Division of Hematology/Oncology, Columbia University Irving Medical Center, New York, NY, USA.
The Patricia Lynch Cancer Center, Holy Name Medical Center, Teaneck, NJ, USA.
Blood Cancer J. 2021 Jan 11;11(1):10. doi: 10.1038/s41408-020-00397-w.
Venetoclax is efficacious in relapsed/refractory t(11;14) multiple myeloma, thus warranting investigation in light-chain amyloidosis (AL). This retrospective cohort includes 43 patients with previously treated AL, from 14 centers in the US and Europe. Thirty-one patients harbored t(11;14), 11 did not, and one t(11;14) status was unknown. Patients received a venetoclax-containing regimen for at least one 21- or 28-day cycle; the median prior treatments was three. The hematologic response rate for all patients was 68%; 63% achieved VGPR/CR. t(11;14) patients had higher hematologic response (81% vs. 40%) and higher VGPR/CR rate (78% vs. 30%, odds ratio: 0.12, 95% CI 0.02-0.62) than non-t(11;14) patients. For the unsegregated cohort, median progression-free survival (PFS) was 31.0 months and median OS was not reached (NR). For t(11;14), median PFS was NR and for non-t(11;14) median PFS was 6.7 months (HR: 0.14, 95% CI 0.04-0.53). Multivariate analysis incorporating age, sex, prior lines of therapy, and disease stage suggested a risk reduction for progression or death in t(11;14) patients. Median OS was NR for either subgroup. The organ response rate was 38%; most responders harbored t(11;14). Grade 3 or higher adverse events occurred in 19% with 7% due to infections. These promising results require confirmation in a randomized clinical trial.
维奈托克对复发/难治性 t(11;14)多发性骨髓瘤有效,因此有必要在轻链淀粉样变性 (AL) 中进行研究。本回顾性队列包括来自美国和欧洲 14 个中心的 43 例先前治疗过的 AL 患者。31 例患者存在 t(11;14),11 例不存在,1 例 t(11;14)状态未知。患者接受至少一个 21 或 28 天周期的维奈托克治疗方案;先前治疗的中位数为三种。所有患者的血液学缓解率为 68%;63%达到 VGPR/CR。t(11;14)患者的血液学缓解率更高(81%对 40%),VGPR/CR 率更高(78%对 30%,比值比:0.12,95%CI 0.02-0.62)。对于未分层队列,中位无进展生存期(PFS)为 31.0 个月,中位总生存期(OS)未达到(NR)。对于 t(11;14),中位 PFS 为 NR,对于非 t(11;14),中位 PFS 为 6.7 个月(HR:0.14,95%CI 0.04-0.53)。纳入年龄、性别、先前治疗线数和疾病分期的多变量分析表明,t(11;14)患者进展或死亡的风险降低。两个亚组的中位 OS 均未达到。器官缓解率为 38%;大多数缓解者存在 t(11;14)。3 级或更高的不良事件发生率为 19%,其中 7%归因于感染。这些有希望的结果需要在随机临床试验中得到证实。