De Novellis Danilo, Palmieri Salvatore, Rocco Stefano, Derudas Daniele, Della Pepa Roberta, Roccotelli Daniela, Esposito Daniela, Masucci Chiara, Gigliotta Emilia, Barone Maria Lucia, Morelli Emanuela, Lazzaro Antonio, Bianco Rosario, Accardi Fabrizio, Marano Luana, Bonanni Matteo, Della Corte Anna Maria, Serio Bianca, Urciuoli Eleonora, Rizzo Michela, Fontana Raffaele, Arcamone Manuela, Iula Rossella, Dandolo Anna, Leone Aldo, Rascato Maria Gabriella, Di Perna Maria, Falcone Antonietta Pia, Morello Lucia, Marcacci Gianpaolo, Rodolfo Nunziata Giuseppe, Frigeri Ferdinando, Califano Catello, Carella Angelo Michele, Risitano Antonio Maria, Annunziata Mario, Pane Fabrizio, Giudice Valentina, Botta Cirino, Selleri Carmine
Hematology and Transplant Center, University Hospital"San Giovanni di Dio e Ruggi d'Aragona", Salerno, Italy.
Department of Medicine, Surgery and Dentistry"Scuola Medica Salernitana", University of Salerno, Baronissi, Italy.
Ann Hematol. 2025 Sep 10. doi: 10.1007/s00277-025-06572-y.
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.
功能性高危多发性骨髓瘤(FHRMM)仍然是一个具有挑战性的疾病实体,预后较差且生存期有限,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回顾性研究中,我们调查了总共62例FHRMM患者的临床特征和预后,这些患者先前接受了基于达雷妥尤单抗的一线四联方案治疗,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%的患者达到非常好的部分缓解(VGPR)或更好。同样,未达到中位无进展生存期(PFS),估计12个月PFS率为54%,中位总生存期(OS)为12个月OS率为72%。与较差PFS相关的因素包括髓外疾病、先前使用来那度胺维持治疗、缺乏ASCT巩固治疗、东部肿瘤协作组(ECOG)评分≥2、疾病晚期以及未使用卡非佐米-来那度胺-地塞米松的挽救治疗。总之,由于缺乏标准化的国际指南,达雷妥尤单抗-硼替佐米-沙利度胺-地塞米松诱导治疗后FHRMM的二线管理极具挑战性且各中心存在差异。基于卡非佐米的方案显示出一些临床益处,尤其是在未使用过来那度胺的患者中;然而,在FHRMM人群中,其预后仍然不理想,这些患者可能从更早期治疗线使用的新型疗法中获益。需要更大规模的前瞻性试验来优化FHRMM的临床管理并改善患者预后。