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Single vs Double Umbilical Cord Blood Transplants in Children With High Risk Leukemia and Myelodysplasia (BMT CTN 0501)

13. Oktober 2021 aktualisiert von: Medical College of Wisconsin

Multi-center, Open Label, Randomized Trial Comparing Single Versus Double Umbilical Cord Blood (UCB) Transplantation in Pediatric Patients With High Risk Leukemia and Myelodysplasia (BMT CTN #0501)

This study is a Phase III, randomized, open-label, multi-center, prospective study of single umbilical cord blood (UCB) transplantation versus double UCB transplantation in pediatric patients with hematologic malignancies.

Studienübersicht

Status

Abgeschlossen

Bedingungen

Intervention / Behandlung

Detaillierte Beschreibung

BACKGROUND:

In nearly every large single center or registry analysis of outcomes after UCB transplantation, cell dose is identified as an important factor influencing the incidence and rate of hematopoietic recovery, risk of transplant-related mortality, and probability of survival. Pilot data suggest that infusion of two partially human leukocyte antigen (HLA)-matched UCB units, which always augments the graft cell dose, is safe and may improve neutrophil recovery and survival. To determine whether the infusion of two UCB units enhances survival, a multi-center, open-label, randomized trial is proposed. As adequate single UCB units can be identified for more than 80% of pediatric recipients (in contrast to less than 30% for adults), this study will be open only to pediatric patients. The population will be restricted to patients with high-risk hematologic malignancy, the most common indication of UCB transplantation in children.

DESIGN NARRATIVE:

Participants will include patients 1 to 21 years of age with a diagnosis of hematological malignancy and with two partially HLA-matched UCB units. Units must be HLA-matched at 3 of 6 HLA-A and B (intermediate resolution molecular typing) and DRB1 (high resolution molecular typing) with each other and 4 of 6 with the recipient. Two appropriately HLA-matched units must be available such that one unit delivers a pre-cryopreserved, nucleated cell dose of at least 2.5 x 10^7 per kilogram and the second unit delivers at least 1.5 x 10^7 per kilogram.

Patients will be randomized no more than 14 days prior to initiation of conditioning. UCB units will be shipped prior to initiation of conditioning.

The preparative regimen will consist of the following:

  • Fludarabine: 25 mg/m2/day IV on Days -10, -9, and -8.
  • Total Body Irradiation (TBI): 165 cGy twice daily on Days -7, -6, -5, and -4.
  • Cyclophosphamide: 60 mg/kg/day x 2 on Days -3 and -2.
  • Day 0 will be the day of the UCB transplant. The Graft-vs-Host-Disease (GVHD) prophylaxis regimen will be mycophenolate mofetil (MMF) 15 mg/kg IV BID on Day -3 to Day + 45 and cyclosporine A (CSA) to maintain level 200-400 ng/mL beginning on Day -3.

Patients will be followed for at least 24 months post-transplant.

Studientyp

Interventionell

Einschreibung (Tatsächlich)

