A phase II study on the role of gemcitabine plus romidepsin (GEMRO regimen) in the treatment of relapsed/refractory peripheral T-cell lymphoma patients
Journal of Hematology & Oncology volume 9, Article number: 38 (2016)
There is no consensus regarding optimal treatment for peripheral T-cell lymphomas (PTCL), especially in relapsed or refractory cases, which have very poor prognosis and a dismal outcome, with 5-year overall survival of 30 %.
A multicenter prospective phase II trial was conducted to investigate the role of the combination of gemcitabine plus romidepsin (GEMRO regimen) in relapsed/refractory PTCL, looking for a potential synergistic effect of the two drugs. GEMRO regimen contemplates an induction with romidepsin plus gemcitabine for six 28-day cycles followed by maintenance with romidepsin for patients in at least partial remission. The primary endpoint was the overall response rate (ORR); secondary endpoints were survival, duration of response, and safety of the regimen.
The ORR was 30 % (6/20) with 15 % (3) complete response (CR) rate. Two-year overall survival was 50 % and progression-free survival 11.2 %. Grade ≥3 adverse events were represented by thrombocytopenia (60 %), neutropenia (50 %), and anemia (20 %). Two patients are still in CR with median response duration of 18 months. The majority of non-hematological toxicities were mild and transient. No treatment-related death occurred and no toxicity led to treatment interruption.
GEMRO combination regimen shows efficacy data similar to those of single-agent romidepsin with additional hematologic toxicities. Synergy observed in preclinical phase did not turn into ability to improve clinical outcomes.
The trial was registered under EudraCT 2012-001404-38; ClinicalTrials.gov number, NCT01822886.
Peripheral T-cell lymphomas (PTCL) comprise a heterogeneous group of lymphoid malignancies arising from mature T-cells which present with different phenotypes and clinical presentations [1, 2]. These aggressive lymphomas are uncommon, constituting 10–12 % of non-Hodgkin’s lymphomas (NHL) in Western countries  but are relatively common in Eastern Asian, constituting about 20 % of mature NHL . There is no consensus regarding optimal treatment for PTCL, especially in relapsed or refractory cases, which have very poor prognosis. High-dose chemotherapy followed by autologous stem cell transplantation (ASCT) has been accepted as a salvage treatment for eligible patients, although the evidence is unclear . Moreover, the overall prognosis remains dismal in patients unsuitable for ASCT. Thus, effective salvage chemotherapy prior to ASCT or optimal therapeutic approach for patients ineligible for ASCT should be investigated in order to improve the prognosis of PTCL patients. Despite the enormous advances in our understanding of aggressive lymphomas, it is clear that progress in PTCL management has lagged well behind other B-cell malignancies. Over the past 5 years, the US Food and Drug Administration (FDA) has approved four drugs for patients with relapsed/refractory PTCL, and, counting the recent Japanese approval of the anti-CCR4 monoclonal antibody for patients with adult T-cell leukemia/lymphoma, five drugs have been approved worldwide [6–10]. These approvals have led to the initiation of no fewer than four randomized clinical studies, exploring the integration of these new agents into standard CHOP (cyclophosphamide–adriamycin–vincristine–prednisone)-based chemotherapy regimens for patients with newly diagnosed PTCL [11–14]. In addition, new waves of studies are exploring the potential benefits of novel drug combinations, an effort to build on the obvious single-agent successes. What has emerged most recently is the recognition that PTCL may be a disease characterized by epigenetic dysregulation: this could explain PTCL sensitivity to histone deacetylase (HDAC) inhibitors and open the door for even more creative combination approaches.
Gemcitabine (2′,2′-difluorodeoxycytidine) is a pyrimidine anti-metabolite with clinical activity in aggressive lymphomas. The overall response rates (ORR) for gemcitabine as a single agent in relapsed/refractory PTCL are up to 50 % [15, 16], while the single-agent activity is lower in relapsed/refractory aggressive B-cell NHL with a reported ORR of 20 % in small series . Gemcitabine-based combinations with other chemotherapeutic agents afford higher response rates, although even toxicity occurrence is higher (especially myelosuppression and infective complications) .
