Dasatinib in Treating Patients With Chronic Myelogenous Leukemia or Acute Lymphoblastic Leukemia
Long-Term Safety and Efficacy of Dasatinib (BMS-354825) in Subjects Who Experienced Clinical Benefit on Protocol CA 180-002
RATIONALE: Dasatinib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth.
PURPOSE: This phase I trial is studying the side effects of dasatinib in treating patients with chronic myelogenous leukemia or acute lymphoblastic leukemia.
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
詳細な説明
OBJECTIVES:
Primary
- Determine the long-term safety and tolerability of dasatinib in patients with Philadelphia chromosome-positive chronic myelogenous leukemia or acute lymphoblastic leukemia resistant or intolerant to imatinib mesylate.
Secondary
- Describe any hematologic or cytogenetic response in patients treated with this drug.
- Determine the duration of hematologic and cytogenetic response in patients using this drug during trial UCLA-0303035.
- Determine the progression-free survival and overall survival of patients treated with this drug.
OUTLINE: This is an open-label, roll-over study of protocol UCLA-0303035.
Patients receive oral dasatinib once or twice daily for 5, 6, or 7 days. Treatment repeats every 7 days in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed periodically for 5 years.
PROJECTED ACCRUAL: A total of 54 patients will be accrued for this study.
研究の種類
研究の種類
入学 (実際)
入学
段階
段階
- フェーズ 1
連絡先と場所
研究場所
-
-
California
-
Los Angeles、California、アメリカ、90095-1781
- Jonsson Comprehensive Cancer Center at UCLA
-
-
参加基準
適格基準
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
DISEASE CHARACTERISTICS:
Diagnosis of one of the following hematologic malignancies:
Chronic phase chronic myelogenous leukemia (CML)
In complete hematologic response after treatment on protocol UCLA-0303035, as indicated by the following criteria:
- WBC ≤ upper limit of normal (ULN)
- Platelet count < 450,000/mm^3
- No blasts or promyelocytes in peripheral blood
- Less than 5% myelocytes plus metamyelocytes in peripheral blood
- Peripheral blood basophils ≤ ULN
- No extramedullary involvement (including no hepatomegaly or splenomegaly)
- Response lasting ≥ 4 weeks after first documentation
Accelerated or blastic phase CML or acute lymphoblastic leukemia
In major hematologic response* after treatment on protocol UCLA-0303035, defined as 1 of the following:
In complete hematologic response*, as indicated by the following criteria:
- WBC ≤ ULN
- Absolute neutrophil count ≥ 1,000/mm^3
- Platelet count ≥ 100,000/mm^3
- No blasts or promyelocytes in peripheral blood
- Bone marrow blasts ≤ 5%
- Less than 5% myelocytes plus metamyelocytes in peripheral blood
- Peripheral blood basophils ≤ ULN
- No extramedullary involvement (including no hepatomegaly or splenomegaly)
No evidence of leukemia, as indicated by the following criteria:
- WBC ≤ ULN
- No blasts or promyelocytes in the peripheral blood
- Bone marrow blasts ≤ 5%
- Less than 5% myelocytes plus metamyelocytes in peripheral blood
- Peripheral blood basophils ≤ ULN
- No extramedullary involvement (including no hepatomegaly or splenomegaly)
- Absolute neutrophil count ≥ 500/mm^3 and < 1,000/mm^3 AND platelet count ≥ 20,000/mm^3 and < 100,000/mm^3
In minor hematologic response* after treatment on protocol UCLA-0303035, as indicated by the following criteria:
- Less than 15% in bone marrow and < 15% in peripheral blood
- Less than 30% blasts plus promyelocytes in bone marrow and < 30% blasts plus promyelocytes in peripheral blood
- Less than 20% basophils in peripheral blood
- No extramedullary disease other than spleen and liver NOTE: *Response confirmed after ≥ 4 weeks allowed provided there is no concurrent anagrelide or hydroxyurea during this time
- Philadelphia chromosome-positive (Ph+) disease
- Resistant or intolerant to prior imatinib mesylate
- Received and benefitted from ≥ 3 months of prior therapy with dasatinib on protocol UCLA-0303035
PATIENT CHARACTERISTICS:
- ECOG performance status 0-2
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception during and for 12 weeks after completion of study treatment
- No serious uncontrolled medical disorder
- No active infection that would preclude study participation
- No uncontrolled angina within the past 3 months
- No diagnosed or suspected congenital long QT syndrome
- No history of clinically significant ventricular arrhythmias (e.g., ventricular tachycardia, ventricular fibrillation, or torsades de pointes)
- QTc ≤ 450 msec on electrocardiogram
- No uncontrolled hypertension
- No dementia or altered mental status the would prohibit the understanding or rendering of informed consent
No history of the following significant bleeding disorders unrelated to CML:
- Diagnosed congenital bleeding disorders (e.g., von Willebrand's disease)
- Diagnosed acquired bleeding disorder in the past year (e.g., acquired antifactor VIII antibodies)
- Not involuntarily incarcerated for either psychiatric or physical (e.g., infectious disease) illness
- No patients who are imprisoned
- No clinical adverse event, laboratory abnormality, or intercurrent illness that may preclude study treatment, in the opinion of the investigator
- Bilirubin < 1.5 mg/dL
- ALT and AST < 2 times upper limit of normal (ULN)
- Creatinine < 1.5 times ULN
PRIOR CONCURRENT THERAPY:
- See Disease Characteristics
No concurrent use of the following drugs that may confer risk of torsades de pointes:
- Quinidine
- Procainamide
- Disopyramide
- Amiodarone
- Sotalol
- Ibutilide
- Dofetilide
- Erythromycin
- Clarithromycin
- Chlorpromazine
- Haloperidol
- Mesoridazine
- Thioridazine
- Pimozide
- Cisapride
- Bepridil
- Droperidol
- Methadone
- Arsenic
- Chloroquine
- Domperidone
- Halofantrine
- Levomethadyl
- Pentamidine
- Sparfloxacin
- Lidoflazine
- No other concurrent treatment for CML except for hydroxyurea for a 2-week duration
- No concurrent medications that inhibit platelet function (e.g., aspirin, dipyridamole, epoprostenol, eptifibatide, clopidogrel, cilostazol, abciximab, ticlopidine, or any nonsteroidal anti-inflammatory drug)* except for hydroxyurea or anagrelide
- No concurrent anticoagulants (e.g., warfarin or heparin/low molecular weight heparin [e.g., danaparoid, dalteparin, tinzaparin, or enoxaparin]) except as prophylaxis for catheter thrombosis and/or heparin flushes for IV lines* NOTE: *Allowed if received previously on UCLA-0303035
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)
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
実験的:ダサチニブ
|
この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
時間枠 |
|---|---|
|
Long term safety and tolerability
時間枠:5 years
|
5 years
|
協力者と研究者
協力者
協力者
捜査官
捜査官
- 主任研究者:Charles Sawyers, MD、Jonsson Comprehensive Cancer Center
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
研究開始
一次修了 (実際)
一次修了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
最初の投稿
学習記録の更新
投稿された最後の更新 (見積もり)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
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
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
その他の研究ID番号
- CDR0000480396
- UCLA-0509010-01
- BMS-CA180039
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