224

Phase

  • Phase 3

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

  • Australien
    • New South Wales
      • Westmead, New South Wales, Australien, 2145
        • Children's Hospital at Westmead
  • Kanada
    • British Columbia
      • Vancouver, British Columbia, Kanada, V5Z 4E3
        • BC Cancer Agency
  • Vereinigte Staaten
    • Alabama
      • Birmingham, Alabama, Vereinigte Staaten, 35294
        • University of Alabama
    • Arizona
      • Phoenix, Arizona, Vereinigte Staaten, 85016
        • Phoenix Children's Hospital
    • California
      • Duarte, California, Vereinigte Staaten, 91010
        • City of Hope National Medical Center
      • Oakland, California, Vereinigte Staaten, 94609
        • Childrens Hospital at Oakland
      • San Diego, California, Vereinigte Staaten, 92123
        • UCSD/Rady Childrens Hospital
      • San Francisco, California, Vereinigte Staaten, 94143
        • University of California, San Francisco (Peds)
    • Colorado
      • Denver, Colorado, Vereinigte Staaten, 80218
        • The Children's Hospital of Denver
    • District of Columbia
      • Washington, District of Columbia, Vereinigte Staaten, 20010
        • Children's National Medical Center
    • Florida
      • Gainesville, Florida, Vereinigte Staaten, 32610
        • University of Florida College of Medicine (Shands)
      • Jacksonville, Florida, Vereinigte Staaten, 32207
        • Nemours Childrens Clinic
      • Miami, Florida, Vereinigte Staaten, 33136
        • University of Miami
      • Saint Petersburg, Florida, Vereinigte Staaten, 33710
        • All Children's Hospital
    • Georgia
      • Atlanta, Georgia, Vereinigte Staaten, 30322-1062
        • Children's Healthcare of Atlanta
    • Indiana
      • Indianapolis, Indiana, Vereinigte Staaten, 46202
        • Indiana University Medical Center
    • Kentucky
      • Louisville, Kentucky, Vereinigte Staaten, 40202
        • University of Louisville/Kosiar Children's Hospital
    • Louisiana
      • New Orleans, Louisiana, Vereinigte Staaten, 70118
        • Children's of New Orleans
    • Massachusetts
      • Boston, Massachusetts, Vereinigte Staaten, 02115
        • DFCI/Children's Hospital of Boston
    • Michigan
      • Ann Arbor, Michigan, Vereinigte Staaten, 48109
        • University of Michigan Medical Center
      • Detroit, Michigan, Vereinigte Staaten, 48201
        • Karmanos Cancer Institute/Children's Hospital of Michigan
    • Minnesota
      • Minneapolis, Minnesota, Vereinigte Staaten, 55455
        • University of Minnesota
    • Mississippi
      • Jackson, Mississippi, Vereinigte Staaten, 39216
        • University of Mississippi
    • Missouri
      • Kansas City, Missouri, Vereinigte Staaten, 64108
        • Children's Mercy Hospital and Clinics
    • New York
      • Valhalla, New York, Vereinigte Staaten, 10595
        • New York Medical College
    • North Carolina
      • Durham, North Carolina, Vereinigte Staaten, 27705
        • Duke University Medical Center
    • Ohio
      • Columbus, Ohio, Vereinigte Staaten, 43205-2696
        • Nationwide Children's Hospital
    • Oregon
      • Portland, Oregon, Vereinigte Staaten, 97239
        • Oregon Health Sciences University
    • Pennsylvania
      • Philadelphia, Pennsylvania, Vereinigte Staaten, 19104
        • Children's Hospital of Philadelphia
    • South Carolina
      • Charleston, South Carolina, Vereinigte Staaten, 29425
        • Medical University of South Carolina
    • Tennessee
      • Nashville, Tennessee, Vereinigte Staaten, 37232-7610
        • Vanderbilt University Medical Center
    • Texas
      • Dallas, Texas, Vereinigte Staaten, 75235
        • Children's Medical Center of Dallas
      • Fort Worth, Texas, Vereinigte Staaten, 76104
        • Cook Childrens Medical Center
      • San Antonio, Texas, Vereinigte Staaten, 78229
        • Texas Transplant Institute
    • Utah
      • Salt Lake City, Utah, Vereinigte Staaten, 84132
        • Utah BMT/University of Utah Medical School
    • Virginia
      • Richmond, Virginia, Vereinigte Staaten, 23298
        • Virgina Commonwealth University
    • Washington
      • Seattle, Washington, Vereinigte Staaten, 98109
        • Fred Hutchinson Cancer Research Center
    • Wisconsin
      • Milwaukee, Wisconsin, Vereinigte Staaten, 53211
        • Medical College of Wisconsin

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

1 Jahr bis 21 Jahre (Kind, Erwachsene)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  • Two partially HLA-matched UCB units. Units must be HLA-matched minimally at 4 of 6 HLA-A and B (at intermediate resolution by molecular typing) and DRB1 (at high resolution by molecular typing) loci with the patient, and the units must be HLA-matched at 3 of 6 HLA- A, B, DRB1 loci with each other (using same resolution of molecular typing as indicated above). Two appropriately HLA-matched units must be available such that one unit delivers a pre-cryopreserved nucleated cell dose of at least 2.5 x 10^7 per kilogram and the second unit at least 1.5 x 10^7 per kilogram.