Romidepsin is an HDAC inhibitor that was approved by FDA in 2011 for the treatment of PTCL in patients who have received at least one prior therapy . A larger, pivotal phase II study on romidepsin in patients with relapsed or refractory PTCL showed an overall response rate of 25 % (complete response [CR] rate of 15 %) without significant differences in response rates between patient subgroups that included major PTCL subtypes . On the basis of these data, there are some trials examining the combination of romidepsin with conventional chemotherapy regimens [11, 19]. Currently, romidepsin is under investigation for patients with PTCL in various combinations, i.e., aurora A kinase inhibitor alisertib , proteasome inhibitors bortezomib , carfilzomib , lenalidomide [23, 24], and pralatrexate .
Starting from these data and due to the still unmet clinical need for patients with relapsed/refractory PTCL, we designed a multicenter phase II study to investigate the role of the combination of gemcitabine plus romidepsin (GEMRO regimen) looking for a potential synergistic effect of the two drugs.
Study population and eligibility criteria
Patients with histologically proven PTCL as per WHO criteria and for whom previous treatments had failed were eligible for this study. Additional inclusion criteria included measurable disease, an absolute neutrophil count >1 × 109/l, hemoglobin >8 g/dl, platelets >100 × 109/l, and normal renal and hepatic functions. All patients had to have an Eastern Cooperative Oncology Group performance status (PS) score of 0–2 at time of enrolment. Patients had not to have received prior gemcitabine or romidepsin therapy.
This was a phase II clinical study on patients with PTCL conducted at 4 Italian centers. The local ethic committee at each centre approved the study protocol and its amendments, in accordance with the Italian law and complying with the Declaration of Helsinki (ethical committee of the coordinating center, Comitato Etico Policlinico S. Orsola-Malpighi Bologna, Italy; reference number 045-2012/U). Patients provided written informed consent before enrolment.
The dose and schedule of this combined regimen were extrapolated by a phase I trial of romidepsin in combination with gemcitabine in patients with pancreatic and other advanced solid tumors . The present phase II study included an induction part with romidepsin 12 mg/m2 i.v. on days 1, 8, and 15 and gemcitabine 800 mg/m2 i.v. on days 1 and 15 for 6 cycles, each cycle to be repeated every 28 days. After this induction phase, patients who obtained at least a partial response (PR) proceeded onto romidepsin maintenance at the dose of 14 mg/m2 i.v. until disease progression.
Clinical evaluations at the time of study entry included medical history and physical examination, complete blood cell count, serum biochemistry, electrocardiogram and echocardiogram, computed tomography (CT) scan of the neck, chest, abdomen, and pelvis, and positron emission tomography (PET) scan of the total body. Bone marrow and lymph node biopsies had not to be if performed before signing the study informed consent as part of standard medical care within 56 days before GEMRO for bone marrow biopsy and within 6 months for lymph node biopsy, respectively.
Patient response was evaluated after 3 cycles of GEMRO and 4 weeks after the end of the induction phase (i.e., after the sixth cycle); in addition, during the maintenance phase with romidepsin, the response evaluation was done every 4 months for the first 2 years. All sites of initial disease were reassessed by CT scan, PET scan, and bone marrow biopsy for patients who had bone marrow involvement. Response assessment was performed according to the Revised Response Criteria for Malignant Lymphoma .
The trial was registered under EudraCT 2012-001404-38; ClinicalTrials.gov number, NCT01822886.
Sample size estimation was performed by Fleming’s single-stage procedure. Defined p0 as the proportion of response below which the treatment does not warrant further investigations and pα as the proportion of responses beyond which a phase 3 trial should be carried out, we set p0 = 0.3 and pα = 0.7. The number of patients required, given a type I error at 0.05 one sided and a power of 80 %, was 18 and the number of successes 13. Taking into account a dropout of 10 %, the number of patients was set at 20.
The primary endpoint of this study was ORR after the induction phase, consisting of the sum of CR and PR rates; the secondary endpoints were duration of the response, progression-free survival (PFS), overall survival (OS), and safety of the GEMRO regimen . Survival curves were estimated using the Kaplan-Meier method. For the safety analyses, frequency of toxicities was reported by type and grade according to the National Cancer Institute Common Terminology Criteria for Adverse Events (version 4.0).
