• Dolores Gallardo-Rincón, Gabriela Alamilla-García, Edgar Montes-Servín, Flavia Morales-Vázquez, Claudia Cano-Blanco, Jaime Coronel-Martínez, Antonio Bahena-González, Raquel Gerson-Cwilich, David Isla-Ortiz, Alfredo Toledo-Leyva, Elizabeth Montes-Servín, David Michel-Tello, and Raquel Espinosa-Romero.
• Departamento de Oncología Médica. Instituto Nacional de Cancerología. Ciudad de México, México.
• Gac Med Mex. 2019 Jan 1; 155 (6): 585-589.

IntroductionMore than the twenty percent of ovarian cancers are hereditary, and most have BRCA mutations. The 30% of Mexican patients with the BRCA1 mutation have the BRCA1 gene exon 9-12del deletion founder mutation (BRCA1 ex9-12del). BRCA-mutated tumors are more sensitive to PARP inhibitors such as olaparib.ObjectiveTo show the clinical experience on the use of olaparib at Instituto Nacional de Cancerología in Mexico.MethodOvarian cancer patients treated with olaparib from November 2016 to December 2018 were studied, and their characteristics, clinical response, progression-free survival (PFS) and toxicities were described.ResultsNineteen patients were assessed, with BRCA1 mutation being found in 78.9%, out of which 21.1% were carriers of the ex9-12del founder mutation. The median of PFS was 12 months; for patients treated on second and third line it was > 15 months, and for those treated with a fourth and subsequent line it was 8.3 months. Patients with the founder mutation had better results. Toxicities were like those reported in previous studies.ConclusionsOlaparib offers greater PFS benefit as maintenance therapy after a first and second relapse. Patients with founder mutation have had sustained PFS.Copyright: © 2019 Permanyer.

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