A comparison of the sarcopenic effect of androgen receptor-axistargeted agents vs. androgen deprivation alone in patients with metastatic prostate cancer
DOI:
https://doi.org/10.5489/cuaj.8245Keywords:
Prostatic Neoplasms, Sarcopenia, Androgen AntagonistsAbstract
INTRODUCTION: 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.
METHODS: Our cohort was comprised of 55 patients diagnosed with metastatic hormone-naive 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.
RESULTS: 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.
CONCLUSIONS: 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 the therapeutic regimen.
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