Lawen Tarek, Masoumi-Ravandi Kaveh, Rendon Ricardo A, Connor Liette, Mason Ross J
Department of Urology, Dalhousie University, Halifax NS, Canada.
Can Urol Assoc J. 2023 Aug;17(8):274-279. doi: 10.5489/cuaj.8245.
Androgen deprivation therapy (ADT) with androgen receptor axis-targeted (ARAT) therapy is the standard of care provided to patients with metastatic prostate cancer. While effective, it results in sequelae, such as loss of skeletal muscle mass. In this study, we compared the sarcopenic effects of abiraterone and enzalutamide, two ARATs used to treat metastatic prostate cancer.
Our cohort was comprised of 55 patients diagnosed with metastatic hormonenaive prostate cancer from 2014-2019. Patients were divided into three treatment groups: gonadotropin-releasing hormone (GnRH ) agonist alone; GnRH agonist combined with abiraterone acetate; and GnRH agonist combined with enzalutamide. We then compared axial computed tomographic (CT) scans at the L3 level before and after the initiation of hormone therapy for each patient. A skeletal muscle index (SMI) was calculated for each patient, and alongside clinical data, was compared between the three groups. One-way analysis of variance (ANOVA) and Fisher's exact test were used to compare means and proportions, respectively.
Baseline clinical characteristics were not significantly different between the three groups. The percent SMI change and number of newly sarcopenic patients were not found to be significantly different between the groups. The only variable that was significantly different across the three groups was time between CT scans.
Although we found no significant difference in the sarcopenic effects of GnRH alone, GnRH with abiraterone, or GnRH with enzalutamide in our cohort of 55 hormone-naive metastatic prostate cancer patients, overall decreases in muscle mass were observed for all three groups. This highlights the importance of muscle-retaining strategies for patients undergoing ADT for metastatic prostate cancer, regardless of therapeutic regimen.
雄激素剥夺疗法(ADT)联合雄激素受体轴靶向(ARAT)疗法是为转移性前列腺癌患者提供的标准治疗方案。虽然该疗法有效,但会导致诸如骨骼肌量减少等后遗症。在本研究中,我们比较了阿比特龙和恩杂鲁胺这两种用于治疗转移性前列腺癌的ARAT药物的肌肉减少症效应。
我们的队列由2014年至2019年期间诊断为转移性激素初治前列腺癌的55名患者组成。患者被分为三个治疗组:单独使用促性腺激素释放激素(GnRH)激动剂;GnRH激动剂联合醋酸阿比特龙;GnRH激动剂联合恩杂鲁胺。然后,我们比较了每位患者激素治疗开始前后L3水平的轴向计算机断层扫描(CT)图像。计算每位患者的骨骼肌指数(SMI),并将其与临床数据一起在三组之间进行比较。分别使用单因素方差分析(ANOVA)和Fisher精确检验来比较均值和比例。
三组之间的基线临床特征无显著差异。未发现各组之间SMI变化百分比和新出现肌肉减少症患者数量有显著差异。三组之间唯一有显著差异的变量是CT扫描之间的时间。
尽管在我们的55名激素初治转移性前列腺癌患者队列中,我们发现单独使用GnRH、GnRH联合阿比特龙或GnRH联合恩杂鲁胺在肌肉减少症效应方面无显著差异,但所有三组均观察到肌肉量总体下降。这凸显了对于接受ADT治疗的转移性前列腺癌患者,无论治疗方案如何,采取肌肉维持策略的重要性。