Sabina Llera, Andrea , Furquim Werneck Abdelhay, Eliana Saul , Artagaveytia, Nora , Daneri-Navarro, Adrian , Muller, Bettina , Velazquez, Carlos , Alcoba, Elsa B. , Alonso, Isabel , Alves da Quinta, Daniela B. , Binato, Renata , Ines Bravo, Alicia , Camejo, Natalia , Maria Carraro, Dirce , Castro, Monica , Castro-Cervantes, Juan M. , Cataldi, Sandra , Cayota, Alfonso , Cerda, Mauricio , Colombo, Alicia , Crocamo, Susanne , Del Toro-Arreola, Alicia , Delgadillo-Cisterna, Raul , Delgado, Lucia , Dreyer-Breitenbach, Marisa , Fejerman, Laura , Fernandez, Elmer A. , Fernandez, Jorge , Fernandez, Wanda , Franco-Topete, Ramon A. , Gabay, Carolina , Gaete, Fancy , Garibay-Escobar, Adriana , Gomez, Jorge , Greif, Gonzalo , Gross, Thomas G. , GUERRERO ALONSO, MARISOL, Henderson, Marianne K. , Lopez-Munoz, Miguel E. , Lopez-Vazquez, Alejandra , Maldonado, Silvina , Moran-Mendoza, Andres J. , Nagai, Maria Aparecida , Oceguera-Villanueva, Antonio , Ortiz-Martinez, Miguel A. , Quintero, Jael , Quintero-Ramos, Antonio , Reis, Rui M. , Retamales, Javier , Rivera-Claisse, Ernesto , Rocha, Dario , Rodriguez, Robinson , Rosales, Cristina , Salas-Gonzalez, Efrain , Sanchotena, Veronica , Segovia, Laura , Martin Sendoya, Juan , Silva-Garcia, Aida A. , Trinchero, Alejandra , Valenzuela, Olivia , Vedham, Vidya , Zagame, Livia , Podhajcer, Osvaldo L. , US-Latin Amer Canc Res Network US-
No
Front. Oncol.
Article
Científica
2
2
4.7
1.138
22/03/2022
000788226200001
PurposesMost molecular-based published studies on breast cancer do not adequately represent the unique and diverse genetic admixture of the Latin American population. Searching for similarities and differences in molecular pathways associated with these tumors and evaluating its impact on prognosis may help to select better therapeutic approaches. Patients and MethodsWe collected clinical, pathological, and transcriptomic data of a multi-country Latin American cohort of 1,071 stage II-III breast cancer patients of the Molecular Profile of Breast Cancer Study (MPBCS) cohort. The 5-year prognostic ability of intrinsic (transcriptomic-based) PAM50 and immunohistochemical classifications, both at the cancer-specific (OSC) and disease-free survival (DFS) stages, was compared. Pathway analyses (GSEA, GSVA and MetaCore) were performed to explore differences among intrinsic subtypes. ResultsPAM50 classification of the MPBCS cohort defined 42 center dot 6% of tumors as LumA, 21 center dot 3% as LumB, 13 center dot 3% as HER2E and 16 center dot 6% as Basal. Both OSC and DFS for LumA tumors were significantly better than for other subtypes, while Basal tumors had the worst prognosis. While the prognostic power of traditional subtypes calculated with hormone receptors (HR), HER2 and Ki67 determinations showed an acceptable performance, PAM50-derived risk of recurrence best discriminated low, intermediate and high-risk groups. Transcriptomic pathway analysis showed high proliferation (i.e. cell cycle control and DNA damage repair) associated with LumB, HER2E and Basal tumors, and a strong dependency on the estrogen pathway for LumA. Terms related to both innate and adaptive immune responses were seen predominantly upregulated in Basal tumors, and, to a lesser extent, in HER2E, with respect to LumA and B tumors. ConclusionsThis is the first study that assesses molecular features at the transcriptomic level in a multicountry Latin American breast cancer patient cohort. Hormone-related and proliferation pathways that predominate in PAM50 and other breast cancer molecular classifications are also the main tumor-driving mechanisms in this cohort and have prognostic power. The immune-related features seen in the most aggressive subtypes may pave the way for therapeutic approaches not yet disseminated in Latin America.
breast cancer; Latin America; PAM50 subtypes; risk of recurrence; biological pathways