Abstract

Cancer cachexia is associated with a poor prognosis. This study aimed to investigate the association between sarcopenia and survival in patients with metastatic hormone-sensitive prostate cancer. We retrospectively evaluated 197 patients diagnosed with metastatic hormone-sensitive prostate cancer in our department and its affiliated institution between January 2008 and December 2015. Sarcopenia was diagnosed according to the sex-specific consensus definition. Castration-resistance prostate cancer-free survival, cancer-specific survival and overall survival from the metastatic hormone-sensitive prostate cancer diagnoses were calculated using the Kaplan-Meier method and compared using the log-rank test. Risk factors affecting the survival outcomes were analyzed using the Cox proportional regression analysis. In total, 163 patients (82.7%) had sarcopenia. Cancer-specific survival and overall survival were significantly shorter in sarcopenic patients than in non-sarcopenic patients (median cancer-specific survival: 77.0months vs. not reached, P=0.0099; overall survival: 72.0months vs. not reached, P=0.0465), whereas castration-resistance prostate cancer-free survival did not significantly differ between the groups (P=0.6063). Multivariate analyses showed that sarcopenia was an independent factor for cancer-specific survival (hazard ratio: 2.18, P=0.0451), together with the Gleason score (hazard ratio: 1.87, P=0.0272) and LATITUDE risk classification (hazard ratio: 2.73, P=0.0008). Moreover, the prognostic association of sarcopenia was remarkable in patients aged <73.0years (cancer-specific survival: 82.0months vs. not reached, P=0.0027; overall survival: 72.0months vs. not reached, P=0.0078 in sarcopenic vs. non-sarcopenic patients), whereas the association was not significant in patients aged ≥73.0years (cancer-specific survival: 76.0 and 75.0months, respectively, P=0.7879; overall survival: 67.0 and 52.0months, respectively, P=0.7263). Sarcopenia was an independent risk factor of cancer-specific survival in patients with metastatic hormone-sensitive prostate cancer, especially in younger patients.

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