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A tertiary center experience of multiple myeloma patients with COVID-19: lessons learned and the path forward

Abstract

Background

The COVID-19 pandemic, caused by SARS-CoV-2 virus, has resulted in over 100,000 deaths in the USA. Our institution has treated over 2000 COVID-19 patients during the pandemic in New York City. The pandemic directly impacted cancer patients and the organization of cancer care. Mount Sinai Hospital has a large and diverse multiple myeloma (MM) population. Herein, we report the characteristics of COVID-19 infection and serological response in MM patients in a large tertiary care institution in New York.

Methods

We performed a retrospective study on a cohort of 58 patients with a plasma-cell disorder (54 MM, 4 smoldering MM) who developed COVID-19 between March 1, 2020, and April 30, 2020. We report epidemiological, clinical, and laboratory characteristics including the persistence of viral detection by polymerase chain reaction (PCR) and anti-SARS-CoV-2 antibody testing, treatments initiated, and outcomes.

Results

Of the 58 patients diagnosed with COVID-19, 36 were hospitalized and 22 were managed at home. The median age was 67 years; 52% of patients were male and 63% were non-White. Hypertension (64%), hyperlipidemia (62%), obesity (37%), diabetes mellitus (28%), chronic kidney disease (24%), and lung disease (21%) were the most common comorbidities. In the total cohort, 14 patients (24%) died. Older age (> 70 years), male sex, cardiovascular risk, and patients not in complete remission (CR) or stringent CR were significantly (p < 0.05) associated with hospitalization. Among hospitalized patients, laboratory findings demonstrated elevation of traditional inflammatory markers (CRP, ferritin, D-dimer) and a significant (p < 0.05) association between elevated inflammatory markers, severe hypogammaglobulinemia, non-White race, and mortality. Ninety-six percent (22/23) of patients developed antibodies to SARS-CoV-2 at a median of 32 days after initial diagnosis. The median time to PCR negativity was 43 (range 19–68) days from initial positive PCR.

Conclusions

Drug exposure and MM disease status at the time of contracting COVID-19 had no bearing on mortality. Mounting a severe inflammatory response to SARS-CoV-2 and severe hypogammaglobulinemia was associated with higher mortality. The majority of patients mounted an antibody response to SARS-CoV-2. These findings pave a path to the identification of vulnerable MM patients who need early intervention to improve outcomes in future outbreaks of COVID-19.

Introduction

The coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), represents a world-wide public health crisis. Patient care has been drastically altered, primarily in epidemic, urban areas. As of May 22, 2020, New York City had nearly 200,000 confirmed cases of COVID-19 with over 16,000 deaths and a patient death rate of 21% [1], with cancer patients comprising about 8% of all COVID-19 fatalities in the state of New York (https://covid19tracker.health.ny.gov/). Mount Sinai Hospital, a tertiary care center in New York City, has treated over 2000 admitted COVID-19 patients thus far. At our cancer center, we actively care for a large and particularly diverse population of over 3000 multiple myeloma (MM) patients. Like many other centers in the region and the world, clinical care at our institution has seen significant changes in an attempt to mitigate the spread of SARS-CoV-2 to vulnerable cancer patients receiving treatment. Balancing the competing risks of treatment delay or alteration versus infection is essential and depends upon understanding the clinical profile of COVID-19 in this vulnerable population.

Limited studies describing the impact of COVID-19 both in the USA [2] and abroad [3,4,5,6] suggest a higher risk of hospitalization and poor outcomes including death in certain subsets of cancer patients. The effect of COVID-19 on patients with MM, the second most common hematological malignancy, is of particularly great concern due to immunosuppression associated with the disease, and at this time remains incompletely understood. MM is a plasma cell malignancy, diagnosed at a median age around 70 years in patients often with multiple comorbidities [7]. MM is associated with both cellular and humoral immune dysfunction and causes a state of generalized immune suppression, leaving patients especially vulnerable to infections [8, 9].

In contrast to the reported immunosuppressive nature of MM, COVID-19 infection has demonstrated a propensity for triggering an uncontrolled immune inflammatory cascade [10,11,12] that bears resemblance to cytokine release syndrome (CRS) seen in patients treated with chimeric antigen receptor (CAR)-T cells and bispecific antibodies [13, 14]. Inflammatory markers and cytokines, including C-reactive protein (CRP), ferritin, and interleukin (IL)-6, have been significantly elevated in multiple cohorts of patients infected with COVID-19 [15,16,17,18].

We aimed to characterize the population of MM patients at our institution who developed COVID-19 in the epicenter of the pandemic in the USA. To address this, we retrospectively analyzed a cohort of 58 MM and smoldering MM (SMM) patients treated at the Mount Sinai Hospital who were diagnosed with COVID-19 between March 1 and April 30, 2020. We have identified several demographic characteristics and comorbidities associated with hospitalization and elevation of certain inflammatory markers associated with increased mortality as described below.

