Lack of tumors in infants with perinatal HIV-1 exposure and fetal/neonatal exposure to zidovudine

被引:79
作者
Hanson, IC
Antonelli, TA
Sperling, RS
Oleske, JM
Cooper, E
Culnane, M
Fowler, MG
Kalish, LA
Lee, SS
McSherry, G
Mofenson, L
Shapiro, DE
机构
[1] Baylor Coll Med, Houston, TX 77030 USA
[2] New England Res Inst, Watertown, MA 02172 USA
[3] Mt Sinai Sch Med, New York, NY USA
[4] Univ Med & Dent New Jersey, Sch Med, Newark, NJ 07103 USA
[5] Boston Med Ctr, Boston, MA USA
[6] NIAID, Pediat Med Branch, Div Aids, NIH, Bethesda, MD 20892 USA
[7] Harvard Univ, Sch Publ Hlth, Stat & Data Anal Ctr, Ctr Biostat AIDS Res, Boston, MA 02115 USA
[8] NICHHD, NIH, Bethesda, MD 20892 USA
关键词
perinatal HIV transmission; zidovudine; perinatal HIV transmission prophylaxis carcinogenesis;
D O I
10.1097/00042560-199904150-00008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Zidovudine (ZDV) therapy during pregnancy and to the neonate reduced perinatal HIV transmission by nearly 70% in Pediatric AIDS Clinical Trials Group (PACTG) protocol 076. ZDV has been reported as positive in several in vitro carcinogenicity screening tests. We evaluated the short-term risk for tumors in 727 children with known ZDV exposure enrolled into the PACTG 076/219 and the Women and Infants Transmission Study (WITS). ZDV exposure in utero (antepartum) occurred in 97% and 99% of infants in PACTG 076/219 or WITS, respectively. Mean follow-up was 38.3 months with 366.9 person years follow-up for PACTC 076/219 and 14.5 months with 743.7 person years follow-up for WITS. No tumors of any nature were observed; relative risk was 0 (95% confidence interval [CI], 0-17.6). These data are reassuring regarding the short-term lack of tumors for ZDV-exposed infants observed to date. Longitudinal, standardized follow-up for infants with in utero antiretroviral exposure is necessary to assess long-term carcinogenicity.
引用
收藏
页码:463 / 467
页数:5
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