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Nilotinib is effective in imatinib-resistant or -intolerant patients with chronic myeloid leukemia in blastic phase
by
Ottmann, O G
, Baccarani, M
, Gillis, K
, Goldberg, S L
, Larson, R A
, Hochhaus, A
, Blakesley, R E
, Giles, F J
, Mahon, F-X
, Gallagher, N J
, Kantarjian, H M
, le Coutre, P D
in
Adolescent
/ Adult
/ Aged
/ Anemia
/ Antineoplastic Agents - adverse effects
/ Antineoplastic Agents - therapeutic use
/ BCR-ABL protein
/ Benzamides
/ Biological and medical sciences
/ Blast Crisis
/ Cancer Research
/ Chromosome aberrations
/ Chronic myeloid leukemia
/ Critical Care Medicine
/ Cytogenetics
/ Development and progression
/ Drug resistance
/ Drug Resistance, Neoplasm
/ Drug therapy
/ Fusion protein
/ Health aspects
/ Hematologic and hematopoietic diseases
/ Hematology
/ Humans
/ Hyperbilirubinemia
/ Hypophosphatemia
/ Imatinib
/ Imatinib Mesylate
/ Inhibitor drugs
/ Intensive
/ Internal Medicine
/ Kinases
/ Leukemia
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - pathology
/ Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
/ Medical genetics
/ Medical sciences
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Mutation
/ Myeloid leukemia
/ Myelosuppression
/ Neutropenia
/ Neutrophils
/ Nilotinib
/ Oncology
/ original-article
/ Patients
/ Piperazines - therapeutic use
/ Protein-Tyrosine Kinases - antagonists & inhibitors
/ Pyrimidines - adverse effects
/ Pyrimidines - therapeutic use
/ Stem cell transplantation
/ Stem cells
/ Survival
/ Survival Analysis
/ Targeted cancer therapy
/ Thrombocytopenia
/ Transplantation
/ Young Adult
2012
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Nilotinib is effective in imatinib-resistant or -intolerant patients with chronic myeloid leukemia in blastic phase
by
Ottmann, O G
, Baccarani, M
, Gillis, K
, Goldberg, S L
, Larson, R A
, Hochhaus, A
, Blakesley, R E
, Giles, F J
, Mahon, F-X
, Gallagher, N J
, Kantarjian, H M
, le Coutre, P D
in
Adolescent
/ Adult
/ Aged
/ Anemia
/ Antineoplastic Agents - adverse effects
/ Antineoplastic Agents - therapeutic use
/ BCR-ABL protein
/ Benzamides
/ Biological and medical sciences
/ Blast Crisis
/ Cancer Research
/ Chromosome aberrations
/ Chronic myeloid leukemia
/ Critical Care Medicine
/ Cytogenetics
/ Development and progression
/ Drug resistance
/ Drug Resistance, Neoplasm
/ Drug therapy
/ Fusion protein
/ Health aspects
/ Hematologic and hematopoietic diseases
/ Hematology
/ Humans
/ Hyperbilirubinemia
/ Hypophosphatemia
/ Imatinib
/ Imatinib Mesylate
/ Inhibitor drugs
/ Intensive
/ Internal Medicine
/ Kinases
/ Leukemia
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - pathology
/ Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
/ Medical genetics
/ Medical sciences
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Mutation
/ Myeloid leukemia
/ Myelosuppression
/ Neutropenia
/ Neutrophils
/ Nilotinib
/ Oncology
/ original-article
/ Patients
/ Piperazines - therapeutic use
/ Protein-Tyrosine Kinases - antagonists & inhibitors
/ Pyrimidines - adverse effects
/ Pyrimidines - therapeutic use
/ Stem cell transplantation
/ Stem cells
/ Survival
/ Survival Analysis
/ Targeted cancer therapy
/ Thrombocytopenia
/ Transplantation
/ Young Adult
2012
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Nilotinib is effective in imatinib-resistant or -intolerant patients with chronic myeloid leukemia in blastic phase
by
Ottmann, O G
, Baccarani, M
, Gillis, K
, Goldberg, S L
, Larson, R A
, Hochhaus, A
, Blakesley, R E
, Giles, F J
, Mahon, F-X
, Gallagher, N J
, Kantarjian, H M
, le Coutre, P D
in
