Abstract
Efficacy and safety of docetaxel (D) vs androgen-receptor signaling inhibitors (ARSi) as second-line therapy (Rx) after progression on alternative ARSi as first-line Rx for patients who are elderly (≥75 years old) with metastatic castration-resistant prostate cancer (mCRPC) in a multicenter international database: A SPARTACUSS–Meet-URO 26 study
Journal of clinical oncology, Vol.41(6_suppl), pp.166-166
02/20/2023
DOI: 10.1200/JCO.2023.41.6_suppl.166
Abstract
166 Background: About 2/3 of all prostate cancer (PCa) deaths occur in patients aged ≥75, who are frequently diagnosed with advanced PCa. ARSi abiraterone acetate (AA) and enzalutamide (E) are the most common 1 st line Rx for patients with mCRPC. Yet, the optimal treatment sequence for the elderly ≥75 after ARSi failure is still unclear. Methods: Using available medical records, patients aged ≥75 who started ARSi as 1 st line Rx for mCRPC within January 2015 - April 2019 and, upon progression, 2 nd line alternative ARSi or D were identified from the IRB approved hospital registries of 10 centers in Europe, North and South America. Patients were categorized by type of 2 nd line Rx for mCRPC into cohorts AA/E and D. Primary endpoints were overall survival (OS) from 1 st line AA/E start, OS and radiographic progression-free survival (rPFS) from 2 nd line Rx start, and safety. The Kaplan Meier method was used to calculate endpoint distributions and medians (95% CI). Results: Of the 122 patients identified, 57 (46.7%) had AA/E and 65 (53.3%) D, as 2 nd line Rx for mCRPC. Median follow-up was 26.3 months (95% CI, 23.1-27.9 months). Cohort AA/E tended to be older (81 vs 78 years; p=0.001) and with high-volume disease (45.5% vs 25.0%; p=0.022) compared to cohort D. No significant difference in OS from 1 st line ARSi onset and OS or rPFS from 2 nd line Rx start was found between the 2 cohorts. Cohort AA/E had longer rPFS than cohort D, albeit not significant (18.5 vs 12.0 months; p=0.13). Rates of adverse events (AEs) of any grade (42.1 vs 53.8; p=0.21) and AEs of grade ≥3 (19.3% vs 18.5%; p=1.0) did not show significant differences between the 2 cohorts. Conclusions: Within the limitations of small cohorts and retrospective design, treatment sequences with 2 nd line AA/E or D after failure of 1 st line alternative ARSi for mCRPC showed similar efficacy and safety in the elderly ≥75 years old.
Details
- Title: Subtitle
- Efficacy and safety of docetaxel (D) vs androgen-receptor signaling inhibitors (ARSi) as second-line therapy (Rx) after progression on alternative ARSi as first-line Rx for patients who are elderly (≥75 years old) with metastatic castration-resistant prostate cancer (mCRPC) in a multicenter international database: A SPARTACUSS–Meet-URO 26 study
- Creators
- Vincenzo Gennusa - Azienda Ospedaliera Universitaria Policlinico "Paolo Giaccone" di PalermoCalogero Saieva - Cancer Risk Factors and Lifestyle Epidemiology Unit – ISPRO, Firenze, ItalyRichard M. Lee-Ying - Tom Baker Cancer Centre, Calgary, AB, CanadaPier Vitale Nuzzo - Cornell UniversityGian Paolo Spinelli - Department of Medico-Surgical Sciences and Biotechnologies, Oncology Unit, Santa Latina, ItalyElisa Zanardi - Ospedale Policlinico San MartinoGiuseppe Fotia - Fondazione IRCCS Istituto Nazionale dei TumoriSabrina Rossetti - Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale"Loana Bueno Valenca - D’Or Institute for Research and EducationAnna Patrikidou - Institut Gustave RoussyLivia Andrade - D’Or Institute for Research and EducationRicardo Pereira Mestre - Istituto Oncologico della Svizzera ItalianaGiuseppe Fornarini - Ospedale Policlinico San MartinoGiuseppe Procopio - Fondazione IRCCS Istituto Nazionale dei TumoriDaniele Santini - Università Campus Bio-MedicoChristopher Sweeney - Harvard UniversityDaniel Yick Chin Heng - University of CalgaryUgo De Giorgi - Istituto Scientifico Romagnolo per lo Studio e la Cura dei TumoriAntonio Russo - University of PalermoEdoardo Francini - Department of Experimental and Clinical Medicine, Firenze, Italy
- Resource Type
- Abstract
- Publication Details
- Journal of clinical oncology, Vol.41(6_suppl), pp.166-166
- DOI
- 10.1200/JCO.2023.41.6_suppl.166
- ISSN
- 0732-183X
- eISSN
- 1527-7755
- Number of pages
- 1
- Language
- English
- Date published
- 02/20/2023
- Academic Unit
- Internal Medicine
- Record Identifier
- 9985223630402771
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