Division of Hematology and Oncology, Department of Medicine, O'Neal Comprehensive Cancer Center, and.
Institute for Cancer Outcomes and Survivorship, University of Alabama at Birmingham, Birmingham, AL.
Blood Adv. 2022 Jul 26;6(14):4122-4131. doi: 10.1182/bloodadvances.2022007247.
Mantle cell lymphoma (MCL) is considered incurable with the available chemoimmunotherapy approaches, and therefore, newer effective targeted therapies such as Bruton tyrosine kinase (BTK) inhibitors are increasingly used in MCL as chronic suppressive therapy, especially in the elderly. We aimed to describe the treatment patterns in MCL at different lines of therapy with a focus on BTK inhibitor use and compare outcomes with known prognostic factors using a nationwide Flatiron Health electronic health record-derived de-identified database. We analyzed patient-level data from the period of 2011 to 2021. In this study of 4336 patients with MCL, we found that bendamustine plus rituximab chemotherapy was the most commonly used frontline regimen (42%). Maintenance rituximab or consolidative autologous stem cell transplant (ASCT) was administered to 31% of all patients. Also, for patients who received ASCT as consolidation therapy, only 34% subsequently received rituximab maintenance. BTK inhibitors were the most preferred agents in second or later lines of therapy (n = 933, 57%), followed by bortezomib, lenalidomide, and venetoclax, respectively. Among patients treated with BTK inhibitors, the median real-world overall survival (rwOS) was 35 months (95% confidence interval [CI], 27-50), 24 months (95% CI, 22-30), and 18 months (95% CI, 14-21) for first line, second line, and third or later line of therapy, respectively. Patients with a deletion 17p/TP53 mutation and blastoid variant MCL had poor outcomes; however, BTK inhibitors appeared to mitigate the negative influence of del17p/TP53-mutated MCL with a hazard ratio of 1.17 (95% CI, 0.88-1.55) on multivariable analysis.
套细胞淋巴瘤(MCL)目前采用的化疗免疫疗法无法治愈,因此,新型有效的靶向治疗药物,如布鲁顿酪氨酸激酶(BTK)抑制剂,在 MCL 中作为慢性抑制性治疗方法被越来越多地应用,尤其适用于老年患者。本研究旨在描述不同治疗线的 MCL 治疗模式,重点介绍 BTK 抑制剂的使用情况,并利用全国范围内的 Flatiron Health 电子病历衍生的去标识数据库,结合已知的预后因素来比较结果。我们分析了 2011 年至 2021 年期间的患者水平数据。在这项涉及 4336 例 MCL 患者的研究中,我们发现苯达莫司汀联合利妥昔单抗化疗是最常用的一线方案(42%)。31%的所有患者接受了利妥昔单抗维持治疗或巩固性自体干细胞移植(ASCT)。此外,对于接受 ASCT 作为巩固治疗的患者,仅有 34%的患者随后接受了利妥昔单抗维持治疗。BTK 抑制剂是二线或三线治疗中最受欢迎的药物(n = 933,57%),其次是硼替佐米、来那度胺和维奈托克。在接受 BTK 抑制剂治疗的患者中,中位真实世界总生存期(rwOS)分别为一线治疗 35 个月(95%CI,27-50)、二线治疗 24 个月(95%CI,22-30)和三线或以上治疗 18 个月(95%CI,14-21)。存在 17p 缺失/TP53 突变和母细胞样变异型 MCL 的患者预后较差;然而,BTK 抑制剂似乎减轻了 del17p/TP53 突变型 MCL 的负面影响,多变量分析的风险比为 1.17(95%CI,0.88-1.55)。