scholarly journals Mantle Cell Lymphoma: Updates in the Management of Relapsed/Refractory Disease

2021 ◽  
Vol 19 (11.5) ◽  
pp. 1331-1333
Author(s):  
Mazyar Shadman

Mantle cell lymphoma remains incurable despite recent treatment advances, and most patients experience relapsed/refractory disease. BTK inhibitors are the preferred choice in the relapsed setting, especially in patients with early relapse. For patients with high-risk features such as TP53 mutation, early referral for CAR T-cell therapy should be considered, even in those with stable disease on a BTK inhibitor. Patients without high-risk features may be monitored and initiate CAR T-cell therapy after clinical disease progression. CAR T-cell therapy is an effective treatment with high rate of complete remissions. For patients who do not achieve a complete remission 3 months after CAR-T therapy, bridging therapy with chemotherapy or targeted therapy agents and referral for allogeneic transplant are recommended.

2021 ◽  
Vol 161 ◽  
pp. S894-S895
Author(s):  
N. Figura ◽  
A. Sim ◽  
S. Dahiya ◽  
F. Lutfi ◽  
A. Rapoport ◽  
...  

2020 ◽  
Vol 382 (14) ◽  
pp. 1331-1342 ◽  
Author(s):  
Michael Wang ◽  
Javier Munoz ◽  
Andre Goy ◽  
Frederick L. Locke ◽  
Caron A. Jacobson ◽  
...  

2020 ◽  
Vol 8 (2) ◽  
pp. e001114 ◽  
Author(s):  
Michael Wang ◽  
Preetesh Jain ◽  
T Linda Chi ◽  
Sheree E Chen ◽  
Amy Heimberger ◽  
...  

Cerebral edema following chimeric antigen receptor (CAR) T-cell therapy can be fatal. ZUMA-2 is a pivotal phase 2, multicenter study evaluating KTE-X19, an autologous anti-CD19 CAR T-cell therapy, in relapsed/refractory mantle cell lymphoma. We describe a 65-year-old patient in ZUMA-2 who developed cerebral edema following CAR T-cell therapy and had complete recovery after multimodality clinical intervention including rabbit antithymocyte globulin (ATG). Biomarker results show early and robust CAR T-cell expansion and related induction of inflammatory cytokines, followed by rapid declines in CAR T-cell and proinflammatory cytokine levels after ATG administration. This clinical profile highlights a potential relevance of ATG in treating severe CAR T-cell-related neurotoxicity.


Cancers ◽  
2021 ◽  
Vol 13 (22) ◽  
pp. 5592
Author(s):  
Edit Porpaczy ◽  
Philipp Wohlfarth ◽  
Oliver Königsbrügge ◽  
Werner Rabitsch ◽  
Cathrin Skrabs ◽  
...  

Refractory/relapsed diffuse large B-cell lymphoma (DLBCL) is associated with poor outcome. The clinical behavior and genetic landscape of DLBCL is heterogeneous and still not fully understood. TP53 mutations in DLBCL have been identified as markers of poor prognosis and are often associated with therapeutic resistance. Chimeric antigen receptor T-cell therapy is an innovative therapeutic concept and represents a game-changing therapeutic option by supporting the patient’s own immune system to kill the tumor cells. We investigated the impact of TP53 mutations on the overall survival of refractory/relapsed DLBCL patients treated with comparable numbers of therapy lines. The minimum number of therapy lines was 2 (median 4), including either anti-CD19 CAR T-cell therapy or conventional salvage therapy. A total of 170 patients with DLBCL and high-grade B-cell lymphoma with MYC, BCL2, and/or BCL6 rearrangements (DHL/THL), diagnosed and treated in our hospital between 2000 and 2021, were included. Twenty-nine of them received CAR T-cell therapy. TP53 mutations were found in 10/29 (35%) and 31/141 (22%) of patients in the CAR T-cell and conventional groups, respectively. Among the 141 patients not treated with CAR T cells, TP53 mutation was an independent prognostic factor for overall survival (OS) (median 12 months with TP53 vs. not reached without TP53 mutation, p < 0.005), but in the CAR T cell treated group, this significance could not be shown (median OS 30 vs. 120 months, p = 0.263). The findings from this monocentric retrospective study indicate that TP53 mutation status does not seem to affect outcomes in DLBCL patients treated with CAR T-cell therapy. Detailed evaluation in large cohorts is warranted.