Methods

Study design, inclusion criteria, and data collection

The study was designed from a register of patients with SMM and MM in any phase of the response, currently receiving treatment or follow-up at the Mount Sinai Hospital. All patients with a confirmed or presumptive diagnosis of COVID-19 between March 1, 2020, and April 30, 2020, were considered potentially relevant. Infection with SARS-CoV-2 was confirmed by Roche Cobas 6800 polymerase chain reaction (PCR) in patients that were treated at the Mount Sinai Hospital. For patients admitted to other hospital systems, inclusion was based on external reporting and follow-up testing confirmation. Similarly, outpatients that reported a positive COVID-19 test to our clinic (e.g., over the phone) were included in the analysis, awaiting collection of their formal test results. Anti-SARS-CoV-2 antibody testing was performed using an anti-IgG assay developed at Mount Sinai Health System Department of Pathology in collaboration with the Icahn School of Medicine at Mount Sinai Department of Microbiology under a Food and Drug Administration (FDA) Emergency Use Authorization. We reviewed clinical charts, nursing records, laboratory findings, and radiological images for patients and obtained demographic data from the electronic medical records. Plasma levels of selected inflammatory cytokines, including IL-1β, IL-6, IL-8, and tumor necrosis factor-α (TNF-α), were assessed using the ELLA rapid detection enzyme-linked immunosorbent assay (ELISA) microfluidic platform and made available through the Mount Sinai data warehouse for hospitalized patients. Treatment response criteria were used as defined by the International Myeloma Working Group (IMWG) [19, 20]. This retrospective study was approved by the institutional review board (IRB) of the Mount Sinai Hospital and is in compliance with the Declaration of Helsinki and International Conference on Harmonization Guidelines for Good Clinical Practice (IRB: GCO#: 11-1433).

Statistical analysis

Continuous variables are presented as a median and interquartile range (IQR). Categorical variables are shown as a percentage and an absolute number of patients. Wherever two outcome groups are compared, Fisher’s exact test was used to determine significance and odds ratios (ORs) were reported for categorical variables and Mann-Whitney U test was used to determine significance for continuous variables. A two-sided alpha < 0.05 was considered statistically significant. All statistical analyses were done using R (version 3.6.1).

Results

Baseline characteristics

Our cohort of 58 patients encompassed 52% males and had a median age of 67 years (IQR: 12.5 years), with 17% of patients older than 75 years (Table 1). The median body mass index (BMI) was 27.6 kg/m2 (with 37% of patients with a BMI > 30 kg/m2). The majority of patients reported being non-White (63%), with 13 (23%) patients of African American and 9 (16%) of Hispanic origin.

Table 1 Demographics and baseline characteristics of patients

The most common comorbidities were hypertension (64%), hyperlipidemia (62%), previous or active smoking (37%), diabetes mellitus type 2 (28%), chronic kidney disease (CKD, estimated glomerular filtration rate (eGFR) < 60 mL/min) (24%), and lung disease (21%), including asthma or chronic obstructive lung disease (COPD). Thirty-two (55%) patients had a high-risk cardiovascular profile (defined as having ≥ 2 of the conditions: hypertension, hyperlipidemia, and diabetes) and 13 (22%) had coronary artery disease (CAD) and/or cerebrovascular disease. Seven (12%) patients had congestive heart failure. Twelve (21%) patients were on therapeutic anticoagulation and 34 (59%) were on aspirin, while 26 (45%) patients were on an angiotensin-converting enzyme (ACE) inhibitor or angiotensin II receptor blocker (ARB).

Myeloma characteristics

The cohort included 54 MM and 4 SMM patients (Table 2). The median time from diagnosis to COVID-19 infection was 29.8 months (IQR: 44.2 months). MM patients had a median of 1.5 (IQR: 2) lines of therapy, and 9 (17%) patients had more than 4 previous lines of treatment. Twenty-two (41%) patients had a prior autologous stem cell transplant (ASCT). The median age of patients with and without prior ASCT was 63.5 and 70 years, respectively. Of all patients, 27 (47%) had an Eastern Cooperative Oncology Group (ECOG) performance status of 0 at the time of COVID-19 infection. The most common myeloma subtype was IgG (59%) followed by IgA (19%), with light chain involvement in 33% of cases. High-risk cytogenetics were present in 22 (39%) patients, with 18 (33%) patients having an international staging system (ISS) of 1, while 14 (26%) and 10 (19%) patients had ISS 2 and 3, respectively, at time of MM diagnosis. At the time of SARS-CoV-2 infection, 3 SMM and 8 MM patients were not on therapy. Among the remaining patients, 28 (48%) patients were being treated with daratumumab, 32 (55%) patients were on immunomodulatory drugs (IMiDs), 22 (38%) were on a proteasome inhibitor (PI), 5 (9%) were on venetoclax, and 30 (52%) patients were on concomitant corticosteroids.

