来那度胺难治性多发性骨髓瘤患者的特征和预后:达拉曲单抗临床试验患者个体层面数据分析。

IF 7.6 1区 医学 Q1 ONCOLOGY
Kwee Yong, Hermann Einsele, Jordan M Schecter, Tito Roccia, William Deraedt, Nikoletta Lendvai, Ana Slaughter, Carolina Lonardi, Kaitlyn Connors, Keqin Qi, Anil Londhe, Robin Carson, Akshay Kharat, Patricia Cost, Satish Valluri, João Mendes, Lida Pacaud, Nitin Patel, Erika Florendo, Binod Dhakal
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引用次数: 0

摘要

背景:蛋白酶体抑制剂(PIs)和来那度胺作为新诊断的多发性骨髓瘤(MM)治疗药物的引入,导致来那度胺难治性患者人数增加。目前关于这一难以治疗人群的治疗方法和疗效的数据十分有限:分析了多项达拉曲单抗研究治疗组的患者个体数据,包括 APOLLO、CASTOR、CANDOR、EQUULEUS、ALCYONE、MAIA、GRIFFIN、POLLUX 和 CASSIOPEIA。纳入的患者均为PI暴露和来那度胺难治患者,接受过1-3种既往疗法(LOT),且东方合作肿瘤组织(Eastern Cooperative Oncology Group)检查结果显示其表现为阳性:在4764名患者中,有915名患者(既往LOT,1次[n=114];2次[n=462];3次[n=339])符合纳入标准。随访时间中位数为 29-7 个月(28-0-31-7 个月)。总体反应率为 55-4%。估计中位 TTNT 为 9-7 个月,中位 PFS 为 10-0 个月,中位 OS 为 27-5 个月。随着先前LOT次数的增加,应答率和PFS均有所下降。反应、TTNT、PFS和OS的预后因素包括国际分期系统分期、基线浆细胞瘤状态、基线血红蛋白、抗CD38难治性状态和细胞遗传学风险状态:来那度胺难治性患者既往接受过1-3次LOT治疗,其PFS和OS均较差,且每增加一次LOT治疗,PFS和OS通常都会恶化,这凸显了该人群对新的有效治疗方法的需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characteristics and outcomes in patients with lenalidomide-refractory multiple myeloma treated with 1-3 prior lines of therapy: Analysis of individual patient-level data from daratumumab clinical trials.

Background: The introduction of proteasome inhibitors (PIs) and lenalidomide as treatment for newly diagnosed multiple myeloma (MM) has led to an increased population of lenalidomide-refractory patients. Limited data are available characterizing current treatments and outcomes in this difficult-to-treat population.

Methods: Individual patient-level data were analyzed from the treatment arms of multiple daratumumab studies, including APOLLO, CASTOR, CANDOR, EQUULEUS, ALCYONE, MAIA, GRIFFIN, POLLUX, and CASSIOPEIA. Included patients were PI exposed and lenalidomide refractory, received 1-3 prior lines of therapy (LOT), and had an Eastern Cooperative Oncology Group performance status < 2. Treatments and outcomes were analyzed by number of prior LOT in the lenalidomide-refractory population. Time to next treatment (TTNT), progression-free survival (PFS), and overall survival (OS) were estimated using the Kaplan-Meier method.

Findings: Out of 4764 patients, 915 patients (prior LOT, one [n = 114]; two [n = 462]; three [n = 339]) met inclusion criteria. Median follow-up was 29·7 months (range 28·0-31·7). The overall response rate was 55·4 %. Estimated median TTNT was 9·7 months, median PFS was 10·0 months, and median OS was 27·5 months. Response rates and PFS decreased as number of prior LOT increased. Prognostic factors for response, TTNT, PFS, and OS included International Staging System stage, baseline plasmacytoma status, baseline hemoglobin, anti-CD38-refractory status, and cytogenetic risk status.

Interpretation: Lenalidomide-refractory patients treated with 1-3 prior LOT have poor PFS and OS, which generally worsen with each additional LOT, highlighting the need for new and effective treatments for this population.

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来源期刊
European Journal of Cancer
European Journal of Cancer 医学-肿瘤学
CiteScore
11.50
自引率
4.80%
发文量
953
审稿时长
23 days
期刊介绍: The European Journal of Cancer (EJC) serves as a comprehensive platform integrating preclinical, digital, translational, and clinical research across the spectrum of cancer. From epidemiology, carcinogenesis, and biology to groundbreaking innovations in cancer treatment and patient care, the journal covers a wide array of topics. We publish original research, reviews, previews, editorial comments, and correspondence, fostering dialogue and advancement in the fight against cancer. Join us in our mission to drive progress and improve outcomes in cancer research and patient care.
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