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Acute myeloid leukemia and myelodysplastic syndrome after adjuvant chemotherapy: A population‐based study among older breast cancer patients

机译:辅助化疗后急性髓性白血病和骨髓增生术综合征:较老乳腺癌患者的群体研究

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BACKGROUND Chemotherapy for early breast cancer is associated with a small risk of developing myelodysplastic syndrome (MDS) and/or acute myeloid leukemia (AML). The aim of this study was to determine the risk of developing AML or MDS after modern adjuvant chemotherapy in older breast cancer patients and to further define the risk of individual chemotherapy regimens. METHODS Patients diagnosed with stage I to III breast cancer from 2003 to 2009 were identified in the Surveillance, Epidemiology, and End Results–Medicare and Texas Cancer Registry–Medicare linked databases. The development of AML/MDS, chemotherapy use, and comorbidities were identified with International Classification of Diseases, Ninth Revision and Healthcare Common Procedure Coding System codes. Analyses included descriptive statistics, cumulative incidences, and Cox proportional hazards models to estimate the hazard of AML/MDS after adjustments for clinically relevant covariates. RESULTS In all, 92,110 patients were included; after a median follow‐up of 85 months, the overall rates per 1000 person‐years were 0.65 for AML and 1.56 for MDS. Patients who received an anthracycline (A) or anthracycline and taxane (A+T) regimen were more likely to develop AML (hazard ratio [HR] for A, 1.70; 95% confidence interval [CI], 1.16‐2.50; HR for A+T, 1.68; 95% CI, 1.22‐2.30) or MDS (HR for A, 2.18; 95% CI, 1.70‐2.80; HR for A+T, 1.62; 95% CI, 1.29‐2.03) than patients who did not receive chemotherapy. Patients using docetaxel and cyclophosphamide (TC) were not at increased risk for AML or MDS. CONCLUSIONS Adjuvant chemotherapy is associated with a small but significant increase in the risk of AML and MDS, especially with regimens that include A. Longer follow‐up is needed to confirm that risk is not increased with the recently adopted TC regimen. Cancer 2018;124:899‐906. ? 2017 American Cancer Society .
机译:背景技术早期乳腺癌的化疗与开发骨髓增生术综合征(MDS)和/或急性髓性白血病(AML)的缺乏患风险。本研究的目的是确定在较旧的乳腺癌患者的现代佐剂化疗后开发AML或MDS的风险,进一步确定单个化疗方案的风险。方法在2003年至2009年诊断为III乳腺癌患者的患者在监测,流行病学和最终结果 - Medicare和德克萨斯州癌症登记处 - Medicare联系数据库中确定了2003年至2009年的乳腺癌。通过国际疾病分类,第九次修订和医疗保健普通程序编码系统代码确定了AML / MDS,化疗使用和可融合的发展。分析包括描述性统计数据,累积发生率和Cox比例危险模型,以估算在临床相关协变量的调整后AML / MD的危害。结果所有,包括92,110名患者;在85个月的中位随访后,每1000人的总体税率为0.65,适用于MDS和1.56。接受蒽环素(A)或蒽环素和紫杉烷(A + T)方案的患者更可能发育AML(危害比[HR],1.70; 95%置信区间[CI],1.16-2.50;人力资源+ T,1.68; 95%CI,1.22-2.30)或MDS(适用于A,2.18; 95%CI,1.70-2.80; HR,适用于A + T,1.62; 95%CI,1.29-2.03)比做的患者没有接受化疗。使用多西紫杉醇和环磷酰胺(TC)的患者不适于AML或MDS的风险。结论佐剂化疗与AML和MDS风险的小而显着增加,特别是与包括A的方案,需要更长的随访,以确认风险不会随着最近通过的TC方案而增加。癌症2018; 124:899-906。还2017年美国癌症协会。

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