Deep PSA response and extended time‐to‐nadir as robust predictors of survival in Asian patients with de novo metastatic hormone‐sensitive prostate cancer receiving upfront intensified treatment

Introduction In de novo metastatic hormone‐sensitive prostate cancer (mHSPC) treated with upfront intensification using androgen receptor signaling inhibitor or chemotherapy (Docetaxel), achieving a PSA nadir less than 0.2 ng/mL, indicative of superior survival in trials, may often be unattainable i...

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Veröffentlicht in:The Prostate 2025-01, Vol.85 (1), p.30-39
Hauptverfasser: Wong, Chris H.‐M., Ko, Ivan C.‐H., Leung, David K.‐W., Siu, Brian, Cheng, Cheuk‐K. K., Lim, Yung‐Y. J., Mok, Hiu T., Kwok, Chun‐F. B., Tang, Cheuk Y., Leung, Steven C.‐H., Chiu, Peter K.‐F., Teoh, Jeremy Y.‐C., Ng, Chi F.
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Sprache:eng
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Zusammenfassung:Introduction In de novo metastatic hormone‐sensitive prostate cancer (mHSPC) treated with upfront intensification using androgen receptor signaling inhibitor or chemotherapy (Docetaxel), achieving a PSA nadir less than 0.2 ng/mL, indicative of superior survival in trials, may often be unattainable in real‐world settings. We explored the predictive value of the degree of PSA decline and time to PSA nadir (TTPN) on oncological outcomes. Methods A prospectively maintained database of consecutive prostate cancer cases in Hong Kong was accessed. Patients diagnosed with de novo mHSPC from 2016 to 2022 and treated with upfront intensification were included in this analysis. Landmark analysis on PSA kinetics at 6‐months following treatment intensification was performed. They were classified based on 1) TTPN (≥6 months vs.
ISSN:0270-4137
1097-0045
1097-0045
DOI:10.1002/pros.24797