Gemtuzumab ozogamicin (Mylotarg) monotherapy for relapsed AML after hematopoietic stem cell transplant: efficacy and incidence of hepatic veno-occlusive disease
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作者:
AD Cohen
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机构:Hematologic Malignancies Program and the Bone Marrow and Stem Cell Transplantation Program,
AD Cohen
SM Luger
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机构:Hematologic Malignancies Program and the Bone Marrow and Stem Cell Transplantation Program,
SM Luger
C Sickles
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机构:Hematologic Malignancies Program and the Bone Marrow and Stem Cell Transplantation Program,
C Sickles
PA Mangan
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机构:Hematologic Malignancies Program and the Bone Marrow and Stem Cell Transplantation Program,
PA Mangan
DL Porter
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机构:Hematologic Malignancies Program and the Bone Marrow and Stem Cell Transplantation Program,
DL Porter
SJ Schuster
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机构:Hematologic Malignancies Program and the Bone Marrow and Stem Cell Transplantation Program,
SJ Schuster
DE Tsai
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机构:Hematologic Malignancies Program and the Bone Marrow and Stem Cell Transplantation Program,
DE Tsai
S Nasta
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机构:Hematologic Malignancies Program and the Bone Marrow and Stem Cell Transplantation Program,
S Nasta
AM Gewirtz
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机构:Hematologic Malignancies Program and the Bone Marrow and Stem Cell Transplantation Program,
AM Gewirtz
EA Stadtmauer
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机构:Hematologic Malignancies Program and the Bone Marrow and Stem Cell Transplantation Program,
EA Stadtmauer
机构:
[1] Hematologic Malignancies Program and the Bone Marrow and Stem Cell Transplantation Program,
[2] University of Pennsylvania Cancer Center,undefined
Gemtuzumab ozogamicin (GO) (Mylotarg, CMA-676) is a novel chemotherapeutic agent consisting of an anti-CD33 monoclonal antibody linked to calicheamicin, and is associated with a 30% response rate in patients with CD33-positive acute myeloid leukemia (AML) in first relapse. GO therapy has a 20% incidence of grade 3 or 4 hepatotoxicity, and has recently been associated with hepatic veno-occlusive disease (VOD). The efficacy and toxicity of GO in patients with AML who have relapsed after hematopoietic stem cell transplant (HSCT) is unknown, as this population was largely excluded from phase II studies. We reviewed the outcomes of eight consecutive patients with AML who received GO following relapse after HSCT. Two (25%) had responses to GO. One patient, who had had two previous HSCT and prior hyperbilirubinemia, developed severe VOD and died 14 days after GO therapy. The other seven patients did not meet diagnostic criteria for VOD. We conclude that GO can be safe and effective in patients who relapse following HSCT, but that caution is warranted in patients with multiple risk factors for VOD.
机构:
Childrens Hosp, Montefiore Albert Einstein Coll Med, Pediat Blood & Marrow Transplantat, New York, NY USAChildrens Hosp, Montefiore Albert Einstein Coll Med, Pediat Blood & Marrow Transplantat, New York, NY USA
Mahadeo, Kris M.
Bajwa, Rajinder P. S.
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机构:
Nationwide Childrens Hosp, Dept Hematol Oncol BMT, Columbus, OH USAChildrens Hosp, Montefiore Albert Einstein Coll Med, Pediat Blood & Marrow Transplantat, New York, NY USA
机构:
Department of Paediatrics and Adolescent Medicine, The University of Hong KongDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong