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多发性骨髓瘤患者在新药时代接受自体移植治疗后生存率提高。

Improved survival of multiple myeloma patients treated with autologous transplantation in the modern era of new medicine.

机构信息

Department of Hematology, Kyoto University Hospital, Kyoto, Japan.

Division of Hematology, Department of Internal Medicine, Aichi Medical University School of Medicine, Nagakute, Japan.

出版信息

Cancer Sci. 2021 Dec;112(12):5034-5045. doi: 10.1111/cas.15163. Epub 2021 Oct 26.

DOI:10.1111/cas.15163
PMID:34644446
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8645729/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/403d/8645729/e48077d47d88/CAS-112-5034-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/403d/8645729/e48077d47d88/CAS-112-5034-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/403d/8645729/626b3e01f240/CAS-112-5034-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/403d/8645729/e7eca146722b/CAS-112-5034-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/403d/8645729/ccbbd6fd9b69/CAS-112-5034-g004.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/403d/8645729/e48077d47d88/CAS-112-5034-g001.jpg

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