Efficacy and safety were evaluated on the basis of intention-to-treatment. All analyses were performed using STATA (version 11.1).
A total of 20 patients with relapsed/refractory PTCL were enrolled and treated between January 2013 and December 2014. The baseline characteristics of the patients in this study are summarized in Table 1. The median age of patients was 55 years (range 24–77 years), and 10 were males (50 %). All patients had a good PS of 0 or 1. Regarding the histology, 10 (50 %) patients had PTCL not otherwise specified (PTCL-NOS), 9 (45 %) patients had angioimmunoblastic T-cell lymphoma (AITL), and 1 (5 %) patient had anaplastic large cell lymphoma (ALCL) anaplastic lymphoma kinase (ALK) negative. No follicular helper T-cell cases were observed. One patient (5 %) was stage II, and 19 patients (95 %) were stage III or IV. In addition, there were 10 patients (50 %) with extranodal involvement, 6 of whom with bone marrow involvement. The 80 % of subjects had an international prognostic index score ≥2. Patients had received a median of two (range, 1–4) prior treatment regimens and 7 (35 %) of patients had failed prior autologous stem cell transplantation. There were 12 refractory cases (60 %) and 8 relapsed cases (40 %).
Response to treatment and outcomes
Patients started GEMRO therapy at a median time from diagnosis of 13.9 months. The median number of cycles received per patient during induction phase was 3 (range 1–6). Six patients withdrew from treatment before the first scheduled restaging due to objective clinical progression of the underlying disease.
At the end the induction phase, the ORR was 30 % (6/20 patients) and included 3 (15 %) CR and 3 (15 %) PR; among the remaining patients, stable disease was observed in one (5 %) case and 13 (65 %) had progressive disease. According to the histologic subsets, among the 6 responders, there were 4 PTCL-NOS (2 CR and 2 PR) and 2 AILT (1 CR and 1 PR). One (an AITL) of the 3 CR patients discontinued the treatment after 4 cycles due to cardiologic problems not related to the therapeutic regimen, and she is currently in CR after 35 months: Fig. 1 shows the rapid and complete disappearance of the lymphoma assessed by PET scan.
All the responders (CRs and PRs), except for the CR patient who stopped the treatment after 4 cycles, underwent maintenance phase with romidepsin. Current median number of cycles in the maintenance phase is 5, but one patient is still on treatment (12th cycle).
During the maintenance period, two PRs had a disease progression after 4 and 5 months, respectively; the third PR patient, after 2 months of maintenance, underwent allotransplant obtaining CR. At this time, 2/3 CRs are in continuous response after 12 and 35 (AILT patient treated with only 4 cycles) months, respectively. One CR patient relapsed after the sixth cycle of maintenance. Median duration of response was 12.4 months, 18 months for CR patients.
At a median follow-up of 18 months, the 2-year OS rate for all patients was 50 % (median reached at 22 months, Fig. 2), the 2-year PFS rate for all patients was 11.2 % with median reached at 2.5 months (Fig. 3). At the latest follow-up, 10 patients were deceased due to lymphoma and 10 patients were still, 3 of whom without disease.
Treatment-related toxicities are shown in Table 2. The most common grade 3 or 4 toxicity was thrombocytopenia, which was observed in 12 patients (60 %); grade 3 or 4 neutropenia was observed in 10 (50 %) patients while grade 3/4 anemia occurred in 20 % of cases. The majority of non-hematological toxicities were mild and transient. There was no grade 4 non-hematological toxicity observed in the study; however, a grade 3 transaminase increase occurred in 3 patients. No treatment-related death occurred and no toxicity led to treatment interruption.
