Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA 91101, USA.
Cancer Epidemiol Biomarkers Prev. 2013 Feb;22(2):313-6. doi: 10.1158/1055-9965.EPI-12-1137. Epub 2013 Jan 4.
While androgen deprivation therapy (ADT) is a common treatment for prostate cancer, little is known regarding its long-term health effects, particularly as it relates to the development of second primary malignancies. Therefore, the goal of this study was to assess the association between ADT use and second primary malignancies among men diagnosed with localized prostate cancer.
We assessed whether use of ADT (specifically, gonadotropin-releasing hormone agonists) was associated with the development of second primary malignancies in a retrospective cohort of 24,038 men ages more than 18 years who were diagnosed with localized prostate cancer between 1998 and 2007, and followed through 2009. We used proportional hazards regression to estimate the risk of developing a second primary cancer among men who were treated with ADT compared with men who were not.
Men who were treated with ADT were not more likely to develop any second primary malignancy compared with those who were not treated with ADT after adjustment for age, race, date of diagnosis, utilization, clinical stage, Gleason score, and radiation therapy [HR, 1.10; 95% confidence interval (CI), 0.98-1.22)]. Radiotherapy, diabetes, and obesity did not modify the association between ADT use and second primary cancer risk.
Our results suggest that among men with localized prostate cancer, ADT is not associated with an increased risk of second primary malignancies.
When evaluating the risks and benefits of using ADT as a treatment for localized prostate cancer, considering the risk of second primary malignancies may not be clinically important.
虽然雄激素剥夺疗法(ADT)是治疗前列腺癌的常用方法,但对于其长期的健康影响,尤其是与第二原发恶性肿瘤的发展关系,知之甚少。因此,本研究旨在评估 ADT 治疗与局部前列腺癌患者第二原发恶性肿瘤之间的关系。
我们评估了在 1998 年至 2007 年间被诊断为局限性前列腺癌且在 2009 年之前接受过治疗的 24038 名年龄超过 18 岁的男性中,ADT(特别是促性腺激素释放激素激动剂)的使用是否与第二原发恶性肿瘤的发生有关。我们使用比例风险回归来估计接受 ADT 治疗的男性与未接受 ADT 治疗的男性相比,发生第二原发癌症的风险。
在调整了年龄、种族、诊断日期、使用率、临床分期、Gleason 评分和放疗后,接受 ADT 治疗的男性与未接受 ADT 治疗的男性相比,发生任何第二原发恶性肿瘤的可能性没有增加[风险比(HR),1.10;95%置信区间(CI),0.98-1.22]。放疗、糖尿病和肥胖并未改变 ADT 使用与第二原发癌症风险之间的关联。
我们的结果表明,在局限性前列腺癌患者中,ADT 治疗与第二原发恶性肿瘤风险的增加无关。
在评估 ADT 作为局部前列腺癌治疗方法的风险和益处时,考虑第二原发恶性肿瘤的风险可能在临床上并不重要。