Sarah Cannon Research Institute, Nashville, Tennessee, USA
Tennessee Oncology, PLLC, Nashville, Tennesse, USA.
Oncologist. 2019 Aug;24(8):1035-e623. doi: 10.1634/theoncologist.2019-0286. Epub 2019 May 9.
The combination of ofatumumab and bendamustine in elderly patients with diffuse large B-cell lymphoma demonstrated modest efficacy compared with standard of care.The poor response may have been due to patient age and the high rate of treatment discontinuation.
This phase II trial evaluated the efficacy of bendamustine and ofatumumab in elderly patients with newly diagnosed diffuse large B-cell lymphoma (DLBCL) who were not candidates for rituximab cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP).
Patients received IV 90 mg/m bendamustine on days 1 and 2 of cycles 1 through 6 and IV 1,000 mg ofatumumab on days 1 and 8 of cycle 1 and on day 1 of cycles 2 through 6. Both drugs were administered at the U.S. Food and Drug Administration-approved dose for combination therapy. All patients received premedications before each infusion of ofatumumab and hematopoietic growth factors. Treatment was administered in 21-day cycles, with restaging after cycle 3 and cycle 6. The primary endpoint was complete response rate (CRR).
Twelve of 21 enrolled patients completed treatment; median age was 83 years. The most common reasons for treatment discontinuation were disease progression (three patients), intercurrent illness (two patients), and death (one patient due to drug-related sepsis and bowel necrosis and one patient due to unknown cause). Thrombocytopenia (14%), neutropenia (10%), diarrhea (10%), vomiting (10%), and dehydration (10%) were the most common grade ≥3 treatment-related adverse events. The overall response rate was 90.5% and the CRR was 33.3%. Median progression-free survival (PFS) and overall survival (OS) were 8.6 and 12.0 months, respectively.
The combination of ofatumumab and bendamustine is feasible in elderly patients with DLBCL.
与标准治疗相比,奥法妥木单抗联合苯达莫司汀在老年弥漫性大 B 细胞淋巴瘤患者中的疗效仅为适度。反应不佳可能归因于患者年龄以及治疗中断率较高。
这项 II 期试验评估了苯达莫司汀联合奥法妥木单抗在不适合利妥昔单抗环磷酰胺、多柔比星、长春新碱和泼尼松(R-CHOP)治疗的新诊断弥漫性大 B 细胞淋巴瘤(DLBCL)老年患者中的疗效。
患者在第 1 周期的第 1 和第 2 天接受静脉注射 90 mg/m2 的苯达莫司汀,在第 1 和第 8 天接受静脉注射 1000mg 的奥法妥木单抗,在第 1 周期的第 2 天和第 2 至第 6 周期的第 1 天接受奥法妥木单抗。两种药物均按联合治疗的美国食品和药物管理局批准剂量给药。所有患者在每次奥法妥木单抗输注前均接受预处理,并在第 3 周期和第 6 周期后进行重新分期。主要终点是完全缓解率(CRR)。
21 名入组患者中有 12 名完成治疗;中位年龄为 83 岁。治疗中断的最常见原因是疾病进展(3 例)、并发疾病(2 例)和死亡(1 例死于药物相关脓毒症和肠坏死,1 例死因不明)。血小板减少症(14%)、中性粒细胞减少症(10%)、腹泻(10%)、呕吐(10%)和脱水(10%)是最常见的 3 级以上治疗相关不良事件。总缓解率为 90.5%,完全缓解率为 33.3%。中位无进展生存期(PFS)和总生存期(OS)分别为 8.6 个月和 12.0 个月。
奥法妥木单抗联合苯达莫司汀在老年 DLBCL 患者中是可行的。