Department of Hematology, Kyoto University Hospital, Kyoto, Japan.
Division of Hematology, Department of Internal Medicine, Aichi Medical University School of Medicine, Nagakute, Japan.
Cancer Sci. 2021 Dec;112(12):5034-5045. doi: 10.1111/cas.15163. Epub 2021 Oct 26.
New drugs for multiple myeloma (MM) have dramatically improved patients' overall survival (OS). Autologous stem cell transplantation (ASCT) remains the mainstay for transplant-eligible MM patients. To investigate whether the post-ASCT prognosis of MM patients has been improved by new drugs, we undertook a retrospective observational analysis using the Transplant Registry Unified Management Program database in Japan. We analyzed 7323 patients (4135 men and 3188 women; median age, 59 years; range 16-77 years) who underwent upfront ASCT between January 2007 and December 2018. We categorized them by when they underwent ASCT according to the drugs' introduction in Japan: group 1 (2007-2010), group 2 (2011-2016), and group 3 (2017-2018). We compared the groups' post-ASCT OS. The 2-year OS rates (95% confidence interval [CI]) of groups 1, 2, and 3 were 85.8% (84.1%-87.4%), 89.1% (88.0%-90.1%), and 92.3% (90.0%-94.2%) (P < .0001) and the 5-year OS (95% CI) rates were 64.9% (62.4%-67.3%), 71.6% (69.7%-73.3%), and not applicable, respectively (P < .0001). A multivariate analysis showed that the post-ASCT OS was superior with these factors: age less than 65 years, performance status 0/1, low International Staging System (ISS) stage, receiving SCT for 180 days or less post-diagnosis, better treatment response pre-ASCT, later year of ASCT, and receiving SCT twice. A subgroup analysis showed poor prognoses for the patients with unfavorable karyotype and poor treatment response post-ASCT. The post-ASCT OS has thus improved over time (group 1 < 2 < 3) with the introduction of new drugs for MM. As the prognosis of high-risk-karyotype patients with ISS stage III remains poor, their treatment requires improvement.
新的多发性骨髓瘤 (MM) 药物显著改善了患者的总生存期 (OS)。自体干细胞移植 (ASCT) 仍然是适合移植的 MM 患者的主要治疗方法。为了研究新药物是否改善了 ASCT 后 MM 患者的预后,我们使用日本移植登记统一管理计划数据库进行了回顾性观察分析。我们分析了 7323 例 (4135 名男性和 3188 名女性;中位年龄 59 岁;年龄范围 16-77 岁) 于 2007 年 1 月至 2018 年 12 月期间接受首次 ASCT 的患者。我们根据新药物在日本的引入时间将他们分为三组:第 1 组 (2007-2010 年)、第 2 组 (2011-2016 年) 和第 3 组 (2017-2018 年)。我们比较了各组患者 ASCT 后的 OS。第 1、2 和 3 组的 2 年 OS 率 (95%置信区间 [CI]) 分别为 85.8% (84.1%-87.4%)、89.1% (88.0%-90.1%) 和 92.3% (90.0%-94.2%) (P<0.0001),5 年 OS 率 (95%CI) 分别为 64.9% (62.4%-67.3%)、71.6% (69.7%-73.3%) 和不适用,分别 (P<0.0001)。多变量分析显示,以下因素与 ASCT 后 OS 改善相关:年龄小于 65 岁、表现状态 0/1、国际分期系统 (ISS) 分期较低、诊断后接受 SCT 治疗 180 天或更短时间、ASCT 前治疗反应较好、ASCT 年份较晚和接受 SCT 两次。亚组分析显示,不良核型和 ASCT 后治疗反应不佳的患者预后较差。随着 MM 新药的引入,ASCT 后 OS 随时间推移逐渐改善 (第 1 组<第 2 组<第 3 组)。然而,由于 ISS 分期 III 期高危核型患者的预后仍然较差,他们的治疗需要改善。