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Post-transplant cyclophosphamide after matched sibling, unrelated and haploidentical donor transplants in patients with acute myeloid leukemia: a comparative study of the ALWP EBMT
by
Sanz, Jaime
, Cornelissen, Jan J.
, Blaise, Didier
, Castagna, Luca
, Labopin, Myriam
, Angelucci, Emanuele
, Ciceri, Fabio
, Galimard, Jacques-Emmanuel
, Afanasyev, Boris
, Savani, Bipin
, Ruggeri, Annalisa
, Meijer, Ellen
, Nagler, Arnon
, Mohty, Mohamad
, Diez-Martin, J. L.
, Koc, Yener
, Rovira, Montserrat
in
Acute leukemia
/ Acute myelocytic leukemia
/ Acute myeloid leukemia
/ Adult
/ Aged
/ Allogeneic stem cell transplant
/ Alternative donor transplants
/ Cancer Research
/ Care and treatment
/ Comparative analysis
/ Cyclophosphamide
/ Cyclophosphamide - therapeutic use
/ Donor Selection
/ Drug dosages
/ Female
/ Graft vs Host Disease - etiology
/ Graft vs Host Disease - prevention & control
/ Graft-versus-host reaction
/ Haploidentical transplant
/ Hematology
/ Hematopoietic Stem Cell Transplantation - adverse effects
/ Humans
/ Immunosuppressive Agents - therapeutic use
/ Leukemia
/ Leukemia, Myeloid, Acute - therapy
/ Male
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Mortality
/ Myeloid leukemia
/ Neutrophils
/ Oncology
/ Patients
/ Peripheral blood
/ Post-transplant cyclophosphamide
/ Prophylaxis
/ Remission
/ Retrospective Studies
/ Siblings
/ Software
/ Stem cell transplantation
/ Stem cells
/ Studies
/ Tissue Donors
/ Transplantation, Haploidentical - adverse effects
/ Transplants & implants
/ Treatment Outcome
/ Young Adult
2020
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Post-transplant cyclophosphamide after matched sibling, unrelated and haploidentical donor transplants in patients with acute myeloid leukemia: a comparative study of the ALWP EBMT
by
Sanz, Jaime
, Cornelissen, Jan J.
, Blaise, Didier
, Castagna, Luca
, Labopin, Myriam
, Angelucci, Emanuele
, Ciceri, Fabio
, Galimard, Jacques-Emmanuel
, Afanasyev, Boris
, Savani, Bipin
, Ruggeri, Annalisa
, Meijer, Ellen
, Nagler, Arnon
, Mohty, Mohamad
, Diez-Martin, J. L.
, Koc, Yener
, Rovira, Montserrat
in
Acute leukemia
/ Acute myelocytic leukemia
/ Acute myeloid leukemia
/ Adult
/ Aged
/ Allogeneic stem cell transplant
/ Alternative donor transplants
/ Cancer Research
/ Care and treatment
/ Comparative analysis
/ Cyclophosphamide
/ Cyclophosphamide - therapeutic use
/ Donor Selection
/ Drug dosages
/ Female
/ Graft vs Host Disease - etiology
/ Graft vs Host Disease - prevention & control
/ Graft-versus-host reaction
/ Haploidentical transplant
/ Hematology
/ Hematopoietic Stem Cell Transplantation - adverse effects
/ Humans
/ Immunosuppressive Agents - therapeutic use
/ Leukemia
/ Leukemia, Myeloid, Acute - therapy
/ Male
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Mortality
/ Myeloid leukemia
/ Neutrophils
/ Oncology
/ Patients
/ Peripheral blood
/ Post-transplant cyclophosphamide
/ Prophylaxis
/ Remission
/ Retrospective Studies
/ Siblings
/ Software
/ Stem cell transplantation
/ Stem cells
/ Studies
/ Tissue Donors
/ Transplantation, Haploidentical - adverse effects
/ Transplants & implants
/ Treatment Outcome
/ Young Adult
2020
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Post-transplant cyclophosphamide after matched sibling, unrelated and haploidentical donor transplants in patients with acute myeloid leukemia: a comparative study of the ALWP EBMT
by
Sanz, Jaime
, Cornelissen, Jan J.
