Evaluation of BM cytomorphology after allo-SCT in patients with AML

Standard

Evaluation of BM cytomorphology after allo-SCT in patients with AML. / Christopeit, M; Miersch, K; Klyuchnikov, Evgeny; Haferlach, T; Binder, Mascha; Zabelina, Tatjana; Ayuketang Ayuk, Francis; Schafhausen, Philippe; Zander, Axel R.; Bokemeyer, Carsten; Kröger, Nicolaus; Bacher, Ulrike.

in: BONE MARROW TRANSPL, Jahrgang 47, Nr. 12, 12, 12.2012, S. 1538-1544.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Christopeit, M, Miersch, K, Klyuchnikov, E, Haferlach, T, Binder, M, Zabelina, T, Ayuketang Ayuk, F, Schafhausen, P, Zander, AR, Bokemeyer, C, Kröger, N & Bacher, U 2012, 'Evaluation of BM cytomorphology after allo-SCT in patients with AML', BONE MARROW TRANSPL, Jg. 47, Nr. 12, 12, S. 1538-1544. https://doi.org/10.1038/bmt.2012.70

APA

Christopeit, M., Miersch, K., Klyuchnikov, E., Haferlach, T., Binder, M., Zabelina, T., Ayuketang Ayuk, F., Schafhausen, P., Zander, A. R., Bokemeyer, C., Kröger, N., & Bacher, U. (2012). Evaluation of BM cytomorphology after allo-SCT in patients with AML. BONE MARROW TRANSPL, 47(12), 1538-1544. [12]. https://doi.org/10.1038/bmt.2012.70

Vancouver

Christopeit M, Miersch K, Klyuchnikov E, Haferlach T, Binder M, Zabelina T et al. Evaluation of BM cytomorphology after allo-SCT in patients with AML. BONE MARROW TRANSPL. 2012 Dez;47(12):1538-1544. 12. https://doi.org/10.1038/bmt.2012.70

Bibtex

@article{ffe32a9e04174a08accb5791f4e1f143,
title = "Evaluation of BM cytomorphology after allo-SCT in patients with AML",
abstract = "Estimation of relapse risk in AML after allo-SCT is critical. The negative impact of increased blast count post transplant is widely accepted. Here, we studied cellularity and dysplasia in BM cytomorphology on days 30 and 100 in 112 AML patients who achieved haematological CR after SCT. Overall cellularity on day 30 was normal in 45.3%, reduced in 37.3% and increased in 17.3% of samples (day 100: normal: 54.8%; reduced: 38.7%; and increased: 6.5%). Dysplasia in ?10% of cells was frequent on day 30 (granulopoiesis: 25.0% of samples; erythropoiesis: 34.6%; and megakaryopoiesis: 47.7%) and also on day 100. Relapses were less frequent in patients with normal BM cellularity on day 30 (7/34; 20.6%) when compared with reduced (9/28; 32.1%) or increased cellularity (10/13; 76.9%; P = 0.001). Estimated 2-year OS was 59.0% for patients with normal overall cellularity, followed by patients with increased (44.0%) and reduced cellularity (31.4%, P = 0.009). In contrast, cellularity at day 100 and dysplasia at days 30 and 100 did not correlate with outcome measures. Thus, in the cohort studied, BM cellularity represents a prognostic parameter for the post-transplant period in AML patients. Dysplasia seems to be an unspecific phenomenon in the cohort analysed.",
keywords = "Adolescent, Adult, Aged, Bone Marrow Cells, Cytodiagnosis, Cytogenetics, Female, Humans, Leukemia, Myeloid, Acute, Male, Middle Aged, Prognosis, Recurrence, Risk Factors, Stem Cell Transplantation, Transplantation Chimera, Treatment Outcome, Young Adult, Journal Article",
author = "M Christopeit and K Miersch and Evgeny Klyuchnikov and T Haferlach and Mascha Binder and Tatjana Zabelina and {Ayuketang Ayuk}, Francis and Philippe Schafhausen and Zander, {Axel R.} and Carsten Bokemeyer and Nicolaus Kr{\"o}ger and Ulrike Bacher",
year = "2012",
month = dec,
doi = "10.1038/bmt.2012.70",
language = "English",
volume = "47",
pages = "1538--1544",
journal = "BONE MARROW TRANSPL",
issn = "0268-3369",
publisher = "NATURE PUBLISHING GROUP",
number = "12",

}

RIS

TY - JOUR

T1 - Evaluation of BM cytomorphology after allo-SCT in patients with AML

AU - Christopeit, M

AU - Miersch, K

AU - Klyuchnikov, Evgeny

AU - Haferlach, T

AU - Binder, Mascha

AU - Zabelina, Tatjana

AU - Ayuketang Ayuk, Francis

AU - Schafhausen, Philippe

AU - Zander, Axel R.

