Treatment patterns and survival outcomes in metastatic castration-resistant prostate cancer in the Brazilian population: LACOG 1818.
Abstract
27 Background: Prostate cancer is the second leading cause of cancer death in men worldwide. In Brazil, 75% of patients (pts) rely on the public healthcare system, where access to novel therapies is limited. This disparity may lead to significant differences in survival outcomes. The LACOG 1818 study aims to address this gap by evaluating survival outcomes and treatment patterns among Brazilian pts diagnosed with metastatic castration resistant prostate cancer (mCRPC) in different healthcare settings (public versus private). Methods: LACOG 1818 is a retrospective cohort that included Brazilian pts from 18 research sites diagnosed with mCRPC between Jan 2014 and Dec 2017. Data on pts demographics, clinicopathological features, treatment patterns, and overall survival (OS) were collected from medical records. The primary endpoint was cause-specific survival (CSS) estimated by Kaplan-Meier method. Comparisons between groups (public vs. private healthcare) were assessed by chi-square and the log-rank tests. Results: From Jan 2020 to Jan 2022, 582 eligible pts were included. The median age was 49 (26-53) years, 259 (45%) were white and 85 (15%) were black/brown. Most had bone metastases (n=499, 86%), followed by non-regional lymph-nodes (n=239, 41%). A total of 323 (55%) pts had public and 259 (45%) had private health coverage. The main modality of castration was biochemical castration (n=442, 76% [public 60% vs. private 96%; p<0.0001]), followed by bilateral orchiectomy (n=140, 24% [public 40% vs. private 4%; p<0.0001]). 499 pts had available data on systemic treatment for mCRPC: 473 (95%) received first line; 247 (49%) second line; and 147 (29%) ≥ 3 lines. 378 (65%) pts received a bone protector agent (63% in public vs. 68% in private; p <0.001). At median follow-up of 59 months (95% CI 54.3-62.1), median OS was 57.1 months (95% CI 47.0-65.2) in overall sample; 44.8 months (95% CI 36.0-57.1) in public versus 65.7 months (95% CI 59.8-79.1) in private (HR 1.4 [95%IC 1.1-1.8] p=0.0051). The median CSS was 73.8 months (95% CI 55.1.-NR) in public versus 102.4 months (95% CI 83.4-102.4) in private (HR 1.9 [95%IC 1.4-2.6] p<0.0001). Conclusions: LACOG 1818 study demonstrated significant disparities in treatment patterns and survival outcomes between public and private settings for Brazilian pts with mCRPC. Pts with private coverage had longer OS and CSS. These findings underscore the need for improved access to novel therapies and comprehensive cancer care in Brazil's public healthcare system to reduce survival disparities. Clinical trial information: NCT04962919 . Private Public P First-line N=221 N= 251 <0.0001 ARPI 132 (60%) 18 (7%) Antiandrogen 30 (13%) 127(51%) Chemotherapy 59 (27%) 106 (42%) Second-line N=132 N=110 <0.0001 ARPI 75 (57%) 25 (23%) Antiandrogen 5 (4%) 22 (20%) Chemotherapy 52 (39%) 63 (57%) ARPI= Antiandrogen receptor pathways inhibitor. Antiandrogen= bicalutamide, flutamide, cyproterone and DES.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (20)
Fernando Cotait Maluf
Hospital Beneficência Portuguesa and Hospital Israelita Albert Einstein, São Paulo, Brazil
Suelen Patrícia dos Santos Martins
Centro de Estudos e Pesquisas de Hematologia e Oncologia (CEPHO), Faculdade de Medicina do ABC (FMABC), São Paulo, Brazil
Deusdedit Cortez Vieira Silva Neto
Irmandade Santa Casa de Misericórdia de São Paulo, São Paulo, Brazil
Daniel da Motta Girardi
Hospital Sírio-Libanês, Brasília, Brazil
Jose Augusto Rinck Jr
A.C. Camargo Cancer Center HC da Unicamp, Campinas, Brazil
Ana Caroline Fonseca Alves
Hospital São Domingos, São Luís, Brazil
Thiago Lins Almeida
Hospital Napoleão Laureano - Universidade Federal da Paraiba (UFPB), João Pessoa, Brazil
Andréa Lopes Ponte de Souza
Instituto de Medicina Integral Professor Fernando Figueira (IMIP) and Instituto Santa Joana de Ensino e Pesquisa - Hospital Santa Joana, Recife, Brazil
Daniel Vilarim Araujo
University of Florida, Gainesville, FL
Aline Bobato Lara Gongora
Hospital do Câncer de Cascavel - União Oeste Paranaense de Estudos e Combate ao Cancer (UOPECCAN), Cascavel, Brazil
Diogo Assed Bastos
Hospital Sírio-Libanês, São Paulo, Brazil
Cristina de Deus Anjos Tavares Sampaio
Clinica Prognóstica - Centro de Pesquisa Clínica Onconeo, Campo Grande, Brazil
Augusto C. A. Mota
Instituto ETICA, Clínica AMO (Assistência Multidisciplinar em Oncologia), Salvador, Brazil
Andre P. Fay
PUCRS School of Medicine, Hospital Nora Teixeira, Porto Alegre, Brazil
Roberto Odebrecht Rocha
Hospital Santa Marcelina, São Paulo, Brazil
Douglas Dias e Silva
Einstein Hospital Israelita, São Paulo, Brazil
Tainá Cabalheiro
Latin American Cooperative Oncology Group (LACOG), Porto Alegre, Brazil
Pablo Barrios
Dana-Farber Cancer Institute, Boston, MA
Gustavo Gössling
Latin American Cooperative Oncology Group (LACOG), Porto Alegre, Brazil
Andrey Soares
Einstein Hospital Israelita, São Paulo, Brazil