Mismatched Donor Cells to Treat Acute Myeloid Leukemia (ATAC-AML-01)
2017年8月28日 更新者:Elizabeth Krakow、Maisonneuve-Rosemont Hospital
Adoptive Transfer of Alloreactive Cells to Treat Patients With Poor-Prognosis Acute Myeloid Leukemia-01
The purpose of this study is to assess the safety and efficacy of infusing immune cells from a donor as treatment for patients with acute myeloid leukemia that is resistant to chemotherapy or who have experienced relapse.
Unlike standard bone marrow or stem cell transplantation which uses donors who are well 'matched' to the patient, this study uses donors whose immune cells are not compatible with the patient.
With standard stem cell or bone marrow transplantation, the well-matched immune cells will attack the leukemia but they also attack the patient's organs (a situation called graft-versus-host disease, which can persist in the long term).
Our hypothesis is that the mismatched donor cells will fight the leukemia but will then be eliminated from the patient's body, so long-term side effects like graft-versus-host disease should not occur.
調査の概要
詳細な説明
The ATAC cell therapy product contains unselected, non-mobilized peripheral blood mononuclear cells from related donors who are mismatched to the recipients at 3 or more (out of 6) HLA loci.
Cohorts of 3 patients will be treated at each of four pre-specified dose levels (T cells per kg recipient weight).
One ATAC infusion is administered 24-48 hours following re-induction chemotherapy (for relapsed or primary refractory AML patients not in remission).
In situations where ATAC infusion is not available immediately following re-induction chemotherapy and patients nonetheless achieve complete remission, one ATAC infusion is given 24-48 hours after consolidation chemotherapy.
研究の種類
介入
入学 (予想される)
12
段階
- フェーズ 1
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究場所
-
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Quebec
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Montreal、Quebec、カナダ、H1T 3M4
- 募集
- Hopital Maisonneuve-Rosemont
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-
参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
18年歳以上 (大人、高齢者)
健康ボランティアの受け入れ
いいえ
受講資格のある性別
全て
説明
Recipient Inclusion Criteria:
- Age ≥ 18 years (no upper age limit, but physician discretion is advised)
- AML that is refractory to 2 courses of induction therapy (that together constitute the 'first-line' therapy) or that has relapsed after a period of morphologic complete remission or morphologic remission with incomplete blood count recovery (CRi)
- Candidacy for intense induction chemotherapy (ECOG 0-2, adequate renal, liver and cardiac function, absence of uncontrolled infections)
- Availability of parents, siblings or children who are HLA haploidentical (and not homozygous for the shared haplotype), who are deemed suitable donors after medical evaluation, and who complete peripheral blood mononuclear cell collection
- No history of autologous or allogeneic stem cell transplant, purine analog chemotherapy or cyclophosphamide, or total body irradiation
- Ability to comprehend the investigational nature of the study and provide informed consent
Recipient Exclusion Criteria:
- Acute promyelocytic leukemia (including those with non-classical rearrangements of RARα)
- History of severe myelodysplastic syndrome clearly preceding the diagnosis of AML (i.e., red cell transfusion dependence or erythropoietin dependence over a 4-month period, or in the absence of a clear cause, any of the following: hemoglobin consistently below 9 g/dL or platelets below 50 x 10^9/L or ANC below 1000/uL on 2 or more occasions 2 weeks apart, or use of G-CSF to maintain the ANC threshold in the absence of infection, in the 3 months preceding the diagnosis of AML). Exception: If ATAC therapy is being considered as a bridge to stem cell transplantation in patients with an available standard transplant donor (familial, unrelated, or cord blood), this exclusion criterion does not apply.