AU - Bokemeyer, Carsten

AU - Kröger, Nicolaus

AU - Bacher, Ulrike

PY - 2012/12

Y1 - 2012/12

N2 - Estimation of relapse risk in AML after allo-SCT is critical. The negative impact of increased blast count post transplant is widely accepted. Here, we studied cellularity and dysplasia in BM cytomorphology on days 30 and 100 in 112 AML patients who achieved haematological CR after SCT. Overall cellularity on day 30 was normal in 45.3%, reduced in 37.3% and increased in 17.3% of samples (day 100: normal: 54.8%; reduced: 38.7%; and increased: 6.5%). Dysplasia in ?10% of cells was frequent on day 30 (granulopoiesis: 25.0% of samples; erythropoiesis: 34.6%; and megakaryopoiesis: 47.7%) and also on day 100. Relapses were less frequent in patients with normal BM cellularity on day 30 (7/34; 20.6%) when compared with reduced (9/28; 32.1%) or increased cellularity (10/13; 76.9%; P = 0.001). Estimated 2-year OS was 59.0% for patients with normal overall cellularity, followed by patients with increased (44.0%) and reduced cellularity (31.4%, P = 0.009). In contrast, cellularity at day 100 and dysplasia at days 30 and 100 did not correlate with outcome measures. Thus, in the cohort studied, BM cellularity represents a prognostic parameter for the post-transplant period in AML patients. Dysplasia seems to be an unspecific phenomenon in the cohort analysed.

AB - Estimation of relapse risk in AML after allo-SCT is critical. The negative impact of increased blast count post transplant is widely accepted. Here, we studied cellularity and dysplasia in BM cytomorphology on days 30 and 100 in 112 AML patients who achieved haematological CR after SCT. Overall cellularity on day 30 was normal in 45.3%, reduced in 37.3% and increased in 17.3% of samples (day 100: normal: 54.8%; reduced: 38.7%; and increased: 6.5%). Dysplasia in ?10% of cells was frequent on day 30 (granulopoiesis: 25.0% of samples; erythropoiesis: 34.6%; and megakaryopoiesis: 47.7%) and also on day 100. Relapses were less frequent in patients with normal BM cellularity on day 30 (7/34; 20.6%) when compared with reduced (9/28; 32.1%) or increased cellularity (10/13; 76.9%; P = 0.001). Estimated 2-year OS was 59.0% for patients with normal overall cellularity, followed by patients with increased (44.0%) and reduced cellularity (31.4%, P = 0.009). In contrast, cellularity at day 100 and dysplasia at days 30 and 100 did not correlate with outcome measures. Thus, in the cohort studied, BM cellularity represents a prognostic parameter for the post-transplant period in AML patients. Dysplasia seems to be an unspecific phenomenon in the cohort analysed.

KW - Adolescent

KW - Adult

KW - Aged

KW - Bone Marrow Cells

KW - Cytodiagnosis

KW - Cytogenetics

KW - Female

KW - Humans

KW - Leukemia, Myeloid, Acute

KW - Male

KW - Middle Aged

KW - Prognosis

KW - Recurrence

KW - Risk Factors

KW - Stem Cell Transplantation

KW - Transplantation Chimera

KW - Treatment Outcome

KW - Young Adult

KW - Journal Article

U2 - 10.1038/bmt.2012.70

DO - 10.1038/bmt.2012.70

M3 - SCORING: Journal article

C2 - 22543745

VL - 47

SP - 1538

EP - 1544

JO - BONE MARROW TRANSPL

JF - BONE MARROW TRANSPL

SN - 0268-3369

IS - 12

M1 - 12

ER -