Favorable long-term follow-up results over 6 years for response, survival, and safety with imatinib mesylate therapy in chronic-phase chronic myeloid leukemia after failure of interferon-α treatment

被引:160
作者
Hochhaus, Andreas [1 ]
Druker, Brian [2 ]
Sawyers, Charles [3 ]
Guilhot, Francois [4 ]
Schiffer, Charles A. [5 ]
Cortes, Jorge [6 ]
Niederwieser, Dietger W. [7 ]
Gambacorti, Carlo [8 ]
Stone, Richard M. [9 ]
Goldman, John [10 ]
Fischer, Thomas [11 ]
O'Brien, Stephen G. [12 ]
Reiffers, Jose J. [13 ]
Mone, Manisha [14 ]
Krahnke, Tillmann [14 ]
Talpaz, Moshe [15 ]
Kantarjian, Hagop M. [6 ]
机构
[1] Univ Heidelberg, Fak Klin Med Mannheim, D-6800 Mannheim, Germany
[2] Oregon Hlth & Sci Univ, Inst Canc, Portland, OR USA
[3] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[4] CHU Poiters, Poitiers, France
[5] Karmanos Canc Inst, Detroit, MI USA
[6] Univ Texas MD Anderson Canc Ctr Houston, Houston, TX USA
[7] Univ Leipzig, D-7010 Leipzig, Germany
[8] Inst Natl Tumuri, Milan, Italy
[9] Childrens Hosp, Dana Farber Canc Inst, Boston, MA 02115 USA
[10] Univ London Imperial Coll Sci & Technol, London, England
[11] Johannes Gutenberg Univ Mainz, D-6500 Mainz, Germany
[12] Univ Newcastle, Newcastle Upon Tyne, Tyne & Wear, England
[13] Univ Victor Segalen, Lab Greffe Moelle, Bordeaux, France
[14] Novartis Pharmaceut, E Hanover, NJ USA
[15] Univ Michigan, Ann Arbor, MI 48109 USA
关键词
D O I
10.1182/blood-2007-07-103523
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Imatinib mesylate, a targeted inhibitor of BCR-ABL tyrosine kinase, is the standard of care for chronic myeloid leukemia (CML). A phase 2 trial of imatinib in late chronic-phase (CP) CML after interferon-a (IFN alpha) failure enrolled 532 patients, 454 with a confirmed diagnosis of CP CML. Median time from diagnosis was 34 months; median duration of imatinib treatment was 65 months. Cumulative best rates of major cytogenetic response (MCyR) and complete cytogenetic response (CCyR) were 67% and 57%, respectively. At the 5-year landmark, 184 (41 %) of the 454 patients are in CCyR. At more than 6 years, 199 (44%) of the 454 patients remain on imatinib. Most responses occurred within 12 months of starting imatinib; however, some patients achieved initial MCyR and CCyR more than 5 years after imatinib initiation. Estimated rates of freedom from progression to accelerated phase (AP) and blastic phase (BP) and overall survival at 6 years were 61% and 76%, respectively. Both freedom from progression to AP/BP and overall survival (OS) were associated with cytogenetic response level at 12 months. No increase in rates of serious adverse events was observed with continuous use of imatinib for up to 6.5 years, compared with earlier time points. Imatinib continues to be an effective and safe therapy for patients with CP CML after failure of IFN.
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收藏
页码:1039 / 1043
页数:5
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