The generally poor outcomes observed in PTCL patients highlight the urgent need for alternative treatment strategies. Several novel approaches have been evaluated in single-arm phase I and II studies, mainly in patients with relapsed/refractory disease, which has a particularly poor prognosis. In a recent registry study , PTCL patients receiving CHOP or CHOP-like regimens as first-line therapy showed poor outcomes: 25 % of patients had refractory disease with a median OS of 2.5 months and 53 % of responding patients relapsed with a median OS of 6 months. There is, consequently, a requirement for effective second-line treatments for relapsed and refractory PTCL. Over recent years, several single-agent therapies have proven to be effective in this setting. Pralatrexate, romidepsin, and belinostat are all approved broadly for PTCL with ORRs in large phase II studies of 29, 25, and 26 %, respectively [6, 7, 9]. Brentuximab vedotin is also approved in relapsed ALCL with an ORR of 86 % in a small phase II trial . In addition, mogamulizumab (approved only in Japan) reported an ORR of 34 % in a small PTCL phase II study .
Regarding the combination of romidepsin and gemcitabine, there were some interesting preclinical data in solid tumors: romidepsin synergistically inhibits cell proliferation with gemcitabine by suppressing removal of incorporated harmful nucleotide analogues of DNA . Despite minimal clinical activity of this combination in solid tumors , romidepsin plus gemcitabine is being studied in several phase I trials underway in patients with PTCL [30, 31].
In our study, we reported an ORR of 30 % with a CR rate of 15 %. The median duration of response was 12 months (range, 9–35 months with median follow-up of 18 months) and the median PFS was reached at 2.5 months. In responding patients, the achievement of CR was associated with prolonged PFS and OS compared with all other outcomes. The safety profile was overall hematologic, and particularly it was represented by thrombocytopenia and neutropenia.
The ORR and CR rates did not differ from data reported on romidepsin as a single agent . At the same time, there was a similar outcome for responding patients as observed in the pivotal phase II study on romidepsin in monotherapy . Remarkably, the median PFS was analogous to those reported for PTCL after relapse or progression, regardless of the treatment, e.g., romidepsin or belinostat [7, 9, 33]. On the other side, the toxicity profile of GEMRO regimen reported additional hematologic toxicities, as previously stated in the phase I study on solid tumors .
One possible reason for these disappointing results could be that cases with extensive and refractory disease were enrolled: 95 % of patients had stage III–IV disease and 60 % patients were refractory. It could be important to revise the GEMRO regimen on the basis of different schedule (dose and timing) of both drugs.
We identified disappointing clinical results with GEMRO plan in relapsed/refractory PTCL. In fact, these preliminary data failed to show a superiority of the GEMRO combination regimen over single-agent romidepsin as salvage treatment in this setting of patients. These data could indicate that synergy observed in preclinical phase does not always turn into ability to improve clinical outcomes. For the next steps, potential modifications of the treatment schedule are requested to allow more substantial delivery of the treatment and subsequent better clinical response.
angioimmunoblastic T-cell lymphoma
anaplastic large cell lymphoma
anaplastic lymphoma kinase
autologous stem cell transplantation
Food and Drug Administration
overall response rate
positron emission tomography
peripheral T-cell lymphoma
peripheral T-cell lymphoma not otherwise specified
Kim K, Kim WS, Jung CW, Im YH, Kang WK, Lee MH, Park CH, Ko YH, Ree HJ, Park K. Clinical features of peripheral T-cell lymphomas in 78 patients diagnosed according to the Revised European-American lymphoma (REAL) classification. Eur J Cancer. 2002;38(1):75–81.
Lopez-Guillermo A, Cid J, Salar A, Lopez A, Montalban C, Castrillo JM, Gonzalez M, Ribera JM, Brunet S, Garcia-Conde J, Fernandez de Sevilla A, Bosch F, Montserrat E. Peripheral T cell lymphomas: initial features, natural history, and prognostic factors in a series of 174 patients diagnosed according to the R.E.A.L. Classification. Ann Oncol. 1998;9(8):849–55.
Reddy NM, Evens AM. Chemotherapeutic advancements in peripheral T-cell lymphoma. Semin Hematol. 2014;51(1):17–24.