Table 2 Myeloma disease characteristics of patients

The disease status at the time of SARS-CoV-2 infection included 15 (26%) patients in complete response (CR) or stringent CR (sCR), 11 (19%), 13 (22%), and 2 (3%) patients who had a very good partial response (VGPR), partial response (PR), and stable disease (SD), respectively, and 9 (16%) who had progressive disease (PD). Response status was not evaluable for 8 (14%) of patients (including 4 SMM patients and 1 newly diagnosed patient).

Biochemical parameters at the last routine clinic visit before presentation with COVID-19 were collected to determine if these steady-state parameters would provide insight into which patients are particularly vulnerable (Table 2). Twenty (35%) patients had leukopenia (< 4 × 109/L) and 7 (12%) lymphocytopenia (grade 3, < 0.5 × 109/L) at their last clinic visit. The monoclonal spike (M-spike) was undetectable in 31 (54%) patients. Median serum IgG level of all patients was 805 mg/dL (IQR: 736 mg/dL) and 37% (21/57) of patients had hypogammaglobulinemia (< 700 mg/dL), while 11% (6/57) of patients had severe (< 400 mg/dL) hypogammaglobulinemia. Immunoparesis, defined as a reduction in one or more of the uninvolved immunoglobulins below the lower limit of normal [21], was present in 89% (51/57) of patients.

Clinical course and biochemical parameters

The most common reported symptoms among all patients were fever (70%), cough (65%), and dyspnea (45%). Thirty-six patients were admitted at a hospital for inpatient care, 23 of which were admitted at our healthcare system and had both clinical and biochemical parameters available, as shown in Table 3. The median time between self-reported symptom onset and admission was 3 days. Among the 23 patients, 16 (70%) were febrile, and 11 (48%) were tachycardic with a heart rate > 100 beats per minute (bpm) at the time of presentation. Ten (43%) patients required immediate oxygen support: 7 needed a nasal cannula or non-rebreather mask, 1 needed high flow oxygen, and 2 were immediately intubated and required mechanical ventilation.

Table 3 Clinical parameters, treatments, and outcomes of patients hospitalized due to COVID-19 at Mount Sinai Hospital

During their hospital stay, 22 (95%) patients developed fever, 18 (78%) tachycardia (> 100 bpm), and 18 (78%) hypoxemia (SpO2 < 93%). Five (22%) patients never required supplemental oxygen, and 10 (40%) needed a nasal cannula or non-rebreather mask at some point during hospitalization. Four (17%) patients were treated with high-flow oxygen, continuous positive airway pressure (CPAP) or bi-level positive airway pressure (BiPAP) machines and five (22%) were eventually intubated. Seven (30%) patients required intensive care unit (ICU) care during their hospitalization. The median length of stay was 22 days. Of the 23 patients admitted to our hospital with COVID-19, seven (30%) died. When we consider the total hospitalized cohort (36 patients, i.e., including patients admitted at other hospitals), the mortality rate was 39% (14 patients). All 14 deaths were due to COVID-19. There were no deaths reported in patients who were not hospitalized among the total cohort.

Patients presented with multiple elevated inflammatory markers, including CRP (median: 89 mg/L), ferritin (median: 595 μg/L), IL-6 (median: 82.4 pg/mL), whereas procalcitonin was normal (median: 0.2 ng/mL). Leukocytes were not elevated (median: 4.3 × 109/L) and the absolute lymphocyte count was low (median 0.6 × 109/L) whereas absolute neutrophil count was within the normal range (median 3.6 × 109/L). On initial presentation, lactate dehydrogenase (LDH, median 249.5 U/L), fibrinogen (median 600 mg/dL), and D-dimer (median 1.2 mg/L) were elevated but transaminases were normal (median aspartate aminotransferase (AST) and alanine aminotransferase (ALT): 24 U/L and 20 U/L, respectively). Peak levels for these markers are shown in Table 3 and temporal trends for a subset of patients are illustrated in Supplementary Figure S1. CRP and ferritin peaked early (within the first 10 days of hospitalization) and subsequently demonstrated a downward trend over time, with a slower decline in ferritin levels notable in patients that eventually died. D-dimer level was transiently elevated in some patients but was persistently and progressively elevated in all patients that eventually died. The inflammatory cytokines IL-1β, IL-6, IL-8, and TNF-α were assessed over the duration of hospitalization at the discretion of the treating physician. Peak levels for IL-6, IL-8, and TNF-α were elevated (median: 128.5 pg/mL, 65.4 pg/mL, and 28.7 pg/mL, respectively), and levels for IL-1β were generally low (median: 0.5 pg/mL).

