Prediction of initial cytogenetic response for subsequent major and complete cytogenetic response to imatinib mesylate therapy in patients with Philadelphia chromosome-positive chronic myelogenous leukemia
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作者:
Kantarjian, H
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机构:Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
Kantarjian, H
Talpaz, M
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机构:Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
Talpaz, M
O'Brien, S
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机构:Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
O'Brien, S
Giles, F
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机构:Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
Giles, F
Rios, MB
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机构:Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
Rios, MB
White, K
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机构:Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
White, K
Garcia-Manero, G
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机构:Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
Garcia-Manero, G
Ferrajoli, A
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机构:Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
Ferrajoli, A
Verstovsek, S
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机构:Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
Verstovsek, S
Wierda, W
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机构:Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
Wierda, W
Kornblau, S
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机构:Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
Kornblau, S
Cortes, J
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机构:Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
Cortes, J
机构:
[1] Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Bioimmunotherapy, Houston, TX 77030 USA
BACKGROUND. Obtaining a major (Philadelphia chromosome [Ph] of < 35%) or a complete cytogenetic response (Ph of 0%) has been associated with excellent long-term survival. Cytogenetic response may continue to improve with therapy. Because early allogeneic stem cell transplantation (SCT) may be associated with a better outcome, early parameters predicting for subsequent cytogenetic responses would optimize the treatment decision-making. METHODS. The current study was performed to analyze whether early cytogenetic responses may be predictive of later major or complete cytogenetic responses to imatinib mesyl ate therapy in patients with Ph-positive chronic myelogenous leukemia (CML). RESULTS. Two hundred sixty-one patients with Ph-positive, chronic-phase CML after failure with interferon therapy who were treated with imatinib mesylate therapy were analyzed. A persistence of 100% Ph-positive cells after ! 6 months of imatinib mesylate therapy was associated with a major cytogenetic response rate of 9-13% and a complete cytogenetic response rate of 0-4%. However, a minor cytogenetic response after 3-12 months of therapy still was associated with high rates of major (68-83%) or complete (35-54%) cytogenetic response rates. CONCLUSIONS. Patients with Ph-positive, chronic-phase CML who have persistent 100% Ph-positive disease after ! 6 months of imatinib mesylate therapy may be offered allogeneic SCT or considered for alternative investigational therapies. Cancer 2003;97:2225-8. (C) 2003 American Cancer Society.
机构:
Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, JapanUniv Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, Japan
Nannya, Yasuhito
Yokota, Hiromitsu
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Univ Tokyo, Grad Sch Med, Dept Clin Lab Med, Tokyo 1138655, JapanUniv Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, Japan
Yokota, Hiromitsu
Sato, Yumiko
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Univ Tokyo, Grad Sch Med, Dept Clin Lab Med, Tokyo 1138655, JapanUniv Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, Japan
Sato, Yumiko
Yamamoto, Go
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Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, JapanUniv Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, Japan
Yamamoto, Go
Asai, Takashi
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Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, JapanUniv Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, Japan
Asai, Takashi
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Ichikawa, Motoshi
Watanabe, Takuro
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Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, JapanUniv Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, Japan
Watanabe, Takuro
Kumano, Keiki
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Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, Japan
Univ Tokyo, Grad Sch Med, Dept Cell Therapy & Transplantat, Tokyo 1138655, JapanUniv Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, Japan
Kumano, Keiki
Hangaishi, Akira
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Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, JapanUniv Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, Japan
Hangaishi, Akira
Takahashi, Tsuyoshi
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Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, JapanUniv Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, Japan
Takahashi, Tsuyoshi
Chiba, Shigeru
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Univ Tokyo, Grad Sch Med, Dept Cell Therapy & Transplantat, Tokyo 1138655, JapanUniv Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, Japan
Chiba, Shigeru
Yatomi, Yutaka
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Univ Tokyo, Grad Sch Med, Dept Clin Lab Med, Tokyo 1138655, JapanUniv Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, Japan
Yatomi, Yutaka
Kurokawa, Mineo
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Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, Japan
Univ Tokyo, Grad Sch Med, Dept Cell Therapy & Transplantat, Tokyo 1138655, JapanUniv Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, Japan
机构:
US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Johnson, JR
Bross, P
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Bross, P
Cohen, M
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Cohen, M
Rothmann, M
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Rothmann, M
Chen, G
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Chen, G
Zajicek, A
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Zajicek, A
Gobburu, J
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Gobburu, J
Rahman, A
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Rahman, A
Staten, A
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Staten, A
Pazdur, R
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA