Use of a five-agent GVHD prevention regimen in recipients of unrelated donor marrow.

Standard

Use of a five-agent GVHD prevention regimen in recipients of unrelated donor marrow. / Zander, A R; Zabelina, Tatjana; Kröger, N; Renges, H; Krüger, W; Löliger, C; Dürken, M; Stockschläder, M; de Wit, M; Wacker-Backhaus, G; Bielack, S; Jaburg, N; Rüssmann, B; Erttmann, Rudolf; Kabisch, H.

In: BONE MARROW TRANSPL, Vol. 23, No. 9, 9, 1999, p. 889-893.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Zander, AR, Zabelina, T, Kröger, N, Renges, H, Krüger, W, Löliger, C, Dürken, M, Stockschläder, M, de Wit, M, Wacker-Backhaus, G, Bielack, S, Jaburg, N, Rüssmann, B, Erttmann, R & Kabisch, H 1999, 'Use of a five-agent GVHD prevention regimen in recipients of unrelated donor marrow.', BONE MARROW TRANSPL, vol. 23, no. 9, 9, pp. 889-893. <http://www.ncbi.nlm.nih.gov/pubmed/10338043?dopt=Citation>

APA

Zander, A. R., Zabelina, T., Kröger, N., Renges, H., Krüger, W., Löliger, C., Dürken, M., Stockschläder, M., de Wit, M., Wacker-Backhaus, G., Bielack, S., Jaburg, N., Rüssmann, B., Erttmann, R., & Kabisch, H. (1999). Use of a five-agent GVHD prevention regimen in recipients of unrelated donor marrow. BONE MARROW TRANSPL, 23(9), 889-893. [9]. http://www.ncbi.nlm.nih.gov/pubmed/10338043?dopt=Citation

Vancouver

Zander AR, Zabelina T, Kröger N, Renges H, Krüger W, Löliger C et al. Use of a five-agent GVHD prevention regimen in recipients of unrelated donor marrow. BONE MARROW TRANSPL. 1999;23(9):889-893. 9.

Bibtex

@article{11b6a7e396b042eb9a524bfae6f7eea0,
title = "Use of a five-agent GVHD prevention regimen in recipients of unrelated donor marrow.",
abstract = "A five-agent GVHD prophylaxis programme consisting of cyclosporin A, methotrexate, anti-thymocyte-globulin, pentaglobin and metronidazol was given to 48 recipients of unrelated donor marrow with chronic myelogenous leukemia, acute leukemia, myelodysplastic syndromes, and familiar lymphocytic hemophagocytosis of an average age of 33.5 (0.6-56) years. GVHD grades II-IV occurred in 18 patients (39%) and grades III-IV in five patients (11%). Chronic GVHD developed in nine patients (23%), three limited and six extensive. Fifteen patients died. Clinical relapse was detected in eight patients. Four patients died as a consequence of the underlying disease and subsequent treatment, 11 patients died of transplant-related causes. After a median follow-up of 19 months, the overall and disease-free survival are 67% and 62%, respectively. Survival by age is as follows: 0-19 years: 12/13 patients; 20-39 years: 14/25 patients; 40-59 years: 7/10 patients. The five-agent GVHD prophylaxis regimen is effective. Matched-unrelated donor transplants can be carried out safely in patients younger than 50 years of age. The results in patients younger than 20 years of age should encourage matched-unrelated donor transplants at earlier stages of the disease.",
author = "Zander, {A R} and Tatjana Zabelina and N Kr{\"o}ger and H Renges and W Kr{\"u}ger and C L{\"o}liger and M D{\"u}rken and M Stockschl{\"a}der and {de Wit}, M and G Wacker-Backhaus and S Bielack and N Jaburg and B R{\"u}ssmann and Rudolf Erttmann and H Kabisch",
year = "1999",
language = "Deutsch",
volume = "23",
pages = "889--893",
journal = "BONE MARROW TRANSPL",
issn = "0268-3369",
publisher = "NATURE PUBLISHING GROUP",
number = "9",

}

RIS

TY - JOUR

T1 - Use of a five-agent GVHD prevention regimen in recipients of unrelated donor marrow.

AU - Zander, A R

AU - Zabelina, Tatjana

AU - Kröger, N

AU - Renges, H

AU - Krüger, W

AU - Löliger, C

AU - Dürken, M

AU - Stockschläder, M

AU - de Wit, M

AU - Wacker-Backhaus, G

AU - Bielack, S

AU - Jaburg, N

AU - Rüssmann, B

AU - Erttmann, Rudolf

AU - Kabisch, H

PY - 1999

Y1 - 1999

N2 - A five-agent GVHD prophylaxis programme consisting of cyclosporin A, methotrexate, anti-thymocyte-globulin, pentaglobin and metronidazol was given to 48 recipients of unrelated donor marrow with chronic myelogenous leukemia, acute leukemia, myelodysplastic syndromes, and familiar lymphocytic hemophagocytosis of an average age of 33.5 (0.6-56) years. GVHD grades II-IV occurred in 18 patients (39%) and grades III-IV in five patients (11%). Chronic GVHD developed in nine patients (23%), three limited and six extensive. Fifteen patients died. Clinical relapse was detected in eight patients. Four patients died as a consequence of the underlying disease and subsequent treatment, 11 patients died of transplant-related causes. After a median follow-up of 19 months, the overall and disease-free survival are 67% and 62%, respectively. Survival by age is as follows: 0-19 years: 12/13 patients; 20-39 years: 14/25 patients; 40-59 years: 7/10 patients. The five-agent GVHD prophylaxis regimen is effective. Matched-unrelated donor transplants can be carried out safely in patients younger than 50 years of age. The results in patients younger than 20 years of age should encourage matched-unrelated donor transplants at earlier stages of the disease.

AB - A five-agent GVHD prophylaxis programme consisting of cyclosporin A, methotrexate, anti-thymocyte-globulin, pentaglobin and metronidazol was given to 48 recipients of unrelated donor marrow with chronic myelogenous leukemia, acute leukemia, myelodysplastic syndromes, and familiar lymphocytic hemophagocytosis of an average age of 33.5 (0.6-56) years. GVHD grades II-IV occurred in 18 patients (39%) and grades III-IV in five patients (11%). Chronic GVHD developed in nine patients (23%), three limited and six extensive. Fifteen patients died. Clinical relapse was detected in eight patients. Four patients died as a consequence of the underlying disease and subsequent treatment, 11 patients died of transplant-related causes. After a median follow-up of 19 months, the overall and disease-free survival are 67% and 62%, respectively. Survival by age is as follows: 0-19 years: 12/13 patients; 20-39 years: 14/25 patients; 40-59 years: 7/10 patients. The five-agent GVHD prophylaxis regimen is effective. Matched-unrelated donor transplants can be carried out safely in patients younger than 50 years of age. The results in patients younger than 20 years of age should encourage matched-unrelated donor transplants at earlier stages of the disease.

M3 - SCORING: Zeitschriftenaufsatz

VL - 23

SP - 889

EP - 893

JO - BONE MARROW TRANSPL

JF - BONE MARROW TRANSPL

SN - 0268-3369

IS - 9

M1 - 9

ER -