一项意大利现实世界的多中心研究,对接受二线治疗的难治性/复发性功能性高风险多发性骨髓瘤患者进行了研究。

IF 2.4 3区 医学 Q2 HEMATOLOGY
Danilo De Novellis, Salvatore Palmieri, Stefano Rocco, Daniele Derudas, Roberta Della Pepa, Daniela Roccotelli, Daniela Esposito, Chiara Masucci, Emilia Gigliotta, Maria Lucia Barone, Emanuela Morelli, Antonio Lazzaro, Rosario Bianco, Fabrizio Accardi, Luana Marano, Matteo Bonanni, Anna Maria Della Corte, Bianca Serio, Eleonora Urciuoli, Michela Rizzo, Raffaele Fontana, Manuela Arcamone, Rossella Iula, Anna Dandolo, Aldo Leone, Maria Gabriella Rascato, Maria Di Perna, Antonietta Pia Falcone, Lucia Morello, Gianpaolo Marcacci, Nunziata Giuseppe Rodolfo, Ferdinando Frigeri, Catello Califano, Angelo Michele Carella, Antonio Maria Risitano, Mario Annunziata, Fabrizio Pane, Valentina Giudice, Cirino Botta, Carmine Selleri
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引用次数: 0

摘要

功能性高风险多发性骨髓瘤(FHRMM)仍然是一个具有挑战性的实体,预后差,生存期有限,对于复发/难治性患者的最佳二线治疗策略尚无国际共识。在这项多中心真实世界的回顾性研究中,我们调查了62例FHRMM患者的临床特征和结果,这些患者之前接受过一线基于daratumumab的四联体方案治疗,或在一线自体干细胞移植(ASCT)后12个月内复发。在我们的队列中,总体缓解率为61%,42%的患者获得了非常好的部分缓解(VGPR)或更好。同样,中位无进展生存期(PFS)未达到,估计12个月PFS率为54%,中位总生存期(OS)为72%。与PFS恶化相关的因素包括髓外疾病、既往来那度胺维持、缺乏ASCT巩固、ECOG评分≥2、疾病晚期和不使用卡非佐米-来那度胺-地塞米松的补救性治疗。总之,由于缺乏标准化的国际指南,达拉图单抗-博尔替佐米-沙利度胺-地塞米松诱导后FHRMM的二线管理是极具挑战性和各中心差异的。以卡非佐米为基础的方案显示出一些临床益处,特别是在lenalidomide-naïve患者中;然而,FHRMM人群的结果仍然不理想,他们可能从早期治疗线的新疗法中受益。需要更大规模的前瞻性试验来优化FHRMM临床管理并改善患者预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Italian real-world multicenter study of patients with refractory/relapsed functional high-risk multiple myeloma patients treated with second-line therapies.

Functional high risk multiple myeloma (FHRMM) remains a challenging entity with poor outcomes and limited survival, and there is no international consensus on optimal second-line therapeutic strategies in relapsed/refractory patients. In this multicenter real-world retrospective study, we investigated clinical characteristics and outcomes of a total of 62 FHRMM patients previously treated with a first-line daratumumab-based quadruplet regimen or who relapsed within 12 months after frontline autologous stem cell transplantation (ASCT). In our cohort, the overall response rate was 61%, with 42% of patients achieving a very good partial response (VGPR) or better. Similarly, median progression-free survival (PFS) was not reached with an estimated 12-month PFS rate of 54%, as well as median overall survival (OS) with a 12-month OS rate of 72%. Factors associated with worse PFS included extramedullary disease, prior lenalidomide maintenance, lack of ASCT consolidation, an ECOG score ≥ 2, advanced disease stage, and salvage therapy without carfilzomib-lenalidomide-dexamethasone. In conclusion, second-line management of FHRMM following daratumumab-bortezomib-thalidomide-dexamethasone induction is highly challenging and variable across centers, due to the lack of standardized international guidelines. Carfilzomib-based regimens demonstrated some clinical benefits, especially in lenalidomide-naïve patients; however, outcomes remained suboptimal in FHRMM population who may benefit from novel therapies administered as earlier treatment lines. Larger prospective trials are needed to optimize FHRMM clinical management and improve patient outcomes.

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来源期刊
Annals of Hematology
Annals of Hematology 医学-血液学
CiteScore
5.60
自引率
2.90%
发文量
304
审稿时长
2 months
期刊介绍: Annals of Hematology covers the whole spectrum of clinical and experimental hematology, hemostaseology, blood transfusion, and related aspects of medical oncology, including diagnosis and treatment of leukemias, lymphatic neoplasias and solid tumors, and transplantation of hematopoietic stem cells. Coverage includes general aspects of oncology, molecular biology and immunology as pertinent to problems of human blood disease. The journal is associated with the German Society for Hematology and Medical Oncology, and the Austrian Society for Hematology and Oncology.
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