  • Acute myelogenous leukemia (AML) at the following stages:

    1. High risk first complete remission (CR1), defined as the following:

      • Having preceding myelodysplasia (MDS)
      • High risk cytogenetics (high risk cytogenetics: del (5q) -5, -7, abn (3q), t (6;9) complex karyotype [at least 5 abnormalities],)the presence of a high FLT3 ITD-AR (> 0.4)
      • Requiring more than 1 cycle of chemotherapy to obtain complete remission (CR);
      • FAB M6
    2. Second or greater CR
    3. First relapse with less than 25% blasts in bone marrow
    4. Morphologic complete remission with incomplete blood count recovery
  • Therapy-related AML for which prior malignancy has been in remission for at least 12 months

  • Acute lymphocytic leukemia (ALL) at the following stages:

    1. High risk first remission, defined as one of the following conditions:

      • Philadelphia chromosome-positive adult lymphoblastic leukemia (Ph+ ALL)
      • Mixed lineage leukemia (MLL) rearrangement with slow early response (defined as having M2 [5-25% blasts] or M3 [more than 25% blasts on bone marrow examination on Day 14 of induction therapy])
      • Hypodiploidy (less than 44 chromosomes or DNA index less than 0.81)
      • End of induction M3 bone marrow
      • End of induction M2 with M2-3 at Day 42
      • Evidence of minimal residual disease (MRD). If a patient's only high risk criterion is MRD, approval by a protocol chair or protocol officer is required for enrollment. For COG centers, this will only be for MRD greater than 1 percent by flow MRD at the end of extended induction.

    2. High risk second remission, defined as one of the following conditions:

      • Philadelphia chromosome-positive adult lymphoblastic leukemia (Ph+ ALL)
      • Bone marrow relapse less than 36 months from induction
      • T-lineage relapse at any time
      • Very early isolated central nervous system (CNS) relapse (6 months from diagnosis)
      • Slow reinduction (M2-3 at Day 28) after relapse at any time
      • Evidence of minimal residual disease (MRD). If a patient's only high risk criterion is MRD, approval by a protocol chair or protocol officer is required for enrollment. For COG centers, this will only be for MRD greater than 1 percent by flow MRD at the end of extended induction.
    3. Any third or subsequent CR
  • NK cell lymphoblastic leukemia in any CR
  • Biphenotypic or undifferentiated leukemia in any CR or if in first relapse must have less than 25% blasts in bone marrow (BM)
  • Myelodysplastic syndrome (MDS) at any stage
  • Chronic myelogenous leukemia (CML) in chronic or accelerated phase
  • All patients with evidence of CNS leukemia must be treated and be in CNS CR to be eligible for study.
  • Patients 16 years old or older must have a Karnofsky score of at least 70% and patients younger than 16 years old must have a Lansky score of at least 70%.

  • Patients with adequate physical function as measured by:

    1. Cardiac: Left ventricular ejection fraction greater than 40% or shortening fraction greater than 26%
    2. Hepatic: Bilirubin no more than 2.5 mg/dL; alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP) no more than 5 times the upper limit of normal (ULN)
    3. Renal: Serum creatinine within normal range for age, or if serum creatinine is outside normal range for age, then renal function (creatinine clearance or GFR) greater than 70 mL/min/1.73 m^2
    4. Pulmonary: Diffusing capacity of the lung for carbon monoxide (DLCO), forced expiratory volume in one second (FEV1), or forced vital capacity (FVC) greater than 50% of predicted value (corrected for hemoglobin); if unable to perform pulmonary function tests, then O2 saturation greater than 92% of room air

Exclusion Criteria:

  • Pregnant (β-positive human chorionic gonadotropin [HCG]) or breastfeeding
  • Evidence of HIV infection or HIV positive serology
  • Current uncontrolled bacterial, viral, or fungal infection (currently taking medication and progression of clinical symptoms)
  • Autologous transplant less than 12 months prior to enrollment
  • Prior autologous transplant for the disease for which the UCB transplant will be performed
  • Prior allogeneic hematopoietic stem cell transplant
  • Active malignancy other than the one for which the UCB transplant is being performed within 12 months of enrollment
  • Inability to receive TBI
  • Requirement of supplemental oxygen
  • HLA-matched related donor able to donate

