Risk models predicting survival after reduced-intensity transplantation for myelofibrosis.

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Risk models predicting survival after reduced-intensity transplantation for myelofibrosis. / Alchalby, Haefaa; Yunus, Dinah-Rohina; Zabelina, Tatjana; Kobbe, Guido; Holler, Ernst; Bornhäuser, Martin; Schwerdtfeger, Rainer; Bethge, Wolfgang; Kvasnicka, Hans Michael; Büsche, Guntram; Ayuketang Ayuk, Francis; Bacher, Ulrike; Zander, Axel R.; Kröger, Nicolaus.

In: BRIT J HAEMATOL, Vol. 157, No. 1, 1, 2012, p. 75-85.

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

Harvard

Alchalby, H, Yunus, D-R, Zabelina, T, Kobbe, G, Holler, E, Bornhäuser, M, Schwerdtfeger, R, Bethge, W, Kvasnicka, HM, Büsche, G, Ayuketang Ayuk, F, Bacher, U, Zander, AR & Kröger, N 2012, 'Risk models predicting survival after reduced-intensity transplantation for myelofibrosis.', BRIT J HAEMATOL, vol. 157, no. 1, 1, pp. 75-85. <http://www.ncbi.nlm.nih.gov/pubmed/22280409?dopt=Citation>

APA

Alchalby, H., Yunus, D-R., Zabelina, T., Kobbe, G., Holler, E., Bornhäuser, M., Schwerdtfeger, R., Bethge, W., Kvasnicka, H. M., Büsche, G., Ayuketang Ayuk, F., Bacher, U., Zander, A. R., & Kröger, N. (2012). Risk models predicting survival after reduced-intensity transplantation for myelofibrosis. BRIT J HAEMATOL, 157(1), 75-85. [1]. http://www.ncbi.nlm.nih.gov/pubmed/22280409?dopt=Citation

Vancouver

Alchalby H, Yunus D-R, Zabelina T, Kobbe G, Holler E, Bornhäuser M et al. Risk models predicting survival after reduced-intensity transplantation for myelofibrosis. BRIT J HAEMATOL. 2012;157(1):75-85. 1.

Bibtex

@article{6d84b31b7d7c4ba5a6d6b882fb130796,
title = "Risk models predicting survival after reduced-intensity transplantation for myelofibrosis.",
abstract = "To define a prognostic model for predicting outcome of reduced-intensity allogeneic stem cell transplantation (RIC-ASCT) for myelofibrosis we evaluated 150 homogeneously treated patients and developed a new risk score for overall survival (OS). In a multivariate Cox model for OS, only JAK2 V617F wild-type, age ?57?years and constitutional symptoms were independently predictive for OS (Hazard Ratio: 2·02; 2·43 and 2·80 respectively). Depending on the presence of one, two or all of these factors, HR of death was 3·08; 4·70 and 16·61 respectively (P?<?0·001). This score was compared to the Lille, Cervantes, International Prognostic Scoring System (IPSS), dynamic IPSS (DIPSS) and modified European Blood and Marrow Transplantation Group (EBMT) scores. Lille score correlated significantly with OS but discriminated poorly between the intermediate and high-risk groups (5-year OS 56% and 51% respectively). IPSS and DIPSS correlated significantly with OS but differences between intermediate-1 and intermediate-2 groups were not significant (5-year OS 78% vs. 78% and 70%, 60% respectively). Modified EBMT and Cervantes models did not predict OS post-ASCT. In conclusion, a simple model which includes: age, JAK2 V617F-status and constitutional symptoms can clearly separate distinct risk groups and can be used in addition to the Lille model to predict OS after RIC-ASCT for myelofibrosis.",
keywords = "Adult, Humans, Male, Aged, Female, Middle Aged, Risk Assessment, Survival Rate, Time Factors, Disease-Free Survival, Mutation, Missense, Amino Acid Substitution, Transplantation, Homologous, *Models, Biological, *Stem Cell Transplantation, *Transplantation Conditioning, Janus Kinase 2/genetics/metabolism, Primary Myelofibrosis/enzymology/genetics/*mortality/*therapy, Adult, Humans, Male, Aged, Female, Middle Aged, Risk Assessment, Survival Rate, Time Factors, Disease-Free Survival, Mutation, Missense, Amino Acid Substitution, Transplantation, Homologous, *Models, Biological, *Stem Cell Transplantation, *Transplantation Conditioning, Janus Kinase 2/genetics/metabolism, Primary Myelofibrosis/enzymology/genetics/*mortality/*therapy",
author = "Haefaa Alchalby and Dinah-Rohina Yunus and Tatjana Zabelina and Guido Kobbe and Ernst Holler and Martin Bornh{\"a}user and Rainer Schwerdtfeger and Wolfgang Bethge and Kvasnicka, {Hans Michael} and Guntram B{\"u}sche and {Ayuketang Ayuk}, Francis and Ulrike Bacher and Zander, {Axel R.} and Nicolaus Kr{\"o}ger",
year = "2012",
language = "English",
volume = "157",
pages = "75--85",
journal = "BRIT J HAEMATOL",
issn = "0007-1048",
publisher = "Wiley-Blackwell",
number = "1",

}

RIS

TY - JOUR

T1 - Risk models predicting survival after reduced-intensity transplantation for myelofibrosis.

