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一项关于递增剂量硼替佐米联合大剂量美法仑作为多发性骨髓瘤患者挽救性自体外周血干细胞移植预处理方案的I/II期研究。

A Phase I/II Study of Escalating Doses of Bortezomib in Conjunction with High-Dose Melphalan as a Conditioning Regimen for Salvage Autologous Peripheral Blood Stem Cell Transplantation in Patients with Multiple Myeloma.

作者信息

Biran Noa, Rowley Scott D, Vesole David H, Zhang Shijia, Donato Michele L, Richter Joshua, Skarbnik Alan P, Pecora Andrew, Siegel David S

机构信息

John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, New Jersey.

John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, New Jersey.

出版信息

Biol Blood Marrow Transplant. 2016 Dec;22(12):2165-2171. doi: 10.1016/j.bbmt.2016.08.017. Epub 2016 Aug 31.

Abstract

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.

摘要

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。

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