1099 – Chemotherapy for breast cancer during pregnancy: evaluation of maternal–fetal safety and therapeutic efficacy

Authors

  • Maria Maria Sanches de Oliveira Pontifícia Universidade Católica de Goiás – Goiânia (GO), Brazil.
  • Alberto Vilela Lopes Dávila Pontifícia Universidade Católica de Goiás – Goiânia (GO), Brazil.
  • Geovanna Aires Silva Pontifícia Universidade Católica de Goiás – Goiânia (GO), Brazil.
  • Maria Eduarda Pereira de Souza Pontifícia Universidade Católica de Goiás – Goiânia (GO), Brazil.
  • Marina Ribeiro Castro Pontifícia Universidade Católica de Goiás – Goiânia (GO), Brazil.

DOI:

https://doi.org/10.29289/25945394V36S11099

Keywords:

breast neoplasms, pregnancy, chemotherapy

Abstract

Introduction: Breast cancer is the most common malignancy diagnosed during pregnancy, creating a therapeutic dilemma
that requires effective maternal treatment while protecting the fetus. Evidence suggests that chemotherapy after the first
trimester, mainly anthracyclines and taxanes, does significantly elevate the risk of congenital malformations, although
prematurity and a low birth weight remain concerns. Long-term child outcomes are still uncertain.
Objective: To assess the safety and efficacy of chemotherapy during pregnancy in patients with breast cancer.
Methodology: An integrative review was conducted via the PubMed database, utilizing MeSH terms related to breast
cancer, pregnancy, chemotherapy, and therapeutic outcomes. English-language studies published from 2015 to 2025 were
included if they evaluated the safety and/or efficacy of chemotherapy during pregnancy. Clinical trials, observational studies, cohorts, case series, and case reports with maternal and fetal data were eligible. Studies on fertility preservation, isolated hormonal therapy, narrative reviews, and nongestational settings were excluded. Main outcomes were disease-free
survival, overall survival, recurrence, prematurity, congenital malformations, and birth weight.
Results: Anthracycline- and taxane-based regimens administered after the first trimester showed maternal oncologic
outcomes comparable to those of nonpregnant patients after adjustment for stage and tumor factors. Serious maternal
events and congenital malformations were uncommon. Still, prematurity, low birth weight, and neonatal intensive care
admission remained important risks, often linked to iatrogenic preterm delivery. Anti-HER2 agents were strongly associated with oligohydramnios or anhydramnios and poorer perinatal outcomes and therefore should be avoided.
Conclusion: Chemotherapy with anthracyclines and taxanes in the second and third trimesters appears to be effective
and relatively safe in pregnancy-associated breast cancer. The main gap in literature is the lack of robust, long-term prospective data on neurocognitive and cardiac outcomes in exposed children. Individualized multidisciplinary care focused
on reducing iatrogenic prematurity is essential.
Ethics: Public data – Literature review.

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Published

2026-10-19

How to Cite

de Oliveira, M. M. S., Dávila, A. V. L., Silva, G. A., de Souza, M. E. P., & Castro, M. R. (2026). 1099 – Chemotherapy for breast cancer during pregnancy: evaluation of maternal–fetal safety and therapeutic efficacy. Mastology, 36(suppl. 1). https://doi.org/10.29289/25945394V36S11099

Issue

Section

Basic Research Section