We describe COVID-19 management comprehensively for the 23 patients hospitalized at our center and their outcome (Table 3). One (4%) patient received remdesivir, 17 (74%) patients received hydroxychloroquine, and 17 (74%) patients received azithromycin. Nineteen (82%) patients were treated with other antibiotics, most commonly a beta-lactam antibiotic ± vancomycin (n = 16) for presumed bacterial superinfection. Six (26%) patients received granulocyte colony-stimulating factor (G-CSF) and 18 (78%) patients received therapeutic anticoagulation, 13 of which had not been on full anticoagulation before COVID-19. Patients were treated with a direct oral anticoagulant (DOAC, n = 3), therapeutic doses of enoxaparin (n = 8), or a heparin drip (n = 2). There were no major bleeding events. Ten (43%) patients were given systemic corticosteroids. One (4%) patient was treated with convalescent plasma. Anti-TNFα, anti-IL-6, and anti-IL-1 therapy were initiated in 1 (4%), 4 (17%), and 2 (9%) patients, respectively. Five patients (22%) were given low-dose selinexor, a selective inhibitor of nuclear export, for its presumed activity against virus host protein interaction [22] and to counter amplification of pro-inflammatory signaling [23].

Antibody serology and repeat PCR testing

We collected data on antibody testing and follow-up PCR testing for patients. As of May 28, 2020, 96% (22/23) of patients have developed antibodies against SARS-CoV-2 at a median time of 32 (range 6–50) days since COVID-19 diagnosis. Titers ranged from 1:160 to 1:2880, with 74% (17/23) exhibiting the most significant titer level of 1:2880, 9% (2/23) with 1:960, 9% (2/23) with 1:320, and 4% (1/23) with 1:160. Antibody titer did not correlate with COVID-19 severity, yet we observed that all 5 MM patients with low titers (< 1:2880) had hypogammaglobulinemia. The one patient who did not develop any antibodies had SMM and was tested 27 days after initial diagnosis. So far, 27 patients have undergone repeat PCR testing; 74% (20/27) are negative and the median time to PCR negativity was 43 (range 19–68) days from initial positive PCR. Among the 22 patients with positive antibody titers, 19 patients had repeat PCR swab and 3 remained positive while 16 were negative.

Clinical associations

In a univariate analysis on all patients, we found that the following variables were significantly associated with hospitalization, as shown in Table 4: age over 70 (OR 7.74, p = 0.007), male sex (OR 3.70, p = 0.030), diabetes mellitus type 2 (OR 6.18, p = 0.016), high cardiovascular risk profile (OR 3.42, p = 0.032), history of CAD (OR ∞, p = 0.009), history of CHF (OR ∞, p = 0.037), use of statins (OR = 12.10, p < 0.001) and use of beta-blockers (OR 9.63, p = 0.002). We also noted significant associations between hospitalization status and grade 3 lymphocytopenia (OR ∞, p = 0.036) at the last clinic visit prior to COVID-19 infection. Patients who had not achieved a CR or sCR were at increased risk of hospitalization (p = 0.013).

Table 4 Univariate associations of selected variables with risk of hospitalization and mortality

Similarly, for hospitalized patients, using a univariate approach, we found a statistically significant association between mortality and these variables: non-White race (OR 10.49, p = 0.011), statin use (OR 6.21, p = 0. 012), severe hypogammaglobulinemia (OR 7.80, p = 0.027), and higher peak levels of D-dimer (p = 0.004), ferritin (p = 0.007), procalcitonin (p = 0.010), and CRP (p = 0.019). The full list of associations is shown in Table 4.

Discussion

Situated in the heart of New York City, our cancer center at Mount Sinai Hospital bore witness to the immense disruption of healthcare services caused by COVID-19. During the initial phase of the pandemic, the goal was to keep patients at home following federal and state guidelines of isolation, social distancing, and strict hand hygiene [24,25,26]. Patients were switched to all oral regimens if possible or had delayed therapy depending on the perceived risk of need for therapy to control myeloma versus exposure to SARS-CoV-2. Yet community transmission of SARS-CoV-2 during the pandemic was inevitable.

