Taxanes for the treatment of breast cancer during pregnancy: an international cohort study.
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Ferrigno Guajardo Ana S, Vaca-Cartagena Bryan F, Mayer Erica L, Bousrih Chayma, Oluchi Oke, Saura Cristina, Peccatori Fedro, Muñoz-Montaño Wendy, Cabrera-Garcia Alvaro, Lambertini Matteo, Corrales Luis, Becerril-Gaitan Andrea, Sella Tal, Newman Alexandra Bili, Pistilli Barbara, Martinez Ashley, Ortiz Carolina, Joval-Ramentol Laia, Scarfone Giovanna, Buonomo Barbara, Lara-Medina Fernando, Sanchez Jacqueline, Arecco Luca, Ramos-Esquivel Allan, Susnjar Snezana, Morgan Gilberto, Villarreal-Garza Cynthia, Azim Hatem A
Аннотация
METHODS: This is a multicenter, international cohort study of breast cancer patients treated with taxanes during pregnancy. A descriptive analysis was undertaken to synthetize available data.
RESULTS: A total of 103 patients were included, most of whom were treated with paclitaxel and anthracyclines given in sequence during gestation (90.1%). The median gestational age at taxane initiation was 28 weeks (range = 12-37 weeks). Grade 3-4 adverse events were reported in 7 of 103 (6.8%) patients. The most common reported obstetric complications were intrauterine growth restriction (n = 8 of 94, 8.5%) and preterm premature rupture of membranes (n = 5 of 94, 5.3%). The live birth rate was 92 of 94 (97.9%), and the median gestational age at delivery was 37 weeks (range = 32-40 weeks). Admission to an intensive care unit was reported in 14 of 88 (15.9%) neonates, and 17 of 70 (24.3%) live births resulted in small for gestational age neonates. Congenital malformations were reported in 2 of 93 (2.2%).
CONCLUSION: Obstetric and neonatal outcomes after taxane exposure during pregnancy were generally favorable and did not seem to differ from those reported in the literature with standard anthracycline-based regimens. This study supports the use of taxanes during gestation when clinically indicated.