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在多发性骨髓瘤中,采用全身骨髓照射和大剂量马法兰序贯进行自体造血细胞移植的 tandem 疗法。

Tandem autologous hematopoietic cell transplantation with sequential use of total marrow irradiation and high-dose melphalan in multiple myeloma.

机构信息

Department of Bone Marrow Transplantation and Onco-Hematology, Maria Skłodowska-Curie National Research Institute of Oncology, Gliwice Branch, Gliwice, Poland.

Department of Radiotherapy, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch, Gliwice, Poland.

出版信息

Bone Marrow Transplant. 2021 Jun;56(6):1297-1304. doi: 10.1038/s41409-020-01181-x. Epub 2020 Dec 18.

Abstract

The goal of this phase II trial was to evaluate safety and efficacy of a tandem autologous hematopoietic cell transplantation (auto-HCT) using sequentially total marrow irradiation (TMI) at the dose of 12 Gy (4 Gy on days -3, -2, and -1) and melphalan 200 mg/m for patients with multiple myeloma (MM). TMI was performed using helical tomotherapy. Additional "boosts" (total 24 Gy) were applied for patients with active lesions as revealed by PET-FDG. Fifty patients with median age 58 years (41-64 years) were included and received tandem auto-HCT. TMI resulted in absolute neutropenia in all patients. Grade 3 infections were reported in 30% patients. Other toxicities were rare. Proportion of patients who achieved at least very good partial response increased from 46% before the first auto-HCT to 82% after tandem transplantation. Complete remission rates changed from 10% to 42%, respectively. The probabilities of overall and progression-free survival at 5 years were 74% and 55%, respectively. No patient died without progression. We conclude that conditioning with TMI ± PET-guided "boosts" represents personalized treatment approach in MM and is characterized by very good toxicity profile. Tandem auto-HCT using TMI in sequence with high-dose melphalan appears safe with encouraging early efficacy.

摘要

这项 II 期试验的目的是评估序贯全骨髓照射(TMI)剂量为 12Gy(-3、-2 和-1 日 4Gy)和 200mg/m 美法仑用于多发性骨髓瘤(MM)患者的串联自体造血细胞移植(auto-HCT)的安全性和疗效。TMI 采用螺旋断层放疗。对于 PET-FDG 显示有活动病灶的患者,额外应用“增敏剂量”(总剂量 24Gy)。50 名中位年龄为 58 岁(41-64 岁)的患者接受了串联自体 HCT。TMI 导致所有患者出现绝对中性粒细胞减少。30%的患者报告了 3 级感染。其他毒性罕见。在第一次自体 HCT 前,至少达到非常好的部分缓解的患者比例为 46%,在串联移植后增加到 82%。完全缓解率分别从 10%增加到 42%。5 年总生存率和无进展生存率分别为 74%和 55%。没有患者无进展死亡。我们得出结论,TMI±PET 引导的“增敏剂量”作为 MM 的个体化治疗方法,具有良好的毒性特征。采用 TMI 序贯大剂量美法仑的串联自体 HCT 安全且早期疗效令人鼓舞。

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