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

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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Journal
The Oncologist
Published
2025-08-29
DOI
https://doi.org/10.1093/oncolo/oyaf248.035
Primary Topic
Prostate Cancer Treatment and Research
Type
article
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article

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

F.M. Djuraev, Alexey R. Zakirov, O Raxmonov, A Jumaev
1 links
The Oncologist
Prostate Cancer Treatment and Research
article

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

F.M. Djuraev, Alexey R. Zakirov, O Raxmonov, A Jumaev
article en

Abstract

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

The OncologistVol. 30(Supplement_1)
Tashkent Pediatric Medical Institute (UZ)
Openalex Percentile: Top 67%
Prostate Cancer Treatment and Research
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