Deep prostate-specific antigen response and overall survival in patients with metastatic castration-sensitive prostate cancer: A systematic review and meta-analysis.

Authors

null

Syed Arsalan Ahmed Naqvi

Mayo Clinic, Phoenix, AZ

Syed Arsalan Ahmed Naqvi , Irbaz Bin Riaz , Manal Imran , Muhammad Daim Bin Zafar , Kunwer Sufyan Faisal , Zaryab Bin Riaz , Parminder Singh , Alan Haruo Bryce

Organizations

Mayo Clinic, Phoenix, AZ, Dana-Farber Cancer Institute, Boston, MA, Dow Medical College, Karachi, Pakistan, Ziauddin Medical University, Karachi, Pakistan, Rashid Latif Medical College, Lahore, Pakistan

Research Funding

No funding received
None.

Background: Preliminary data suggests that patients with metastatic castration-sensitive prostate cancer (mCSPC) who achieve deep prostate-specific antigen (PSA) response may have improved survival. This finding may have implications for developing treatment de-escalation strategies. Thus, we assessed the overall survival by deep PSA response in mCSPC patients receiving intensified treatments. Methods: MEDLINE and EMBASE were systematically searched from each database’s inception through 1st October 2022. Trials assessing androgen deprivation therapy intensification (doublets, triplets) and reporting overall survival (OS) by deep PSA response were considered eligible for inclusion. Deep PSA response was defined as the PSA level of less than 0.1 or 0.2 ng/ml within eight months after initiation of intensified treatment. Precomputed effect estimates of OS (deep PSA response vs no deep PSA response) were pooled using an inverse-variance approach after logarithmic transformation; a random-effects meta-analysis was conducted within the Bayesian framework using empirical informative priors for heterogeneity parameter as specified by Turner et al. Summary effect was expressed as hazard ratios (HR) with the corresponding 95% credible intervals (CrI). A sensitivity analysis was conducted using the Der Simonian-Lairds random-effects meta-analysis with Hartung-Knapp (HK) adjustment. Results: Five RCTs (PEACE-1, ARASENS, CHAARTED, LATITUDE, TITAN) with 2533 patients were included in this systematic review. A total of 1335 patients experienced a deep PSA response, while 1218 did not achieve a deep PSA response after the initiation of intensified treatment. The pooled incidence of deep PSA response was 49.45% (95% confidence interval: 37.75-61.18). Bayesian meta-analysis showed significantly improved OS in overall mCSPC patient population who achieved a deep PSA response after intensified treatment with either triplet or doublet therapy as compared to those who did not achieve a deep PSA response (HR: 0.39; 95% CI: 0.30-0.50) as shown. The results were consistent with HK adjustment. Conclusions: Excellent overall survival in patients with deep PSA response may offer an opportunity to guide treatment de-escalation trials in carefully selected mCSPC patients.

Anticipated absolute effects
OutcomeParticipants (trials)Hazard ratio (95% CrI)Risk without deep PSA responseRisk difference with deep PSA response
Overall survival1980 (4 trials)HR 0.39 (0.30 to 0.50)347 deaths per 1,000194 fewer deaths per 1,000; (227 fewer to 155 fewer)

The PEACE-1 trial did not provide analyzable estimates and hence was not included in the analysis.

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Abstract Details

Meeting

2023 ASCO Genitourinary Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session A: Prostate Cancer

Track

Prostate Cancer - Advanced,Prostate Cancer - Localized

Sub Track

Therapeutics

Citation

J Clin Oncol 41, 2023 (suppl 6; abstr 195)

DOI

10.1200/JCO.2023.41.6_suppl.195

Abstract #

195

Poster Bd #

G8

Abstract Disclosures