Meyer Cancer Center, Weill Cornell Medicine, New York, NY.
Department of Medicine, New York Presbyterian Hospital, New York, NY.
Blood. 2019 Mar 14;133(11):1201-1204. doi: 10.1182/blood-2018-11-886457. Epub 2019 Jan 28.
Single-agent ibrutinib is active in patients with previously treated mantle cell lymphoma (MCL); however, nearly half of all patients experience treatment failure during the first year. We previously demonstrated that prolonged early G1 cell cycle arrest induced by the oral, specific CDK4/6 inhibitor palbociclib can overcome ibrutinib resistance in primary human MCL cells and MCL cell lines expressing wild-type Bruton's tyrosine kinase (BTK). Therefore, we conducted a phase 1 trial to evaluate the dosing, safety, and preliminary activity of palbociclib plus ibrutinib in patients with previously treated mantle cell lymphoma. From August 2014 to June 2016, a total of 27 patients (21 men, 6 women) were enrolled. The maximum tolerated doses were ibrutinib 560 mg daily plus palbociclib 100 mg on days 1 to 21 of each 28-day cycle. The dose-limiting toxicity was grade 3 rash. The most common grade 3 to 4 toxicities included neutropenia (41%), thrombocytopenia (30%), hypertension (15%), febrile neutropenia (15%), and lung infection (11%). The overall and complete response rates were 67% and 37%, and with a median follow-up of 25.6 months, the 2-year progression-free survival was 59.4% and the 2-year response duration was 69.8%. A phase 2 multicenter clinical trial to further characterize efficacy is now ongoing. The current trial was registered at www.clinicaltrials.gov as #NCT02159755.
单药伊布替尼在既往治疗的套细胞淋巴瘤(MCL)患者中具有活性;然而,几乎一半的患者在第一年期间经历治疗失败。我们之前证明,口服、特异性 CDK4/6 抑制剂帕博西尼诱导的早期 G1 细胞周期阻滞延长可克服原发性人 MCL 细胞和表达野生型布鲁顿酪氨酸激酶(BTK)的 MCL 细胞系中的伊布替尼耐药。因此,我们进行了一项 1 期试验,以评估帕博西尼联合伊布替尼在既往治疗的套细胞淋巴瘤患者中的剂量、安全性和初步疗效。从 2014 年 8 月至 2016 年 6 月,共入组 27 例患者(21 例男性,6 例女性)。最大耐受剂量为伊布替尼 560mg 每日一次,帕博西尼 100mg 每日一次,每 28 天周期的第 1 至 21 天。剂量限制毒性为 3 级皮疹。最常见的 3 级至 4 级毒性包括中性粒细胞减少(41%)、血小板减少(30%)、高血压(15%)、发热性中性粒细胞减少(15%)和肺部感染(11%)。总有效率和完全缓解率分别为 67%和 37%,中位随访 25.6 个月,2 年无进展生存率为 59.4%,2 年缓解持续时间为 69.8%。目前正在进行一项多中心 2 期临床试验以进一步确定疗效。该试验已在 www.clinicaltrials.gov 上注册,编号为#NCT02159755。