Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Health Services Research, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cancer. 2018 Mar 1;124(5):899-906. doi: 10.1002/cncr.31144. Epub 2017 Dec 13.
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.
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.
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.
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.
早期乳腺癌的化疗与骨髓增生异常综合征(MDS)和/或急性髓系白血病(AML)的发生风险小有关。本研究的目的是确定在老年乳腺癌患者中接受现代辅助化疗后 AML 或 MDS 的发生风险,并进一步确定个体化疗方案的风险。
在 Surveillance, Epidemiology, and End Results-Medicare 和 Texas Cancer Registry-Medicare 链接数据库中,确定了 2003 年至 2009 年间诊断为 I 期至 III 期乳腺癌的患者。使用国际疾病分类第 9 版和医疗保健通用程序编码系统代码确定 AML/MDS 的发生、化疗使用和合并症。分析包括描述性统计、累积发生率和 Cox 比例风险模型,以在调整临床相关协变量后估计 AML/MDS 的风险。
共纳入 92110 例患者;中位随访 85 个月后,每 1000 人年的总发生率分别为 AML 0.65 例和 MDS 1.56 例。接受蒽环类药物(A)或蒽环类药物和紫杉烷(A+T)方案的患者发生 AML 的风险更高(A 组的风险比 [HR],1.70;95%置信区间 [CI],1.16-2.50;A+T 组的 HR,1.68;95%CI,1.22-2.30)或 MDS(A 组的 HR,2.18;95%CI,1.70-2.80;A+T 组的 HR,1.62;95%CI,1.29-2.03)比未接受化疗的患者更高。使用多西他赛和环磷酰胺(TC)的患者发生 AML 或 MDS 的风险没有增加。
辅助化疗与 AML 和 MDS 的风险小但显著增加相关,尤其是包含 A 的方案。需要更长时间的随访来证实最近采用的 TC 方案不会增加风险。癌症 2018;124:899-906。©2017 年美国癌症协会。