Stavudine - A review of its pharmacodynamic and pharmacokinetic properties and clinical potential in HIV infection

被引:92
作者
Lea, AP
Faulds, D
机构
[1] Adis International Limited, Auckland
[2] Adis International Limited, Auckland 10, 41 Centorian Drive, Mairangi Bay
关键词
D O I
10.2165/00003495-199651050-00009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Stavudine is a nucleoside analogue which undergoes intracellular phosphorylation to its active metabolite, stavudine-5'-triphosphate. At clinically relevant concentrations, the active metabolite restricts HIV replication by inhibiting the inclusion of thymidine-5'-triphosphate into proviral DNA by HIV reverse transcriptase, and/or by causing DNA chain termination. Viral resistance to stavudine does not commonly develop during treatment. Where it has developed, up to a 12-fold increase in resistance has been observed in clinical isolates from patients treated with stavudine for long periods. Stavudine 40mg twice daily and zidovudine 200mg 3 times daily were compared in 822 patients at various stages of HIV infection who had previously received long term zidovudine therapy. Stavudine was superior for both primary and surrogate end-points including clinical progression, treatment failure, increase in CD4+ cell counts and bodyweight gain. In a larger study, stavudine 40mg twice daily provided greater benefit than stavudine 20mg twice daily in terms of weight gain, haematological findings and the number of hospitalisations in 11 784 patients intolerant of, resistant to, zidovudine and didanosine. Peripheral neuropathy is the major dose-limiting adverse event associated with stavudine therapy and occurred more frequently with stavudine than zidovudine. However, haematological adverse events were observed less frequently with stavudine than with zidovudine. Thus, stavudine is effective in alleviating signs and symptoms of HIV infection in patients intolerant of, or no longer responding to, zidovudine or didanosine. It is also more effective than zidovudine in slowing disease progression in patients previously treated with zidovudine for long periods. The results of studies which will reveal the role of stavudine therapy in untreated patients and in combination with other anti-HIV agents are awaited with interest.
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页码:846 / 864
页数:19
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共 114 条
  • [61] GENOTYPIC AND PHENOTYPIC ANALYSIS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 ISOLATES FROM PATIENTS ON PROLONGED STAVUDINE THERAPY
    LIN, PF
    SAMANTA, H
    ROSE, RE
    PATICK, AK
    TRIMBLE, J
    BECHTOLD, CM
    REVIE, DR
    KHAN, NC
    FEDERICI, ME
    LI, H
    LEE, A
    ANDERSON, RE
    COLONNO, RJ
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1994, 170 (05) : 1157 - 1164
  • [62] LIN TS, 1987, BIOCHEM PHARMACOL, V36, P2713
  • [63] MACLEOD CM, 1994, J CLIN PHARMACOL, V34, P1025
  • [64] THE T4 GENE ENCODES THE AIDS VIRUS RECEPTOR AND IS EXPRESSED IN THE IMMUNE-SYSTEM AND THE BRAIN
    MADDON, PJ
    DALGLEISH, AG
    MCDOUGAL, JS
    CLAPHAM, PR
    WEISS, RA
    AXEL, R
    [J]. CELL, 1986, 47 (03) : 333 - 348
  • [65] 1-(2,3-DIDEOXY-BETA-D-GLYCERO-PENT-2-ENOFURANOSYL)THYMINE - A HIGHLY POTENT AND SELECTIVE ANTI-HIV AGENT
    MANSURI, MM
    STARRETT, JE
    GHAZZOULI, I
    HITCHCOCK, MJM
    STERZYCKI, RZ
    BRANKOVAN, V
    LIN, TS
    AUGUST, EM
    PRUSOFF, WH
    SOMMADOSSI, JP
    MARTIN, JC
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1989, 32 (02) : 461 - 466
  • [66] COMPARISON OF INVITRO BIOLOGICAL PROPERTIES AND MOUSE TOXICITIES OF 3 THYMIDINE ANALOGS ACTIVE AGAINST HUMAN-IMMUNODEFICIENCY-VIRUS
    MANSURI, MM
    HITCHCOCK, MJM
    BUROKER, RA
    BREGMAN, CL
    GHAZZOULI, I
    DESIDERIO, JV
    STARRETT, JE
    STERZYCKI, RZ
    MARTIN, JC
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1990, 34 (04) : 637 - 641
  • [67] MARS ME, 1995, 35 INT C NAT AG CHEM, P226
  • [68] MARTIN JC, 1990, ANN NY ACAD SCI, V616, P22
  • [69] INHIBITION OF HIV-ASSOCIATED REVERSE-TRANSCRIPTASE BY SUGAR-MODIFIED DERIVATIVES OF THYMIDINE 5'-TRIPHOSPHATE IN COMPARISON TO CELLULAR DNA POLYMERASE-ALPHA AND POLYMERASE-BETA
    MATTHES, E
    LEHMANN, C
    SCHOLZ, D
    VONJANTALIPINSKI, M
    GAERTNER, K
    ROSENTHAL, HA
    LANGEN, P
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1987, 148 (01) : 78 - 85
  • [70] Mellors J. W., 1995, International Antiviral News, V3, P8