套细胞淋巴瘤
苯达莫司汀
来那度胺
美罗华
硼替佐米
医学
肿瘤科
内科学
淋巴瘤
多发性骨髓瘤
作者
Mitchell R. Smith,Opeyemi A. Jegede,Peter Martin,Brian G. Till,Samir Parekh,David T. Yang,Eric D. Hsi,Thomas E. Witzig,Sandeep S. Davé,David W. Scott,Curtis A. Hanson,Lale Kostakoglu Shields,Nizar Abdel‐Samad,Carla Casulo,Nancy L. Bartlett,Paolo F. Caimi,Tareq Al Baghdadi,Kristie A. Blum,Mark D. Romer,David J. Inwards
出处
期刊:Blood
[Elsevier BV]
日期:2024-05-31
卷期号:144 (10): 1083-1092
被引量:3
标识
DOI:10.1182/blood.2024023962
摘要
While initial therapy of mantle cell lymphoma (MCL) is not standardized, bendamustine-rituximab (BR) is commonly used in older patients. Rituximab (R) maintenance following induction is often utilized. Thus, the open-label, randomized phase II ECOG-ACRIN Cancer Research Group E1411 trial was designed to test two questions: 1) Does addition of bortezomib to BR induction (BVR) and/or 2) addition of lenalidomide to rituximab (LR) maintenance improve progression-free survival (PFS) in patients with treatment-naïve MCL? From 2012-2016, 373 previously untreated patients, 87% ≥ 60 years old, were enrolled in this trial. At a median follow up of 7.5 years, there is no difference in the median PFS of BR compared to BVR (5.5 yrs vs. 6.4 yrs, HR 0.90, 90% CI 0.70, 1.16). There were no unexpected additional toxicities with BVR treatment compared to BR, with no impact on total dose/duration of treatment received. Independent of the induction treatment, addition of lenalidomide to rituximab did not significantly improve PFS, with median PFS in R vs LR (5.9 yrs vs 7.2 yrs, HR 0.84 90% CI 0.62, 1.15). The majority of patients completed the planned 24 cycles of LR at the scheduled dose. In summary, adding bortezomib to BR induction does not prolong PFS in treatment-naïve MCL, and LR maintenance was not associated with longer PFS compared with rituximab alone following BR. Nonetheless, the > 5 year median PFS outcomes in this prospective cooperative group trial indicate the efficacy of BR followed by rituximab maintenance as highly effective initial therapy for older MCL patients. (NCT01415752)
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