAS  Article  PubMed  Google Scholar 

  81. 81.

    Shuch B, et al. Understanding pathologic variants of renal cell carcinoma: distilling therapeutic opportunities from biologic complexity. Eur Urol. 2015;67(1):85–97.

    Article  PubMed  Google Scholar 

  82. 82.

    Hackshaw MD, et al. Prescribing preferences in the first-line treatment for patients with metastatic renal cell carcinoma in the United States. Clin Genitourin Cancer, 2016.

Download references


Not applicable.


This report required no funding.

Availability of data and materials

Data sharing is not applicable to this article as no datasets were generated or analyzed during the current study.

Authors’ contributions

KZ, CF, and SW contributed to the writing of the manuscript and creating of the table. All authors read and approved the final manuscript.

Competing interests

S. Wu is a speaker for Exelixis, Novartis, and Pfizer. Other authors declare no competing interests.

Consent for publication

Not applicable.

Ethics approval and consent to participate

Not applicable.

Author information



Corresponding author

Correspondence to Shenhong Wu.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Zarrabi, K., Fang, C. & Wu, S. New treatment options for metastatic renal cell carcinoma with prior anti-angiogenesis therapy. J Hematol Oncol 10, 38 (2017).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI:


  • Renal cell carcinoma
  • Anti-angiogenesis
  • Lenvatinib
  • Cabozantinib
  • Nivolumab