Imatinib Mesylate in Treating Patients With Chronic Myelogenous Leukemia
A Phase II Study of Gleevec in Ph+ Chronic Phase Chronic Myelogenous Leukemia
調査の概要
詳細な説明
OBJECTIVES:
I. Determine the response rate in patients with Philadelphia chromosome positive chronic phase chronic myelogenous leukemia treated with imatinib mesylate.
II. Determine the disease-free survival of patients treated with this drug. III. Determine the pharmacokinetics of this drug in these patients. IV. Determine the toxic effects of this drug in these patients. V. Determine the rates of hematological, cytogenetic, and molecular response and time to response in patients treated with this drug.
OUTLINE: This is a multicenter study. Patients are stratified according to disease (chronic myelogenous leukemia [CML] in first chronic phase after failing interferon therapy or demonstrating intolerance to interferon [closed to accrual as of 12/05/03] vs CML relapsing after stem cell transplantation or in second or subsequent chronic phase [closed to accrual as of 7/29/05] vs newly diagnosed CML in first chronic phase with no prior treatment [closed to accrual as of 7/29/05] vs newly diagnosed CML in first chronic phase with no prior treatment).
Patients receive oral imatinib mesylate once daily on days 1-28. Courses repeat every 28 days for 1 year in the absence of disease progression or unacceptable toxicity. Patients who fail to achieve a complete hematologic response after 3 courses or a partial or complete cytogenic response after 6 courses are removed from the study.
PROJECTED ACCRUAL: A total of 109 patients (30 for stratum I [closed to accrual as of 12/05/03] and stratum II [closed to accrual as of 7/29/05], 34 for stratum III [closed to accrual as of 7/29/05], and 45 for stratum IV) will be accrued for this study within 2 years.
研究の種類
入学 (実際)
段階
- フェーズ2
連絡先と場所
研究場所
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California
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Arcadia、California、アメリカ、91006-3776
- Children's Oncology Group
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Diagnosis of Philadelphia chromosome positive (Ph+) chronic phase chronic myelogenous leukemia (CML)
Stratum I (closed to accrual as of 12/05/03):
CML in first chronic phase with resistance to interferon alfa (IFN-A) therapy defined as one of the following:
- WBC count at least 20,000/mm^3 after at least 3 months of treatment with an IFN-A-containing regimen
- Rising WBC count (at least 100% increase to a level of at least 20,000/mm^3) by two samples at least two weeks apart while receiving treatment with an IFN-A-containing regimen
- At least 66% Ph+ cells in bone marrow after 1 year of IFN-A therapy
- At least 30% increase in Ph+ cells in bone marrow after IFN-A-induced cytogenetic response while continuing to receive IFN-A therapy
- Intolerance to interferon therapy defined as more than two grade 2 toxic effects or any grade 3 toxic effect related to interferon therapy, except grade 3 fever, that is persistent beyond the first 28-day course of therapy and unresponsive to standard supportive care interventions
Stratum II (closed to accrual as of 7/29/05): CML recurring after stem cell transplantation or in second or subsequent chronic phase
- No molecular relapse (only evidence is detection of bcr-abl rearrangement with normal bone marrow and blood morphology and normal standard cytogenetic analysis)
- Stratum III (closed to accrual as of 7/29/05): Newly diagnosed CML in first chronic phase with no prior treatment except hydroxyurea
- Stratum IV: Newly diagnosed CML in first chronic phase with no prior treatment except hydroxyurea
No accelerated or blast phase defined as one or more of the following:
- WBC doubling time less than 5 days
- Chloroma
- Medullary fibrosis
- More than 10% blasts in peripheral blood or bone marrow
- More than 20% promyelocytes in peripheral blood or bone marrow
- More than 20% basophils and eosinophils in peripheral blood
- Performance status - ECOG 0-2
- At least 8 weeks
- See Disease Characteristics
- Shortening fraction ≥ 27% by echocardiogram OR ejection fraction ≥ 50% by radionuclide angiogram
- Bilirubin no greater than 1.5 times normal
- ALT less than 3.0 times normal
- Albumin greater than 2 g/dL
- Creatinine no greater than 1.5 times normal
- Creatinine clearance or radioisotope glomerular filtration rate at least 70 mL/min
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
- No uncontrolled infection
- No CNS toxicity greater than grade 2
- See Disease Characteristics
- No prior immunotherapy (for patients in stratum III [closed to accrual as of 7/29/05] and stratum IV only)
- At least 3 months since prior stem cell transplantation (SCT) (patients with allogeneic SCT must have no active graft-versus-host disease [GVHD] and have stable use of steroids) (for patients in stratum II only )
- At least 1 week since prior growth factors
- At least 1 week since prior biologic therapy, including interferon alfa (for patients in stratum I [closed to accrual as of 12/05/03] and stratum II only)
- Recovered from prior immunotherapy
- No concurrent immunomodulating agents
- See Disease Characteristics
- No prior chemotherapy (for patients in stratum III [closed to accrual as of 7/29/05] and stratum IV only)
- At least 6 weeks since prior busulfan or nitrosoureas
- At least 7 days since prior hydroxyurea
- At least 7 days since prior low-dose cytarabine (less than 30 mg/m^2 every 12 to 24 hours)
- At least 14 days since prior moderate-dose cytarabine (100-200 mg/m^2 for 5 to 7 days)
- At least 28 days since prior high-dose cytarabine (1-3 g/m^2 every 12 to 24 hours for 6 to 12 doses)
- At least 21 days since all other cytotoxic chemotherapy
- Recovered from prior chemotherapy
- No concurrent chemotherapy
- No concurrent steroids other than for controlled GVHD in patients with prior allogeneic SCT
- No prior radiotherapy (for patients in stratum III [closed to accrual as of 7/29/05] and stratum IV only)
- At least 2 weeks since prior local palliative (small port) radiotherapy*
- At least 3 months since prior craniospinal radiotherapy or radiotherapy to 50% or more of pelvis*
- At least 6 weeks since prior substantial bone marrow radiotherapy*
- Recovered from prior radiotherapy
- No prior imatinib mesylate
- No concurrent enzyme-activating anticonvulsants
- No concurrent warfarin
- No concurrent naturopathic agents or herbal medicines
- No other concurrent investigational agents
- Concurrent low-molecular weight heparin allowed
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
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実験的:Treatment (imatinib mesylate)
Patients receive oral imatinib mesylate once daily on days 1-28.
Courses repeat every 28 days for 1 year in the absence of disease progression or unacceptable toxicity.
Patients who fail to achieve a complete hematologic response after 3 courses or a partial or complete cytogenic response after 6 courses are removed from the study.
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相関研究
相関研究
他の名前:
経口投与
他の名前:
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
時間枠 |
|---|---|
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回答率
時間枠:5年まで
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5年まで
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無病生存
時間枠:5年まで
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5年まで
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National Cancer Institute Common Toxicity Criteria (NCI CTC) v2.0 に従って分類された毒性
時間枠:5年まで
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5年まで
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Time to achieve hematological cytogenetic and molecular response
時間枠:Up to 12 months
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Studied in a multivariate model using a Cox proportional hazards regression model.
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Up to 12 months
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イベントフリーサバイバル
時間枠:最長5年
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最長5年
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協力者と研究者
捜査官
- 主任研究者:Martin Champagne、Children's Oncology Group
出版物と役立つリンク
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- NCI-2012-01867
- U10CA098543 (米国 NIH グラント/契約)
- AAML0123
- CDR0000069161 (レジストリ識別子:PDQ (Physician Data Query))
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