Sun Li-Min, Lin Cheng-Li, Lin Ming-Chia, Liang Ji-An, Kao Chia-Hung
From the Department of Radiation Oncology, Zuoying Branch of Kaohsiung Armed Forces General Hospital, Kaohsiung (LMS); Management Office for Health Data, China Medical University Hospital, Taichung (C-LL); College of Medicine, China Medical University, Taichung (C-LL); Department of Nuclear Medicine, E-Da Hospital, I-Shou University, Kaohsiung (M-CL); Graduate Institute of Clinical Medical Science, School of Medicine, College of Medicine, China Medical University, Taichung (J-AL, C-HK); Department of Radiation Oncology (J-AL); and Department of Nuclear Medicine and PET Center, China Medical University Hospital, Taichung, Taiwan (C-HK).
Medicine (Baltimore). 2015 May;94(17):e737. doi: 10.1097/MD.0000000000000737.
This study explored which kinds of cancer are related to a higher incidence of subsequent myelodysplastic syndrome (MDS) after radiotherapy (RT) and chemotherapy (CT).We performed a nested case-control study by using data from the Taiwanese National Health Insurance (NHI) system. The case group included cancer patients who developed MDS. For the control group, 4 cancer patients without MDS were frequency-matched with each MDS case by age, sex, year of cancer diagnosis, and MDS index year. A multivariable logistic regression analysis was conducted, and odds ratios (ORs) and 95% confidence intervals (CIs) were estimated.Overall, cancer patients who received RT or CT exhibited secondary MDS more frequently than did those who did not (RT: OR = 1.53; 95% CI = 1.33-1.77; CT: OR = 1.51; 95% CI = 1.25-1.82). Analysis by cancer site showed that RT increased the risk of MDS for patients with stomach, colorectal, liver, breast, endometrial, prostate, and kidney cancers. By contrast, CT was more likely to increase the risk of MDS for patients with lung, endometrial, and cervical cancers. Further analysis revealed that RT and CT seemed to have a positive interaction. The major limitation of this study was the lack of certain essential data in the NHI Research Database, such as data regarding cancer stage and treatment dose details.This population-based nested case-control study determined that RT and CT predisposed patients in Taiwan to the development of MDS. This effect was more prominent when both modalities were used.
本研究探讨了哪些癌症与放疗(RT)和化疗(CT)后发生骨髓增生异常综合征(MDS)的较高发生率相关。我们利用台湾国民健康保险(NHI)系统的数据进行了一项巢式病例对照研究。病例组包括发生MDS的癌症患者。对照组中,4名无MDS的癌症患者按年龄、性别、癌症诊断年份和MDS索引年份与每例MDS病例进行频数匹配。进行了多变量逻辑回归分析,并估计了比值比(OR)和95%置信区间(CI)。总体而言,接受RT或CT的癌症患者发生继发性MDS的频率高于未接受者(RT:OR = 1.53;95% CI = 1.33 - 1.77;CT:OR = 1.51;95% CI = 1.25 - 1.82)。按癌症部位分析表明,RT增加了胃癌、结直肠癌、肝癌、乳腺癌、子宫内膜癌、前列腺癌和肾癌患者发生MDS的风险。相比之下,CT更有可能增加肺癌、子宫内膜癌和宫颈癌患者发生MDS的风险。进一步分析显示,RT和CT似乎存在正向相互作用。本研究的主要局限性是NHI研究数据库中缺乏某些关键数据,如癌症分期和治疗剂量细节等数据。这项基于人群的巢式病例对照研究确定,RT和CT使台湾患者易发生MDS。当两种治疗方式都使用时,这种效应更为显著。