- ICH GCP
- Реестр клинических исследований США
- Клиническое испытание NCT07566377
Cord Blood Transplantation in Children and Young Adults With Blood Cancer
Cord Blood Transplantation in Children and Young Adults With Hematologic Malignancies
Обзор исследования
Статус
Условия
Тип исследования
Регистрация (Оцененный)
Фаза
- Фаза 2
Контакты и местонахождение
Контакты исследования
- Имя: Andromachi Scaradavou, MD
- Номер телефона: 833-MSK-KIDS
- Электронная почта: ScaradaA@mskcc.org
Учебное резервное копирование контактов
- Имя: Jaap Jan Boelens, MD, PhD
- Номер телефона: 833-MSK-KIDS
- Электронная почта: boelensj@mskcc.org
Места учебы
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New York
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New York, New York, Соединенные Штаты, 10065
- Рекрутинг
- Memorial Sloan Kettering Cancer Center (All Protocol Activities)
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Контакт:
- Andromachi Scaradavou, MD
- Номер телефона: 1-833-MSK-KIDS
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Критерии участия
Критерии приемлемости
Возраст, подходящий для обучения
- Ребенок
- Взрослый
Принимает здоровых добровольцев
Описание
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.
Учебный план
Как устроено исследование?
Детали дизайна
- Основная цель: Уход
- Распределение: Нерандомизированный
- Интервенционная модель: Параллельное назначение
- Маскировка: Нет (открытая этикетка)
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
|
Экспериментальный: 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.
Другие имена:
Cyclophosphamide is an alkylating agent that prevents cell division by cross-linking DNA strands and decreasing DNA synthesis.
Другие имена:
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
Другие имена:
Clofarabine, a purine (deoxyadenosine) nucleoside analog, is metabolized to clofarabine 5'-triphosphate.
Другие имена:
Busulfan is a bifunctional alkylating agent known chemically as 1,4- butanediol, dimethanesulfonate.
Другие имена:
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.
Другие имена:
Tacrolimus inhibits T-lymphocyte activation
Другие имена:
Mycophenolate exhibits a cytostatic effect on T and B lymphocytes.
Другие имена:
Cyclosporine is a calcineurin inhibitor that inhibits production and release of interleukin II and inhibits interleukin II-induced activation of resting T-lymphocytes.
|
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Экспериментальный: 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.
Другие имена:
Cyclophosphamide is an alkylating agent that prevents cell division by cross-linking DNA strands and decreasing DNA synthesis.
Другие имена:
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
Другие имена:
Clofarabine, a purine (deoxyadenosine) nucleoside analog, is metabolized to clofarabine 5'-triphosphate.
Другие имена:
Busulfan is a bifunctional alkylating agent known chemically as 1,4- butanediol, dimethanesulfonate.
Другие имена:
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.
Другие имена:
Tacrolimus inhibits T-lymphocyte activation
Другие имена:
Mycophenolate exhibits a cytostatic effect on T and B lymphocytes.
Другие имена:
Cyclosporine is a calcineurin inhibitor that inhibits production and release of interleukin II and inhibits interleukin II-induced activation of resting T-lymphocytes.
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Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
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Disease-free Survival (DFS)
Временное ограничение: 1 year
|
Disease-free Survival (DFS) at 1 year after CBT
|
1 year
|
Соавторы и исследователи
Следователи
- Главный следователь: Andromachi Scaradavou, MD, Memorial Sloan Kettering Cancer Center
Публикации и полезные ссылки
Полезные ссылки
Даты записи исследования
Изучение основных дат
Начало исследования (Действительный)
Первичное завершение (Оцененный)
Завершение исследования (Оцененный)
Даты регистрации исследования
Первый отправленный
Впервые представлено, что соответствует критериям контроля качества
Первый опубликованный (Действительный)
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
Последнее отправленное обновление, отвечающее критериям контроля качества
Последняя проверка
Дополнительная информация
Термины, связанные с этим исследованием
Ключевые слова
Дополнительные соответствующие термины MeSH
- Новообразования
- Заболевания иммунной системы
- Новообразования по гистологическому типу
- Гематологические заболевания
- Лимфатические заболевания
- Лимфопролиферативные заболевания
- Иммунопролиферативные заболевания
- Лейкоз, миелоидный
- Заболевания костного мозга
- Лейкемия, лимфоидная
- Гемики и лимфатические заболевания
- Лейкемия
- Лейкоз, Миелоидный, Острый
- Лимфома
- Клетки-предшественники лимфобластный лейкоз-лимфома
- Лимфома, неходжкинская
- Миелодиспластические синдромы
- Болезнь Ходжкина
- Трансплантат против болезни хозяина
- Пептиды
- Аминокислоты, пептиды и белки
- Средние соединения
- Органические химические вещества
- Гетероциклические соединения, 1-кольцо
- Гетероциклические соединения
- Гетероциклические соединения, 2-кольцо
- Гетероциклические соединения, слитое кольцо
- Следственные методы
- Терапия
- Жирные кислоты
- Липиды
- Нуклеиновые кислоты, нуклеотиды и нуклеозиды
- Углеводороды, ациклические
- Углеводороды
- Кислоты, ациклические
- Карбоновые кислоты
- Полициклические соединения
- Пурины
- Алканы
- Спирты
- Бутиленгликол
- Гликоль
- Мезилаты
- Алкансульфонаты
- Алкансульфоновые кислоты
- Сульфоновые кислоты
- Серные кислоты
- Макролиды
- Лактоны
- Фосфорамид горчицы
- Азотные соединения горчицы
- Горчичные соединения
- Углеводороды, галогенированные
- Фосфорамиды
- Соединения органофосфора
- Нуклеозиды
- Арабинонуклеозиды
- Лучевая терапия
- Макроциклические соединения
- Триэтиленфосфорамид
- Азиридины
- Азирины
- Пептиды, циклические
- Капуаты
- Циклоспорины
- Рибонуклеотиды
- Нуклеотиды
- Адениновые нуклеотиды
- Пуриновые нуклеотиды
- Клофарабин
- Циклофосфамид
- Микофеноловая кислота
- Такролимус
- Циклоспорин
- Бусульфан
- Тиотепа
- флударабин
- Флударабин фосфат
- Облучение всего тела
Другие идентификационные номера исследования
- 26-168
Планирование данных отдельных участников (IPD)
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Описание плана IPD
Информация о лекарствах и устройствах, исследовательские документы
Изучает лекарственный продукт, регулируемый FDA США.
Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.
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