There were no deaths among myeloma patients with milder symptoms who were managed entirely as outpatients with COVID-19 in this cohort. The mortality rates of the overall cohort (n = 58), MM patients admitted to Mount Sinai Hospital (n = 23), and all admitted MM patients (n = 36) were 24%, 30%, and 39%, respectively. These figures are in line with the overall mortality seen in New York, where the estimated mortality among hospitalized patients over 45 years old is 37% as of May 25, 2020 [1, 27]. Interestingly, the mortality among our cohort of MM patients was lower than the 54.6% seen in a cohort of 75 MM patients treated in Britain [28]. We acknowledge that the apparent mortality differences between different countries and health systems may be affected by the local epidemiology, hospitalization, and resource utilization rates and potential differences in the escalation of care. However, in both of these populations, there appeared to be a trend toward increased mortality in patients of non-White/Caucasian background. This has been consistently seen in the USA, where death rates for COVID-19 are several fold higher in patients of Black and Hispanic origins [29,30,31].

MM specific disease characteristics and the type of MM treatment were not associated with increased mortality. In contrast, we observed that age and cardiovascular risk factors (diabetes, CAD, CHF) were significantly associated with patient hospitalization for COVID-19. The data from our cohort showed that non-White background, severe (< 400 mg/dL) hypogammaglobulinemia, and statin use were significantly associated with mortality. This information would indicate that during the post pandemic phase, we do not have to change the management of myeloma patients. However, earlier diagnosis of COVID-19 and prompt intervention especially for the vulnerable population identified above is warranted to reduce the risk of mortality. As we reopen and move forward into a post-COVID-19 era, we will need to remain vigilant, particularly for select patient groups, and await effective COVID-19 treatments while balancing the need to manage patients’ myeloma.

We were able to capture the evolution of inflammatory markers for patients who were admitted to the inpatient service, and we found a significant association with mortality in patients who had elevated D-dimer, CRP, or ferritin. Many COVID-19 patients treated at our institution also received a rapid panel for cytokine testing as part of a larger study to characterize the inflammatory profile of COVID-19 illness. Among our cohort of hospitalized patients, those who died appeared to exhibit rather elevated pro-inflammatory cytokines, consistent in principle with what was seen in a large COVID-19 cohort analyzed at the Mount Sinai Health System [32]. It is possible that a CRS-like syndrome, similar though not identical to one seen in MM patients treated with CAR-T cells [13, 33] and bispecific antibodies [34, 35], occurs in a significant portion of MM patients afflicted with COVID-19. Various agents including but not limited to anti-IL-6 [36] monoclonal antibodies and JAK inhibitors [37] are presently under investigation to address potential components of immune dysregulation in COVID-19. We noted that patients who died from COVID-19 had alarmingly elevated D-dimer levels compared to survivors (median of 18.24 mg/L vs 1.96 mg/L). Emerging research suggests that the overwhelming immune activation during SARS-CoV-2 infection is a potent catalyst for significant arterial and venous thromboembolism leading to strokes and pulmonary emboli [15, 38], and serum pro-inflammatory cytokines including IL-1β, TNF-α, and IL-6 have been tied to endothelial damage underlying thrombus formation seen in COVID-19 [39]. To counter this possibility, a large majority of patients admitted to our institution in this cohort received therapeutic anticoagulation and none suffered bleeding events. Our data regarding inflammatory markers raises the question if the process driving severe D-dimer elevation in MM patients with COVID-19 is the same or is separate from the CRS-like process seen in many COVID-19 patients.

Data on the persistence of SARS-CoV-2 by PCR and development of specific antibody response to the virus in potentially immunocompromised cancer patients have thus far been lacking. A significant majority of tested patients among this cohort cleared infection by PCR and developed antibodies despite a very high proportion of patients who fit the definition of classical myeloma-associated immunoparesis. Immunoparesis alone was not significantly associated with hospitalization or mortality and importantly did not appear to affect the development of anti-SARS-CoV-2 antibodies. Looking forward, we will need to determine if the development of antibodies confers protection against reinfection.

This study has the limitations of single institution, retrospective reporting of a smaller cohort of patients. Serological data were not available for a minority of the patients who were hospitalized at outside institutions. The observations reported here have to be confirmed by a larger series of data collected from multiple institutions and such efforts are underway. Few patients received COVID-19-directed treatment on clinical trials. The role of recently emergency approved anti-viral agent remdesivir, or convalescent plasma should be explored in the high-risk population with myeloma.

Conclusions

In this study of patients treated for myeloma at the Mount Sinai Hospital, we provide a detailed analysis of a cohort of 58 MM and SMM patients who developed COVID-19. Although several demographic factors and comorbidities increased the risk of hospitalization and mortality, myeloma therapy and immunoparesis did not influence outcomes. In fact, survival was comparable to the overall population of New York during the pandemic, and patients generally mounted a significant antibody response to SARS-CoV-2. The data herein supports the need to maintain proactive management of MM patients by balancing their need for therapy with the increased risk of hospitalization and death in a subset of MM patients with COVID-19.

