NTP专著:与妊娠期间癌症化疗使用相关的发育影响和妊娠结局。

NTP monograph Pub Date : 2013-05-01
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引用次数: 0

摘要

美国国家毒理学计划(NTP)健康评估和翻译办公室(OHAT)对人类怀孕期间使用癌症化疗对发育的影响和妊娠结局进行了评估。最终的NTP专著于2013年5月完成(可在http:// ntp.niehs.nih.gov/go/36495获得)。据报道,怀孕期间癌症的发病率为每10万名孕妇中有17至100人。化疗是治疗癌症的常用方法;然而,大多数化疗药物被归类为已知或可疑的人类致畸物。国家毒理学规划选择在怀孕期间使用癌症化疗进行评估,因为:(1)缺乏对人类怀孕期间使用癌症化疗后妊娠结局的全面综述,包括发育动物毒理学文献与人类观察性研究的整合;(2)由于怀孕期间诊断出的癌症的预期发病率随着女性怀孕年龄的推迟,化疗对妊娠期间暴露于癌症化疗的后代的发育影响日益引起公众的兴趣。在目前使用的大约110种癌症化疗药物中,NTP专著包括在1261例妊娠中使用的56种药物的数据,这些药物的妊娠结局已被记录。总体而言,NTP评估发现,癌症化疗治疗似乎与:(1)与妊娠中期和/或妊娠晚期暴露相比,妊娠早期暴露后的主要畸形率更高;(2)妊娠中期和/或妊娠晚期暴露后的死产率增加;羊水异常低水平(主要归因于曲妥珠单抗);(3)胎儿生长受损和骨髓抑制,数据也不充分。在怀孕期间用化疗治疗癌症似乎不会增加自发性早产,也不会损害孩子早期的正常生长发育。此外,国家毒理学规划专著提供了个别癌症化疗药物的背景资料(例如,胎盘和母乳转运的证据,动物的发育毒性),并简要回顾了怀孕期间妇女中七种常诊断癌症的患病率和预后。最后,国家毒理学规划专著指出了在解释这一观察性文献基础上的健康结果所面临的挑战,并讨论了可能采取的措施,以提高对怀孕期间癌症化疗对发育影响的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
NTP Monograph: Developmental Effects and Pregnancy Outcomes Associated With Cancer Chemotherapy Use During Pregnancy.

The National Toxicology Program (NTP) Office of Health Assessment and Translation (OHAT) conducted an evaluation of the developmental effects and pregnancy outcomes associated with cancer chemotherapy use during pregnancy in humans. The final NTP monograph was completed in May 2013 (available at http:// ntp.niehs.nih.gov/go/36495). The incidence of cancer during pregnancy has been reported to occur from 17 to 100 per 100,000 pregnant women. Chemotherapy is a common treatment for cancer; however, most chemotherapy agents are classified as known or suspected human teratogens. Cancer chemotherapy use during pregnancy was selected for evaluation by the NTP because of the: (1) paucity of comprehensive reviews on the pregnancy outcomes following cancer chemotherapy use during pregnancy in humans, including the integration of the developmental animal toxicology literature with the observational studies in humans, and (2) growing public interest in the developmental effects of chemotherapy on offspring exposed to cancer chemotherapy during gestation due to the expected incidence of cancer diagnosed during pregnancy as women delay pregnancy to later ages. Of the approximately 110 cancer chemotherapeutic agents currently in use, the NTP monograph includes data on 56 agents used during 1,261 pregnancies for which pregnancy outcomes were documented. Overall, the NTP evaluation found that treatment with chemotherapy for cancer appeared to be associated with: (1) a higher rate of major malformations following exposure during the first trimester compared to exposure in the second and/or third trimester; (2) an increase the rate of stillbirth following exposure in the second and/ or third trimester; abnormally low levels of amniotic fluid (primarily attributable to Trastuzumab); and (3), also data are insufficient, impaired fetal growth and myelosuppression. Treatment with chemotherapy for cancer during pregnancy did not appear to increase spontaneous preterm birth, or impair normal growth and development of offspring during early life. In addition, the NTP monograph provides background materials on individual cancer chemotherapeutic agents (e.g., evidence for placenta and breast milk transport, developmental toxicity in animals), and a brief review of the prevalence and prognosis of seven frequently diagnosed cancers in women during pregnancy. Finally, the NTP monograph identifies challenges in interpreting the health outcomes from this observational literature base and discussed possible actions to improve the understanding of the developmental effects of chemotherapy treatment for cancer administered during pregnancy.

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