Washington University in St Louis School of Medicine, St Louis, MO, 63110.
Washington University in St Louis School of Medicine, St Louis, MO, 63110.
Clin Lymphoma Myeloma Leuk. 2023 Jul;23(7):552-560. doi: 10.1016/j.clml.2023.04.003. Epub 2023 Apr 24.
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.
套细胞淋巴瘤(MCL)是一种中度侵袭性淋巴瘤亚型,通常被认为无法治愈。对于年轻、健康的患者,标准治疗方法仍然是各种基于高剂量阿糖胞苷的诱导方案,随后进行自体造血细胞移植和 3 年的利妥昔单抗维持治疗。尽管有相当不错的结果,中位无进展生存期在 7 到 9 年之间,但大多数患者最终仍会复发,这表明需要提高缓解诱导策略的安全性和耐受性。
鉴于苯达莫司汀/利妥昔单抗(BR)在老年 MCL 患者中的显著疗效,我们开发了一种诱导方案,该方案模仿北欧方案,但用 BR 替代 R-CHOP。在第二项试点研究中,我们将第二代布鲁顿酪氨酸激酶抑制剂(BTKi)阿卡替尼纳入该方案。这两项研究的主要终点都是干细胞动员成功率。
在这两项研究中,所有患者都成功地进行了干细胞采集。
来自我们单机构试点研究的经验表明,与交替使用 BR 和阿糖胞苷/利妥昔单抗(CR)相比,连续使用 BR 和 CR 更容易管理,而且从毒性和随后的剂量调整角度来看也是如此。来自 FitMCL 1.0 和 2.0 两项试点研究的安全性和疗效数据相似。这些试点研究提供了初步的安全性数据,支持开展 NCTN 试验 EA4181,评估三种不同的诱导方案,包括是否使用阿卡替尼。