多发性骨髓瘤的生物复发:西班牙真实世界中的治疗结果和治疗策略

IF 7.6 2区 医学 Q1 HEMATOLOGY
HemaSphere Pub Date : 2024-07-04 DOI:10.1002/hem3.81
Adrián Alegre, Mercedes Gironella, Fernando Escalante, Juan M. Bergua, Carmen Martínez-Chamorro, Aurelio López, Esther González, Abelardo Bárez, Nieves Somolinos, Ernesto P. Persona, Alexia S. Cabrera, Alfons Soler, Belén I. Rodríguez, Joaquín M. López, Yolanda González, Verónica C. Giménez, Antonia Sampol, Carolina Muñoz, David Vilanova, Marta Durán, Carlos Fernández de Larrea, Spanish Myeloma Group (GEM_PETHEMA)
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引用次数: 0

摘要

关于复发/难治性多发性骨髓瘤(RRMM)患者在生物学复发/进展(BR)后开始治疗的最佳时机的建议尚不明确。这项观察性、前瞻性、多中心登记研究旨在根据西班牙RRMM成年患者的常规治疗方法,评估在生物复发与无症状临床复发(ClinR)时开始治疗对进展时间(TTP)的影响。患者既往接受过两次或两次以下的治疗,且至少有过一次部分应答。记录了基线特征和治疗结果,并分析了存活率。根据研究者的标准,在225名患者中,110人接受了BR治疗(TxBR组),115人接受了ClinR治疗(TxClinR组)。与 TxClinR 组相比,TxBR 组 ECOG 较高、既往未完全缓解 (CR) 和第二次复发的患者比例明显较高。与 TxBR 组相比,TxClinR 组的疗效(包括 TTP)有所改善。与 TxBR 组(32.5 个月)相比,TxClinR 组的无进展生存期(56.2 个月)有所延长(p = 0.0137),中位总生存期也有所延长(p = 0.0897)。与非 CR 复发患者(32.9 个月)和第二次复发患者(25.2 个月)相比,CR 复发患者(50.4 个月)和第一次复发患者(38.7 个月)的中位 TTP 明显更长。对于预后不良的RRMM患者,医生似乎更早开始治疗。先前对抗MM治疗的反应和先前的治疗次数被认为是预后因素,而从CR复发和首次复发与较长的进展时间有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Biological relapse in multiple myeloma: Outcome and treatment strategies in a Spanish real-world setting

Biological relapse in multiple myeloma: Outcome and treatment strategies in a Spanish real-world setting

Recommendations regarding the best time to start treatment in patients with relapsed/refractory multiple myeloma (RRMM) after biological relapse/progression (BR) are unclear. This observational, prospective, multicenter registry aimed to evaluate the impact on time to progression (TTP) of treatment initiation at BR versus at symptomatic clinical relapse (ClinR) based on the Spanish routine practice in adult patients with RRMM. Patients had two or less previous treatment lines and at least one previous partial response. Baseline characteristics and treatment outcomes were recorded, and survival was analyzed. Of 225 patients, 110 were treated at BR (TxBR group) and 115 at ClinR (TxClinR group) according to the investigators' criteria. The proportion of patients with higher ECOG, previous noncomplete remission (CR), and second relapse were significantly higher in the TxBR group compared to the TxClinR group. TheTxClinR group showed improved outcomes, including TTP, compared to the TxBR group. Progression-free survival increased in the TxClinR group (56.2 months) compared to the TxBR group (32.5 months) (p = 0.0137), and median overall survival also increased (p = 0.0897). Median TTP was significantly longer in patients relapsing from a CR (50.4 months) and in their first relapse (38.7 months) compared to those relapsing from a non-CR response (32.9 months) and in their second relapse (25.2 months). Physicians seemed to start treatment earlier in RRMM patients with poor prognosis features. Previous responses to anti-MM treatment and the number of prior treatment lines were identified as prognosis factors, whereby relapse from CR and first relapse were associated with a longer time to progression.

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来源期刊
HemaSphere
HemaSphere Medicine-Hematology
CiteScore
6.10
自引率
4.50%
发文量
2776
审稿时长
7 weeks
期刊介绍: HemaSphere, as a publication, is dedicated to disseminating the outcomes of profoundly pertinent basic, translational, and clinical research endeavors within the field of hematology. The journal actively seeks robust studies that unveil novel discoveries with significant ramifications for hematology. In addition to original research, HemaSphere features review articles and guideline articles that furnish lucid synopses and discussions of emerging developments, along with recommendations for patient care. Positioned as the foremost resource in hematology, HemaSphere augments its offerings with specialized sections like HemaTopics and HemaPolicy. These segments engender insightful dialogues covering a spectrum of hematology-related topics, including digestible summaries of pivotal articles, updates on new therapies, deliberations on European policy matters, and other noteworthy news items within the field. Steering the course of HemaSphere are Editor in Chief Jan Cools and Deputy Editor in Chief Claire Harrison, alongside the guidance of an esteemed Editorial Board comprising international luminaries in both research and clinical realms, each representing diverse areas of hematologic expertise.
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