Analysis of patients with metastatic castration-resistant prostate cancer (mCRPC) treated with carboplatin-paclitaxel after multiple lines of treatment.

Authors

null

Elisa María Fernández Pérez

Hospital Universitario Virgen de Valme, Sevilla, Spain

Elisa María Fernández Pérez , Isabel Beltrán Guerra , Adrian Sánchez Vegas , Carlos Enrique Robles , Gloria Lourenzo Aguilera , Marta Fernández Carcaño , Carlos Ayala De Miguel , Sebastián Díaz López , Guillermo García González , Leonid Bachurin , Javier Rico López , Jose Fuentes Pradera , Jeronimo Jimenez Castro , María Rodríguez de la Borbolla , Pilar López Álvarez , María José Gómez Reina , Manuel Chaves Conde Sr., Eva Fernández Parra

Organizations

Hospital Universitario Virgen de Valme, Sevilla, Spain

Research Funding

No funding sources reported

Background: Metastatic castration-resistant prostate cancer (mCRPC) occurs in men with advanced disease progressing to androgen deprivation therapy, with serum testosterone < 50 ng/dL. In this setting, several active therapies are available, such as chemotherapy and androgen receptor-targeted agents. We analyzed the efficacy of the carboplatin - paclitaxel (C-P) combination in mCRPC patients after several lines of treatment. Methods: In this retrospective observational study, we analyzed the clinical data of 43 patients with mCRPC who received treatment with biweekly C-P between 2015-2022 at the Hospital Universitario Virgen de Valme. The data collected refer to the baseline characteristics of the patients at the start of treatment (age, functional status), stage at diagnosis and treatments received in first and successive lines, among others. The response variables analyzed were both overall survival (OS) and progression-free survival (PFS). Treatment-derived toxicity was collected. The data were processed with IBM-SPSS Statistics v. 25. The information was collected from Diraya Estación Clínica v 4.0.80 and Farmis-Oncofarm. Results: As of September 2022, data had been collected for 43 men with mCRPC. Histology was adenocarcinoma in all cases. At the start of C-P treatment: 48.9% of patients were in good functional status (ECOG ≤ 1), median age was 71 years and 62.8% had received at least 3 lines of treatment. Patients received C-P for a median of 12 weeks: 76.7% showed clinical improvement and 44.2% had PSA decline, with PSA decline ≥ 30% in 27.5% of patients. The median OS (mOS) was 8 months (95% CI 6.46-9.54) and the median PFS was 14 weeks. By Kaplan-Meier survival analysis, we compared mOS as a function of PSA: response/non-response, the differences being statistically significant: 11 (95% CI=6.22-15.78) vs. 6 (95% CI=4.21-7.79) months, respectively (Log Rank 0.001). The main toxicity was hematological. Conclusions: The C-P combination may be an effective treatment option in patients with mCRPC refractory to various lines of therapy, with PSA being a good marker of response to treatment.

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Abstract Details

Meeting

2024 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 42, 2024 (suppl 4; abstr 144)

DOI

10.1200/JCO.2024.42.4_suppl.144

Abstract #

144

Poster Bd #

F15

Abstract Disclosures