Identificador persistente para citar o vincular este elemento: https://accedacris.ulpgc.es/jspui/handle/10553/157770
Título: BRCA1 mRNA expression and outcome to neoadjuvant cisplatin-based chemotherapy in bladder cancer
Autores/as: Font, A.
Taron, M.
Gago, J.L.
Costa, C.
Sánchez, J.J.
Carrato, C.
Mora, M.
Celiz, P.
Pérez, L.
Rodríguez Abreu, Delvys 
Gimenez-Capitan, A.
Quiroga, V.
Benlloch, S.
Ibarz, L.
Rosell, R.
Clasificación UNESCO: 32 Ciencias médicas
320713 Oncología
320806 Quimioterapia
Palabras clave: Bladder cancer
BRCA1 mRNA expression
Cisplatin
Customized chemotherapy
Pathological response, et al.
Fecha de publicación: 2011
Publicación seriada: Annals of Oncology 
Resumen: Background: Neoadjuvant chemotherapy has shown a modest benefit in muscle-invasive bladder cancer patients; however, the subset of patients most likely to benefit has not been identified. BRCA1 plays a central role in DNA repair pathways and low BRCA1 expression has been associated with sensitivity to cisplatin and longer survival in lung and ovarian cancer patients. Patients and methods: We assessed BRCA1 messenger RNA expression levels in paraffin-embedded pre-treatment tumor samples obtained by transurethral resection from 57 patients with locally advanced bladder cancer subsequently treated with neoadjuvant cisplatin-based chemotherapy. BRCA1 levels were divided into terciles and correlated with pathological response and survival. Results: A significant pathological response (pT0-1) was attained in 66% (24 of 39) of patients with low/intermediate BRCA1 levels compared with 22% (4 of 18) of patients with high BRCA1 levels (P = 0.01). Median survival was 168 months in patients with low/intermediate levels and 34 months in patients with high BRCA1 levels (P = 0.002). In the multivariate analysis for survival, only BRCA1 expression levels and lymphovascular invasion emerged as independent prognostic factors. Conclusions: Our data suggest that BRCA1 expression may predict the efficacy of cisplatin-based neoadjuvant chemotherapy and may help to customize therapy in bladder cancer patients.
URI: https://accedacris.ulpgc.es/jspui/handle/10553/157770
ISSN: 0923-7534
DOI: 10.1093/annonc/mdq333
Fuente: Annals of Oncology [ISSN 0923-7534], v. 22(1), pp. 139-144 (Enero 2011)
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