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Single Cord Blood Transplant
Unrelated donor, single umbilical cord blood unit transplant; conditioning regimen: Total Body Irradiation/cyclophosphamide/fludarabine; GVHD prophylaxis: Cyclosporine A/Mycophenolate Mofetil
Biologisch: Single Umbilical Cord Blood Unit Transplant
Unrelated donor, single umbilical cord blood unit; conditioning regimen: TBI/cyclophosphamide/fludarabine; GVHD prophylaxis: cyclosporine/MMF
Strahlung: Total Body Irradiation
The TBI will be delivered from either a linear accelerator or cobalt source at a dose rate of between 4 and 26 cGy/minute using energies of between 1 and 25 MV.
Andere Namen:
  • TBI
Arzneimittel: Cyclophosphamide
Cyclophosphamide 60 mg/kg/day will be administered as a 2 hour intravenous infusion with a high volume fluid flush on Days -3 and -2.
Andere Namen:
  • Cytoxan®
Arzneimittel: Fludarabine
Fludarabine 25 mg/m2/day will be administered over 30-60 minutes intravenous infusion on Days -10 through -8. Fludarabine will not be dose adjusted for body weight.
Andere Namen:
  • Fludara
Arzneimittel: Cyclosporine A
CSA will be administered beginning on Day -3 and doses will be adjusted to maintain a level of 200-400 ng/mL by TDX method (or 100-250 ng/mL by Tandem MS or equivalent level for other CSA testing methods). CSA can be administered per institutional practice.
Andere Namen:
  • CSA
Arzneimittel: Mycophenolate Mofetil
MMF will be given at a dose of 1 gram IV q 8 hours if > 50 kg or 15 mg/kg IV q 8 hours if < 50 kg beginning the morning of Day -3.
Andere Namen:
  • MMF, Cellcept®
Experimental: Double Cord Blood Transplant
Unrelated donor, double umbilical cord blood unit transplant; Conditioning regimen: Total Body Irradiation/cyclophosphamide/fludarabine; GVHD prophylaxis: Cyclosporine A/Mycophenolate Mofetil
Strahlung: Total Body Irradiation
The TBI will be delivered from either a linear accelerator or cobalt source at a dose rate of between 4 and 26 cGy/minute using energies of between 1 and 25 MV.
Andere Namen:
  • TBI
Arzneimittel: Cyclophosphamide
Cyclophosphamide 60 mg/kg/day will be administered as a 2 hour intravenous infusion with a high volume fluid flush on Days -3 and -2.
Andere Namen:
  • Cytoxan®
Arzneimittel: Fludarabine
Fludarabine 25 mg/m2/day will be administered over 30-60 minutes intravenous infusion on Days -10 through -8. Fludarabine will not be dose adjusted for body weight.
Andere Namen:
  • Fludara
Arzneimittel: Cyclosporine A
CSA will be administered beginning on Day -3 and doses will be adjusted to maintain a level of 200-400 ng/mL by TDX method (or 100-250 ng/mL by Tandem MS or equivalent level for other CSA testing methods). CSA can be administered per institutional practice.
Andere Namen:
  • CSA
Arzneimittel: Mycophenolate Mofetil
MMF will be given at a dose of 1 gram IV q 8 hours if > 50 kg or 15 mg/kg IV q 8 hours if < 50 kg beginning the morning of Day -3.
Andere Namen:
  • MMF, Cellcept®
Biologisch: Double Umbilical Cord Blood Unit Transplant
Unrelated donor, double umbilical cord blood unit; Conditioning regimen: TBI/cyclophosphamide/fludarabine; GVHD prophylaxis: cyclosporine/MMF

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Percentage of Participants With Overall Survival
Zeitfenster: 1 year post-randomization
Overall survival is defined as survival of death from any cause.
1 year post-randomization

