A trial of shortened zidovudine regimens to prevent mother-to-child transmission of human immunodeficiency virus type 1

被引:261
作者
Lallemant, M
Jourdain, G
Le Coeur, S
Kim, S
Koetsawang, S
Comeau, AM
Phoolcharoen, W
Essex, M
McIntosh, K
Vithayasai, V
机构
[1] Inst Rech Dev, Epidemiol Clin, Paris, France
[2] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[3] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[4] Inst Natl Etud Demog, Paris, France
[5] Mahidol Univ, Family Hlth Res Ctr, Bangkok 10700, Thailand
[6] Univ Massachusetts, Sch Med, New England Newborn Screening Program, Boston, MA 02125 USA
[7] Minist Publ Hlth, Bangkok, Thailand
[8] Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA
[9] Chiang Mai Univ, Sch Med, Dept Microbiol, Chiang Mai 50000, Thailand
关键词
D O I
10.1056/NEJM200010053431401
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The optimal duration of zidovudine administration to prevent perinatal transmission of human immunodeficiency virus type 1 (HIV-1) should be determined to facilitate its use in areas where resources are limited. Methods: We conducted a randomized, double-blind equivalence trial of four regimens of zidovudine starting in the mother at 28 weeks' gestation, with 6 weeks of treatment in the infant (the long-long regimen), which is similar to protocol 076; zidovudine starting at 35 weeks' gestation, with 3 days of treatment in the infant (the short-short regimen); a long-short regimen; and a short-long regimen. The mothers received zidovudine orally during labor. The infants were fed formula and were tested for HIV DNA at 1, 45, 120, and 180 days. After the first interim analysis, the short-short regimen was stopped. Results: A total of 1437 women were enrolled. At the first interim analysis, the rates of HIV transmission were 4.1 percent for the long-long regimen and 10.5 percent for the short-short regimen (P=0.004); at this point the short-short regimen was stopped. For the entire study period, the transmission rates were 6.5 percent (95 percent confidence interval, 4.1 to 8.9 percent) for the long-long regimen, 4.7 percent (95 percent confidence interval, 2.4 to 7.0 percent) for the long-short regimen, and 8.6 percent (95 percent confidence interval, 5.6 to 11.6 percent) for the short-long regimen. The rate of in utero transmission was significantly higher with the two regimens with shorter maternal treatment (5.1 percent) than with the two with longer maternal treatment (1.6 percent). Conclusions: The short-short zidovudine regimen is inferior to the long-long regimen and leads to a higher rate of perinatal HIV transmission. The long-short, short-long, and long-long regimens had equivalent efficacy. However, the higher rate of in utero transmission with the short-long regimen suggests that longer treatment of the infant cannot substitute for longer treatment of the mother. (N Engl J Med 2000;343:982-91.) (C) 2000, Massachusetts Medical Society.
引用
收藏
页码:982 / 991
页数:10
相关论文
共 16 条
  • [1] PROVING THE NULL HYPOTHESIS IN CLINICAL-TRIALS
    BLACKWELDER, WC
    [J]. CONTROLLED CLINICAL TRIALS, 1982, 3 (04): : 345 - 353
  • [2] REDUCTION OF MATERNAL-INFANT TRANSMISSION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 WITH ZIDOVUDINE TREATMENT
    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
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (18) : 1173 - 1180
  • [3] Intrapartum and neonatal single-dose nevirapine compared with zidovudine for prevention of mother-to-child transmission of HIV-1 in Kampala, Uganda: HIVMET 012 randomised trial
    Guay, LA
    Musoke, P
    Fleming, T
    Bagenda, D
    Allen, M
    Nakabiito, C
    Sherman, J
    Bakaki, P
    Ducar, C
    Deseyve, M
    Emel, L
    Mirochnick, M
    Fowler, MG
    Mofenson, L
    Miotti, P
    Dransfield, K
    Bray, D
    Mmiro, F
    Jackson, JB
    [J]. LANCET, 1999, 354 (9181) : 795 - 802
  • [4] International Conference on Harmonization (ICH), 1997, FED REG, V62, P25691
  • [5] JOURDAIN G, 2000, 7 C RETR OPP INF SAN
  • [6] Defining the time of fetal or perinatal acquisition of human immunodeficiency virus type 1 infection on the basis of age at first positive culture
    Kalish, LA
    Pitt, J
    Lew, J
    Landesman, S
    Diaz, C
    Hershow, R
    Hollinger, FB
    Pagano, M
    Smeriglio, V
    Moye, J
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1997, 175 (03) : 712 - 715
  • [7] KHONGPHATTHANAY. M, 1999, 2 C GLOB STRAT PREV
  • [8] LALLEMANT M, 1999, 2 C GLOB STRAT PREV
  • [9] MAKUCH R, 1978, CANCER TREAT REP, V62, P1037
  • [10] Advances and research directions in the prevention of mother-to-child HIV-1 transmission
    Mofenson, LM
    McIntyre, JA
    [J]. LANCET, 2000, 355 (9222) : 2237 - 2244