BRaziLian outcomE for metAStatic breasT Cancer

Overview

Given the certain benefit in efficacy of adding CDK 4/6 inhibitor to first line endocrine therapy in metastatic breast cancer HR+ HER2- , the aim of this project is to evaluate whether patients without private health insurance may have worse outcomes than privately insured women due to limited access to such class of drugs during their treatments. Prospective observational study with 300 patients divided into two groups, one with patients from the public health system and the second with patients treated in the private service. Patients will be recruited in different regions of Brazil and will be followed for 24 months, stratified according to the use or not of the CDK 4/6 inhibitors.

In Brazil, breast cancer is the most common carcinoma in women, non- melanoma skin carcinomas. 66,280 new cases of breast cancer were estimated for each year of the 2020-2022 triennium, which represents 29.7% of all cancers. It is the main cause of cancer death in women and mortality rates remain high due to the large number of cases diagnosed in advanced stages (around 40%). According to data from Concord-3, five-year survival estimates in the country were 75.2% (73.9 - 76.5) for the period from 2010 to 2014. However, the 5-year survival rate in the same period was over 85% in 25 countries and reached approximately 90% in North America and Oceania (3). The survival rate in low- and middle-income countries is remarkably different. This disparity in survival reflects the unequal access of the population to breast screening, difficulty in diagnosis, delayed treatment and limited access to first-line systemic therapy for advanced and metastatic tumors. Notwithstanding, with the development of new, expensive drugs, breast cancer survival differences between Brazil and high-income countries may increase if the access to new agents is not assured. One of the most important changes in the hormone positive breast cancer, recently identified, was the greatly increased function of proteins that stimulate cells to grow and multiply, known as CDK4 and 6 (Cyclin-Dependent Kinase). These are normal parts of the human cell, but in this type of tumor they work much faster than they should, making the tumor grow. Recent studies showed benefit with new target therapies that lower recurrence and progression, as cyclin-dependent kinases 4 and 6 (CDK 4/6) inhibitors with endocrine therapies in hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)- negative advanced breast cancer has shown substantial improvements in progression- free survival (PFS). Palbociclib (IBRANCE®) is a first-in-class oral inhibitor of cyclin-dependent kinases 4 and 6 that blocks G1-to S-phase progression. There is a strong in-vitro and clinical evidence suggesting that the dual inhibition of CDK 4/6 and ER signaling is a highly effective therapeutic strategy in HR+ MBC. In the phase 2 PALOMA-1 trial, the addition of palbociclib to letrozole significantly improved progression-free survival in women with advanced estrogen receptor-positive and HER2-negative breast cancer. Subsequently, in the phase III trial that included postmenopausal patients with metastatic, HR-positive, HER2-negative breast cancer who had not received prior treatment for advanced disease, an improvement in PFS (24.8 vs. 14.5 months; hazard ratio \[HR\] 0.58, 95% CI 0.46-0.72) and objective response rate (ORR; 42 vs. 35 percent) was seen with the combination of palbociclib and letrozole compared with letrozole alone. The National Comprehensive Cancer Network (NCCN) Panel recommends first line therapy for HR-positive HER2-negative with aromatase inhibitor (AI) in combination with CDK 4/6 inhibitor (palbociclib, ribociclib, or abemaciclib) in postmenopausal women or premenopausal women receiving ovarian ablation or ovarian function suppression with an LHRH agonist, combinations of aromatase inhibitors with CDK 4/6 inhibitors (8). However, the situation is rather different in many countries, including Brazil, where the population has limited access to these medications. The health system in Brazil is organized in two types of assistance: the public system, known as Unified Health System (SUS), where the policies and costs are regulated by the State, and a private system, where the coverage is regulated by the National Supplementary Health Agency (ANS) through agreements with health insurance plans. Nowadays, 75% of the Brazilian population is attended by the public system versus 25% in the Supplementary Health Service. The commercialization of CDK 4/6 inhibitors was only released in the national territory in 2018, but until nowadays it is not accessible for the majority of patients. Of note, patients in the public health system do not gain access to this class of drugs and those with private insurances usually settle a lawsuit to obtain the treatment once CDK 4/6 inhibitors are not covered by the National Supplementary Health Agency. Thus, the disparity in the access to these important treatments due to socioeconomic differences probably results in worse outcomes according to health care coverage.