Bendamustine/Rituximab Plus Cytarabine/Rituximab, With or Without Acalabrutinib, for the Initial Treatment of Transplant-Eligible Mantle Cell Lymphoma Patients: Pooled Data From Two Pilot Studies

套细胞淋巴瘤 医学 美罗华 耐受性 养生 内科学 肿瘤科 阿糖胞苷 苯达莫司汀 自体干细胞移植 移植 外科 不利影响 淋巴瘤 化疗
作者
Dilan A. Patel,Fei Wan,Kathryn Trinkaus,Daniel Guy,Natasha Edwin,Marcus P. Watkins,Nancy L. Bartlett,Amanda F. Cashen,Todd A. Fehniger,Armin Ghobadi,Neha-Mehta Shah,Brad S. Kahl
出处
期刊:Clinical Lymphoma, Myeloma & Leukemia [Elsevier BV]
卷期号:23 (7): 552-560
标识
DOI:10.1016/j.clml.2023.04.003
摘要

Mantle cell lymphoma (MCL) is a moderately aggressive lymphoma subtype, generally viewed as incurable. For younger, fit patients, the standard of care remains various high-dose cytarabine-based induction regimens followed by autologous hematopoietic cell transplant and 3 years of rituximab maintenance. Despite reasonably good outcomes, with median progression-free survival in the range of 7 to 9 years, most patients eventually relapse, indicating a need to improve the safety and tolerability of remission induction strategies.Given the impressive activity of bendamustine/rituximab (BR) in older patients with MCL, we developed an induction regimen modeled after the Nordic Regimen but substituted BR in place of R-CHOP. In a second pilot study, we incorporated the second-generation Bruton tyrosine kinase inhibitor (BTKi), acalabrutinib, into the regimen. The primary endpoint of both studies was stem cell mobilization success rate.All patients successfully underwent stem cell harvest in both studies.The experience from our single institution pilot study suggested that sequential rather than alternating BR and cytarabine/rituximab (CR) was easier to administer from the standpoint of toxicities and subsequent dose modifications. Safety and efficacy data from the 2 pilot studies, FitMCL 1.0 and 2.0, were similar. The pilot studies provided preliminary safety data supporting the development of the NCTN trial EA4181, assessing three different induction regimens with or without acalabrutinib.
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