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基于机器学习的序贯分析,以辅助新诊断多发性骨髓瘤患者在硼替佐米联合美法仑泼尼松方案(VMP)和来那度胺联合地塞米松方案(RD)之间进行选择

ML-based sequential analysis to assist selection between VMP and RD for newly diagnosed multiple myeloma.

作者信息

Park Sung-Soo, Lee Jong Cheol, Byun Ja Min, Choi Gyucheol, Kim Kwan Hyun, Lim Sungwon, Dingli David, Jeon Young-Woo, Yahng Seung-Ah, Shin Seung-Hwan, Min Chang-Ki, Koo Jamin

机构信息

Catholic Research Network for Multiple Myeloma, Catholic Hematology Hospital, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea.

Department of Hematology, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul, 06591, Republic of Korea.

出版信息

NPJ Precis Oncol. 2023 May 20;7(1):46. doi: 10.1038/s41698-023-00385-w.

Abstract

Optimal first-line treatment that enables deeper and longer remission is crucially important for newly diagnosed multiple myeloma (NDMM). In this study, we developed the machine learning (ML) models predicting overall survival (OS) or response of the transplant-ineligible NDMM patients when treated by one of the two regimens-bortezomib plus melphalan plus prednisone (VMP) or lenalidomide plus dexamethasone (RD). Demographic and clinical characteristics obtained during diagnosis were used to train the ML models, which enabled treatment-specific risk stratification. Survival was superior when the patients were treated with the regimen to which they were low risk. The largest difference in OS was observed in the VMP-low risk & RD-high risk group, who recorded a hazard ratio of 0.15 (95% CI: 0.04-0.55) when treated with VMP vs. RD regimen. Retrospective analysis showed that the use of the ML models might have helped to improve the survival and/or response of up to 202 (39%) patients among the entire cohort (N = 514). In this manner, we believe that the ML models trained on clinical data available at diagnosis can assist the individualized selection of optimal first-line treatment for transplant-ineligible NDMM patients.

摘要

对于新诊断的多发性骨髓瘤(NDMM)患者而言,能够实现更深、更长时间缓解的最佳一线治疗至关重要。在本研究中,我们开发了机器学习(ML)模型,用于预测接受硼替佐米联合美法仑加泼尼松(VMP)或来那度胺联合地塞米松(RD)这两种方案之一治疗的不适合移植的NDMM患者的总生存期(OS)或反应。诊断期间获得的人口统计学和临床特征用于训练ML模型,该模型可实现特定治疗的风险分层。当患者接受其低风险的方案治疗时,生存期更佳。在VMP低风险和RD高风险组中观察到OS的最大差异,该组接受VMP与RD方案治疗时的风险比为0.15(95%CI:0.04-0.55)。回顾性分析表明,使用ML模型可能有助于提高整个队列(N = 514)中多达202名(39%)患者的生存期和/或反应。通过这种方式,我们相信基于诊断时可用临床数据训练的ML模型可以帮助为不适合移植的NDMM患者个体化选择最佳一线治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10cf/10199943/7919e9c74e0d/41698_2023_385_Fig1_HTML.jpg

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