Cord Blood Transplantation in Children and Young Adults With Blood Cancer
Cord Blood Transplantation in Children and Young Adults With Hematologic Malignancies
調査の概要
状態
研究の種類
入学 (推定)
段階
- フェーズ2
連絡先と場所
研究連絡先
- 名前:Andromachi Scaradavou, MD
- 電話番号:833-MSK-KIDS
- メール:ScaradaA@mskcc.org
研究連絡先のバックアップ
- 名前:Jaap Jan Boelens, MD, PhD
- 電話番号:833-MSK-KIDS
- メール:boelensj@mskcc.org
研究場所
-
-
New York
-
New York、New York、アメリカ、10065
- 募集
- Memorial Sloan Kettering Cancer Center (All Protocol Activities)
-
コンタクト:
- Andromachi Scaradavou, MD
- 電話番号:1-833-MSK-KIDS
-
-
参加基準
適格基準
就学可能な年齢
- 子
- 大人
健康ボランティアの受け入れ
説明
Inclusion Criteria:
A patient cannot be considered eligible for this study unless ALL of the following conditions are met.
° Disease type
Cohort 1, High Risk Disease: Patients with age ≤ 26 years at the time of informed consent with no available and suitably matched related or unrelated donor within 4 weeks, with one of the following diagnoses:
I. Acute myelogenous leukemia (AML):
Complete first remission (CR1) with blast count < 5% by bone marrow morphology at high risk for relapse such as any of the following:
- Known prior diagnosis of myelodysplasia (MDS)
- High risk cytogenetics (e.g., those associated with MDS, abnormalities of 5, 7, 8, complex karyotype) and/or high-risk molecular abnormalities (e.g., TP53)
- Requirement for 2 or more inductions to achieve CR1
- Therapy-related AML (t-AML) or therapy-related myeloid neoplasm (t-MN) (including after therapy for other malignancy, and/or gene therapy or cell therapy)
- Presence of Minimal/Measurable Residual Disease (MRD+) by cytogenetics, flow cytometry or molecular methods (at End of Induction or End of Consolidation)
- Other high-risk features not defined above.
- Complete second remission (CR2) or subsequent remission, with blast count < 5% by bone marrow morphology
- Presence of MRD by multiparameter flow cytometry at pre-transplant evaluation is acceptable.
II. Acute lymphoblastic leukemia (ALL):
Complete first remission (CR1) with MRD negative status by multicolor flow cytometry, at high risk for relapse such as any of the following:
- Presence of any high risk cytogenetic abnormalities such as t(9;22), t(1;19), t(4;11) or other, KMT2A (11q23) or other high risk molecular abnormality
- Failure to achieve complete remission (CR) after four weeks of induction therapy (transplant to follow antibody therapy and/or CAR T cells)
- Persistence or recurrence of MRD on therapy (Transplant to follow antibody therapy and/or CAR T cells)
- T-ALL in CR even with presence of MRD
- Other high-risk features not defined above
Complete second remission (CR2) or subsequent remission with MRD negative status by multiparameter flow cytometry.
- Relapse in less than 36 months from CR1
- Relapse for T-ALL
- Patients after antibody therapy (e.g., blinatumomab, inotuzumab, other) and/or CAR-T cell therapy that resulted in MRD negative status by multiparameter flow cytometry.
III. Other acute leukemias:
- Leukemias of ambiguous lineage or of other types with < 5% blasts by bone marrow morphology.
- Patients with persistent/relapsed disease with cytogenetic, flow cytometric or molecular aberrations in < 5% of cells.
- Chronic myelogenous leukemia: Patients with history of blast crisis or accelerated phase.
- Any leukemia that developed after gene therapy or cell therapy
IV. Myelodysplastic Syndrome (MDS):
- Any IPSS risk category with life-threatening cytopenia(s).
- Any IPSS risk category with high risk cytogenetic/molecular findings (5, 7, 8, complex karyotype, or TP53)
V. Non-Hodgkin lymphoma (NHL) or Hodgkin lymphoma (HL) at high risk of relapse or progression if not in remission:
- Patients with aggressive histology (such as, but not limited to, diffuse large B-cell NHL, mantle cell NHL, and T-cell NHL) in CR.
- Patients with indolent B cell NHL (such as, but not limited to, follicular, small cell or marginal zone NHL) will have 2nd or subsequent progression with stable disease/ CR/ PR with no single lesion equal to or more than 5 cm.
- Patients with HL without progression of disease (POD) after salvage chemotherapy with no single lesion ≥5 cm.
Cohort 2: Very High-Risk disease:
Patients in CR (bone marrow blasts <5% by morphology) who had prior allogeneic transplant and disease recurrence. The second transplant will take place at least 4 months after the first.
- Acute myelogenous leukemia (AML) or Myelodysplastic Syndrome (MDS): Relapse after previous transplant, in CR after induction therapy. MRD positive status by multi-parameter flow cytometry is accepted.
