Gill David, Gaston David, Bailey Erin, Hahn Andrew, Gupta Sumati, Batten Julia, Alex Anitha, Boucher Kenneth, Stenehjem David, Agarwal Neeraj
Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Department of Pharmacotherapy, College of Pharmacy, University of Utah, Salt Lake City, UT.
Clin Genitourin Cancer. 2017 Aug;15(4):e599-e602. doi: 10.1016/j.clgc.2016.12.008. Epub 2017 Jan 5.
Abiraterone acetate has been approved for metastatic castration-resistant prostate cancer (mCRPC). Coadministration with prednisone has been recommended to prevent the toxicity from secondary mineralocorticoid excess, such as hypertension, hypokalemia, and edema. However, the use of prednisone is often not desired by patients because of the potential for detrimental effects of long-term therapy with corticosteroids, especially in those with comorbidities such as diabetes or who have received previous immunotherapeutic agents. Eplerenone is a nonsteroidal mineralocorticoid antagonist demonstrated to abrogate mineralocorticoid excess. In the present retrospective study, we report our real-world experience with the use of eplerenone with abiraterone in men with mCRPC who wished to avoid concomitant prednisone therapy.
The incidence and grade (Common Terminology Criteria for Adverse Events, version 4) of mineralocorticoid excess toxicities, baseline demographics, disease characteristics, and progression-free survival (PFS) were collected retrospectively. The patient population included men with mCRPC treated with abiraterone, who were not willing to receive corticosteroids, and thus received eplerenone. Their data were compared with the data from those treated with abiraterone and prednisone during the same period. Continuous variables were assessed using the Wilcoxon rank sum test or Student t test, and categorical variables were assessed using Fischer's exact test or χ test, as appropriate. PFS was compared using the Kaplan-Meier method.
Of the 106 men treated with abiraterone, 40 received eplerenone and 66 received prednisone. The baseline and disease characteristics, incidence and grade of adverse events related to the syndrome of mineralocorticoid excess, and the median PFS were similar in both cohorts.
In a real-world population of men with mCRPC treated with abiraterone, corticosteroids can be avoided by concomitant treatment with eplerenone. These data require further validation.
醋酸阿比特龙已被批准用于转移性去势抵抗性前列腺癌(mCRPC)。建议与泼尼松联合使用以预防继发性盐皮质激素过多引起的毒性,如高血压、低钾血症和水肿。然而,患者通常不希望使用泼尼松,因为长期使用皮质类固醇可能产生有害影响,特别是在患有合并症(如糖尿病)或曾接受过免疫治疗药物的患者中。依普利酮是一种非甾体类盐皮质激素拮抗剂,已证明可消除盐皮质激素过多。在本回顾性研究中,我们报告了在希望避免同时使用泼尼松治疗的mCRPC男性患者中使用依普利酮联合阿比特龙的真实世界经验。
回顾性收集盐皮质激素过多毒性的发生率和分级(不良事件通用术语标准,第4版)、基线人口统计学、疾病特征和无进展生存期(PFS)。患者群体包括接受阿比特龙治疗但不愿意接受皮质类固醇的mCRPC男性患者,因此接受了依普利酮治疗。将他们的数据与同期接受阿比特龙和泼尼松治疗的患者的数据进行比较。连续变量使用Wilcoxon秩和检验或Student t检验进行评估,分类变量根据情况使用Fischer精确检验或χ检验进行评估。使用Kaplan-Meier方法比较PFS。
在106例接受阿比特龙治疗的男性患者中,40例接受了依普利酮,66例接受了泼尼松。两个队列的基线和疾病特征、与盐皮质激素过多综合征相关的不良事件的发生率和分级以及中位PFS相似。
在接受阿比特龙治疗的mCRPC男性真实世界人群中,联合使用依普利酮可避免使用皮质类固醇。这些数据需要进一步验证。