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Six-year follow-up of patients receiving imatinib for the first-line treatment of chronic myeloid leukemia
by
Hughes, T P
, Hochhaus, A
, Radich, J P
, Mone, M
, Rudoltz, M
, Müller, M C
, O'Brien, S G
, Foroni, L
, Branford, S
, Larson, R A
, Druker, B J
, Goldman, J M
, Guilhot, F
, Gathmann, I
in
administration & dosage
/ BCR-ABL Positive
/ Benzamides
/ Biological and medical sciences
/ Blast crisis
/ Cancer Research
/ chemically induced
/ Chronic
/ Chronic myeloid leukemia
/ Clinical Medicine
/ complications
/ Critical Care Medicine
/ Cytarabine
/ Cytogenetics
/ Diagnosis
/ Disease Progression
/ Drug therapy
/ Follow-Up Studies
/ Heart Failure
/ Heart Failure - chemically induced
/ Hematologic and hematopoietic diseases
/ Hematology
/ Humans
/ Imatinib
/ Imatinib Mesylate
/ Inhibitor drugs
/ Intensive
/ Interferon
/ Internal Medicine
/ Klinisk medicin
/ Leukemia
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - complications
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - mortality
/ Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
/ Medical sciences
/ Medicine
/ Medicine & Public Health
/ mortality
/ Myelogenous
/ Myeloid leukemia
/ Neoplasms
/ Neoplasms, Second Primary - chemically induced
/ Oncology
/ original-article
/ Patients
/ Piperazines
/ Piperazines - administration & dosage
/ Piperazines - toxicity
/ Pyrimidines
/ Pyrimidines - administration & dosage
/ Pyrimidines - toxicity
/ Remission Induction
/ Second Primary
/ Survival
/ Survival Analysis
/ Targeted cancer therapy
/ Toxicity
/ Treatment Outcome
/ α-Interferon
2009
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Six-year follow-up of patients receiving imatinib for the first-line treatment of chronic myeloid leukemia
by
Hughes, T P
, Hochhaus, A
, Radich, J P
, Mone, M
, Rudoltz, M
, Müller, M C
, O'Brien, S G
, Foroni, L
, Branford, S
, Larson, R A
, Druker, B J
, Goldman, J M
, Guilhot, F
, Gathmann, I
in
administration & dosage
/ BCR-ABL Positive
/ Benzamides
/ Biological and medical sciences
/ Blast crisis
/ Cancer Research
/ chemically induced
/ Chronic
/ Chronic myeloid leukemia
/ Clinical Medicine
/ complications
/ Critical Care Medicine
/ Cytarabine
/ Cytogenetics
/ Diagnosis
/ Disease Progression
/ Drug therapy
/ Follow-Up Studies
/ Heart Failure
/ Heart Failure - chemically induced
/ Hematologic and hematopoietic diseases
/ Hematology
/ Humans
/ Imatinib
/ Imatinib Mesylate
/ Inhibitor drugs
/ Intensive
/ Interferon
/ Internal Medicine
/ Klinisk medicin
/ Leukemia
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - complications
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - mortality
/ Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
/ Medical sciences
/ Medicine
/ Medicine & Public Health
/ mortality
/ Myelogenous
/ Myeloid leukemia
/ Neoplasms
/ Neoplasms, Second Primary - chemically induced
/ Oncology
/ original-article
/ Patients
/ Piperazines
/ Piperazines - administration & dosage
/ Piperazines - toxicity
/ Pyrimidines
/ Pyrimidines - administration & dosage
/ Pyrimidines - toxicity
/ Remission Induction
/ Second Primary
/ Survival
/ Survival Analysis
/ Targeted cancer therapy
/ Toxicity
/ Treatment Outcome
/ α-Interferon
2009
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Six-year follow-up of patients receiving imatinib for the first-line treatment of chronic myeloid leukemia
by
Hughes, T P
, Hochhaus, A
, Radich, J P
, Mone, M
, Rudoltz, M
, Müller, M C
, O'Brien, S G
, Foroni, L
, Branford, S
, Larson, R A
, Druker, B J
, Goldman, J M
, Guilhot, F
, Gathmann, I
in
administration & dosage
/ BCR-ABL Positive
/ Benzamides
/ Biological and medical sciences
/ Blast crisis
/ Cancer Research
/ chemically induced
/ Chronic
/ Chronic myeloid leukemia
/ Clinical Medicine
/ complications
/ Critical Care Medicine
/ Cytarabine
/ Cytogenetics
/ Diagnosis
/ Disease Progression
/ Drug therapy
/ Follow-Up Studies
/ Heart Failure
/ Heart Failure - chemically induced
/ Hematologic and hematopoietic diseases
/ Hematology
/ Humans
/ Imatinib
/ Imatinib Mesylate
/ Inhibitor drugs
/ Intensive
/ Interferon
/ Internal Medicine
/ Klinisk medicin
/ Leukemia
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - complications
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - mortality
/ Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
/ Medical sciences
/ Medicine
/ Medicine & Public Health
/ mortality
/ Myelogenous
/ Myeloid leukemia
/ Neoplasms
/ Neoplasms, Second Primary - chemically induced
/ Oncology
/ original-article
/ Patients
/ Piperazines
/ Piperazines - administration & dosage
/ Piperazines - toxicity
/ Pyrimidines
/ Pyrimidines - administration & dosage
/ Pyrimidines - toxicity
/ Remission Induction
/ Second Primary
/ Survival
/ Survival Analysis
/ Targeted cancer therapy
/ Toxicity
/ Treatment Outcome
/ α-Interferon
2009
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Six-year follow-up of patients receiving imatinib for the first-line treatment of chronic myeloid leukemia
Journal Article
Six-year follow-up of patients receiving imatinib for the first-line treatment of chronic myeloid leukemia
2009
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Overview
Imatinib mesylate is considered standard of care for first-line treatment of chronic phase chronic myeloid leukemia (CML-CP). In the phase III, randomized, open-label International Randomized Study of Interferon vs STI571 (IRIS) trial, previously untreated CML-CP patients were randomized to imatinib (
n
=553) or interferon-α (IFN) plus cytarabine (
n
=553). This 6-year update focuses on patients randomized to receive imatinib as first-line therapy for newly diagnosed CML-CP. During the sixth year of study treatment, there were no reports of disease progression to accelerated phase (AP) or blast crisis (BC). The toxicity profile was unchanged. The cumulative best complete cytogenetic response (CCyR) rate was 82%; 63% of all patients randomized to receive imatinib and still on study treatment showed CCyR at last assessment. The estimated event-free survival at 6 years was 83%, and the estimated rate of freedom from progression to AP and BC was 93%. The estimated overall survival was 88%––or 95% when only CML-related deaths were considered. This 6-year update of IRIS underscores the efficacy and safety of imatinib as first-line therapy for patients with CML.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ Biological and medical sciences
/ Chronic
/ Heart Failure - chemically induced
/ Hematologic and hematopoietic diseases
/ Humans
/ Imatinib
/ Leukemia
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - complications
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - mortality
/ Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
/ Medicine
/ Neoplasms, Second Primary - chemically induced
/ Oncology
/ Patients
/ Piperazines - administration & dosage
/ Pyrimidines - administration & dosage
/ Survival
/ Toxicity
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