- Acute lymphoblastic leukemia (ALL): Relapse after previous transplant, in CR after induction therapy and/or antibody therapy/CAR T cells. MRD positive status after targeted therapy, as evaluated by multi-parameter flow cytometry is accepted.
- Other: patients with leukemia or lymphoma, who, in the opinion of their physician, are not likely to have reduction in disease burden with further chemotherapy.
Patients with relapsed/refractory disease at either first or second allogeneic transplant, with up to 30% bone marrow blasts by multiparameter flow cytometry or morphology. ° Relapse after previous transplant with < 30% blasts by bone marrow morphology, or with cytogenetic, flow cytometric, or molecular abnormalities in < 30% of bone marrow cells, after induction therapy.
° Primary refractory or relapsed AML with < 30% blasts by bone marrow morphology or with cytogenetic, flow cytometric, or molecular abnormalities in < 30% of bone marrow cells.
° Age 0-26 years at the time of informed consent
° Performance: Karnofsky (≥16 years) or Lansky score (<16 years) of ≥70% (see Appendix A).
° Not Pregnant and Not Nursing
° Required Organ Function
- Bilirubin ≤ 1.5 mg/dL (unless benign congenital hyperbilirubinemia).
- ALT ≤ 3 x upper limit of normal.
Pulmonary function (FVC, FEV1 and DLCO corrected for hemoglobin) ≥ 50% predicted.
- In young children unable to perform pulmonary function testing: pulse oximetry >92% in room air, and a normal CT of the chest (if CT is not normal, the child needs to be evaluated and cleared by pediatric pulmonary physician).
- Left ventricular ejection fraction > 50%.
- Age-adjusted Hematopoietic Cell Transplantation-Comorbidity Index (aaHCT-CI) ≤ 7.
- Female patients of childbearing potential must have a negative serum pregnancy test within 7 days of enrolment and must be willing to use an effective contraceptive method while enrolled in the study.
- Renal: Serum creatinine (SCr) ≤ 1.5 x normal for age. If SCr is outside the normal range, then CrCl > 50 mL/min (calculated or estimated) or estimated GFR (mL/min/1.73m2) >30% of predicted normal for age.
Normal GFR by Age : Mean GFR +- SD (mL/min/1.73m^2) 1 week : 40.6 + / - 14.8 2-8 weeks : 65.8 + / - 24.8 >8 weeks : 95.7 + / - 21.7 2-12 years : 133.0 + / - 27.0 13-21 years (males) : 140.0 + / - 30.0 13-21 years (females) : 126.0 + / - 22.0
GFR, glomerular filtration rate; SD, standard deviation; Greater than 2 years old: Normal GFR is 100 mL/ min; Infants: GFR must be corrected for body surface area.
Exclusion Criteria:
Exclusion criteria for both cohorts:
° Inadequate performance status/ organ function.
° Active CNS leukemic involvement.
- Chloroma >2 cm.
- Active and uncontrolled infection (bacterial/fungal/viral) at time of transplant.
- HIV infection.
- Seropositivity for HTLV-1.
- Pregnancy or breast feeding.
- Patient or guardian unable to give informed consent or unable to comply with the treatment protocol including appropriate supportive care, long-term follow-up, and research tests.
- Any abnormal condition or lab result that is considered by the PI capable or altering patient's condition or study outcome.
Cohort 2 Very High-Risk Disease (additional to above):
° Allogeneic HCT in the preceding 4 months.
Note (1): Prior checkpoint inhibitors/blockade in the last 12 months: eligibility to be discussed with study PI.
Note (2): For patients with known HBV and/or HCV infection :
- For patients with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated.
- Patients with a history of hepatitis C virus (HCV) infection must have been treated and cured. For patients with HCV infection who are currently on treatment, they are eligible if they have an undetectable HCV viral load.
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:並列代入
- 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:Cohort 1: Patients with High-Risk Disease
Participants in complete remission (CR; bone marrow blasts <5% by morphology) with no prior allogeneic transplant, who require allogeneic transplantation and do not have human leukocyte antigen (HLA)-matched related or unrelated donors readily available within 4 weeks. For participants with AML/MDS, MRD (Measurable/Minimal Residual Disease) positive status at the time of transplant is accepted (evaluated by multiparameter flow cytometry); participants with ALL need to be in MRD negative status (evaluated by multiparameter flow cytometry). |
Cord Blood [(HPC(CB)] products are minimally manipulated unrelated allogeneic cord blood units that have been collected, processed and stored in public Cord Blood banks
Hyper-fractionated TBI is administered by a linear accelerator at a dose rate of <20 cGy/minute.
Treatment planning begins with simulation.
他の名前:
Cyclophosphamide is an alkylating agent that prevents cell division by cross-linking DNA strands and decreasing DNA synthesis.
