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Treatment of severe acute graft‐versus‐host disease with anti‐thymocyte globulin
Author(s) -
Remberger Mats,
Aschan Johan,
Barkholt Lisbeth,
Tollemar Jan,
Ringdén Olle
Publication year - 2001
Publication title -
clinical transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 76
eISSN - 1399-0012
pISSN - 0902-0063
DOI - 10.1034/j.1399-0012.2001.150301.x
Subject(s) - medicine , anti thymocyte globulin , hematopoietic stem cell transplantation , graft versus host disease , gastroenterology , globulin , immunology , transplantation
Severe acute graft‐versus‐host disease (GVHD) is one of the major complications after haematopoietic stem‐cell transplantation (HSCT). Treatment of severe GVHD is difficult and the condition is often fatal. One proposed method of improving the therapy is to include anti‐thymocyte globulin (ATG). Here, we will report our results in 29 patients using ATG as part of treatment for severe steroid‐resistant acute GVHD. Four patients suffered from grade II, 13 from grade III and 12 from grade IV GVHD. Median time to grade II GVHD was 24 d (range 7–91 d) and to grade III was 29 d (range 8–55 d) after HSCT. Five different ATG preparations were used, rabbit ATG (R‐ATG), BMA 031, OKT ® ‐3, ATG‐Fresenius and Thymoglobuline ® . All patients had skin involvement, 26 also had gut involvement and 25 had liver involvement. The rate of response to treatment was best in skin involvement (72%), while liver and gut involvement showed lower response rates (38%). Eleven patients survived more than 90 d, 7 of them developed chronic GVHD, 1 developed mild GVHD, 1 developed moderate GVHD and 5 developed severe GVHD. Survival at 100 d was 37% and at 1 yr it was 12%. Most patients died of GVHD, with virus or fungal infections as contributing causes of death.
To conclude, treatment of severe acute GVHD is difficult and ATG, in our hands, adds nothing to conventional pharmacological treatment.