AU - Alchalby, Haefaa

AU - Yunus, Dinah-Rohina

AU - Zabelina, Tatjana

AU - Kobbe, Guido

AU - Holler, Ernst

AU - Bornhäuser, Martin

AU - Schwerdtfeger, Rainer

AU - Bethge, Wolfgang

AU - Kvasnicka, Hans Michael

AU - Büsche, Guntram

AU - Ayuketang Ayuk, Francis

AU - Bacher, Ulrike

AU - Zander, Axel R.

AU - Kröger, Nicolaus

PY - 2012

Y1 - 2012

N2 - To define a prognostic model for predicting outcome of reduced-intensity allogeneic stem cell transplantation (RIC-ASCT) for myelofibrosis we evaluated 150 homogeneously treated patients and developed a new risk score for overall survival (OS). In a multivariate Cox model for OS, only JAK2 V617F wild-type, age ?57?years and constitutional symptoms were independently predictive for OS (Hazard Ratio: 2·02; 2·43 and 2·80 respectively). Depending on the presence of one, two or all of these factors, HR of death was 3·08; 4·70 and 16·61 respectively (P?<?0·001). This score was compared to the Lille, Cervantes, International Prognostic Scoring System (IPSS), dynamic IPSS (DIPSS) and modified European Blood and Marrow Transplantation Group (EBMT) scores. Lille score correlated significantly with OS but discriminated poorly between the intermediate and high-risk groups (5-year OS 56% and 51% respectively). IPSS and DIPSS correlated significantly with OS but differences between intermediate-1 and intermediate-2 groups were not significant (5-year OS 78% vs. 78% and 70%, 60% respectively). Modified EBMT and Cervantes models did not predict OS post-ASCT. In conclusion, a simple model which includes: age, JAK2 V617F-status and constitutional symptoms can clearly separate distinct risk groups and can be used in addition to the Lille model to predict OS after RIC-ASCT for myelofibrosis.

AB - To define a prognostic model for predicting outcome of reduced-intensity allogeneic stem cell transplantation (RIC-ASCT) for myelofibrosis we evaluated 150 homogeneously treated patients and developed a new risk score for overall survival (OS). In a multivariate Cox model for OS, only JAK2 V617F wild-type, age ?57?years and constitutional symptoms were independently predictive for OS (Hazard Ratio: 2·02; 2·43 and 2·80 respectively). Depending on the presence of one, two or all of these factors, HR of death was 3·08; 4·70 and 16·61 respectively (P?<?0·001). This score was compared to the Lille, Cervantes, International Prognostic Scoring System (IPSS), dynamic IPSS (DIPSS) and modified European Blood and Marrow Transplantation Group (EBMT) scores. Lille score correlated significantly with OS but discriminated poorly between the intermediate and high-risk groups (5-year OS 56% and 51% respectively). IPSS and DIPSS correlated significantly with OS but differences between intermediate-1 and intermediate-2 groups were not significant (5-year OS 78% vs. 78% and 70%, 60% respectively). Modified EBMT and Cervantes models did not predict OS post-ASCT. In conclusion, a simple model which includes: age, JAK2 V617F-status and constitutional symptoms can clearly separate distinct risk groups and can be used in addition to the Lille model to predict OS after RIC-ASCT for myelofibrosis.

KW - Adult

KW - Humans

KW - Male

KW - Aged

KW - Female

KW - Middle Aged

KW - Risk Assessment

KW - Survival Rate

KW - Time Factors

KW - Disease-Free Survival

KW - Mutation, Missense

KW - Amino Acid Substitution

KW - Transplantation, Homologous

KW - Models, Biological

KW - Stem Cell Transplantation

KW - Transplantation Conditioning

KW - Janus Kinase 2/genetics/metabolism

KW - Primary Myelofibrosis/enzymology/genetics/mortality/therapy

KW - Adult

KW - Humans

KW - Male

KW - Aged

KW - Female

KW - Middle Aged

KW - Risk Assessment

KW - Survival Rate

KW - Time Factors

KW - Disease-Free Survival

KW - Mutation, Missense

KW - Amino Acid Substitution

KW - Transplantation, Homologous

KW - Models, Biological

KW - Stem Cell Transplantation

KW - Transplantation Conditioning

KW - Janus Kinase 2/genetics/metabolism

KW - Primary Myelofibrosis/enzymology/genetics/mortality/therapy

M3 - SCORING: Journal article

VL - 157

SP - 75

EP - 85

JO - BRIT J HAEMATOL

JF - BRIT J HAEMATOL

SN - 0007-1048

IS - 1

M1 - 1

ER -