ArticleAmerican journal of cancer research2026
Robot-assisted radical prostatectomy reduces biochemical recurrence risk and improves urinary continence recovery compared with laparoscopic approach in high-risk localized prostate cancer after neoadjuvant therapy: a real-world propensity score-matched analysis.
Article in American journal of cancer research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
This retrospective study compared the oncological and functional outcomes of robot-assisted radical prostatectomy (RARP) versus laparoscopic radical prostatectomy (LRP) in 523 patients with high-risk localized prostate cancer (HR-LPC) receiving neoadjuvant therapy (NAT). After 1:1 propensity score matching (PSM), 218 patients per group were included. Multivariate Cox regression confirmed that RARP was independently associated with a significantly lower biochemical recurrence (BCR) risk compared with LRP (after PSM: HR=0.626, 95% CI 0.471-0.833, P=0.001), a finding that remained robust across all sensitivity analyses. Subgroup analyses identified significant BCR protection by RARP in patients with preoperative PSA ≥20 ng/mL (P=0.001), pathological T stage pT2-pT3a (P=0.002), biopsy ISUP grade 4 (P=0.005), negative lymph nodes (P<0.001), ADT monotherapy (P=0.007), and age ≥65 years (P=0.002), with no significant heterogeneity across subgroups (all P-interaction >0.05). RARP also demonstrated perioperative advantages over LRP, including less intraoperative blood loss (median 239.5 vs. 399.5 mL, P<0.001), lower transfusion rate (4.59% vs. 12.39%, P=0.003), and shorter hospital stay (median 7 vs. 9 days, P<0.001), while pathological outcomes were comparable between groups (all P>0.05). Regarding functional recovery, RARP achieved significantly higher urinary continence rates at postoperative months 1 (33.5% vs. 21.1%, P=0.005), 3 (53.2% vs. 38.5%, P=0.003), 6 (74.8% vs. 60.6%, P=0.002), and 12 (84.9% vs. 73.9%, P=0.006), with a median continence recovery time of 3 months versus 6 months in the LRP group (P<0.001). These findings suggest that RARP offers meaningful oncological and functional advantages over LRP in HR-LPC patients undergoing NAT.
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