D. Satge et al., ANTENATAL THERAPEUTIC DRUG EXPOSURE AND FETAL NEONATAL TUMORS - REVIEW OF 89 CASES/, Paediatric and perinatal epidemiology, 12(1), 1998, pp. 84-117
Although case reports on the association between neonatal tumours and
maternal therapeutic drug use during pregnancy are cited regularly, no
systematic review has been published. In a systematic search of the l
iterature on fetal and neonatal tumours, we identified 36 malignant an
d 54 benign tumours in 89 fetuses and neonates prenatally exposed to v
arious drugs. Six associations with in utero exposure are noteworthy:
(1) phenytoin and neuroblastoma, as already suspected; (2) antibiotics
and leukaemias; (3) hormonal treatment and vascular tumours; (4) acet
aminophen (paracetamol) and fusocellular sarcoma; (5) acetaminophen in
combination with petroleum products and hepatoblastoma; and (6) dicyc
lomine hydrochloride and teratomas. In view of the high level of consu
mption of drugs by pregnant women and the rarity of neonatal tumours,
a possible carcinogenic effect is difficult to establish. However, som
e associations already observed in older infants, children and adults
after antenatal and postnatal exposure to the same drugs are of note.
We suggest that these drugs may act as carcinogens or as co-carcinogen
s in association with other physical and chemical agents and/or a part
icular genetic background. We therefore feel it is important to encour
age the systematic collection, registration and publication of case re
ports on this subject. The hypotheses generated thereby could then be
tested by formal epidemiological studies.