Adolescent
/ Adult
/ Aged
/ Anemia
/ Antineoplastic Agents - adverse effects
/ Antineoplastic Agents - therapeutic use
/ BCR-ABL protein
/ Benzamides
/ Biological and medical sciences
/ Blast Crisis
/ Cancer Research
/ Chromosome aberrations
/ Chronic myeloid leukemia
/ Critical Care Medicine
/ Cytogenetics
/ Development and progression
/ Drug resistance
/ Drug Resistance, Neoplasm
/ Drug therapy
/ Fusion protein
/ Health aspects
/ Hematologic and hematopoietic diseases
/ Hematology
/ Humans
/ Hyperbilirubinemia
/ Hypophosphatemia
/ Imatinib
/ Imatinib Mesylate
/ Inhibitor drugs
/ Intensive
/ Internal Medicine
/ Kinases
/ Leukemia
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - pathology
/ Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
/ Medical genetics
/ Medical sciences
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Mutation
/ Myeloid leukemia
/ Myelosuppression
/ Neutropenia
/ Neutrophils
/ Nilotinib
/ Oncology
/ original-article
/ Patients
/ Piperazines - therapeutic use
/ Protein-Tyrosine Kinases - antagonists & inhibitors
/ Pyrimidines - adverse effects
/ Pyrimidines - therapeutic use
/ Stem cell transplantation
/ Stem cells
/ Survival
/ Survival Analysis
/ Targeted cancer therapy
/ Thrombocytopenia
/ Transplantation
/ Young Adult
2012
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Nilotinib is effective in imatinib-resistant or -intolerant patients with chronic myeloid leukemia in blastic phase
Journal Article
Nilotinib is effective in imatinib-resistant or -intolerant patients with chronic myeloid leukemia in blastic phase
2012
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Overview
Nilotinib is a selective inhibitor of BCR-ABL approved for use in newly diagnosed and imatinib-resistant or -intolerant patients with chronic myeloid leukemia (CML) in chronic phase. In this study, 400 mg of nilotinib was administered twice daily to the patients with myeloid (MBP,
n
=105) or lymphoid blastic phase (LBP,
n
=31) CML. After a minimum follow-up of 24 months, major hematologic responses were observed in 60% (MBP) and 59% (LBP) of patients. Major cytogenetic responses (MCyR) were attained in 38% (MBP) and 52% (LBP) of patients; and complete cytogenetic responses in 30% and 32%, respectively. Median duration of MCyR was 10.8 (MBP) and 3.2 months (LBP). Median overall survival was 10.1 (MBP) and 7.9 (LBP) months with 12- and 24-month survival of 42% (MBP 44%, LBP 35%) and 27% (MBP 32%, LBP 10%), respectively. Twelve MBP patients and two LBP patients received subsequent stem cell transplantation. Myelosuppression was frequent, with grade 3/4 neutropenia, thrombocytopenia, and anemia in 68%, 63% and 47% of patients, respectively. Grade 3/4 hypophosphatemia, hyperbilirubinemia and lipase elevation were observed in 15%, 11% and 11% of patients, respectively. Nilotinib has significant efficacy in patients with BP CML, but given the limited long-term survival of these patients, novel agents are needed.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ Adult
/ Aged
/ Anemia
/ Antineoplastic Agents - adverse effects
/ Antineoplastic Agents - therapeutic use
/ Biological and medical sciences
/ Hematologic and hematopoietic diseases
/ Humans
/ Imatinib
/ Kinases
/ Leukemia
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - pathology
/ Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
/ Medicine
/ Mutation
/ Oncology
/ Patients
/ Piperazines - therapeutic use
/ Protein-Tyrosine Kinases - antagonists & inhibitors
/ Pyrimidines - adverse effects
/ Pyrimidines - therapeutic use
/ Survival
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