- Grade 2-3/3 fibrosis in the diagnostic bone marrow biopsy
- DLCO < 40% predicted
- Left ventricular ejection fraction < 40% (evaluated by ECHO or MUGA)
- AST/SGOT > 2.5 x ULN
- Bilirubin > 1.5 x ULN
- Creatinine > 1.5 x ULN
- Creatinine clearance < 50 mL/min
- HIV positive
- Major anticipated illness or organ failure incompatible with survival from chemotherapy
- Concurrent second primary cancer or a prior malignancy that required cytotoxic treatment within the past 12 months, other than cervical carcinoma in-situ or prostate cancer in-situ
- Severe psychiatric illness or mental deficiency sufficiently severe as to make compliance with the treatment unlikely and informed consent impossible
- Any congenital or acquired immunodeficiency that would possibly permit permanent engraftment of donor cells
- Receiving systemic steroid therapy or systemic immunosuppression such as cyclosporine or TNF-inhibitors
- Prior or concurrent receipt of any marketed or investigational agent deemed on an ad hoc basis to cause immunomodulation, pose a threat of permanent engraftment or increase the risk of GVHD.
Donor inclusion criteria:
- Mismatched family donor (incompatibility at 3 loci HLA-A, B and DR of the unshared haplotype, or higher-order incompatibility)
- Age ≥ 16 and ≤ 80 years
- Fit to undergo apheresis (normal blood counts, normotensive and no history of stroke).
- Donor has been tested negative for HIV-1, HIV-2, hepatitis B virus (HBV, surface and core antigen), hepatitis C virus, human T-lymphotropic virus types I/II, and Treponema pallidum (syphilis).
- ECOG performance status of 2 or less.
- Adequate veins for leukapheresis or agree to placement of a temporary central venous catheter.
- Donor must provide written informed consent.
- Where multiple equally-suitable donors are available, sex mismatched donors will be preferred.
Donor exclusion criteria:
- Medically uncontrolled coronary heart disease
- Myocardial infarction within the last 3 months
- History of seizure
- History of stroke
- History of malignancy (except basal cell or squamous carcinoma of the skin, or positive PAP smear and subsequent negative follow-up)
- Presence of a transmissible disease (such as HIV seropositivity)
- Presence of a major illness or a suspected systemic dysfunction
- Presence of an an active inflammatory or autoimmune disorder
- Female donors who are pregnant or nursing
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
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:ATAC Therapy
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Unselected peripheral blood mononuclear cells given 24-48 hours after induction or consolidation chemotherapy
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 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Safety
時間枠:60 days (up to 2 years)
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Maximum tolerated cell dose: Dose at which < 33% of patients experienced dose-limiting toxicity.
If no DLT occurs, then dose titration will stop at a pre-specified number of T cells/kg.
Four dose-level cohorts are planned.
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60 days (up to 2 years)
|
二次結果の測定
結果測定 |
時間枠 |
|---|---|
|
Treatment-related mortality
時間枠:Continuous up to 2 years
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Continuous up to 2 years
|
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Non-relapse mortality
時間枠:Continuous up to 2 years
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Continuous up to 2 years
|
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Incidence of graft-versus-host disease
時間枠:Continuous up to 2 years
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Continuous up to 2 years
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Duration of cytopenias
時間枠:Monitored continuously from ATAC infusion until peripheral blood count recovery or maximum 2 years (whichever is earlier)
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Monitored continuously from ATAC infusion until peripheral blood count recovery or maximum 2 years (whichever is earlier)
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Overall survival
時間枠:Continuous up to 2 years
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Continuous up to 2 years
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Complete and incomplete remissions (CR, CRi)
時間枠:Day 60 post cell infusion
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Day 60 post cell infusion
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Relapse-free survival
時間枠:Continuous up to 2 years
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Continuous up to 2 years
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協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
捜査官
- スタディチェア:Jean-Sébastien Delisle, MD,PhD、Hôpital Maisonneuve-Rosemont and Université de Montréal
- 主任研究者:Elizabeth Krakow, MD、Hôpital Maisonneuve-Rosemont and Université de Montréal
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始
2012年9月1日
一次修了 (予想される)
2018年12月1日
研究の完了 (予想される)
2018年12月1日
試験登録日
最初に提出
2013年2月10日
QC基準を満たした最初の提出物
2013年2月13日
最初の投稿 (見積もり)
2013年2月15日
学習記録の更新
投稿された最後の更新 (実際)
2017年8月30日
QC基準を満たした最後の更新が送信されました
2017年8月28日
最終確認日
2017年8月1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。