Institut universitaire d'hémato-oncologie et de thérapie cellulaire, Hôpital Maisonneuve-Rosemont, Montréal, Québec, Canada.
Université de Montréal, Montréal, Québec, Canada.
Cancer Med. 2024 Nov;13(21):e70332. doi: 10.1002/cam4.70332.
Young patients ≤ 50 years old with multiple myeloma (MM) account for about 10% of cases and are underrepresented in the literature.
We explored disease characteristics, treatments, and outcomes following modern therapies of young MM patients using the Canadian Myeloma Research Group (CMRG) database. We included 493 patients ≤ 50 years old diagnosed with MM or plasma cell leukemia without concurrent amyloidosis or POEMS syndrome from January 1, 2010, to July 1, 2022.
The median age was 46 years old (range: 25.6-50). Most patients fell into the R-ISS II category (72.7%), and 24.1% had high-risk cytogenetics. The majority of patients (89.9%) received a proteasome inhibitor-based first-line treatment, 92.1% received a stem cell transplant, and 65.6% had maintenance therapy post-autologous stem cell transplant (ASCT). Median follow-up from initial treatment to patients' last follow-up was 48.5 (range: 0-155) months. Median progression-free survival (PFS) was 45.0 months (95% CI: 40.2-50.0). Maintenance therapy post-ASCT improved median PFS to 52.3 months (95% CI: 43.1-68.2), compared to 23.6 months (95% CI: 20.0-34.8) without maintenance [p < 0.001].
Although the overall survival has not yet been reached in this young population, our reported median PFS of only 45 months highlights the urgent need to develop innovative treatments to induce more profound and durable responses.
50 岁以下的多发性骨髓瘤(MM)年轻患者占所有病例的 10%左右,但在文献中代表性不足。
我们使用加拿大骨髓瘤研究组(CMRG)数据库研究了年轻 MM 患者在接受现代治疗后的疾病特征、治疗方法和结局。我们纳入了 2010 年 1 月 1 日至 2022 年 7 月 1 日期间诊断为 MM 或浆细胞白血病、无同时性淀粉样变性或 POEMS 综合征的 493 例≤50 岁的患者。
中位年龄为 46 岁(范围:25.6-50)。大多数患者属于 R-ISS II 类别(72.7%),24.1%有高危细胞遗传学特征。大多数患者(89.9%)接受了基于蛋白酶体抑制剂的一线治疗,92.1%接受了干细胞移植,65.6%在自体干细胞移植(ASCT)后接受了维持治疗。从初始治疗到患者最后一次随访的中位随访时间为 48.5 个月(范围:0-155)。中位无进展生存期(PFS)为 45.0 个月(95%CI:40.2-50.0)。ASCT 后维持治疗使中位 PFS 提高至 52.3 个月(95%CI:43.1-68.2),而未进行维持治疗的患者中位 PFS 为 23.6 个月(95%CI:20.0-34.8)[p<0.001]。
尽管该年轻人群的总生存尚未达到,但我们报告的中位 PFS 仅为 45 个月,这突出表明迫切需要开发创新治疗方法以诱导更深刻和持久的反应。