Yoon SO, Suh C, Lee DH, Chi HS, Park CJ, Jang SS, Shin HR, Park BH, Huh J. Distribution of lymphoid neoplasms in the Republic of Korea: analysis of 5318 cases according to the World Health Organization classification. Am J Hematol. 2010;85(10):760–4.
d’Amore F, Relander T, Lauritzsen GF, Jantunen E, Hagberg H, Anderson H, Holte H, Österborg A, Merup M, Brown P, Kuittinen O, Erlanson M, Østenstad B, Fagerli UM, Gadeberg OV, Sundström C, Delabie J, Ralfkiaer E, Vornanen M, Toldbod HE. Up-front autologous stem-cell transplantation in peripheral T-cell lymphoma: NLG-T-01. J Clin Oncol. 2012;30(25):3093–9.
O’Connor OA, Pro B, Pinter-Brown L, Bartlett N, Popplewell L, Coiffier B, Lechowicz MJ, Savage KJ, Shustov AR, Gisselbrecht C, Jacobsen E, Zinzani PL, Furman R, Goy A, Haioun C, Crump M, Zain JM, Hsi E, Boyd A, Horwitz S. Pralatrexate in patients with relapsed or refractory peripheral T-cell lymphoma: results from the pivotal PROPEL study. J Clin Oncol. 2011;29:1182–9.
Coiffier B, Pro B, Prince HM, Foss F, Sokol L, Greenwood M, Caballero D, Borchmann P, Morschhauser F, Wilhelm M, Pinter-Brown L, Padmanabhan S, Shustov A, Nichols J, Carroll S, Balser J, Balser B, Horwitz S. Results from a pivotal, open-label, phase II study of romidepsin in relapsed or refractory peripheral T-cell lymphoma after prior systemic therapy. J Clin Oncol. 2012;30:631–6.
Pro B, Advani R, Brice P, Bartlett NL, Rosenblatt JD, Illidge T, Matous J, Ramchandren R, Fanale M, Connors JM, Yang Y, Sievers EL, Kennedy DA, Shustov A. Brentuximab vedotin (SGN-35) in patients with relapsed or refractory systemic anaplastic large-cell lymphoma: results of a phase II study. J Clin Oncol. 2012;30:2190–6.
O’Connor OA, Horwitz S, Masszi T, Van Hoof A, Brown P, Doorduijn J, Hess G, Jurczak W, Knoblauch P, Chawla S, Bhat G, Choi MR, Walewski J, Savage K, Foss F, Allen LF, Shustov A. Belinostat in patients with relapsed or refractory peripheral T-cell lymphoma: results of the Pivotal Phase II BELIEF (CLN-19) Study. J Clin Oncol. 2015;33(23):2492–9.
Ogura M, Ishida T, Hatake K, Taniwaki M, Ando K, Tobinai K, Fujimoto K, Yamamoto K, Miyamoto T, Uike N, Tanimoto M, Tsukasaki K, Ishizawa K, Suzumiya J, Inagaki H, Tamura K, Akinaga S, Tomonaga M, Ueda R. Multicenter phase II study of mogamulizumab (KW-0761), a defucosylated anti-cc chemokine receptor 4 antibody, in patients with relapsed peripheral T-cell lymphoma and cutaneous T-cell lymphoma. J Clin Oncol. 2014;32(11):1157–63.
Dupuis J, Morschhauser F, Ghesquières H, Tilly H, Casasnovas O, Thieblemont C, Ribrag V, Bossard C, Bras FL, Bachy E, Hivert B, Nicolas-Virelizier E, Jardin F, Bastie JN, Amorim S, Lazarovici J, Martin A, Coiffier B. Combination of romidepsin with cyclophosphamide, doxorubicin, vincristine, and prednisone in previously untreated patients with peripheral T-cell lymphoma: a non-randomised, phase 1b/2 study. Lancet Haematol. 2015;2(4):e160–5.
Buckstein R, Fraser G, Cheung M, Kukreti VJj Kuruvilla J, Imrie K, Piliotis E, Pond G, Windsor J, Ghorab Z, Shuoprasad K, Turner R, Meyer RM, Pritchard K, Walker S, Levine M, Crump M. Alemtuzumab and CHOP chemotherapy for the treatment of aggressive histology peripheral t cell lymphomas: a multi-center phase I study. Clin Lymphoma Myeloma Leuk. 2016;16(1):18–28. e4.
