189 Background: The phase 3 EMBARK trial (NCT02319837) assessed enzalutamide plus leuprolide (enza combo), leuprolide alone (LA), and enzalutamide monotherapy (enza mono) in patients (pts) with prostate cancer and high-risk biochemical recurrence. EMBARK demonstrated significant improvements for metastasis-free survival (enza combo and enza mono) and overall survival (enza combo). A key feature of EMBARK was tx suspension after 37 weeks in pts with PSA 250 ng/dL. Results for T recovery to baseline and >175 ng/dL are shown (Table). Conclusions: Approximately 1 in 25 pts treated with enza combo for 9 months had PSA 175 ng/dL † , n (%) 72 (20.4) 33 (9.3) 29 (8.2) 35 (9.9) 17 (4.8) 12 (3.4) 15 (4.2) 8 (2.3) 5 (1.4) T >250 ng/dL ‡ , n (%) 44 (12.5) 21 (5.9) 23 (6.5) 25 (7.1) 15 (4.2) 10 (2.8) 13 (3.7) 5 (1.4) 4 (1.1) T ≥baseline § , n (%) 21 (5.9) 11 (3.1) 18 (5.1) 16 (4.5) 10 (2.8) 10 (2.8) 9 (2.5) 3 (0.8) 4 (1.1) No T assessment, n (%) 6 (1.7) 5 (1.4) 2 (0.6) 8 (2.3) 3 (0.8) <jats:td c
Shore et al. (Sun,) studied this question.
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