Velcade (Bortezomib - PS341) in the Treatment of Patients Over 18 Years With Ph+ Leukemia
A Phase II Study of Velcade (Bortezomib - PS341) in the Treatment of Patients Over 18 Years With Ph+ Leukemia
Ph+ leukemias (i.e.Chronic Myelogenous Leukemia (CML) and (Ph+) Acute Lymphoblastic Leukemia are malignant clonal disorder of the hemopoietic stem cell due to reciprocal translocation of genetic material between chromosome 9 and 22 giving rise to the translocation t(9;22) (q2.2; q2.1). The translocation causes the formation of a new hybrid gene (bcr-abl) that codes for a 185 kb or 210 kb cytoplasmic protein (P185 and P210 respectively) that by autophosphorylation activates a number of signaling pathways involved in cell proliferation, maturation, apoptosis and adhesion, leading to the malignant cell transformation1-3. The course of the disease goes on through a chronic phase (CP), usually lasting some years, that is characterized by a massive myeloid hyperplasia with hyperleukocytosis and splenomegaly. The CP is almost always followed by an accelerated or blastic phase (ABP) where the leukemic process acquires the characteristics of acute leukemia. The ABP usually lasts some months and terminates with the death of the patient3.
The frequency of CML in western countries ranges between 10 and 15 per million persons (age - standardized). It is rare in children. The median age is 55 years.
Current treatment of CML includes conventional chemotherapy, allogeneic bone marrow transplantation (allo BMT), alpha-interferon (alpha-IFN)and imatinib.
調査の概要
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
-
-
-
Bologna、イタリア、40138
- Policlinico "S.Orsola-Malpighi"-Istituto di Ematologia "L e A Seragnoli"
-
-
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 for chronic phase patients :
- Age >/=18 years
- Ph positive
- Absence of a CHR after 3 months on imatinib
- Loss of a previously obtained CHR on imatinib alone
- Absence of a CCgR within 12 months on imatinib alone
- Loss of a previously obtained CCgR on imatinib alone
- Written informed consent
Exclusion Criteria for chronic phase patients :
- Age <18
- Performance status (ECOG/WHO) > 2 (see Appendix 2)
- Inability to provide written informed consent
- Pregnancy
- Accelerated or blastic phase
- Formal refusal of any recommendation of a safe contraception
- Alcohol or drug addiction
- Altered hepatic or renal function as defined by AST/ALT or bilirubin > 3 times upper normal limits (UNL)
- Serum creatinine > 265 umol/l or >3.0 mg/dl
- Any other disease or condition that by the advise of the responsible physician would make the treatment dangerous for the patient or would make the patient ineligible for the study, including physical, psychiatric, social and behavioural problems.
Inclusion criteria for accelerated and blastic phase or acute lymphoblastic leukemia Ph+ patients:
- Age >/=18 years
- Ph positive
- Loss of a previous hematological response to imatinib alone, with further progression to ABP (see section 14 for definitions)
- Performance status (ECOG/WHO)
- Written informed consent
Exclusion criteria for accelerated and blastic phase or acute lymphoblastic leukemia Ph+ patients:
- Age <18
- Performance status (ECOG/WHO) > 2 (see Appendix 2)
- Inability to provide written informed consent
- Pregnancy
- Chronic Phase disease
- Formal refusal of any recommendation of a safe contraception
- Alcohol or drug addiction
- Altered hepatic or renal function as defined by AST/ALT or bilirubin > 3 times upper normal limits (UNL)
- Serum creatinine > 265 umol/l or >3.0 mg/dl
- Any other disease or condition that by the advise of the responsible physician would make the treatment dangerous for the patient or would make the patient ineligible for the study, including physical, psychiatric, social and behavioural problems.
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:非ランダム化
- 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)
協力者と研究者
スポンサー
捜査官
- 主任研究者:Giovanni Martinelli, MD、Istituto di Ematologia "L e A Seragnoli" Policlinico S.Orsola-Malpighi di Bologna
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 (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
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
ボルテゾミブの臨床試験
-
Intergroupe Francophone du MyelomePfizer募集