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
相关论文
共 15 条
[1]  
[Anonymous], 1998, MMWR Recomm Rep, V47, P1
[2]  
[Anonymous], 1994, MMWR Recomm Rep, V43, P1
[3]   A transplacental carcinogenicity bioassay in CD-1 mice with zidovudine [J].
Ayers, KM ;
Torrey, CE ;
Reynolds, DJ .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1997, 38 (02) :195-198
[4]   Nonclinical toxicology studies with zidovudine: Genetic toxicity tests and carcinogenicity bioassays in mice and rats [J].
Ayers, KM ;
Clive, D ;
Tucker, WE ;
Hajian, G ;
deMiranda, P .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1996, 32 (02) :148-158
[5]   REDUCTION OF MATERNAL-INFANT TRANSMISSION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 WITH ZIDOVUDINE TREATMENT [J].
CONNOR, EM ;
SPERLING, RS ;
GELBER, R ;
KISELEV, P ;
SCOTT, G ;
OSULLIVAN, MJ ;
VANDYKE, R ;
BEY, M ;
SHEARER, W ;
JACOBSON, RL ;
JIMENEZ, E ;
ONEILL, E ;
BAZIN, B ;
DELFRAISSY, JF ;
CULNANE, M ;
COOMBS, R ;
ELKINS, M ;
MOYE, J ;
STRATTON, P ;
BALSLEY, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (18) :1173-1180
[6]   After AIDS clinical trial 076: The changing pattern of zidovudine use during pregnancy, and the subsequent reduction in the vertical transmission of human immunodeficiency virus in a cohort of infected women and their infants [J].
Cooper, ER ;
Nugent, RP ;
Diaz, C ;
Pitt, J ;
Hanson, C ;
Kalish, LA ;
Mendez, H ;
Zorrilla, C ;
Hershow, R ;
Moye, J ;
Smeriglio, V ;
Fowler, MG ;
Rich, K ;
Turpin, D ;
PachecoAcosta, E ;
Tuomala, R ;
Mesthene, D ;
Fox, H ;
Higgins, A ;
Landesman, S ;
Moroso, G ;
Willoughby, A ;
Sheon, A ;
McKinlay, S ;
Sherrieb, K .
JOURNAL OF INFECTIOUS DISEASES, 1996, 174 (06) :1207-1211
[7]  
Fiscus SA, 1996, JAMA-J AM MED ASSOC, V275, P1483, DOI 10.1001/jama.275.19.1483
[8]  
GURNEY JG, 1995, CANCER, V75, P2186, DOI 10.1002/1097-0142(19950415)75:8<2186::AID-CNCR2820750825>3.0.CO
[9]  
2-F
[10]   Acceptability and impact of zidovudine for prevention of mother-to-child human immunodeficiency virus-1 transmission in France [J].
Mayaux, MJ ;
Teglas, JP ;
Mandelbrot, L ;
Berrebi, A ;
Gallais, H ;
Matheron, S ;
Ciraru-Vigneron, N ;
Parnet-Mathieu, F ;
Bongain, A ;
Rouzioux, C ;
Delfraissy, JF ;
Blanche, S .
JOURNAL OF PEDIATRICS, 1997, 131 (06) :857-862