Donor lymphocyte infusions and second transplantation as salvage treatment for relapsed myelofibrosis after reduced-intensity allografting.

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Donor lymphocyte infusions and second transplantation as salvage treatment for relapsed myelofibrosis after reduced-intensity allografting. / Klyuchnikov, Evgeny; Holler, Ernst; Bornhäuser, Martin; Kobbe, Guido; Nagler, Arnon; Shimoni, Avichai; Könecke, Christian; Wolschke, Christine; Bacher, Ulrike; Zander, Axel R.; Kröger, Nicolaus.

in: BRIT J HAEMATOL, Jahrgang 159, Nr. 2, 2, 2012, S. 172-181.

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@article{7a0b6eee4b964ef99e6135a19fe6e908,
title = "Donor lymphocyte infusions and second transplantation as salvage treatment for relapsed myelofibrosis after reduced-intensity allografting.",
abstract = "Thirty myelofibrosis patients (21 males, nine females) with relapse (n = 27) or graft-rejection (n = 3) after dose-reduced allografting underwent a salvage strategy including donor lymphocyte infusions (DLIs) and/or second allogeneic haematopoietic stem cell transplantation (HSCT). Twenty-six patients received a median number of three (range, 1-5) DLIs in a dose-escalated mode starting with a median dose of 1·2 × 10(6) (range, 0·003-8 × 10(6) ) up to median dose of 40 × 10(6) T-cells/kg (range, 10-130 × 10(6) ). 10/26 patients (39%) achieved complete response (CR) to DLIs. Acute (grade II-IV) and chronic graft-versus-host (GvHD) disease occurred in 12% and 36% cases. Thirteen non-responders to DLI and four patients who did not receive DLI due to graft-rejection or acute transformation of the blast phase underwent a second allogeneic HSCT from alternative (n = 15) or the same (n = 2) donor. One patient (6%) experienced primary graft-failure and died. Acute (II-IV) and chronic GvHD were observed in 47% and 46% of patients. Overall responses after second HSCT were seen in 12/15 patients (80%: CR: n = 9, partial response: n = 3). The 1-year cumulative incidence of non-relapse mortality for recipients of a second allograft was 6%, and the cumulative incidence of relapse was 24%. After a median follow-up of 27 months, the 2-year overall survival and progression-free survival for all 30 patients was 70% and 67%, respectively. In conclusion, our two-step strategy, including DLI and second HSCT for non-responding or ineligible patients, is an effective and well-tolerated salvage approach for patients relapsing after reduced-intensity allograft after myelofibrosis.",
keywords = "Adult, Humans, Male, Aged, Female, Middle Aged, Survival Rate, Follow-Up Studies, Disease-Free Survival, Acute Disease, Transplantation, Homologous, Salvage Therapy, *Hematopoietic Stem Cell Transplantation, *Living Donors, Graft vs Host Disease/mortality/therapy, *Lymphocyte Transfusion, Primary Myelofibrosis/*mortality/*therapy, Adult, Humans, Male, Aged, Female, Middle Aged, Survival Rate, Follow-Up Studies, Disease-Free Survival, Acute Disease, Transplantation, Homologous, Salvage Therapy, *Hematopoietic Stem Cell Transplantation, *Living Donors, Graft vs Host Disease/mortality/therapy, *Lymphocyte Transfusion, Primary Myelofibrosis/*mortality/*therapy",
author = "Evgeny Klyuchnikov and Ernst Holler and Martin Bornh{\"a}user and Guido Kobbe and Arnon Nagler and Avichai Shimoni and Christian K{\"o}necke and Christine Wolschke and Ulrike Bacher and Zander, {Axel R.} and Nicolaus Kr{\"o}ger",
year = "2012",
language = "English",
volume = "159",
pages = "172--181",
journal = "BRIT J HAEMATOL",
issn = "0007-1048",
publisher = "Wiley-Blackwell",
number = "2",

}

RIS

TY - JOUR

T1 - Donor lymphocyte infusions and second transplantation as salvage treatment for relapsed myelofibrosis after reduced-intensity allografting.

AU - Klyuchnikov, Evgeny

AU - Holler, Ernst

AU - Bornhäuser, Martin

AU - Kobbe, Guido

AU - Nagler, Arnon

AU - Shimoni, Avichai

AU - Könecke, Christian

AU - Wolschke, Christine

AU - Bacher, Ulrike

AU - Zander, Axel R.