Availability of data and materials

The datasets analyzed during the current study are not publicly available due to the US Federal Health Insurance Portability and Accountability Act (HIPAA) compliance, but a de-identified dataset may be available from the corresponding author on reasonable request.

Abbreviations

ACE:

Angiotensin-converting enzyme

ALT:

Alanine aminotransferase

ARB:

Angiotensin II receptor blocker

ASCT:

Autologous stem cell transplant

AST:

Aspartate aminotransferase

BiPAP:

Bi-level positive airway pressure

BMI:

Body mass index

bpm:

Beats per minute

CAD:

Coronary artery disease

CAR:

Chimeric antigen receptor

CHF:

Congestive heart failure

CKD:

Chronic kidney disease

COPD:

Chronic obstructive lung disease

COVID-19:

Coronavirus disease 2019

CPAP:

Continuous positive airway pressure

CR:

Complete response

CRS:

Cytokine release syndrome

CRP:

C-reactive protein

DOAC:

Direct oral anticoagulant

ECOG:

Eastern Cooperative Oncology Group

eGFR:

Estimated glomerular filtration rate

ELISA:

Enzyme-linked immunosorbent assay

G-CSF:

Granulocyte colony-stimulating factor

HIPAA:

Health Insurance Portability and Accountability Act

IMWG:

International Myeloma Working Group

ICU:

Intensive care unit

IL:

Interleukin

IMiD:

Immunomodulatory drug

IRB:

Institutional review board

IQR:

Interquartile range

ISS:

International staging system

LDH:

Lactate dehydrogenase

MM:

Multiple myeloma

OR:

Odd’s ratio

PCR:

Polymerase chain reaction

PD:

Progressive disease

PI:

Proteasome inhibitor

PR:

Partial response

SARS-CoV-2:

Severe acute respiratory syndrome coronavirus 2

sCR:

Stringent complete response

SD:

Stable disease

SMM:

Smoldering multiple myeloma

TNF-α:

Tumor necrosis factor-α

VGPR:

Very good partial response

References

  1. 1.

    Richardson S, Hirsch JS, Narasimhan M, et al. Presenting characteristics, comorbidities, and outcomes among 5700 patients hospitalized with COVID-19 in the New York City area. JAMA. 2020.

  2. 2.

    Robilotti EV, Babady NE, Mead PA, et al. Determinants of severity in cancer patients with COVID-19 illness. medRxiv. 2020; 2020.05.04.20086322.

  3. 3.

    Dai M, Liu D, Liu M, et al. Patients with cancer appear more vulnerable to SARS-COV-2: a multicenter study during the COVID-19 outbreak. Cancer Discov. 2020.

  4. 4.

    Liang W, Guan W, Chen R, et al. Cancer patients in SARS-CoV-2 infection: a nationwide analysis in China. Lancet Oncol. 2020;21:335–7.

    CAS  Article  Google Scholar 

  5. 5.

    Yu J, Ouyang W, Chua MLK, Xie C. SARS-CoV-2 transmission in patients with cancer at a tertiary care hospital in Wuhan, China. JAMA Oncol. 2020.

  6. 6.

    Zhang L, Zhu F, Xie L, et al. Clinical characteristics of COVID-19-infected cancer patients: a retrospective case study in three hospitals within Wuhan, China. Ann Oncol. 2020.

  7. 7.

    Kyle RA, Rajkumar SV. Multiple myeloma. Blood. 2008;111:2962–72.

    CAS  Article  Google Scholar 

  8. 8.

    Lee SJ, Borrello I. Role of the immune response in disease progression and therapy in multiple myeloma. Cancer Treat Res. 2016;169:207–25.

    CAS  Article  Google Scholar 

  9. 9.

    Kumar SK, Anderson KC. Immune therapies in multiple myeloma. Clin Cancer Res. 2016;22:5453–60.

    CAS  Article  Google Scholar 

  10. 10.

    Ingraham NE, Lotfi-Emran S, Thielen BK, et al. Immunomodulation in COVID-19. Lancet Respir Med.

  11. 11.

    Mehta P, McAuley DF, Brown M, et al. COVID-19: consider cytokine storm syndromes and immunosuppression. Lancet. 2020.

  12. 12.

    Merad M, Martin JC. Pathological inflammation in patients with COVID-19: a key role for monocytes and macrophages. Nat Rev Immunol. 2020.

  13. 13.

    Liu D, Zhao J. Cytokine release syndrome: grading, modeling, and new therapy. J Hematol Oncol. 2018;11:121.

    Article  Google Scholar 

  14. 14.