2020 ◽  
Vol 4 (23) ◽  
pp. 5925-5928
Author(s):  
Timothy J. Voorhees ◽  
Nilanjan Ghosh ◽  
Natalie Grover ◽  
Jared Block ◽  
Catherine Cheng ◽  
...  

Key Points CD30 CAR T-cell therapy promoted a prolonged remission in a patient with multiply relapsed EATL.


Blood ◽  
2021 ◽  
Vol 138 (Supplement 1) ◽  
pp. 570-570
Author(s):  
Geoffrey Shouse ◽  
Rachel Tran ◽  
Jesse Osborn ◽  
Lihua E Budde

Abstract Introduction: CAR T-cell therapy has revolutionized the treatment of relapsed/refractory B cell lymphomas, providing hope to patients who previously faced dismal outcomes. Despite unprecedented efficacy including high response rates and a significant proportion of durable responses, significant toxicities are still prevalent. Toxicities related to immune therapy including cytokine release syndrome (CRS) and immune effector cell associated neurotoxicity syndrome (ICANS) along with infections and hematologic toxicity, complicate the post CAR T-cell infusion course. Innate patient-related factors including presence of comorbidities, advanced physiologic age, and poor fitness, likely contribute to poor short-term outcomes, however no validated risk scores incorporating these factors have been validated in patients receiving CAR T-cell therapy for lymphoma. In the present study we identified the ability of a patient to walk 500 feet (ft) or more during the 6 Minute Walk Test (6MWT) at baseline as a predictive marker for poor short-term outcomes after CAR T-cell infusion. Methods: We retrospectively analyzed charts of 78 patients who received commercially available CAR T-cell products for the treatment of lymphoma between May, 2019 and March, 2021 who had baseline assessment by physical therapy at the time of admission for CAR T-cell therapy. CRS and ICANS were scored by ASTCT guidelines. Demographics were analyzed with descriptive statistics. Univariate analysis was performed by Chi Squared. Results: The analysis included 78 patients with a median age of 63 (range, 21-82), 37% (n=29) were female. Patients were treated for DLBCL (64%, n=50), transformed follicular lymphoma (tFL; 29%, n=23), primary mediastinal B cell lymphoma (PMBCL; 4%, n=3), and mantle cell lymphoma (MCL; 3%, n=2). Patients received axicabtagene ciloleucel (94%, n=73), tisagenlecleucel (4%, n=3), or brexucabtagene autoleucel (3%, n=2). Patients had a median of 3 prior lines of therapy (range 2-7) and 53% (n=42) received bridging chemotherapy. Among the 70 patients who completed the 6MWT, the mean distance was 909 ft (range, 20-2045), 8 patients were unable to compete the assessment due to debility and were included in the analysis as a 0 distance. Patients who were unable to complete 500 feet (n=17) were deemed to have poor endurance (PE). The PE group of patients were 3.6 times more likely to have a prolonged length of stay (p=0.02), while they were 1.5 times less likely to be alive at 100 days post CAR T infusion (p = 0.002). Patients also tended to have higher rates of ICANS (76% vs 41%), lower overall response rates (ORR) (78% vs 98%), and higher 30 day mortality (18% vs 2%), although these did not reach statistical significance, p=0.08, 0.06, and 0.07, respectively. CRS did not appear to be related to PE status, neither did age, or prior lines of therapy. Conclusions: Within the limitations of a retrospective study, we demonstrate that the baseline physical therapy-assessed measure of function and endurance, namely the 6MWT, correlates with several critical short-term outcomes in CAR T patients with lymphoma. These include prolonged length of stay, survival at day 100, and there is suggested correlation with ORR, ICANS, and 30-day survival as well. These findings illustrate the potential for early recognition of deconditioned patients that may do poorly after CAR T-cell therapy. Identification of these patients could allow for therapeutic interventions prior to CAR T infusion or during their post-infusion hospital stay, designed to enhance their strength and endurance, and potentially improve these short-term outcomes. Prospective intervention studies are planned based on these findings. Disclosures Shouse: Kite Pharma: Speakers Bureau; Beigene: Honoraria. Budde: Kite Pharma: Consultancy; AstraZeneca: Research Funding; Genentech: Consultancy, Research Funding.