AU - Kröger, Nicolaus

PY - 2012

Y1 - 2012

N2 - Thirty myelofibrosis patients (21 males, nine females) with relapse (n = 27) or graft-rejection (n = 3) after dose-reduced allografting underwent a salvage strategy including donor lymphocyte infusions (DLIs) and/or second allogeneic haematopoietic stem cell transplantation (HSCT). Twenty-six patients received a median number of three (range, 1-5) DLIs in a dose-escalated mode starting with a median dose of 1·2 × 10(6) (range, 0·003-8 × 10(6) ) up to median dose of 40 × 10(6) T-cells/kg (range, 10-130 × 10(6) ). 10/26 patients (39%) achieved complete response (CR) to DLIs. Acute (grade II-IV) and chronic graft-versus-host (GvHD) disease occurred in 12% and 36% cases. Thirteen non-responders to DLI and four patients who did not receive DLI due to graft-rejection or acute transformation of the blast phase underwent a second allogeneic HSCT from alternative (n = 15) or the same (n = 2) donor. One patient (6%) experienced primary graft-failure and died. Acute (II-IV) and chronic GvHD were observed in 47% and 46% of patients. Overall responses after second HSCT were seen in 12/15 patients (80%: CR: n = 9, partial response: n = 3). The 1-year cumulative incidence of non-relapse mortality for recipients of a second allograft was 6%, and the cumulative incidence of relapse was 24%. After a median follow-up of 27 months, the 2-year overall survival and progression-free survival for all 30 patients was 70% and 67%, respectively. In conclusion, our two-step strategy, including DLI and second HSCT for non-responding or ineligible patients, is an effective and well-tolerated salvage approach for patients relapsing after reduced-intensity allograft after myelofibrosis.

AB - Thirty myelofibrosis patients (21 males, nine females) with relapse (n = 27) or graft-rejection (n = 3) after dose-reduced allografting underwent a salvage strategy including donor lymphocyte infusions (DLIs) and/or second allogeneic haematopoietic stem cell transplantation (HSCT). Twenty-six patients received a median number of three (range, 1-5) DLIs in a dose-escalated mode starting with a median dose of 1·2 × 10(6) (range, 0·003-8 × 10(6) ) up to median dose of 40 × 10(6) T-cells/kg (range, 10-130 × 10(6) ). 10/26 patients (39%) achieved complete response (CR) to DLIs. Acute (grade II-IV) and chronic graft-versus-host (GvHD) disease occurred in 12% and 36% cases. Thirteen non-responders to DLI and four patients who did not receive DLI due to graft-rejection or acute transformation of the blast phase underwent a second allogeneic HSCT from alternative (n = 15) or the same (n = 2) donor. One patient (6%) experienced primary graft-failure and died. Acute (II-IV) and chronic GvHD were observed in 47% and 46% of patients. Overall responses after second HSCT were seen in 12/15 patients (80%: CR: n = 9, partial response: n = 3). The 1-year cumulative incidence of non-relapse mortality for recipients of a second allograft was 6%, and the cumulative incidence of relapse was 24%. After a median follow-up of 27 months, the 2-year overall survival and progression-free survival for all 30 patients was 70% and 67%, respectively. In conclusion, our two-step strategy, including DLI and second HSCT for non-responding or ineligible patients, is an effective and well-tolerated salvage approach for patients relapsing after reduced-intensity allograft after myelofibrosis.

KW - Adult

KW - Humans

KW - Male

KW - Aged

KW - Female

KW - Middle Aged

KW - Survival Rate

KW - Follow-Up Studies

KW - Disease-Free Survival

KW - Acute Disease

KW - Transplantation, Homologous

KW - Salvage Therapy

KW - Hematopoietic Stem Cell Transplantation

KW - Living Donors

KW - Graft vs Host Disease/mortality/therapy

KW - Lymphocyte Transfusion

KW - Primary Myelofibrosis/mortality/therapy

KW - Adult

KW - Humans

KW - Male

KW - Aged

KW - Female

KW - Middle Aged

KW - Survival Rate

KW - Follow-Up Studies

KW - Disease-Free Survival

KW - Acute Disease

KW - Transplantation, Homologous

KW - Salvage Therapy

KW - Hematopoietic Stem Cell Transplantation

KW - Living Donors

KW - Graft vs Host Disease/mortality/therapy

KW - Lymphocyte Transfusion

KW - Primary Myelofibrosis/mortality/therapy

M3 - SCORING: Journal article

VL - 159

SP - 172

EP - 181

JO - BRIT J HAEMATOL

JF - BRIT J HAEMATOL

SN - 0007-1048

IS - 2

M1 - 2

ER -