    Lee DW, Santomasso BD, Locke FL, et al. ASTCT Consensus grading for cytokine release syndrome and neurologic toxicity associated with immune effector cells. Biol Blood Marrow Transplant. 2019;25:625–38.

    CAS  Article  Google Scholar 

  15. 15.

    Zhang C, Wu Z, Li J-W, Zhao H, Wang G-Q. The cytokine release syndrome (CRS) of severe COVID-19 and interleukin-6 receptor (IL-6R) antagonist Tocilizumab may be the key to reduce the mortality. Int J Antimicrob Agents. 2020;105954.

  16. 16.

    Mehta P, McAuley DF, Brown M, Sanchez E, Tattersall RS, Manson JJ. COVID-19: consider cytokine storm syndromes and immunosuppression. Lancet (London, England). 2020;395:1033–4.

    CAS  Article  Google Scholar 

  17. 17.

    Huang C, Wang Y, Li X, et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet (London, England). 2020;395:497–506.

    CAS  Article  Google Scholar 

  18. 18.

    Gong J, Dong H, Xia SQ, et al. Correlation analysis between disease severity and inflammation-related parameters in patients with COVID-19 pneumonia. medRxiv. 2020; 2020.02.25.20025643.

  19. 19.

    Rajkumar SV, Dimopoulos MA, Palumbo A, et al. International Myeloma Working Group updated criteria for the diagnosis of multiple myeloma. Lancet Oncol. 2014;15:e538–48.

    Article  Google Scholar 

  20. 20.

    Kumar S, Paiva B, Anderson KC, et al. International Myeloma Working Group consensus criteria for response and minimal residual disease assessment in multiple myeloma. Lancet Oncol. 2016;17:e328–e46.

    Article  Google Scholar 

  21. 21.

    Sørrig R, Klausen TW, Salomo M, et al. Smoldering multiple myeloma risk factors for progression: a Danish population-based cohort study. Eur J Haematol. 2016;97:303–9.

    Article  Google Scholar 

  22. 22.

    Widman DG, Gornisiewicz S, Shacham S, Tamir S. In vitro toxicity and efficacy of verdinexor, an exportin 1 inhibitor, on opportunistic viruses affecting immunocompromised individuals. PLoS One. 2018;13:e0200043.

    Article  Google Scholar 

  23. 23.

    Wu M, Gui H, Feng Z, et al. KPT-330, a potent and selective CRM1 inhibitor, exhibits anti-inflammation effects and protection against sepsis. Biochem Biophys Res Commun. 2018;503:1773–9.

    CAS  Article  Google Scholar 

  24. 24.

    Al Saleh AS, Sher T, Gertz MA. Multiple myeloma in the time of COVID-19. Acta Haematol. 2020:1–7.

  25. 25.

    Society IM. Recommendations for the management of myeloma patients during the COVID-19 pandemic; 2020.

    Google Scholar 

  26. 26.

    Malard F, Mohty M. Management of patients with multiple myeloma during the COVID-19 pandemic. Lancet Haematol. 2020.

  27. 27.

    COVID-19: Data. 2020. at https://www1.nyc.gov/site/doh/covid/covid-19-data.page.).

  28. 28.

    Cook G, Ashcroft AJ, Pratt G, et al. Real-world assessment of the clinical impact of symptomatic infection with severe acute respiratory syndrome coronavirus (COVID-19 disease) in patients with Multiple Myeloma receiving systemic anti-cancer therapy. Br J Haematol.

  29. 29.

    Gross CP, Essien UR, Pasha S, Gross JR, Wang S-Y, Nunez-Smith M. Racial and ethnic disparities in population level COVID-19 mortality. medRxiv. 2020; 2020.05.07.20094250.

  30. 30.

    Henning-Smith C, Tuttle M, Kozhimannil KB. Unequal distribution of COVID-19 risk among rural residents by race and ethnicity. J Rural Health. 2020.

  31. 31.

    Howard G, Safford MM, Moy CS, et al. Racial differences in the incidence of cardiovascular risk factors in older Black and White adults. J Am Geriatr Soc. 2017;65:83–90.

    Article  Google Scholar 

  32. 32.

    Diane Marie Del Valle M, Seunghee Kim-Schulze PD, Hsin-Hui Huang PD, et al. An inflammatory cytokine signature helps predict COVID-19 severity and death. MEDRXIV. 2020;115758.

  33. 33.

    Jatiani SS, Aleman A, Madduri D, et al. Myeloma CAR-T CRS management with IL-1R antagonist anakinra. Clin Lymphoma MyelomaLeukemia. 2020.

  34. 34.

    Dai H, Wu Z, Jia H, et al. Bispecific CAR-T cells targeting both CD19 and CD22 for therapy of adults with relapsed or refractory B cell acute lymphoblastic leukemia. J Hematol Oncol. 2020;13:30.