Blood ◽  
2019 ◽  
Vol 134 (Supplement_1) ◽  
pp. 4137-4137
Author(s):  
Joanna C Yang ◽  
Karen Chau ◽  
Michael Scordo ◽  
Craig S. Sauter ◽  
Joachim Yahalom

Introduction: For patients with relapsed or primary refractory (rel/ref) diffuse large B-cell lymphoma (DLBCL) who respond to salvage chemotherapy, high-dose chemotherapy and autologous hematopoietic cell transplantation (HDT-AHCT) is considered standard of care. Patients with refractory disease to salvage chemotherapy, defined as stable disease (SD) or progressive disease (PD), by functional imaging are ineligible for HDT-AHCT, and have a poor prognosis. In practice, we have attempted to salvage these patients with radiation therapy (RT) to residual sites of active disease prior to consolidative HDT-AHCT. The outcome of this unique combined modality salvage paradigm has not been previously reported. Methods: We retrospectively reviewed all patients with rel/ref DLBCL who received salvage chemotherapy followed by salvage RT and HDT-AHCT between the years of 2000 and 2017 at a single center. Only patients with SD or PD as defined on the 5-point Deauville scale after salvage chemotherapy and who had at least 1 year of follow-up were included in this analysis. The second-line age-adjusted International Prognostic Index (sAAIPI) was determined at the time of initiation of salvage chemotherapy.Survival functions were estimated by the Kaplan-Meier method and compared using a log-rank test. Results: Thirty-six patients, 12 with relapsed and 24 with primary refractory disease, with a median age of 44 years (range: 19-68 years) were analyzed. Twenty-three patients had DLBCL while 13 had primary mediastinal B-cell lymphoma (PMBCL). The majority of patients had KPS 80-100 (n=32, 89%), 0-1 extranodal sites (n=30, 83%), and normal LDH (n=21, 58%). The sAAIPI scores for this cohort were as follows: 0 (n=10), 1 (n=21), 2 (n=4), and 3 (n=1). All patients received salvage chemotherapy with subsequent functional imaging showing SD (n=32) and PD (n=4) and then went on to receive salvage RT to the sites of active disease. Median RT dose was 39.6Gy (range: 30-54Gy). Six patients also received TBI as part of their conditioning regimen prior to HDT-AHCT. With median follow up of 4.0 years (range: 1.0-12.3 years) for survivors, 4-year relapse-free survival (RFS) was 75.6% and 4-year overall survival (OS) was 80.3% (Figure 1a). There was no significant difference in 4-year RFS for patients with relapsed versus primary refractory disease (80.2% vs 74.8%, p=0.59). PMBCL patients had better RFS than DLBCL patients (92.3% vs 67.8%, p=0.12). Using the composite sAAIPI score was highly prognostic with worse outcomes for patients with higher risk sAAIPI scores. By sAAIPI score, 4-year RFS was 80.0% for a score of 0, 90.2% for a score of 1, and 0% for scores of 2 and 3. Patients with low- and low-intermediate risk sAAIPI scores of 0 and 1 had improved RFS as compared to patients with sAAIPI scores of 2 and 3 (87.0% vs 0%, p<0.0001 (Figure 1b). Conclusions: Patients with chemorefractory rel/ref DLBCL who have had minimal or no response to systemic salvage therapy may benefit from salvage RT to the residual PET-avid disease followed by HDT-AHCT, particularly if their sAAIPI score is ≤ 1. The outcome of this retrospective cohort is markedly superior to outcomes described in the literature for this high-risk population and represents a promising treatment paradigm to be further explored. Emerging data suggest similar patients may benefit from CAR T-cell therapy. Given the limited availability and high cost of CAR T-cell therapy, we suggest there may be a role for sequencing this combined-modality salvage paradigm prior to CAR T-cell therapy in order to provide these poor-risk patients with an additional line of therapy. Disclosures Scordo: Angiocrine Bioscience, Inc.: Consultancy; McKinsey & Company: Consultancy. Sauter:Sanofi-Genzyme: Consultancy, Research Funding; GSK: Consultancy; Spectrum Pharmaceuticals: Consultancy; Novartis: Consultancy; Genmab: Consultancy; Precision Biosciences: Consultancy; Kite/Gilead: Consultancy; Celgene: Consultancy; Juno Therapeutics: Consultancy, Research Funding.


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