他の名前:
Fludarabine phosphate is rapidly dephosphorylated to 2- fluoro-ara- A and then phosphorylated intracellularly by deoxycytidine kinase to the active triphosphate, 2- fluoro-ara-ATP
他の名前:
Clofarabine, a purine (deoxyadenosine) nucleoside analog, is metabolized to clofarabine 5'-triphosphate.
他の名前:
Busulfan is a bifunctional alkylating agent known chemically as 1,4- butanediol, dimethanesulfonate.
他の名前:
Thiotepa is an alkylating agent which produces cross-linking of DNA strands leading to inhibition of DNA, RNA, and protein synthesis; thiotepa is cell-cycle independent.
他の名前:
Tacrolimus inhibits T-lymphocyte activation
他の名前:
Mycophenolate exhibits a cytostatic effect on T and B lymphocytes.
他の名前:
Cyclosporine is a calcineurin inhibitor that inhibits production and release of interleukin II and inhibits interleukin II-induced activation of resting T-lymphocytes.
|
|
実験的:Cohort 2: Patients with Very High-Risk Disease
|
Cord Blood [(HPC(CB)] products are minimally manipulated unrelated allogeneic cord blood units that have been collected, processed and stored in public Cord Blood banks
Hyper-fractionated TBI is administered by a linear accelerator at a dose rate of <20 cGy/minute.
Treatment planning begins with simulation.
他の名前:
Cyclophosphamide is an alkylating agent that prevents cell division by cross-linking DNA strands and decreasing DNA synthesis.
他の名前:
Fludarabine phosphate is rapidly dephosphorylated to 2- fluoro-ara- A and then phosphorylated intracellularly by deoxycytidine kinase to the active triphosphate, 2- fluoro-ara-ATP
他の名前:
Clofarabine, a purine (deoxyadenosine) nucleoside analog, is metabolized to clofarabine 5'-triphosphate.
他の名前:
Busulfan is a bifunctional alkylating agent known chemically as 1,4- butanediol, dimethanesulfonate.
他の名前:
Thiotepa is an alkylating agent which produces cross-linking of DNA strands leading to inhibition of DNA, RNA, and protein synthesis; thiotepa is cell-cycle independent.
他の名前:
Tacrolimus inhibits T-lymphocyte activation
他の名前:
Mycophenolate exhibits a cytostatic effect on T and B lymphocytes.
他の名前:
Cyclosporine is a calcineurin inhibitor that inhibits production and release of interleukin II and inhibits interleukin II-induced activation of resting T-lymphocytes.
|
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 |
|---|---|---|
|
Disease-free Survival (DFS)
時間枠:1 year
|
Disease-free Survival (DFS) at 1 year after CBT
|
1 year
|
協力者と研究者
捜査官
- 主任研究者:Andromachi Scaradavou, MD、Memorial Sloan Kettering 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 (実際)
一次修了 (推定)
研究の完了 (推定)
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 (実際)
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
本研究に関する用語
キーワード
追加の関連 MeSH 用語
- 新生物
- 免疫系疾患
- 組織型別の新生物
- 血液疾患
- リンパ疾患
- リンパ増殖性疾患
- 免疫増殖性疾患
- 白血病、骨髄性
- 骨髄疾患
- 白血病、リンパ
- ヘミックおよびリンパ疾患
- 白血病
- 白血病、骨髄性、急性
- リンパ腫
- 前駆細胞リンパ芽球性白血病-リンパ腫
- リンパ腫、非ホジキン
- 骨髄異形成症候群
- ホジキン病
- 移植片対宿主病
- ペプチド
- アミノ酸、ペプチド、およびタンパク質
- 硫黄化合物
- 有機化学物質
- 複素環化化合物、1リング
- 複素環化化合物
- 複素環化化合物、2リング
- 複素環化化合物、融合リング
- 調査手法
- 治療
- 脂肪酸
- 脂質
- 核酸、ヌクレオチド、およびヌクレオシド
- 炭化水素、非環式
- 炭化水素
- 酸、非環式
- カルボン酸
- 多環式化合物
- プリン
- アルカン
- アルコール
- ブチレングリコール
- グリコール
- メシル酸塩
- アルカンスルホン酸塩
- アルカンスルホン酸
- スルホン酸
- 硫酸
- マクロライド
- ラクトン
- ホスホルアミドマスタード
- 窒素マスタード化合物
- マスタード化合物
- 炭化水素、ハロゲン化
- ホスホラミド
- 有機リン化合物
- ヌクレオシド
- アラビノヌクレオシド
- 放射線療法
- 大環性化合物
- トリエチレンフォスリンアミド
- アジリジン
- アジリン
- ペプチド、周期的
- カプロート
- シクロスポリン
- リボヌクレオチド
- ヌクレオチド
- アデニンヌクレオチド
- プリンヌクレオチド
- クロファラビン
- シクロホスファミド
- ミコフェノール酸
- タクロリムス
- シクロスポリン
- ブスルファン
- チオテパ
- フルダラビン
- フルダラビンリン酸
- 全身照射
その他の研究ID番号
- 26-168
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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