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PMID: 14534335 Published · ppublish English Clinical Trial Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Frequency of major molecular responses to imatinib or interferon alfa plus cytarabine in newly diagnosed chronic myeloid leukemia.

The New England journal of medicine ·Vol. 349 ·No. 15 ·2003-10-09 ·Pages 1423-32

Hughes TP, Kaeda J, Branford S, Rudzki Z, Hochhaus A, Hensley ML, Gathmann I, Bolton AE, van Hoomissen IC, Goldman JM, Radich JP, International Randomised Study of Interferon versus STI571 IRIS Study Group

Abstract

In a randomized trial, 1106 patients with chronic myeloid leukemia (CML) in chronic phase were assigned to imatinib or interferon alfa plus cytarabine as initial therapy. We measured levels of BCR-ABL transcripts in the blood of all patients in this trial who had a complete cytogenetic remission. Levels of BCR-ABL transcripts were measured by a quantitative real-time polymerase-chain-reaction assay. Results were expressed relative to the median level of BCR-ABL transcripts in the blood of 30 patients with untreated CML in chronic phase. In patients who had a complete cytogenetic remission, levels of BCR-ABL transcripts after 12 months of treatment had fallen by at least 3 log in 57 percent of those in the imatinib group and 24 percent of those in the group given interferon plus cytarabine (P=0.003). On the basis of the rates of complete cytogenetic remission of 68 percent in the imatinib group and 7 percent in the group given interferon plus cytarabine at 12 months, an estimated 39 percent of all patients treated with imatinib but only 2 percent of all those given interferon plus cytarabine had a reduction in BCR-ABL transcript levels of at least 3 log (P<0.001). For patients who had a complete cytogenetic remission and a reduction in transcript levels of at least 3 log at 12 months, the probability of remaining progression-free was 100 percent at 24 months, as compared with 95 percent for such patients with a reduction of less than 3 log and 85 percent for patients who were not in complete cytogenetic remission at 12 months (P<0.001). The proportion of patients with CML who had a reduction in BCR-ABL transcript levels of at least 3 log by 12 months of therapy was far greater with imatinib treatment than with treatment with interferon plus cytarabine. Patients in the imatinib group with this degree of molecular response had a negligible risk of disease progression during the subsequent 12 months.

MeSH Terms
Actuarial Analysis Adolescent Adult Aged Antineoplastic Agents/therapeutic use Antineoplastic Combined Chemotherapy Protocols/therapeutic use Benzamides Biomarkers, Tumor/blood Cytarabine/therapeutic use Disease-Free Survival Female Fusion Proteins, bcr-abl/blood Humans Imatinib Mesylate Interferon-alpha/therapeutic use Leukemia, Myelogenous, Chronic, BCR-ABL Positive/blood,drug therapy Male Middle Aged Piperazines/therapeutic use Pyrimidines/therapeutic use Remission Induction Reverse Transcriptase Polymerase Chain Reaction Transcription, Genetic/drug effects
Chemicals
Antineoplastic Agents Benzamides Biomarkers, Tumor Interferon-alpha Piperazines Pyrimidines Cytarabine Imatinib Mesylate Fusion Proteins, bcr-abl
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Hughes Tim P
Institute of Medical and Veterinary Science, Adelaide, SA, Australia. [email protected]
Kaeda Jaspal
Branford Susan
Rudzki Zbigniew
Hochhaus Andreas
Hensley Martee L
Gathmann Insa
Bolton Ann E
van Hoomissen Iris C
Goldman John M
Radich Jerald P
International Randomised Study of Interferon versus STI571 (IRIS) Study Group
Article Info
Journal
The New England journal of medicine
Abbr.
N Engl J Med
ISSN
1533-4406
Published
2003-10-09
Pages
1423-32
Language
English
Region
United States
NLM ID
0255562
Subset
IM
Corrections
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