5-Azacytidine for the treatment of patients with acute myeloid leukemia or myelodysplastic syndrome who relapse after allo-SCT: a retrospective analysis.

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5-Azacytidine for the treatment of patients with acute myeloid leukemia or myelodysplastic syndrome who relapse after allo-SCT: a retrospective analysis. / Czibere, A; Bruns, I; Kröger, Nicolaus; Platzbecker, U; Lind, J; Zohren, F; Fenk, R; Germing, U; Schröder, T; Gräf, T; Haas, R; Kobbe, G.

In: BONE MARROW TRANSPL, Vol. *45*, No. 5, 5, 2009, p. 872-876.

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

Harvard

Czibere, A, Bruns, I, Kröger, N, Platzbecker, U, Lind, J, Zohren, F, Fenk, R, Germing, U, Schröder, T, Gräf, T, Haas, R & Kobbe, G 2009, '5-Azacytidine for the treatment of patients with acute myeloid leukemia or myelodysplastic syndrome who relapse after allo-SCT: a retrospective analysis.', BONE MARROW TRANSPL, vol. *45*, no. 5, 5, pp. 872-876. <http://www.ncbi.nlm.nih.gov/pubmed/19820729?dopt=Citation>

APA

Czibere, A., Bruns, I., Kröger, N., Platzbecker, U., Lind, J., Zohren, F., Fenk, R., Germing, U., Schröder, T., Gräf, T., Haas, R., & Kobbe, G. (2009). 5-Azacytidine for the treatment of patients with acute myeloid leukemia or myelodysplastic syndrome who relapse after allo-SCT: a retrospective analysis. BONE MARROW TRANSPL, *45*(5), 872-876. [5]. http://www.ncbi.nlm.nih.gov/pubmed/19820729?dopt=Citation

Vancouver

Bibtex

@article{cf1aadcacf624099b4bfeb0502c3f350,
title = "5-Azacytidine for the treatment of patients with acute myeloid leukemia or myelodysplastic syndrome who relapse after allo-SCT: a retrospective analysis.",
abstract = "Patients with AML or myelodysplastic syndrome who relapse after allo-SCT have a poor prognosis. In the search for novel treatment strategies for these patients, we conducted a multicenter retrospective analysis and identified 22 patients treated with the DNA-methylation inhibitor 5-azacytidine (5-Aza). Patients received a median number of two cycles 5-Aza (range 1-8) at a dose of 100 mg/m(2) over 5 days following relapse. Eighteen patients (82%) also received a median number of two donor lymphocyte infusions (DLI, range 1-5). Sixteen patients (72%) responded to 5-Aza treatment and five patients (23%) achieved a CR. 5-Aza-induced CR lasted for 433 days (median, range 114-769). Median survival and the estimated 2-year survival rate were 144 days and 23%, respectively. Acute GVHD after DLI was seen in six patients (33%) and four of these patients developed chronic GVHD of the skin. There were no treatment-related deaths. Patients who achieved halving of leukocyte counts after the first 5-Aza cycle had a superior median survival of 802 days compared with 135 days (P=0.0025) in all other patients. On univariate analysis, the achievement of this halving of leukocyte counts was identified as a significant predictor of survival.Bone Marrow Transplantation advance online publication, 12 October 2009; doi:10.1038/bmt.2009.266.",
author = "A Czibere and I Bruns and Nicolaus Kr{\"o}ger and U Platzbecker and J Lind and F Zohren and R Fenk and U Germing and T Schr{\"o}der and T Gr{\"a}f and R Haas and G Kobbe",
year = "2009",
language = "Deutsch",
volume = "*45*",
pages = "872--876",
journal = "BONE MARROW TRANSPL",
issn = "0268-3369",
publisher = "NATURE PUBLISHING GROUP",
number = "5",

}

RIS

TY - JOUR

T1 - 5-Azacytidine for the treatment of patients with acute myeloid leukemia or myelodysplastic syndrome who relapse after allo-SCT: a retrospective analysis.

AU - Czibere, A

AU - Bruns, I

AU - Kröger, Nicolaus

AU - Platzbecker, U

AU - Lind, J

AU - Zohren, F

AU - Fenk, R

AU - Germing, U

AU - Schröder, T

AU - Gräf, T

AU - Haas, R

AU - Kobbe, G

PY - 2009

Y1 - 2009

N2 - Patients with AML or myelodysplastic syndrome who relapse after allo-SCT have a poor prognosis. In the search for novel treatment strategies for these patients, we conducted a multicenter retrospective analysis and identified 22 patients treated with the DNA-methylation inhibitor 5-azacytidine (5-Aza). Patients received a median number of two cycles 5-Aza (range 1-8) at a dose of 100 mg/m(2) over 5 days following relapse. Eighteen patients (82%) also received a median number of two donor lymphocyte infusions (DLI, range 1-5). Sixteen patients (72%) responded to 5-Aza treatment and five patients (23%) achieved a CR. 5-Aza-induced CR lasted for 433 days (median, range 114-769). Median survival and the estimated 2-year survival rate were 144 days and 23%, respectively. Acute GVHD after DLI was seen in six patients (33%) and four of these patients developed chronic GVHD of the skin. There were no treatment-related deaths. Patients who achieved halving of leukocyte counts after the first 5-Aza cycle had a superior median survival of 802 days compared with 135 days (P=0.0025) in all other patients. On univariate analysis, the achievement of this halving of leukocyte counts was identified as a significant predictor of survival.Bone Marrow Transplantation advance online publication, 12 October 2009; doi:10.1038/bmt.2009.266.

AB - Patients with AML or myelodysplastic syndrome who relapse after allo-SCT have a poor prognosis. In the search for novel treatment strategies for these patients, we conducted a multicenter retrospective analysis and identified 22 patients treated with the DNA-methylation inhibitor 5-azacytidine (5-Aza). Patients received a median number of two cycles 5-Aza (range 1-8) at a dose of 100 mg/m(2) over 5 days following relapse. Eighteen patients (82%) also received a median number of two donor lymphocyte infusions (DLI, range 1-5). Sixteen patients (72%) responded to 5-Aza treatment and five patients (23%) achieved a CR. 5-Aza-induced CR lasted for 433 days (median, range 114-769). Median survival and the estimated 2-year survival rate were 144 days and 23%, respectively. Acute GVHD after DLI was seen in six patients (33%) and four of these patients developed chronic GVHD of the skin. There were no treatment-related deaths. Patients who achieved halving of leukocyte counts after the first 5-Aza cycle had a superior median survival of 802 days compared with 135 days (P=0.0025) in all other patients. On univariate analysis, the achievement of this halving of leukocyte counts was identified as a significant predictor of survival.Bone Marrow Transplantation advance online publication, 12 October 2009; doi:10.1038/bmt.2009.266.

M3 - SCORING: Zeitschriftenaufsatz

VL - *45*

SP - 872

EP - 876

JO - BONE MARROW TRANSPL

JF - BONE MARROW TRANSPL

SN - 0268-3369

IS - 5

M1 - 5

ER -