Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2005-5-12
pubmed:abstractText
Alemtuzumab is a powerful lymphocyte depleting antibody currently being evaluated in solid organ transplantation. This paper describes 5-year results of a single center study of alemtuzumab as induction in renal transplantation. Thirty-three renal transplant recipients received 20 mg alemtuzumab on day 0 and 1, followed by half-dose cyclosporin monotherapy (trough concentration 75-125 ng/mL) from day 3. They were compared in a retrospective contemporaneous-controlled manner with 66 kidney transplant recipients transplanted in the same period and center who received conventional immunosuppression with cyclosporin, azathioprine and prednisolone. In the alemtuzumab group 12% of recipients died compared to 17% in the control group (p = 0.48); likewise graft loss was similar in both groups (21% vs. 26%, respectively, p = 0.58). Incidence of acute rejection was also comparable at 5 years (31.5% vs. 33.6%), although the pattern of rejection was different with 14% patients in the alemtuzumab group experiencing rejection over 1 year post-transplant compared to none in the control group. There was no significant difference between groups in terms of infection or serious adverse events. While acknowledging the limitations of a relatively small single-center study, results suggest that alemtuzumab induction allowed satisfactory long-term patient and graft survival equivalent to that seen with standard triple immunosuppression, while avoiding steroid therapy.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1600-6135
pubmed:author
pubmed:issnType
Print
pubmed:volume
5
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1347-53
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:15888040-Adult, pubmed-meshheading:15888040-Aged, pubmed-meshheading:15888040-Anti-Inflammatory Agents, pubmed-meshheading:15888040-Antibodies, Monoclonal, pubmed-meshheading:15888040-Antibodies, Monoclonal, Humanized, pubmed-meshheading:15888040-Antibodies, Neoplasm, pubmed-meshheading:15888040-Antineoplastic Agents, pubmed-meshheading:15888040-Azathioprine, pubmed-meshheading:15888040-Cyclosporine, pubmed-meshheading:15888040-Drug Therapy, Combination, pubmed-meshheading:15888040-Female, pubmed-meshheading:15888040-Follow-Up Studies, pubmed-meshheading:15888040-Graft Survival, pubmed-meshheading:15888040-Humans, pubmed-meshheading:15888040-Immunosuppressive Agents, pubmed-meshheading:15888040-Kidney Transplantation, pubmed-meshheading:15888040-Male, pubmed-meshheading:15888040-Middle Aged, pubmed-meshheading:15888040-Postoperative Complications, pubmed-meshheading:15888040-Prednisolone, pubmed-meshheading:15888040-Remission Induction, pubmed-meshheading:15888040-Retrospective Studies, pubmed-meshheading:15888040-Safety, pubmed-meshheading:15888040-Time Factors, pubmed-meshheading:15888040-Treatment Outcome
pubmed:year
2005
pubmed:articleTitle
Alemtuzumab (CAMPATH 1H) induction therapy in cadaveric kidney transplantation--efficacy and safety at five years.
pubmed:affiliation
University of Cambridge, Department of Surgery, Addenbrooke's Hospital, UK. cjew2@cam.ac.uk
pubmed:publicationType
Journal Article, Comparative Study