Treatment Outcomes and Roles of Transplantation and Maintenance Rituximab in Patients With Previously Untreated Mantle Cell Lymphoma: Results From Large Real-World Cohorts

Author:

Martin Peter1ORCID,Cohen Jonathon B.2ORCID,Wang Michael3ORCID,Kumar Anita4ORCID,Hill Brian5,Villa Diego6ORCID,Switchenko Jeffrey M.7ORCID,Kahl Brad8ORCID,Maddocks Kami9,Grover Natalie S.10ORCID,Qi Keqin11ORCID,Parisi Lori12,Daly Katherine12,Zhu Angeline12,Salles Gilles4ORCID

Affiliation:

1. Weill Cornell Medicine, New York-Presbyterian Hospital, New York, NY

2. Department of Hematology, Winship Cancer Institute, Emory University, Atlanta, GA

3. Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX

4. Memorial Sloan Kettering Cancer Center, New York, NY

5. Department of Hematology and Medical Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH

6. BC Cancer Centre for Lymphoid Cancer and University of British Columbia, Vancouver, British Columbia, Canada

7. Department of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, Atlanta, GA

8. Division of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO

9. Arthur G James Comprehensive Cancer Center, The Ohio State University, Columbus, OH

10. Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC

11. Janssen Research and Development, Titusville, NJ

12. Janssen Research and Development, Oncology, Raritan, NJ

Abstract

PURPOSE Commonly used first-line (1L) treatments for mantle cell lymphoma include high-dose cytarabine-based induction followed by autologous stem-cell transplant (ASCT) for younger patients and several chemoimmunotherapy regimens for older patients. Continuous debates exist on the role of ASCT in younger patients and maintenance rituximab (MR) after bendamustine plus rituximab (BR). METHODS Retrospective data from 4,216 patients with mantle cell lymphoma in the Flatiron Health electronic record-derived deidentified database diagnosed between 2011 and 2021, mostly in US community oncology settings, were evaluated for treatment patterns and outcomes. The efficacy findings with ASCT and MR were validated in an independent cohort of 1,168 patients from 12 academic centers. RESULTS Among 3,614 patients with documented 1L treatment, BR was the most used. Among 1,265 patients age < 65 years, 30.5% received cytarabine-based induction and 23.5% received ASCT. There was no significant association between ASCT and real-world time to next treatment (hazard ratio [HR], 0.84; 95% CI, 0.68 to 1.03; P = .10) or overall survival (HR, 0.86; 95% CI, 0.63 to 1.18; P = .4) among ASCT-eligible patients. Among MR-eligible patients, MR after BR versus BR alone was associated with a longer real-world time to next treatment (HR, 1.96; 95% CI, 1.61 to 2.38; P < .001) and overall survival (HR, 1.51; 95% CI, 1.19 to 1.92; P < .001). The efficacy findings were consistent in the validation cohort. CONCLUSION In this large cohort of patients treated primarily in the US community setting, only one in four young patients received cytarabine or ASCT consolidation, suggesting the need to develop treatments that can be delivered effectively in routine clinical practice. Together with the validation cohort, data support future clinical trials exploring regimens without ASCT consolidation in young patients, whereas MR should be considered for patients after 1L BR and rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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