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Outcomes of transplant-eligible and transplant-ineligible patients with mantle cell lymphoma in Ontario.

Blood neoplasia 2026 Vol.3(2) p. 100184 🔓 OA Lymphoma Diagnosis and Treatment
OpenAlex 토픽 · Lymphoma Diagnosis and Treatment Chronic Lymphocytic Leukemia Research Viral-associated cancers and disorders

Suleman A, Ante Z, Liu N, Crump M, Chan KKW, Cheung MC, Prica A

📝 환자 설명용 한 줄

The frontline treatment of patients with mantle cell lymphoma (MCL) varies in practice.

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • 표본수 (n) 303

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APA Adam Suleman, Zharmaine Ante, et al. (2026). Outcomes of transplant-eligible and transplant-ineligible patients with mantle cell lymphoma in Ontario.. Blood neoplasia, 3(2), 100184. https://doi.org/10.1016/j.bneo.2025.100184
MLA Adam Suleman, et al.. "Outcomes of transplant-eligible and transplant-ineligible patients with mantle cell lymphoma in Ontario.." Blood neoplasia, vol. 3, no. 2, 2026, pp. 100184.
PMID 41994328

Abstract

The frontline treatment of patients with mantle cell lymphoma (MCL) varies in practice. We conducted a retrospective, population-based study of patients with MCL from 2005 to 2020. We defined transplant-eligible (TE) patients as those aged <70 years who received R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone) or R-CHOP/R-DHAP (rituximab, dexamethasone, high-dose cytarabine and dexamethasone) and transplant-ineligible (TI) patients as those aged ≥70 years and treated with bendamustine-rituximab (BR) or other chemoimmunotherapy regimens. The primary outcome was 5-year overall survival (OS), and secondary outcomes included toxicities and health care use. We identified 426 TE patients, of whom 254 received R-CHOP and 172 received R-CHOP/R-DHAP. More patients who received R-CHOP/R-DHAP also received an autologous stem cell transplant (ASCT). The 5-year OS for patients treated with R-CHOP/R-DHAP was 70.5% compared with 62.0% for patients treated with R-CHOP, regardless of transplant status. R-CHOP/R-DHAP had more hospital admissions for fever, infection, neutropenia, and renal toxicity. TI patients received BR (n = 303) or historical regimens (n = 189). BR was associated with lower mortality. After adjustment, maintenance rituximab was associated with significantly lower mortality (hazard ratio, 0.33; 95% confidence interval, 0.24-0.44). More patients treated with BR had hospital admissions for febrile neutropenia. In this large population-based study, R-CHOP/R-DHAP before ASCT showed a trend toward improved 5-year OS. BR did not result in superior OS after adjustment, suggesting other regimens followed by rituximab maintenance may be reasonable.