16 Data from ENZAMET in patients with previous local treatment showed a trend toward better overall survival (HR: 0.72; CI: 0.47–1.09) and significantly longer clinical progression-free survival (HR: 0.42; CI: 0.31–0.57) for the addition of enzalutamide to ADT. 15 In conclusion, enzalutamide represents an option for synchronous and metachronous omHSPC.
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Management and treatment options for patients with de novo and recurrent hormone-sensitive oligometastatic prostate cancer.
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However, Hove improvement in overall survival closely failed to reach significance (HR: 0.40; CI: 0.15–1.03), which again might be caused by the few events (n = 18) that occurred in this small subgroup (n = 144). 14 In brief, the addition of apalutamide to ADT offers a therapeutic option for synchronous and metachronous omHSPC patients. 3.2.3.