Puvvada Soham D, Guillen-Rodriguez José, Kumar Abhijeet, Inclán Lora, Heard Kara, Rivera Xavier I, Anwer Faiz, Schatz Jonathan H, Mahadevan Daruka, Persky Daniel O
Division of Hematology-Oncology, Department of Medicine, University of Arizona Cancer Center, Tucson, AZ.
Division of Hematology-Oncology, Department of Medicine, University of Arizona Cancer Center, Tucson, AZ.
Clin Lymphoma Myeloma Leuk. 2018 Jan;18(1):58-64. doi: 10.1016/j.clml.2017.09.001. Epub 2017 Sep 19.
Mantle-cell lymphoma (MCL) and indolent non-Hodgkin lymphoma (iNHL) are incurable heterogeneous diseases characterized by relapse. There is a need for newer treatments in MCL and iNHL, especially in the relapsed/refractory (R/R) setting. We therefore investigated the novel combination of bortezomib (Velcade), cladribine, and rituximab (VCR) in front-line and R/R settings in MCL and iNHL (NCT00980395).
Eligible patients included adults with biopsy-proven CD20-positive MCL and iNHL who met the criteria for treatment. Rituximab 375 mg/m intravenous (IV) day 1, cladribine 4 mg/m IV days 1 to 5, and bortezomib 1.3 mg/m IV days 1 and 4 were administered every 28 days for 6 cycles.
Twenty-four patients were enrolled onto the study with a median follow-up of 38.5 months. Median age was 66.5 years, and 46% had MCL. The most common adverse events were hematologic, with febrile neutropenia in 3 patients. Neuropathy was noted in 17% of patients, of which 8% was grade 3 or above. The overall response rate was 92%. For the entire cohort, and for MCL patients, the median progression-free survival and the median overall survival were not reached. The 2-year progression-free survival was 82% for the MCL group and 54% for the iNHL group; it was 80% for treatment-naive patients and 57% for R/R patients.
VCR is effective in MCL and iNHL. Although hematologic toxicity can be an issue, this study demonstrates a high response rate to a novel combination and provides an alternative option in transplant-ineligible R/R MCL and iNHL.
套细胞淋巴瘤(MCL)和惰性非霍奇金淋巴瘤(iNHL)是无法治愈的异质性疾病,其特征为复发。MCL和iNHL需要更新的治疗方法,尤其是在复发/难治(R/R)情况下。因此,我们研究了硼替佐米(万珂)、克拉屈滨和利妥昔单抗(VCR)在MCL和iNHL的一线及R/R情况下的新型联合方案(NCT00980395)。
符合条件的患者包括经活检证实为CD20阳性MCL和iNHL且符合治疗标准的成年人。第1天静脉注射(IV)利妥昔单抗375 mg/m²,第1至5天静脉注射克拉屈滨4 mg/m²,第1天和第4天静脉注射硼替佐米1.3 mg/m²,每28天给药1次,共6个周期。
24例患者入组本研究,中位随访时间为38.5个月。中位年龄为66.5岁,46%的患者患有MCL。最常见的不良事件为血液学方面的,3例患者出现发热性中性粒细胞减少。17%的患者出现神经病变,其中8%为3级或以上。总缓解率为92%。对于整个队列以及MCL患者,中位无进展生存期和中位总生存期均未达到。MCL组的2年无进展生存率为82%,iNHL组为54%;初治患者为80%,R/R患者为57%。
VCR方案在MCL和iNHL中有效。尽管血液学毒性可能是一个问题,但本研究表明该新型联合方案具有较高的缓解率,并为不符合移植条件的R/R MCL和iNHL提供了一种替代选择。