LAUSR

PurposeGynecologic malignancies are often detected in advanced stages, requiring chemotherapy with taxane/platinum combinations, which may cause severe toxicities, such as neutropenia and peripheral neuropathy. Gene polymorphisms are suspected as possible causes for the interindividual variability on chemotherapy toxicities.ObjectiveTo evaluate the role of ABCB1 1236C>T, 3435C>T; CYP2C8*3; CYP3A5*3C variants on paclitaxel/carboplatin toxicities.MethodsA cohort of 503 gynecologic cancer patients treated with paclitaxel/carboplatin at the Brazilian National Cancer Institute (INCA-Brazil) was recruited (2013–2017). Polymorphisms were genotyped by real-time PCR, and toxicities were evaluated by patients’ interviews at each chemotherapy cycle and by data collection from electronic records. The association of clinical features and genotypes with severe toxicities was estimated using Pearson’s Chi square tests and multiple regression analyses, with calculation of adjusted odds ratios (ORadjusted), and respective 95% confidence intervals (95% CI).ResultsCYP2C8*3 was significantly associated with increased risks of severe (grades 3–4) neutropenia (ORadjusted 2.11; 95% CI 1.24–3.6; dominant model) and severe thrombocytopenia (ORadjusted 4.93; 95% CI 1.69–14.35; recessive model), whereas ABCB1 variant genotypes (ORadjusted 2.13; 95% CI 1.32–3.42), in association with CYP2C8*3 wild type (GG) (ORadjusted 1.93; 95% CI 1.17–3.19), were predictive of severe fatigue.ConclusionsThe present study suggests that CYP2C8*3 is a potential predictor of hematological toxicities related to paclitaxel/carboplatin treatment. Since hematological toxicities, especially neutropenia, may lead to dose delay or treatment interruption, such prognostic evaluation may contribute to clinical management of selected patients with paclitaxel-based chemotherapy.