Biran Noa, Rowley Scott D, Vesole David H, Zhang Shijia, Donato Michele L, Richter Joshua, Skarbnik Alan P, Pecora Andrew, Siegel David S
John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, New Jersey.
John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, New Jersey.
Biol Blood Marrow Transplant. 2016 Dec;22(12):2165-2171. doi: 10.1016/j.bbmt.2016.08.017. Epub 2016 Aug 31.
Escalating doses of bortezomib with high-dose melphalan was evaluated as as a conditioning regimen for autologous stem cell transplantation (ASCT) in patients with relapsed or refractory multiple myeloma (MM). MM patients with less than a partial remission (PR) (or 50% reduction) compared to their pretransplantation paraprotein parameters after a prior ASCT with melphalan conditioning, or who were in relapse after a prior autologous transplantation, were eligible for study. Bortezomib was dose escalated in steps of 1, 1.3, and 1.6 mg/m (3 × 3 design) on days -4 and -1 before transplantation with melphalan 200 mg/m given on day -2. Thirty-two patients were enrolled: 12 in the phase I dose escalation phase and an additional 20 in phase II to gain additional experience with the regimen. Twenty-four (75%) patients were Durie Salmon stage III, and 12 (37.5%) had >2 prior lines of therapy. The overall response rate (≥PR) was 44% with 22% complete remission. Two-year overall survival and progression-free survival were 76% and 39%, respectively, with a median follow-up of 31.7 months. The most common grade 3 and 4 nonhematologic adverse events were neutropenic fever (25%), nausea (18.8%), and mucositis (9.4%). Serious adverse events included intensive care unit admission (9.4%), seizure (3.1%), prolonged diarrhea (3.1%), and Guillain-Barre syndrome (3.1%). Two patients (6%) died of sepsis. There was no emergent peripheral neuropathy nor increase in any pre-existing peripheral neuropathy. The addition of bortezomib to melphalan as conditioning for salvage ASCT was well tolerated. More importantly, it can provide durable remission for patients who have a suboptimal response to prior single-agent melphalan conditioning for ASCT, without requiring a reduction in the dose of melphalan. Larger randomized prospective studies to determine the effect of combination conditioning are being conducted.
对复发或难治性多发性骨髓瘤(MM)患者,评估硼替佐米剂量递增联合大剂量美法仑作为自体干细胞移植(ASCT)预处理方案的效果。在接受过美法仑预处理的ASCT后,与移植前副蛋白参数相比未达到部分缓解(PR)(或降低50%)的MM患者,或既往自体移植后复发的患者符合研究条件。在移植前第-4天和-1天,硼替佐米剂量按1、1.3和1.6mg/m逐步递增(3×3设计),第-2天给予美法仑200mg/m。共纳入32例患者:12例进入I期剂量递增阶段,另外20例进入II期以积累该方案更多经验。24例(75%)患者为Durie Salmon III期,12例(37.5%)既往接受过>2线治疗。总缓解率(≥PR)为44%,完全缓解率为22%。两年总生存率和无进展生存率分别为76%和39%,中位随访时间为31.7个月。最常见的3级和4级非血液学不良事件为中性粒细胞减少性发热(25%)、恶心(18.8%)和黏膜炎(9.4%)。严重不良事件包括入住重症监护病房(9.4%)、癫痫发作(3.1%)、长期腹泻(3.1%)和吉兰-巴雷综合征(3.1%)。2例患者(6%)死于败血症。未出现新发性周围神经病变,也未使任何既往存在的周围神经病变加重。硼替佐米联合美法仑作为挽救性ASCT的预处理耐受性良好。更重要的是,对于既往接受单药美法仑预处理的ASCT疗效欠佳的患者,该方案可提供持久缓解,且无需降低美法仑剂量。正在进行更大规模的随机前瞻性研究以确定联合预处理的效果。