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Daclizumab to prevent rejection after cardiac transplantation.

Hershberger, Ray E (author)
Starling, Randall C (author)
Eisen, Howard J (author)
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Bergh, Claes-Håkan, 1951 (author)
Gothenburg University,Göteborgs universitet,Hjärt-kärlinstitutionen,Wallenberglaboratoriet,Cardiovascular Institute,Wallenberg Laboratory
Kormos, Robert L (author)
Love, Robert B (author)
Van Bakel, Adrian (author)
Gordon, Robert D (author)
Popat, Rina (author)
Cockey, Louise (author)
Mamelok, Richard D (author)
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 (creator_code:org_t)
2005
2005
English.
In: The New England journal of medicine. - 1533-4406. ; 352:26, s. 2705-13
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • BACKGROUND: Daclizumab, a humanized monoclonal antibody against the interleukin-2 receptor, reduced the risk of rejection without increasing the risk of infection among renal-transplant recipients and, in a single-center trial, among cardiac-transplant recipients. We conducted a multicenter, placebo-controlled, double-blind study to confirm these results in cardiac-transplant patients. METHODS: We randomly assigned 434 recipients of a first cardiac transplant treated with standard immunosuppression (cyclosporine, mycophenolate mofetil, and corticosteroids) to receive five doses of daclizumab or placebo. The primary end point was a composite of moderate or severe cellular rejection, hemodynamically significant graft dysfunction, a second transplantation, or death or loss to follow-up within six months. RESULTS: By six months, 104 of 218 patients in the placebo group had reached the primary end point, as compared with 77 of the 216 patients in the daclizumab group (47.7 percent vs. 35.6 percent, P=0.007), a 12.1 percent absolute risk reduction and a 25 percent relative reduction. The rate of rejection was lower in the daclizumab group than in the placebo group (41.3 percent vs. 25.5 percent). Among patients reaching the primary end point, the median time to the end point was almost three times as long in the daclizumab group as in the placebo group during the first 6 months (61 vs. 21 days) and at 1 year (96 vs. 26 days). More patients in the daclizumab group than in the placebo group died of infection (6 vs. 0) when they received concomitant cytolytic therapy. CONCLUSIONS: Daclizumab was efficacious as prophylaxis against acute cellular rejection after cardiac transplantation. Because of the excess risk of death, concurrent or anticipated use of cytolytic therapy with daclizumab should be avoided.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kirurgi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Surgery (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)

Keyword

Adolescent
Adrenal Cortex Hormones
therapeutic use
Adult
Aged
Antibodies
Monoclonal
adverse effects
therapeutic use
Cyclosporine
therapeutic use
Double-Blind Method
Drug Therapy
Combination
Female
Graft Rejection
epidemiology
prevention & control
Heart Transplantation
mortality
Humans
Immunoglobulin G
adverse effects
therapeutic use
Immunosuppressive Agents
adverse effects
therapeutic use
Logistic Models
Male
Middle Aged
Mycophenolic Acid
analogs & derivatives
therapeutic use
Opportunistic Infections
epidemiology
microbiology
mortality
Survival Analysis

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ref (subject category)
art (subject category)

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