Johnston PB, Cashen AF, Nikolinakos PG, Beaven AW, Barta SK, Bhat G, Song T, Choi MR, Allen LF, de Vos S, Oki Y, Deng C, Foss FM. Safe and effective treatment of patients with peripheral T-cell lymphoma (PTCL) with the novel HDAC inhibitor, belinostat, in combination with CHOP: results of the Bel-CHOP Phase 1 Trial. Blood. 2015;124(supplement):abstract 253.
Advani RH, Ansell SM, Lechowicz MJ, Beaven AW, Loberiza F, Carson KR, Evens AM, Foss F, Horwitz S, Pro B, Pinter-Brown LC, Smith SM, Shustov AR, Savage KJ, M Vose J. A phase II study of cyclophosphamide, etoposide, vincristine and prednisone (CEOP) alternating with pralatrexate (P) as front line therapy for patients with peripheral T-cell lymphoma (PTCL): final results from the T- cell consortium trial. Br J Haematol. 2016;172(4):535–44.
Zinzani PL, Magagnoli M, Bendandi M, Orcioni GF, Gherlinzoni F, Albertini P, Pileri SA, Tura S. Therapy with gemcitabine in pretreated peripheral T-cell lymphoma patients. Ann Oncol. 1998;9(12):1351–3.
Zinzani PL, Venturini F, Stefoni V, Fina M, Pellegrini C, Derenzini E, Gandolfi L, Broccoli A, Argnani L, Quirini F, Pileri S, Baccarani M. Gemcitabine as single agent in pretreated T-cell lymphoma patients: evaluation of the long-term outcome. Ann Oncol. 2010;21(4):860–3.
Savage DG, Rule SA, Tighe M, Garrett TJ, Oster MW, Lee RT, Ruiz J, Heitjan D, Keohan ML, Flamm M, Johnson SA. Gemcitabine for relapsed or resistant lymphoma. Ann Oncol. 2000;11(5):595–7.
Dong M, He XH, Liu P, Qin Y, Yang JL, Zhou SY, Yang S, Zhang CG, Gui L, Zhou LQ, Shi YK. Gemcitabine-based combination regimen in patients with peripheral T-cell lymphoma. Med Oncol. 2013;30(1):351.
Delarue R, Zinzani PL, Hertzberg MS, Kim WS, Caballero D, Pezzutto A, Andre M, Gomes Da Silva M, Gaulard P, Coiffier B. ROCHOP study: a phase III randomized study of CHOP compared to romidepsin-CHOP in untreated peripheral T-cell lymphoma. J Clin Oncol. 2013;31(suppl):TPS8616a.
Fanale MA, Fredrick B, Hagemeister FB, Fayad L, Oki Y, Fowler N, Romaguera J, Shah N, Chuang H, Feng L, Horowitz SB, Wesson E, Hutto TY, Muzzafar T, Samaniego F, Davis RE. A phase I trial of alisertib plus romidepsin for relapsed/refractory aggressive B- and T-cell lymphomas. Blood. 2014;124(supplement):abstract 1744.
Holkova B, Kmieciak M, Bose P, Ma S, Kimball A, Tombes MB, Shrader E, Wan W, Weir-Wiggins C, Stoddert E, Singh AG, Dean A, Conine S, Sankala H, Roberts JD, Shea TC, Grant S. Phase 1 study of bortezomib and romidepsin in patients with chronic lymphocytic leukemia/small lymphocytic lymphoma, indolent B-cell lymphoma, peripheral T-cell lymphoma, or cutaneous T-cell lymphoma: updated results. Blood. 2014;124(supplement):abstract 3050.
https://clinicaltrials.gov/ct2/show/NCT01738594. Accessed 16 February 2016.
Lunning MA, Ruan J, Nair S, Boruchov AM, Byrne R, Gerecitano JF, Hamlin PA, Inserra B, Leonard J, Lynch P, Matasar MJ, Moskowitz AJ, Moskowitz C, Myskowski PL, Nolan P, Palomba ML, Quefeld C, Straus DJ, Zelenetz AD, Horwitz SM. A phase I/II trial of the combination of romidepsin and lenalidomide in patients with relapsed/refractory lymphoma and myeloma: phase 1 results. J Clin Oncol. 2014;32(supplement):abstract 8582.
