多发性骨髓瘤患者发生第二原发恶性肿瘤的结果。
Outcome of Second Primary Malignancies Developing in Multiple Myeloma Patients.
发表日期:2023 Sep 01
作者:
Irit Avivi, David H Vesole, Julio Davila-Valls, Lidia Usnarska-Zubkiewicz, Magdalena Olszewska-Szopa, Vibor Milunovic, Bartłomiej Baumert, Bogumiła Osękowska, Anna Kopińska, Massimo Gentile, Borja Puertas-Martinez, Paweł Robak, Edvan Crusoe, Luis Gerardo Rodriguez-Lobato, Małgorzata Gajewska, Gergely Varga, Michel Delforge, Yael Cohen, Alessandro Gozzetti, Camila Pena, Chaim Shustik, Gabor Mikala, Klara Zalac, H Denis Alexander, Peter Barth, Katja Weisel, Joaquín Martínez-López, Anna Waszczuk-Gajda, Mateusz Krzystański, Artur Jurczyszyn
来源:
Stem Cell Research & Therapy
摘要:
多发性骨髓瘤(MM)患者患有二次原发性恶性肿瘤(SMPs)的风险增加。本跨国级“真实世界”回顾性研究分析了患有SMPs的MM患者的特征和结果。共分析了165名患者:男性占62.4%;有先前癌症病史者占8.5%;其中113名患者出现实体SMPs,主要为≥2期;52名患者出现血液系统SMP(血液-SPM),主要为MDS/AML。血液-SPM患者年龄较轻(p = 0.05),先前进行过自体干细胞移植(p = 0.012)的频率较高。年龄较大(>65岁)且接受过更多治疗的患者发生SMP的时间较短。在SPM检测时有100名患者正在接受积极治疗。52名患者停止治疗,15名患者替换其他抗MM疗法,33名患者继续进行治疗。停止治疗在被诊断为血液-SPM的患者中占主导地位(76%)。SPM检测后的中位生存时间为8.5个月,死亡的主要原因是SPM。恶劣的ECOG状态预示着较短的生存时间(PS 3 对比 0,HR = 5.74,2.32-14.21,p < 0.001),而血红蛋白正常水平的预测值HR = 0.43,0.19-0.95,p = 0.037)预示着较长的生存时间。随着生存时间的持续改善,更多MM患者可能会出现SPM。SPM诊断后的生存时间较短,因此,频繁的监测和早期检测对改善结局至关重要。
There is an increased risk of second primary malignancies (SMPs) in patients with multiple myeloma (MM). This multinational 'real-world' retrospective study analyzed the characteristics and outcomes of MM patients that developed SPMs.165 patients were analyzed: 62.4% males; 8.5% with a prior cancer; 113 with solid SPMs, mainly ≥stage 2; and 52 with hematological SPM (hemato-SPM), mainly MDS/AML. Patients with hemato-SPM were younger (p = 0.05) and more frequently had a prior AutoHCT (p = 0.012). The time to SPM was shorter in the older (>65 years) and more heavily pretreated patients. One hundred patients were actively treated at the time of SPM detection. Treatment was discontinued in 52, substituted with another anti-MM therapy in 15, and continued in 33 patients. Treatment discontinuation was predominant in the patients diagnosed with hemato-SPM (76%). The median OS following SPM detection was 8.5 months, and the main cause of death was SPM. A poor ECOG status predicted a shorter OS (PS 3 vs. 0, HR = 5.74, 2.32-14.21, p < 0.001), whereas a normal hemoglobin level (HR = 0.43, 0.19-0.95, p = 0.037) predicted longer OS.With the continuing improvement in OS, a higher proportion of MM patients might develop SPM. The OS following SPM diagnosis is poor; hence, frequent surveillance and early detection are imperative to improve outcomes.