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在德国,接受蛋白酶体抑制剂治疗的复发性/难治性多发性骨髓瘤患者的特征和结局。

Patient Characteristics and Outcomes of Relapsed/Refractory Multiple Myeloma in Patients Treated with Proteasome Inhibitors in Germany.

机构信息

Oncology Cologne, Center for Hematology and Oncology, Cologne, Germany,

Health Economics, Amgen Ltd., Uxbridge, United Kingdom.

出版信息

Oncol Res Treat. 2020;43(9):449-459. doi: 10.1159/000509018. Epub 2020 Jul 21.

Abstract

INTRODUCTION

Real-world data reflects treatments and outcomes in clinical practice in contrast with controlled clinical trials. This study evaluates real-life multiple myeloma (MM) patients receiving proteasome inhibitor (PI)-based treatments in the second or third therapy line in 2017 in Germany.

METHODS

This is a retrospective chart review on adult relapsed/refractory MM patients treated with ≥1 dose of a PI-based regimen in either the second or the third line of therapy. Participating physicians had ≥3 years of clinical experience in treating symptomatic MM patients and used PI according to the label.

RESULTS

Distinct patient profiles for each PI-based regimen emerged. Younger, fitter, transplant-eligible patients received novel PI triplets such as carfilzomib in combination with lenalidomide and dexamethasone (KRd) or IRd. Patients receiving lenalidomide in first-line therapy mostly received lenalidomide-free regimens in second-line therapy. In high-risk patients, no clear treatment patterns could be ascertained. The complete response rates were highest with KRd (13.0%), followed by carfilzomib in combination with dexamethasone (Kd) (5.7%) and bortezomib (4.8%). The very good partial response rates were highest with IRd (76.9%), followed by KRd (53.7%), Kd (25.7%), and bortezomib (20.5%). None of the KRd- or IRd-treated patients responded below a partial response.

DISCUSSION/CONCLUSION: Clear patient profiles for each PI type were observed. In second-line therapy, younger, fitter, transplant-eligible patients received novel-PI-based triplets, e.g., KRd or IRd. Patients treated with lenalidomide in first-line therapy mostly received lenalidomide-sparing regimens in second-line therapy. In high-risk patients no clear treatment patterns could be ascertained due to the limited sample size.

摘要

简介

真实世界的数据反映了临床实践中的治疗方法和结果,与对照临床试验形成对比。本研究评估了 2017 年在德国接受基于蛋白酶体抑制剂(PI)的治疗的二线或三线治疗的多发性骨髓瘤(MM)患者的真实世界数据。

方法

这是一项回顾性图表审查,纳入了接受≥1 剂基于 PI 方案治疗的二线或三线治疗的成年复发性/难治性 MM 患者。参与研究的医生具有≥3 年治疗有症状 MM 患者的临床经验,并根据标签使用 PI。

结果

每种基于 PI 的方案都出现了不同的患者特征。年轻、健康、适合移植的患者接受了新型 PI 三联疗法,如卡非佐米联合来那度胺和地塞米松(KRd)或 IRd。在一线治疗中接受来那度胺治疗的患者,在二线治疗中大多接受了无来那度胺的方案。在高危患者中,无法确定明确的治疗模式。KRd 的完全缓解率最高(13.0%),其次是卡非佐米联合地塞米松(Kd)(5.7%)和硼替佐米(4.8%)。IRd 的非常好的部分缓解率最高(76.9%),其次是 KRd(53.7%)、Kd(25.7%)和硼替佐米(20.5%)。没有接受 KRd 或 IRd 治疗的患者的缓解率低于部分缓解。

讨论/结论:观察到每种 PI 类型的患者特征明显。在二线治疗中,年轻、健康、适合移植的患者接受了新型 PI 三联疗法,例如 KRd 或 IRd。在一线治疗中接受来那度胺治疗的患者,在二线治疗中大多接受了无来那度胺的方案。在高危患者中,由于样本量有限,无法确定明确的治疗模式。

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