Cancer during pregnancy: an analysis of 215 patients emphasizing the obstetrical and the neonatal outcomes
- PMID: 19841323
- DOI: 10.1200/JCO.2009.23.2801
Cancer during pregnancy: an analysis of 215 patients emphasizing the obstetrical and the neonatal outcomes
Abstract
Purpose: The aim of this study was to assess the management and the obstetrical and neonatal outcomes of pregnancies complicated by cancer.
Patients and methods: In an international collaborative setting, patients with invasive cancer diagnosed during pregnancy between 1998 and 2008 were identified. Clinical data regarding the cancer diagnosis and treatment and the obstetric and neonatal outcomes were collected and analyzed.
Results: Of 215 patients, five (2.3%) had a pregnancy that ended in a spontaneous miscarriage and 30 (14.0%) pregnancies were interrupted. Treatment was initiated during pregnancy in 122 (56.7%) patients and postpartum in 58 (27.0%) patients. The most frequently encountered cancer types were breast cancer (46%), hematologic malignancies (18%), and dermatologic malignancies (10%). The mean gestational age at delivery was 36.3 +/- 2.9 weeks. Delivery was induced in 71.7% of pregnancies, and 54.2% of children were born preterm. In the group of patients prenatally exposed to cytotoxic treatment, the prevalence of preterm labor was increased (11.8%; P = .012). Furthermore, in this group a higher proportion of small-for-gestational-age children (birth weight below 10th percentile) was observed (24.2%; P = .001). Of all neonates, 51.2% were admitted to a neonatal intensive care unit, mainly (85.2%) because of prematurity. There was no increased incidence of congenital malformations.
Conclusion: Pregnant cancer patients should be treated in a multidisciplinary setting with access to maternal and neonatal intensive care units. Prevention of iatrogenic prematurity appears to be an important part of the treatment strategy.
Comment in
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Treatment of cancer during pregnancy: the need for tailored strategies.J Clin Oncol. 2010 Jun 20;28(18):e302-3; author reply e304. doi: 10.1200/JCO.2010.28.0628. Epub 2010 May 10. J Clin Oncol. 2010. PMID: 20458035 No abstract available.
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