, Blaise, Didier
, Castagna, Luca
, Labopin, Myriam
, Angelucci, Emanuele
, Ciceri, Fabio
, Galimard, Jacques-Emmanuel
, Afanasyev, Boris
, Savani, Bipin
, Ruggeri, Annalisa
, Meijer, Ellen
, Nagler, Arnon
, Mohty, Mohamad
, Diez-Martin, J. L.
, Koc, Yener
, Rovira, Montserrat
in
Acute leukemia
/ Acute myelocytic leukemia
/ Acute myeloid leukemia
/ Adult
/ Aged
/ Allogeneic stem cell transplant
/ Alternative donor transplants
/ Cancer Research
/ Care and treatment
/ Comparative analysis
/ Cyclophosphamide
/ Cyclophosphamide - therapeutic use
/ Donor Selection
/ Drug dosages
/ Female
/ Graft vs Host Disease - etiology
/ Graft vs Host Disease - prevention & control
/ Graft-versus-host reaction
/ Haploidentical transplant
/ Hematology
/ Hematopoietic Stem Cell Transplantation - adverse effects
/ Humans
/ Immunosuppressive Agents - therapeutic use
/ Leukemia
/ Leukemia, Myeloid, Acute - therapy
/ Male
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Mortality
/ Myeloid leukemia
/ Neutrophils
/ Oncology
/ Patients
/ Peripheral blood
/ Post-transplant cyclophosphamide
/ Prophylaxis
/ Remission
/ Retrospective Studies
/ Siblings
/ Software
/ Stem cell transplantation
/ Stem cells
/ Studies
/ Tissue Donors
/ Transplantation, Haploidentical - adverse effects
/ Transplants & implants
/ Treatment Outcome
/ Young Adult
2020
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Post-transplant cyclophosphamide after matched sibling, unrelated and haploidentical donor transplants in patients with acute myeloid leukemia: a comparative study of the ALWP EBMT
Journal Article
Post-transplant cyclophosphamide after matched sibling, unrelated and haploidentical donor transplants in patients with acute myeloid leukemia: a comparative study of the ALWP EBMT
2020
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Overview
Background
The use of post-transplant cyclophosphamide (PTCy) is highly effective in preventing graft-versus-host disease (GVHD) in the haploidentical (Haplo) transplant setting and is being increasingly used in matched sibling (MSD) and matched unrelated (MUD) transplants. There is no information on the impact of donor types using homogeneous prophylaxis with PTCy.
Methods
We retrospectively compared outcomes of adult patients with acute myeloid leukemia (AML) in first complete remission (CR1) who received a first allogeneic stem cell transplantation (SCT) with PTCy as GVHD prophylaxis from MSD (
n
= 215), MUD (
n
= 235), and Haplo (
n
= 789) donors registered in the EBMT database between 2010 and 2017.
Results
The median follow-up was 2 years. Haplo-SCT carried a significantly increased risk of acute grade II–IV GVHD (HR 1.6; 95% CI 1.1–2.4) and NRM (HR 2.6; 95% CI 1.5–4.5) but a lower risk of relapse (HR 0.7; 95% CI 0.5–0.9) that translated to no differences in LFS (HR 1.1; 95% CI 0.8–1.4) or GVHD/relapse-free survival (HR 1; 95% CI 0.8–1.3). Interestingly, the use of peripheral blood was associated with an increased risk of acute (HR 1.9; 95% CI 1.4–2.6) and chronic GVHD (HR 1.7; 95% CI 1.2–2.4) but a lower risk of relapse (HR 0.7; 95% CI 0.5–0.9).
Conclusions
The use of PTCy in patients with AML in CR1 receiving SCT from MSD, MUD, and Haplo is safe and effective. Haplo-SCT had increased risk of acute GVHD and NRM and lower relapse incidence but no significant difference in survival.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
Subject
/ Adult
/ Aged
/ Allogeneic stem cell transplant
/ Alternative donor transplants
/ Cyclophosphamide - therapeutic use
/ Female
/ Graft vs Host Disease - etiology
/ Graft vs Host Disease - prevention & control
/ Hematopoietic Stem Cell Transplantation - adverse effects
/ Humans
/ Immunosuppressive Agents - therapeutic use
/ Leukemia
/ Leukemia, Myeloid, Acute - therapy
/ Male
/ Medicine
/ Oncology
/ Patients
/ Post-transplant cyclophosphamide
/ Siblings
/ Software
/ Studies
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