Chemotherapy and cardiotoxicity in older breast cancer patients: A population-based study

被引:267
作者
Doyle, JJ
Neugut, AI
Jacobson, JS
Grann, VR
Hershman, DL
机构
[1] Columbia Univ, Herbert Irving Comprehens Canc Ctr, Coll Phys & Surg, New York, NY 10032 USA
[2] Columbia Univ, Dept Med, New York, NY 10032 USA
[3] Columbia Univ, Dept Epidemiol, New York, NY 10032 USA
[4] Columbia Univ, Dept Biostat, Mailman Sch Publ Hlth, New York, NY 10032 USA
[5] New York Presbyterian Hosp, New York, NY USA
关键词
D O I
10.1200/JCO.2005.02.5841
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Adjuvant chemotherapy, especially with anthracyclines, is known to cause acute and chronic cardiortoxicity in breast cancer patients. We studied the cardiac effects of chemotherapy in a population-based sample of breast cancer patients aged >= 65 years with long-term follow-up. Patients and Methods In the Surveillance, Epidemiology, and End Results (SEEB)-Medicare database, we analyzed treatments and outcomes among women >= 65 years of age who were diagnosed with stage I to III breast cancer from January 1, 1992 to December 31, 1999. Propensity scores were used to control for baseline heart disease (HD) and other known predictors of chemotherapy, and Cox proportional hazards models were used to estimate the risk of cardiomyopathy (CM), congestive heart failure (CHF), and HD after chemotherapy. Results Of 31,748 women with stage I to III breast cancer, 5,575 (18%) received chemotherapy. Chemotherapy was associated with younger age, fewer comorbidities, hormone receptor negativity, multiple primary tumors, and advanced disease. Patients who received chemotherapy were less likely than other patients to have pre-existing HID (45% v 55%, respectively; P <.001). The hazard ratios for CM, CHF, and HD for patients treated with doxorubicin (DOX) compared with patients who received no chemotherapy were 2.48 (95% CI, 2.10 to 2.93), 1.38 (95% CI, 1.25 to 1.52), and 1.35 (95% CI, 1.26 to 1.44), respectively. The relative risk of cardiotoxicity among patients who received DOX compared with untreated patients remained elevated 5 years after diagnosis. Conclusion When baseline HID was taken into account, chemotherapy, especially with anthracyclines, was associated with a substantially increased risk of CM. As the number of long-term survivors grows, identifying and minimizing the late effects of treatment will become increasingly important.
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页码:8597 / 8605
页数:9
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