Liang Dong, Yan Yurong, Wang Qiaoli, Bai Shenrui, Xu Weiling, Feng Demei, Bu Yuying, Zeng Min, Nie Xiaomiao, Feng Yuan, Chen Xiaoqin, Xia Zhongjun, Liang Yang, Jin Fengyan, Wang Hua
State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Hematology Department, First Hospital of Jilin University, Changchun, China.
Hematol Oncol. 2025 Jul;43(4):e70112. doi: 10.1002/hon.70112.
This study aimed to discuss the clinical outcomes of extramedullary multiple myeloma in the era of novel agents, based on the largest dataset regarding extramedullary multiple myeloma in China. This study included 597 patients without extramedullary disease (EMD) (non-EMD), 324 with extramedullary bone-related disease (EMB) and 138 with de novo extramedullary extraosseous disease (EME). There were no significant differences in overall survival (OS, p = 0.638) or progression-free survival (PFS, p = 0.195) between non-EMD and EMB patients. However, de novo EME patients exhibited significantly worse OS (p < 0.01) and PFS (p < 0.01) compared to both EMB and non-EMD groups. Among non-EMD and EMB patients, those with ≥ 2 high-risk cytogenetic abnormalities (HRA) experienced extremely poor prognoses, categorizing them as ultra-high-risk multiple myeloma. Similarly, de novo EME patients with ≥ 1 HRA demonstrated very poor outcomes and should also be considered ultra-high risk. Notably, single transplantation was shown to mitigate the adverse prognosis of de novo EME patients. Furthermore, the daratumumab bortezomib lenalidomide dexamethasone (DVRD) quadruplet regimen showed potential as effective frontline therapies for de novo EME patients, offering hope for improved treatment outcomes in this challenging subgroup. These findings suggest that de novo EME represents an extremely poor prognosis and should be treated as a distinct entity within the multiple myeloma population. Furthermore, the results indicate that EMB may need to be excluded from the current EMD definition to better delineate these subgroups and guide therapeutic strategies.
本研究旨在基于中国关于髓外多发性骨髓瘤的最大数据集,探讨新型药物时代髓外多发性骨髓瘤的临床结局。本研究纳入了597例无髓外疾病(EMD)的患者(非EMD组)、324例有髓外骨相关疾病(EMB)的患者和138例初发髓外骨外疾病(EME)的患者。非EMD组和EMB组患者的总生存期(OS,p = 0.638)或无进展生存期(PFS,p = 0.195)无显著差异。然而,与EMB组和非EMD组相比,初发EME患者的OS(p < 0.01)和PFS(p < 0.01)明显更差。在非EMD组和EMB组患者中,那些有≥2种高危细胞遗传学异常(HRA)的患者预后极差,将他们归类为超高危多发性骨髓瘤。同样,有≥1种HRA的初发EME患者预后也非常差,也应被视为超高危。值得注意的是,单次移植被证明可减轻初发EME患者的不良预后。此外,达雷妥尤单抗、硼替佐米、来那度胺、地塞米松(DVRD)四联方案显示出作为初发EME患者有效一线治疗方案的潜力,为改善这一具有挑战性亚组的治疗结局带来了希望。这些发现表明,初发EME代表预后极差的情况,应作为多发性骨髓瘤人群中的一个独特实体进行治疗。此外,结果表明可能需要将EMB从当前的EMD定义中排除,以更好地划分这些亚组并指导治疗策略。