Quality of life in patients with newly diagnosed chronic phase chronic myeloid leukemia on imatinib versus interferon alfa plus low-dose cytarabine: Results from the IRIS study

被引:141
作者
Hahn, EA
Glendenning, GA
Sorensen, MV
Hudgens, SA
Druker, BJ
Larson, RA
O'Brien, SG
Dobrez, DG
Hensley, ML
Cella, D
机构
[1] Evanston NW Healthcare, Ctr Outcomes Res & Educ, Evanston, IL 60201 USA
[2] Univ Chicago, Chicago, IL 60637 USA
[3] Novartis Pharmaceut, E Hanover, NJ USA
[4] Oregon Hlth & Sci Univ, Portland, OR 97201 USA
[5] Ctr Hosp Univ Poitiers, Poitiers, France
[6] Univ Newcastle, Newcastle Upon Tyne, Tyne & Wear, England
[7] Novartis AG, Basel, Switzerland
关键词
D O I
10.1200/JCO.2003.12.154
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose : Quality of life (QOL) outcomes in patients with chronic myeloid leukemia (CML) were evaluated in an international phase III study. Patients and Methods: Newly diagnosed patients with chronic phase CML were randomly assigned to imatinib or interferon alfa plus subcutaneous low-dose cytarabine (IFN+LDAC). Cross-over to the other treatment was permitted because of intolerance or lack of efficacy. Patients completed cancer-specific QOL (Functional Assessment of Cancer Therapy-Biologic Response Modifiers) and utility (Euro QoL-5D) questionnaires at baseline and during treatment (n = 1,049). The primary QOL end point was the Trial Outcome Index (TOI; a measure of physical function and well-being). Secondary end points included social and family well-being (SFWB), emotional well-being (EWB), and the utility score. Primary analyses were intention to treat with secondary analyses accounting for cross-over. Results: Patients receiving IFN+LDAC experienced a large decline in the TOI, whereas those receiving imatinib maintained their baseline level. Treatment differences at each visit were significant (P < .001) and clinically relevant in favor of imatinib. Mean SFWB, EWB, and utility scores were also significantly better for those patients taking imatinib. Patients who crossed over to imatinib experienced a large increase in TOI; significant (P < .001) differences were observed between patients who did and did not cross over in favor of imatinib. Conclusion: Imatinib offers clear QOL advantages compared with IFN+LDAC as first-line treatment of chronic phase CML. In addition, patients who cross over to imatinib from IFN+LDAC experience a significant improvement in QOL compared with patients who continue to take IFN+LDAC. (C) 2003 by American Society of Clinical Oncology.
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收藏
页码:2138 / 2146
页数:9
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