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自体干细胞移植治疗 17p 缺失型多发性骨髓瘤。

Autologous stem cell transplantation in the treatment of multiple myeloma with 17p deletion.

机构信息

Department of Hematology, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, Bydgoszcz, Poland.

Department of Clinical Hematology, Jagiellonian University Medical College, Kraków, Poland

出版信息

Pol Arch Intern Med. 2020 Feb 27;130(2):106-111. doi: 10.20452/pamw.15139. Epub 2020 Jan 14.

Abstract

INTRODUCTION

Deletion of chromosome 17p [del(17p)] in patients with multiple myeloma is associated with a poor prognosis. High‑dose chemotherapy followed by autologous stem cell transplantation (ASCT) remains the standard of treatment in this population.

OBJECTIVES

The aim of the study was to compare the treatment outcomes with high‑dose chemotherapy and ASCT with standard treatment in patients with del(17p).

PATIENTS AND METHODS

We collected data from 12 Polish centers between 2011 and 2017. The records of 97 patients with p53 deletion were assessed, including 29 individuals treated with ACST and 68 receiving standard treatment alone.

RESULTS

During the follow‑up, 45 patients died and the overall survival (OS) for the whole group was 33 months (range, 1-66 months), with a median progression‑free survival (PFS) of 13 months (range, 1-46 months). The prognostic factors of OS in a multivariable analysis were calcium levels at diagnosis within the reference range (hazard ratio [HR], 0.24; 95% CI, 0.12-0.48) and at least partial remission achieved after the first‑line treatment (HR, 0.25; 95% CI, 0.12-0.51). Treatment with ASCT was an important factor in improving survival (HR, 3.23; 95% CI, 1.52-6.84). Abnormal kidney function at the time of diagnosis reduced the PFS (HR, 0.46; 95% CI, 0.22-0.94). When the analysis was limited only to patients who could be candidates for ASCT, the survival benefit of the procedure was lost (P = 0.21).

CONCLUSIONS

Patients with multiple myeloma with del(17p) do not benefit from high‑dose chemotherapy followed by ACST.

摘要

简介

多发性骨髓瘤患者的 17 号染色体缺失(del(17p))与预后不良相关。大剂量化疗后自体干细胞移植(ASCT)仍然是该人群的标准治疗方法。

目的

本研究旨在比较 del(17p)患者接受大剂量化疗和 ASCT 与标准治疗的治疗结果。

患者和方法

我们收集了 2011 年至 2017 年 12 个波兰中心的数据。评估了 97 例 p53 缺失患者的记录,包括 29 例接受 ASCT 治疗和 68 例单独接受标准治疗的患者。

结果

在随访期间,45 名患者死亡,全组总生存率(OS)为 33 个月(范围 1-66 个月),中位无进展生存率(PFS)为 13 个月(范围 1-46 个月)。多变量分析中 OS 的预后因素包括诊断时钙水平在参考范围内(风险比 [HR],0.24;95%置信区间,0.12-0.48)和一线治疗后至少达到部分缓解(HR,0.25;95%置信区间,0.12-0.51)。ASCT 治疗是改善生存的重要因素(HR,3.23;95%置信区间,1.52-6.84)。诊断时肾功能异常降低了 PFS(HR,0.46;95%置信区间,0.22-0.94)。当仅对可接受 ASCT 的患者进行分析时,该程序的生存获益丧失(P=0.21)。

结论

del(17p)多发性骨髓瘤患者不能从大剂量化疗后接受 ASCT 中获益。

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