Circulating hsa-miR-29c-3p and VEGF-A levels predict the response to FOLFIRI plus aflibercept in elderly metastatic colorectal cancer patients

BACKGROUND: Metastatic colorectal cancer (mCRC) patients who progress on oxaliplatin-based chemotherapy benefit from second-line treatment with FOLFIRI plus the antiangiogenic drug aflibercept. However, the absence of validated biomarkers for antiangiogenic therapies remains a challenge. In this con...

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Detalles Bibliográficos
Autores: Toledano-Fonseca, Marta, Cano-Osuna, María Teresa, Élez, Elena, Soto-Alsar, Javier, Páez, David, Fernández-Montes, Ana, Graña, Begoña, Salud, Antonieta, Yubero, Alfonso, Macías, Ismael, Quintero, Guillermo, López-López, Carlos, Fernández-Rodríguez, Teresa, García-Ortiz, María Victoria, Sastre, Javier, García-Alfonso, Pilar, Rodríguez-Ariza, Antonio, Aranda, Enrique
Tipo de recurso: artículo
Fecha de publicación:2025
País:España
Institución:Conselleria de Salut i Consum del Govern de les Illes Balears
Repositorio:Docusalut
Idioma:inglés
OAI Identifier:oai:docusalut.com:20.500.13003/25580
Acceso en línea:https://hdl.handle.net/20.500.13003/25580
Access Level:acceso abierto
Palabra clave:FOLFIRI
VEGF‐A
aflibercept
antiangiogenic therapy
circulating miRNAs
metastatic colorectal cancer
Descripción
Sumario:BACKGROUND: Metastatic colorectal cancer (mCRC) patients who progress on oxaliplatin-based chemotherapy benefit from second-line treatment with FOLFIRI plus the antiangiogenic drug aflibercept. However, the absence of validated biomarkers for antiangiogenic therapies remains a challenge. In this context, we previously reported that combining plasma VEGF-A levels, a circulating microRNA profile, and patient clinical characteristics predicts outcomes in FOLFIRI plus aflibercept treatment. In the present study, we now report biomarkers of response to FOLFIRI plus aflibercept in elderly mCRC patients who progressed after first-line oxaliplatin-based chemotherapy. METHODS: The study included 154 mCRC patients over 70 years of age enrolled in the clinical phase II trial AFEMA. Plasma samples were obtained before FOLFIRI plus aflibercept treatment, and circulating levels of VEGF-A and 13 miRNAs were analysed. RESULTS: The levels of VEGF-A and five of these 13 miRNAs (miR-193-3b, miR-432-5p, miR-29c-3p, miR-93-5p, miR-30a-3p) enabled the stratification of patients based on progression-free survival and time-to-treatment failure. Specifically, combining miR-29c-3p with VEGF-A improved prognostic accuracy. CONCLUSION: Our study underscores the value of integrating miR-29c-3p analysis with VEGF-A as a biomarker strategy to advance the management of elderly mCRC patients receiving FOLFIRI plus aflibercept, improving outcome predictions and enabling more personalised therapeutic strategies.