Mehta-Shah N, Lunning MA, Ruan J, Niar S, Boruchov AM, Moskovitz AJ, Gerecitano JF, Hamlin PA, Leonard JP, Lynch P, Matasar MJ, Moskovitz C, Portlock C, Younes A, Myskowski P, Nolan P, Palomba ML, Vredenburgh J, Querfeld C, Strauss DJ, Zelenetz A, Schroder H, Rademaker J, Schaffer W, Horwitz SM. A phase I/II trial of the combination of romidepsin and lenalidomide in patients with relapsed/refractory lymphoma and myeloma. Hematol Oncol. 2015;33(supplement):abstract 016.
https://clinicaltrials.gov/ct2/show/NCT01947140 Accessed 16 February 2016.
Jones SF, Infante JR, Spigel DR, Peacock NW, Thompson DS, Greco FA, McCulloch W, Burris HA 3rd. Phase 1 results from a study of romidepsin in combination with gemcitabine in patients with advanced solid tumors. Cancer Invest. 2012;30(6):481–6.
Cheson BD, Pfistner B, Juweid ME, Gascoyne RD, Specht L, Horning SJ, Coiffier B, Fisher RI, Hagenbeek A, Zucca E, Rosen ST, Stroobants S, Lister TA, Hoppe RT, Dreyling M, Tobinai K, Vose JM, Connors JM, Federico M, Diehl V. International Harmonization Project on Lymphoma. Revised response criteria for malignant lymphoma. J Clin Oncol. 2007;25(5):579–86.
Ellin F, Landström J, Jerkeman M, Relander T. Real-world data on prognostic factors and treatment in peripheral T-cell lymphomas: a study from the Swedish Lymphoma Registry. Blood. 2014;124(10):1570–7.
Chai G, Li L, Zhou W, Wu L, Zhao Y, Wang D, Lu S, Yu Y, Wang H, McNutt MA, Hu YG, Chen Y, Yang Y, Wu X, Otterson GA, Zhu WG. HDAC inhibitors act with 5-aza-2'-deoxycytidine to inhibit cell proliferation by suppressing removal of incorporated abases in lung cancer cells. PLoS One. 2008;3(6):e2445.
https://clinicaltrials.gov/ct2/show/NCT02181218 Accessed 16 February 2016.
https://clinicaltrials.gov/ct2/show/NCT01846390 Accessed 16 February 2016.
Coiffier B, Pro B, Prince HM, Foss F, Sokol L, Greenwood M, Caballero D, Morschhauser F, Wilhelm M, Pinter-Brown L, Padmanabhan Iyer S, Shustov A, Nielsen T, Nichols J, Wolfson J, Balser B, Horwitz S. Romidepsin for the treatment of relapsed/refractory peripheral T-cell lymphoma: pivotal study update demonstrates durable responses. J Hematol Oncol. 2014;7:11.
Mak V, Hamm J, Chhanabhai M, Shenkier T, Klasa R, Sehn LH, Villa D, Gascoyne RD, Connors JM, Savage KJ. Survival of patients with peripheral T-cell lymphoma after first relapse or progression: spectrum of disease and rare long-term survivors. J Clin Oncol. 2013;31(16):1970–6.
Italian Lymphoma Foundation (Fondazione Italiana Linfomi Onlus, FIL) supported the study.
The authors declare that they have no competing interests.
CP, AD, AC, FM, DD, FS, UV, PC, and PLZ performed the research; CP and PLZ designed the research study; LA and PLZ analyzed the data; CP, AD, AC, FM, DD, FS, UV, LA, PC, and PLZ interpreted the data; CP, LA, and PLZ wrote the paper; CP, AD, AC, FM, DD, FS, UV, LA, PC, and PLZ revised and approved the final manuscript. All authors read and approved the final manuscript.
About this article
Cite this article
Pellegrini, C., Dodero, A., Chiappella, A. et al. A phase II study on the role of gemcitabine plus romidepsin (GEMRO regimen) in the treatment of relapsed/refractory peripheral T-cell lymphoma patients. J Hematol Oncol 9, 38 (2016). https://doi.org/10.1186/s13045-016-0266-1