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Maternal and Neonatal Outcomes in Women with a History of Chemotherapy Exposure: a Population-based Study of 8 Million Obstetric Admissions

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Date 2022 May 6
PMID 35523971
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Abstract

Purpose: With improvement in cancer care and fertility preservation, increasing numbers of cancer survivors are requiring obstetrical care. The objective of our study was to evaluate the effect of history of chemotherapy exposure on maternal and neonatal outcomes.

Methods: A retrospective population-based cohort study was conducted using the Healthcare Cost and Utilization Project-Nationwide Inpatient Sample (HCUP-NIS) to obtain data on maternal and newborn outcomes in a cohort of births occurring between the years 2006 and 2015. The annual and overall prevalence of chemotherapy exposure was calculated among pregnant women, and multivariate logistic regression models were used to estimate the effect of history of exposure to chemotherapy on the risk of adverse maternal and newborn outcomes.

Results: Of 7,907,139 birth admissions, 613 had a history of chemotherapy exposure for an overall incidence of 7.75 per 100,000 admissions. The prevalence of chemotherapy exposure in pregnancy increased during the study period (P < 0.001). Women with a history of chemotherapy were more likely to suffer from obstetric and medical complications including pre-eclampsia, chorioamnionitis, postpartum hemorrhage, and venous thromboembolism as well as an increased risk in overall mortality (OR 9.39, 95% CI 1.31-67.32). No differences were observed in the incidence of adverse neonatal outcomes, including stillbirth, intra-uterine growth restriction, or preterm birth.

Conclusion: Women with history of chemotherapy have higher incidence of pregnancy complications and maternal death, with no differences in fetal or newborn outcomes.

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Anderson C, Baggett C, Engel S, Getahun D, Cannizzaro N, Mitra S JNCI Cancer Spectr. 2023; 8(1).

PMID: 38127994 PMC: 10868397. DOI: 10.1093/jncics/pkad106.

References
1.
Swerdlow A, Higgins C, Smith P, Cunningham D, Hancock B, Horwich A . Myocardial infarction mortality risk after treatment for Hodgkin disease: a collaborative British cohort study. J Natl Cancer Inst. 2007; 99(3):206-14. DOI: 10.1093/jnci/djk029. View

2.
Black K, Nichols H, Eng E, Rowley D . Prevalence of preterm, low birthweight, and small for gestational age delivery after breast cancer diagnosis: a population-based study. Breast Cancer Res. 2017; 19(1):11. PMC: 5282806. DOI: 10.1186/s13058-017-0803-z. View

3.
Ma H, Liu J, Yan W . Accuracy and Reliability of Lung Ultrasound to Diagnose Transient Tachypnoea of the Newborn: Evidence from a Meta-analysis and Systematic Review. Am J Perinatol. 2020; 39(9):973-979. DOI: 10.1055/s-0040-1721134. View

4.
Koren G, Carey N, Gagnon R, Maxwell C, Nulman I, Senikas V . RETIRED: Cancer chemotherapy and pregnancy. J Obstet Gynaecol Can. 2013; 35(3):263-278. DOI: 10.1016/S1701-2163(15)30999-3. View

5.
Framarino-Dei-Malatesta M, Sammartino P, Napoli A . Does anthracycline-based chemotherapy in pregnant women with cancer offer safe cardiac and neurodevelopmental outcomes for the developing fetus?. BMC Cancer. 2017; 17(1):777. PMC: 5696726. DOI: 10.1186/s12885-017-3772-9. View