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IUC23223-77 Triplet therapy in metastatic hormone-sensitive prostate cancer in Asian patients

Alexey R. ZakirovTashkent Medical Park by Urologic Complex ,F.M. DjuraevTashkent Medical Park by Urologic Complex ,O RaxmonovTashkent Medical Park by Urologic Complex ,A JumaevTashkent Medical Park by Urologic Complex ,
The Oncologistjournal2025en
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Abstract Background Two randomized trials demonstrated a survival benefit of triplet therapy, androgen deprivation therapy plus androgen receptor pathway inhibitor plus docetaxel over doublet therapy (ADT plus docetaxel), thus changing treatment strategies in metastatic hormone-sensitive prostate cancer (mHSPC). Methods We conducted the real-world analysis comprising 92 mHSPC patients from 3 Tashkent medical centers, among them 75% of patients received abiraterone and 16.5% daroluramide treatment. Baseline characteristics and clinical parameters during triplet therapy were documented. Results Of them, 78.2% patients with synchronous and 21.8% with metachronous disease were included. 82.6% had high-volume disease diagnosed by conventional imaging (47.8%) or PSMA PET-CT (52.2%). While docetaxel and ARPI were administered consistent with pivotal trials, prednisolone, prophylactic gCSF and osteoprotective agents were not applied according to guidelines in 31.5%, 43,5%, and 25% of patients, respectively. Importantly, a nonsimultaneous onset of chemotherapy and ARPI, performed in 51% of patients, was associated with significantly worse treatment response (P = .015, HR 0.245). Starting ARPI before chemotherapy was associated with a significantly higher probability for progression (P = .023, HR 15.781) than vice versa. Strikingly, 15.2% (abiraterone) and 25.0% (darolutamide) low-volume patients, as well as 14.1% (abiraterone) and 20.6% (darolutamide) metachronous patients, received triplet therapy. Adverse events (AE) occurred in 60.8% with grades 3 to 5 in 15% of patients without age-related differences. All patients achieved a PSA decline of 99% and imaging response was confirmed in 88% of abiraterone and 75% of daroluramide patients. Conclusions Triplet therapy arrived in clinical practice primarily for synchronous high-volume mHSPC. Regardless of the selected therapy regimen, treatment is highly effective and tolerable. Preferably, therapy should be administered simultaneously; however, if not possible, chemotherapy should be started first

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