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Percentage of Participants With Disease-free Survival
Zeitfenster: 1 year post-randomization
Disease-free survival is defined as survival without relapse of the primary disease.
1 year post-randomization
Percentage of Participants With Neutrophil and Platelet Engraftment
Zeitfenster: Days 42 and 100
Neutrophil engraftment is defined as achieving an absolute neutrophil count greater than 500x10^6/liter for three consecutive measurements on different days. The first of the three days will be designated the day of neutrophil engraftment. Platelet engraftment is defined as achieving platelet counts greater than 50,000/microliter for consecutive measurements over 7 days without requiring platelet transfusions. The first of the 7 days will be designated the day of platelet engraftment. Subjects must not have had platelet transfusions during the preceding 7 days.
Days 42 and 100
Time to Neutrophil and Platelet Engraftment
Zeitfenster: 2 years post-transplant
Platelet engraftment is defined as achieving platelet counts greater than 50,000/microliter for consecutive measurements over 7 days without requiring platelet transfusions. The first of the 7 days will be designated the day of platelet engraftment. Subjects must not have had platelet transfusions during the preceding 7 days.
2 years post-transplant
Percentage of Participants With Acute Graft-versus-host Disease (GVHD)
Zeitfenster: Day 100 post-randomization

Acute GVHD is graded according to the scoring system proposed by Przepiorka et al.1995:

Skin stage:

0: No rash

  1. Rash <25% of body surface area
  2. Rash on 25-50% of body surface area
  3. Rash on > 50% of body surface area
  4. Generalized erythroderma with bullous formation

Liver stage (based on bilirubin level)*:

0: <2 mg/dL

  1. 2-3 mg/dL
  2. 3.01-6 mg/dL
  3. 6.01-15.0 mg/dL
  4. >15 mg/dL

GI stage*:

0: No diarrhea or diarrhea <500 mL/day

  1. Diarrhea 500-999 mL/day or persistent nausea with histologic evidence of GVHD
  2. Diarrhea 1000-1499 mL/day
  3. Diarrhea >1500 mL/day
  4. Severe abdominal pain with or without ileus * If multiple etiologies are listed for liver or GI, the organ system is downstaged by 1.

GVHD grade:

0: All organ stages 0 or GVHD not listed as an etiology I: Skin stage 1-2 and liver and GI stage 0 II: Skin stage 3 or liver or GI stage 1 III: Liver stage 2-3 or GI stage 2-4 IV: Skin or liver stage 4
Day 100 post-randomization
Percentage of Participants With Chronic GVHD
Zeitfenster: 1 year post-randomization
Incidences of chronic GVHD will be graded per Shulman et al. 1980. This reference categorizes chronic GVHD as either limited or extensive. For this outcome, participants developing either type are considered to have a chronic GVHD event.
1 year post-randomization
Number of Infections Per Participant
Zeitfenster: 2 years post-randomization
2 years post-randomization
Percentage of Participants With Relapse
Zeitfenster: 1 year post-randomization
Relapse is defined by either morphological or cytogenetic evidence of AML, ALL, CML, or MDS consistent with pre-transplant features. Testing for recurrent malignancy in the blood, marrow or other sites will be used to assess relapse after transplantation.
1 year post-randomization
Percentage of Participants With Treatment-related Mortality
Zeitfenster: 1 year post-randomization
Treatment related mortality is defined as death without relapse of the primary disease.
1 year post-randomization
Number of Participants With Engraftment Syndrome
Zeitfenster: Day 100 post-transplant
Day 100 post-transplant

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Medical College of Wisconsin

Mitarbeiter

National Cancer Institute (NCI)
National Heart, Lung, and Blood Institute (NHLBI)
National Marrow Donor Program
Blood and Marrow Transplant Clinical Trials Network

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Allgemeine Veröffentlichungen

Nützliche Links

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

1. Dezember 2006

Primärer Abschluss (Tatsächlich)

1. März 2014

Studienabschluss (Tatsächlich)

1. Oktober 2014

Studienanmeldedaten

Zuerst eingereicht

14. Dezember 2006

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

14. Dezember 2006

Zuerst gepostet (Schätzen)

18. Dezember 2006

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

28. Oktober 2021

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

13. Oktober 2021

Zuletzt verifiziert

1. Oktober 2021

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Schlüsselwörter

Zusätzliche relevante MeSH-Bedingungen

Andere Studien-ID-Nummern

  • BMTCTN0501
  • 5U24CA076518 (US NIH Stipendium/Vertrag)
  • 2U01HL069294 (US NIH Stipendium/Vertrag)

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

JA

Beschreibung des IPD-Plans

Findings were published in a manuscript.

IPD-Sharing-Zeitrahmen

Within 6 months of official study closure at participating sites.

IPD-Sharing-Zugriffskriterien

Available to the public.

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