Cytotoxic chemotherapy during the first trimester of pregnancy poses a significant risk of teratogenicity and fetal abnormalities.
Supports avoiding cytotoxic chemotherapy in the first trimester; leaves open optimal regimens and later-trimester safety.
OCCASIONALLY, because of clinical considerations, cytotoxic drug therapy is necessary during pregnancy, or unfortunately a patient conceives while under treatment. It is known that the human fetus is the most susceptible to teratogenic agents, such as x-radiation¹and rubella virus,²during the first trimester, and it seems probable that this is also the case for cytotoxic chemotherapy.³It is important to assess the risks to which the fetus is subjected under these circumstances. The teratogenicity of antineoplastic agents has been proved in laboratory animals. Similar phenomena are seen in human fetal development when such drugs are administered during the first trimester of pregnancy. Aminopterin, which has been used in the past as an abortifacient, has been reported to cause profound abnormalities in a high percentage of fetuses.²Alkylating agents, especially cyclophosphamide, when administered during the first trimester, have been associated with major and minor abnormalities, including
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Charles L. Murray (1984) studied this question.
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