Study of Dasatinib to Treat Philadelphia Positive Acute Lymphoblastic Leukemia (DASA-TRAS)
Multicenter, Non-randomized Phase II Pilot Study to Assess the Efficacy and Safety of Dasatinib After Allogeneic Stem Cell Transplantation in Patients With de Novo Philadelphia Positive (Bcr-abl +) Acute Lymphoblastic Leukemia
Study hypothesis:
Treatment with dasatinib 100 mg QD is safe and efficacious when given to patients with Ph+ ALL in the post SCT setting.
調査の概要
詳細な説明
Participants - inclusion criteria
- Adult patients ≥ 18 years.
- Diagnostic confirmation of de novo Ph+ ALL.
- Patients in first/second CR (assessed by cytology, karyotyping and/or FISH) at transplantation.
- Patients with sustained hematologic and cytogenetic CR at the time of study entry.
- Any modality of allogeneic SCT.
- Patients are in days between 120 until 180 after allogeneic SCT with stable graft.
- Ability to understand and voluntarily sign the informed consent form.
- Women of childbearing potential (WOCBP) must be using an adequate method of contraception to avoid pregnancy and have a negative pregnancy test, a maximum of 48 hours prior to study drug start.
Participants - exclusion criteria:
- Patients with ECOG 3-4 at study entry
Any of the following laboratory abnormalities:
- Absolute neutrophil count < 1.5 x 109/l or platelets < 75 x 109/l
- Serum creatinine > 2.0 mg/dl (177 mmol/l).
- Serum glutamic oxalacetic transaminase (SGOT) or serum glutamate pyruvate transaminase (SGPT) > 5,0 x upper limit of normal (ULN).
- Total bilirubin > 3 mg/dl.
- Known HIV infection or any other uncontrolled infection at study entry
- Known pleural effusion of any grade at study entry.
- Morphologic or cytogenetic or molecular relapse at study entry
- Evidence of digestive dysfunction that could prevent administration of study therapy
- Prior therapy with dasatinib during >21 days
- Other concurrent malignancy at study entry
- Uncontrolled or significant cardiovascular disease, including myocardial infarction within 6 months, uncontrolled angina within 3 months, prolonged QT interval, congestive heart failure within 3 months and clinically significant ventricular arrhythmias
- Any psychiatric condition that could prevent patient from signing the informed consent o could put the patient at an unacceptable risk in case of participating in the trial
- Subjects enrolled in another clinical trial at study entry. If patients have received other investigational agent, a minimum of 30 days wash-out period must have elapsed.
Primary Outcome measures
The primary objective of this study is to assess the efficacy of dasatinib maintenance in terms of Disease Free Survival at 2 years in patients with Ph+ ALL who receive maintenance with dasatinib after allogeneic SCT.
Secondary Outcome measures
.To assess the efficacy of maintenance with dasatinib in terms of duration of hematologic, cytogenetic and molecular remission, Relapse rate at 2 years, survival at 2 years, overall DFS, and Overall Survival (OS).
·To assess the safety and tolerability of dasatinib maintenance regimen after allogeneic SCT
Regarding the secondary objective "To assess the safety and tolerability of dasatinib maintenance regimen after allogeneic SCT", such safety analysis includes the frequency of all adverse events and laboratory abnormalities as well as frequency of dose interruptions, dose reductions and treatment discontinuation for drug-related toxicity. Frequency tables will be reported using the "All treated subjects" dataset. Safety will be reported for all treated patients and assessed by baseline findings, AEs and SAEs (definition, pattern, seriousness and intensity according to NCI CTCAE v3.0, relationship with dasatinib and outcome). Hematologic toxicity will be analyzed separately.
研究の種類
入学 (予想される)
段階
- フェーズ2
連絡先と場所
研究場所
-
-
-
Valencia、スペイン、46009
- Hospital La Fe
-
-
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:
- Adult patients ≥ 18 years
- Diagnostic confirmation of de novo Ph+ ALL
- Patients in first/second CR (assessed by cytology, karyotyping and/or FISH) at transplantation
- Patients with sustained hematologic and cytogenetic CR at the time of study entry
- Any modality of allogeneic SCT
- Patients are in days between 120 until 180 after allogeneic SCT with stable graft.
- Ability to understand and voluntarily sign the informed consent form
- Women of childbearing potential (WOCBP) must be using an adequate method of contraception to avoid pregnancy and have a negative pregnancy test, a maximum of 48 hours prior to study drug start
Exclusion Criteria:
- Patients with ECOG 3-4 at study entry
Any of the following laboratory abnormalities:
- Absolute neutrophil count < 1.5 x 109/l or platelets < 75 x 109/l
- Serum creatinine > 2.0 mg/dl (177 mmol/l).
- Serum glutamic oxalacetic transaminase (SGOT) or serum glutamate pyruvate transaminase (SGPT) > 5,0 x upper limit of normal (ULN).
- Total bilirubin > 3 mg/dl.
- Known HIV infection or any other uncontrolled infection at study entry
- Known pleural effusion of any grade at study entry.
- Morphologic or cytogenetic or molecular relapse at study entry
- Evidence of digestive dysfunction that could prevent administration of study therapy
- Prior therapy with dasatinib during >21 days
- Other concurrent malignancy at study entry
- Uncontrolled or significant cardiovascular disease, including myocardial infarction within 6 months, uncontrolled angina within 3 months, prolonged QT interval, congestive heart failure within 3 months and clinically significant ventricular arrhythmias
- Any psychiatric condition that could prevent patient from signing the informed consent o could put the patient at an unacceptable risk in case of participating in the trial
- Subjects enrolled in another clinical trial at study entry. If patients have received other investigational agent, a minimum of 30 days wash-out period must have elapsed.
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 |
|---|---|
|
実験的:ダサチニブ
|
Treatment with 100 mg QD of dasatinib (Sprycel®) administered orally as continuous daily dosing (CDD).
他の名前:
|
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 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
The efficacy of dasatinib
時間枠:at 2 years
|
The primary objective of this study is to assess the efficacy of dasatinib maintenance in terms of Disease Free Survival at 2 years in patients with Ph+ ALL who receive maintenance with dasatinib after allogeneic SCT.
|
at 2 years
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
To assess the efficacy of maintenance with dasatinib in terms of duration of hematologic, cytogenetic and molecular remission
時間枠:at 2 years
|
To assess the efficacy of maintenance with dasatinib in terms of duration of hematologic, cytogenetic and molecular remission, Relapse rate at 2 years, survival at 2 years, overall DFS, and Overall Survival (OS).
|
at 2 years
|
|
To assess the safety and tolerability of dasatinib maintenance regimen after allogeneic SCT
時間枠:at 2 years
|
To assess the safety and tolerability of dasatinib maintenance regimen after allogeneic SCT
|
at 2 years
|
協力者と研究者
捜査官
- 主任研究者:Guillermo Sanz, Doctor、Hospital La Fe de Valencia
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
研究の完了 (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 (実際)
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
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