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Chemotherapy, Total-Body Irradiation, Donor Natural Killer Cell Infusion, Aldesleukin, and UCB Transplant in Treating Patients With Relapsed or Refractory AML

3 grudnia 2017 zaktualizowane przez: Masonic Cancer Center, University of Minnesota

Haploidentical Donor NK Cell Adoptive Therapy and Double T Cell Depleted Umbilical Cord Blood Transplantation With Post-Transplant IL-2 Immune Therapy For Refractory Acute Myeloid Leukemia

RATIONALE: Giving chemotherapy and total-body irradiation before a donor umbilical cord blood stem cell transplant helps stop the growth of cancer cells. It may also stop the patient's immune system from rejecting the donor's stem cells. When the healthy stem cells and natural killer cells from a donor are infused into the patient they may help the patient's bone marrow make stem cells, red blood cells, white blood cells, and platelets. Giving interleukin-2 (IL-2, aldesleukin) after transplant may stimulate the natural killer cells to kill any remaining cancer cells.

PURPOSE: This phase II trial is studying the side effects of giving combination chemotherapy together with total-body irradiation followed by interleukin-2 (IL-2, aldesleukin), and umbilical cord blood transplant and to see how well it works in treating patients with relapsed or refractory acute myeloid leukemia.

Przegląd badań

Szczegółowy opis

OBJECTIVES:

Primary

  • To determine the rate of neutrophil engraftment and grade III-IV acute graft-versus-host disease (GVHD) following a T cell depleted (TCD) umbilical cord blood (UCB) transplantation without post-transplant immunosuppression followed by administration of interleukin-2 (IL-2, aldesleukin) (every other day) days +3 to +13 to expand NK cells in vivo.

Secondary

  • To evaluate the safety of this regimen as assessed by monitoring the rates of graft failure, acute GVHD, and transplant-related mortality (TRM).
  • To perform quantitative, phenotypic, and functional assessments of the in vivo expanded UCB-derived NK cells on (day +72).
  • To assess clinical disease response (leukemia clearance and complete remission) and survival duration in these patients.
  • To evaluate the tolerability of aldesleukin in these patients.
  • To evaluate the tolerance of IL-2

OUTLINE:

  • Preparative regimen: Patients receive fludarabine phosphate intravenously (IV) over 1 hour on days -7 to -5 and cyclophosphamide IV on days -7 and -6. Patients undergo total-body irradiation twice daily on days -5 to -2.
  • Transplantation: Patients undergo T-cell depleted umbilical cord blood (UCB) transplantation on day 0.
  • IL-2 (Aldesleukin) therapy: Patients receive aldesleukin subcutaneously on days +3 6 doses every other day) and +60 (6 doses every other day).

Patients are followed periodically for up to 2 years after transplant.

Typ studiów

Interwencyjne

Zapisy (Rzeczywisty)

2

Faza

  • Faza 2

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

    • Minnesota
      • Minneapolis, Minnesota, Stany Zjednoczone, 55455
        • University of Minnesota Children's Hospital - Fairview

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

Nie starszy niż 45 lat (Dziecko, Dorosły)

Akceptuje zdrowych ochotników

Nie

Płeć kwalifikująca się do nauki

Wszystko

Opis

Inclusion Criteria:

  • Aged 0 to 45 years who meet one of the following criteria:

    • Primary induction failure defined as no complete remission (CR) after two or three induction cycles (no blast limit).
    • Relapsed acute myeloid leukemia (AML) with low disease burden

      • For patients 19 through 45 years of age: must have less than 10% marrow blasts at time of enrollment for patients who did not receive re-induction or measured at least 28 days from the start of re-induction therapy. Patients who have relapsed more than 12 months following a prior hematopoietic cell transplant (HCT) and did not reach CR following one re-induction cycle but have less than 10% marrow blasts are eligible.
      • For patients 0 through 18 years of age: must have less than 50% marrow blasts after no more than 3 induction attempts
    • CR3 or greater. This will include CRp defined as CR without platelet recovery to 100,000/mcL.
    • CR1 or CR2 with high risk features (therapy induced, prior myelodysplastic syndrome (MDS) or myeloproliferative disease (MPD), high risk cytogenetic or molecular phenotype) with no available alternate (sibling, URD or UCB) donors.
  • Patients with prior central nervous system (CNS) involvement are eligible provided that it has been treated and is in remission. CNS therapy (chemotherapy or radiation) should continue as medically indicated during the protocol.
  • Have acceptable organ function within 14 days of enrollment defined as:

    • Renal: creatinine ≤ 2.0 mg/dL (adult patients) or calculated creatinine clearance > 40 ml/min (pediatric patients)
    • Hepatic: bilirubin, AST/ALT, ALP ≤ 5 x upper limit of normal
    • Pulmonary function: DLCOcorr > 50% of normal, (oxygen saturation [>92%] can be used in child where PFT's cannot be obtained)
    • Cardiac: left ventricular ejection fraction ≥ 45%
  • Karnofsky score (adults) > 70% or Lansky score > 50% (pediatrics)
  • Women of childbearing potential must agree to use adequate contraception (diaphragm, birth control pills, injections, intrauterine device [IUD], surgical sterilization, subcutaneous implants, or abstinence, etc.) for the duration of treatment.
  • All patients will be questioned about prior exposure to antibody therapy (including OKT3, rituximab, trastuzumab, and gemtuzumab) without affect to eligibility. Patients with prior exposure will have a blood sample collected for human anti-mouse antibody (HAMA). For patients with no prior antibody therapy exposure, no further action will be taken.
  • Not receiving prednisone or other immunosuppressive medications
  • Voluntary written consent