    Article  Google Scholar 

  35. 35.

    Costa LJ WS, Bermúdez A. First clinical study of the B-cell maturation antigen (BCMA) 2 + 1 T cell engager (TCE) CC-93269 in patients (pts) with relapsed/refractory multiple myeloma (RRMM): interim results of a phase 1 multicenter trial. Abstract #143. American Society of Hematology. Orlando: ASH Annual Meeting Proceedings; 2019.

  36. 36.

    Xu X, Han M, Li T, et al. Effective treatment of severe COVID-19 patients with tocilizumab. Proc Natl Acad Sci. 2020;117:10970–5.

    CAS  Article  Google Scholar 

  37. 37.

    Cao Y, Wei J, Zou L, et al. Ruxolitinib in treatment of severe coronavirus disease 2019 (COVID-19): A multicenter, single-blind, randomized controlled trial. J Allergy Clin Immunol. 2020.

  38. 38.

    Tseng C-TK, Perrone LA, Zhu H, Makino S, Peters CJ. Severe acute respiratory syndrome and the innate immune responses: modulation of effector cell function without productive infection. J Immunol. 2005;174:7977–85.

    CAS  Article  Google Scholar 

  39. 39.

    Bryce C, Grimes Z, Pujadas E, et al. Pathophysiology of SARS-CoV-2: targeting of endothelial cells renders a complex disease with thrombotic microangiopathy and aberrant immune response. The Mount Sinai COVID-19 autopsy experience. medRxiv. 2020; 2020.05.18.20099960.

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Acknowledgements

We would like to acknowledge all the staff and families for the selfless efforts in caring for patients who developed COVID-19, and the strength and courage of all patients affected by the pandemic.

Funding

There is no outside funding declared for this study.

Author information

Affiliations

Authors

Contributions

Conceptualization, BW, OVO, THM, SJ, SP, and DM; Methodology, OVO; Investigation, BW, OVO, THM, DV, and SG; Writing—original draft, BW, OVO, THM; Writing—review & editing, all authors; Funding acquisition, SJ.; Resources, MM, SJ, SP, and DM; Supervision, MM, SJ, SP, and DM. The authors read and approved the final manuscript.

Corresponding author

Correspondence to Deepu Madduri.

Ethics declarations

Ethics approval and consent to participate

This study was performed in accordance with the Declaration of Helsinki and International Conference on Harmonization Guidelines for Good Clinical Practice (IRB: GCO#: 11-1433).

Consent for publication

Not applicable.

Competing interests

A.C.: Advisory board and consulting fees from Amgen, Antegene, Celgene, Janssen, Karyopharm, Millennium/Takeda, Novartis Pharmaceuticals, Oncopeptides, Sanofi; research funding from Amgen, Celgene, Janssen, Millennium/Takeda, Novartis Pharmaceuticals, Pharmacyclics. S. J.: Advisory board and consulting fees from Celgene, Bristol-Myers Squibb, Janssen Pharmaceuticals and Merck. H. J. C: Employed by the Multiple Myeloma Research Foundation, advisory board and consulting fees from Genetech, Celgene, Bristol Myers Squibb, GlaxoSmithKline and received research funding from Takeda, Celgene, and Genetech. D. M.: Advisory board and consulting fees from Janssen, Celgene, Bristol Myers Squibb, Takeda, Legend, GlaxoSmithKline, Kinevant, and Foundation Medicine. B.W.: Consulting fees from Sanofi Genzyme. J. R.: Speaking fees from Celgene and Janssen, advisory board and consulting fees from Celgene, Janssen, Bristol Myers Squibb, Oncopeptides, Adaptive Biotechnologies, X4 Pharmaceuticals, Karyopharm, and Antegene. S. P.: Consulting fees from Foundation Medicine, research funding from Celgene and Karyopharm, supported by 1R01CA244899-01A1. All other authors declare no potential conflict of interest.

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Supplementary information

Additional file 1: Figure S1.

Evolution of selected inflammatory biomarkers in a subset of patients (n = 12) hospitalized at the Mount Sinai Hospital for which the data was available. Different measurements from the same patient are connected. A linear regression line is plotted for the subgroup of patients that survived (blue, n = 8) and died (red, n = 4), respectively.

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Wang, B., Van Oekelen, O., Mouhieddine, T.H. et al. A tertiary center experience of multiple myeloma patients with COVID-19: lessons learned and the path forward. J Hematol Oncol 13, 94 (2020). https://doi.org/10.1186/s13045-020-00934-x

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Keywords

  • Multiple myeloma
  • Smoldering multiple myeloma
  • COVID-19
  • SARS
  • SARS-Cov-2
  • New York
  • Pandemic