Exclusion Criteria:

  • Active infection at time of enrollment or documented fungal infection within 3 months
  • Evidence of HIV infection or known HIV positive serology
  • Pregnant or breast feeding. The agents used in this study may be teratogenic to a fetus and there is no information on the excretion of agents into breast milk. All females of childbearing potential must have a blood test or urine study within 2 weeks prior to registration to rule out pregnancy.
  • If ≤ 18 years old, prior myeloablative transplant within the last 6 months. If > 18 years old prior myeloablative allotransplant or autologous transplant
  • Extensive prior therapy including > 12 months of any alkylator chemotherapy (etoposide >100 mg/m^2 x 5 days, cyclophosphamide >1 gm/m^2 or mitoxantrone >8 gm/m^2) delivered at 3-4 week intervals or > 6 months alkylator therapy (as above) with extensive radiation (determined by Radiation Oncology, e.g. mantle irradiation for Hodgkin's) and/or prior radiation therapy that makes a patient ineligible for total body irradiation (TBI).

Criteria for Second Course of IL-2 (begin day +60):

  • No Graft-Versus-Host Disease (GVHD), active infection or any other severe medical co-morbidity
  • Absolute neutrophil count (ANC) > 1000 without growth factor support
  • No grade 4 toxicity (except fevers) attributed to IL-2 during course #1

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Nie dotyczy
  • Model interwencyjny: Zadanie dla jednej grupy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: UCBT With Post-Transplant IL-2
Patients receive cyclophosphamide, fludarabine phosphate, total-body irradiation, T cell depleted umbilical cord blood transplantation (UCBT), followed by interleukin-2 (IL-2, aldesleukin) every other day beginning day +3 for a total of 6 doses and again on day +60 every other day for 6 doses.
IL-2 will be administered (9 million units; 5 million units if weight is less than 45 kg) every other day beginning on day +3 for a total of 6 doses and again on day +60 every other day for 6 doses.
Inne nazwy:
  • IŁ-2
  • interleukina-2
60 mg/kg over 1 hour intravenously (IV) on days -7 and -6.
Inne nazwy:
  • Cytoksan
25 mg/m^2 intravenously (IV) over 1 hour on days -7 through -5.
Inne nazwy:
  • Fludara
  • Fludarabina
On day 0, transplantation will occur with double T-cell depleted (TCD) umbilical cord blood (UCB) units
Inne nazwy:
  • UCBT
administered on days -5 through -2; 330 cGy daily
Inne nazwy:
  • TBI

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Number of Patients With Neutrophil Engraftment
Ramy czasowe: Day 42
Number of patient with absolute neutrophils >500*10^8/kg by 42 days post transplant.
Day 42
Number of Patients With Grade III-IV Acute Graft-Versus-Host (GVHD) Disease
Ramy czasowe: Day 100 Post Transplant

Number of patients with Grade III-IV GVHD. Graft-versus-host disease (GVHD) is a complication that can occur after a stem cell or bone marrow transplant in which the newly transplanted material attacks the transplant recipient's body.

Acute GVHD usually happens within the first 3 months after transplant.

Day 100 Post Transplant

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Incidence of Primary Graft Failure
Ramy czasowe: Day 42
Incidence of graft failure defined as an absolute neutrophil count of less than 500/uL and a bone marrow that is less than 5% cellular (marrow aplasia) on day 42.
Day 42
Number of Patients With Acute Graft-Versus-Host (GVHD) Disease
Ramy czasowe: Day 100 Post Transplant

Number of patients with any grade of GVHD. Graft-versus-host disease (GVHD) is a complication that can occur after a stem cell or bone marrow transplant in which the newly transplanted material attacks the transplant recipient's body.

Acute GVHD usually happens within the first 3 months after transplant.

Day 100 Post Transplant
Number of Patients With Transplant-Related Death (TRD)
Ramy czasowe: 1 Year Post Transplant
Number of patients whose death is related to study treatment received. TRD is defined as the number of patients that die without prior relapse.
1 Year Post Transplant
Number of Patients With Complete Remission of Disease
Ramy czasowe: Day 100
Disease response will be measured by rate of leukemic clearance (clearance of blasts in blood at timepoint 0) and complete remission (less than 5% blasts and recovery of hematopoiesis).
Day 100
Median Overall Survival
Ramy czasowe: Month 6
Average number of days the patients were alive after receiving UCB transplantation.
Month 6
Number of Patients With Successful Natural Killer Expansion
Ramy czasowe: Day 72 Post Transplant
Successful in vivo donor NK cell expansion will be defined as an absolute circulating donor-derived NK cell count of >100 cells/μl.
Day 72 Post Transplant

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów

1 stycznia 2009

Zakończenie podstawowe (Rzeczywisty)

1 marca 2010

Ukończenie studiów (Rzeczywisty)

1 października 2011

Daty rejestracji na studia

Pierwszy przesłany

27 marca 2009

Pierwszy przesłany, który spełnia kryteria kontroli jakości

27 marca 2009

Pierwszy wysłany (Oszacować)

30 marca 2009

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

28 grudnia 2017

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

3 grudnia 2017

Ostatnia weryfikacja

1 grudnia 2017

Więcej informacji

Terminy związane z tym badaniem

Inne numery identyfikacyjne badania

  • 2008LS110
  • MT2008-36 (Inny identyfikator: Blood and Marrow Transplantation Program)
  • 0810M51781 (Inny identyfikator: IRB, University of Minnesota)

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

Badania kliniczne na aldesleukin

3
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