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TerminatedNCT00916045Updated Feb 11, 2015

Pilot Study of Unrelated Cord Blood Transplantation

A Phase 2 interventional study of Thiotepa and Fludarabine in Leukemia, Myeloid, Acute, Myelodysplastic Syndromes and Leukemia, Lymphoblastic, Acute, sponsored by King's College Hospital NHS Trust. Terminated at 1 site in United Kingdom. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2015-02-11.

Sponsored by King's College Hospital NHS Trust · Phase 2, Interventional, and Treatment

Why this study was terminated
Recruitment issues
Phase
Phase 2
Study type
Interventional
Enrollment
40
Allocation
Non-randomized
Ages
18 Years to 70 Years
Sex
All
01

Study summary

The purpose of this study is to determine the safety and feasibility of unrelated double and single cord blood transplantation in patients with haematological malignancies using reduced-intensity or myeloablative conditioning regimens.

02

Conditions studied

  • Leukemia, Myeloid, Acute
  • Myelodysplastic Syndromes
  • Leukemia, Lymphoblastic, Acute
  • Lymphoma, Non-Hodgkin
  • Hodgkin Disease
  • Chronic Lymphocytic Leukemia
03

In context

Leukemia, Myeloid, Acute

3,035 studies on the registry are indexed under Leukemia, Myeloid, Acute; 746 are open to participants now.

This study's planned enrollment of 40 is close to the median of 40 across 2,561 interventional studies indexed under Leukemia, Myeloid, Acute.

Browse Leukemia, Myeloid, Acute studies →

Lead sponsor

King's College Hospital NHS Trust is the lead sponsor of 171 studies on the registry; 56 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

DISEASE INCLUSION CRITERIA:

In general this encompasses all haematological disorders where a volunteer unrelated donor transplant is clinically indicated.

  1. Acute, chronic leukaemia or myelodysplastic syndrome for which allogeneic transplantation is considered as the best treatment option.

    1. Acute myeloid leukaemia (AML) in first complete remission (CR1) with one of the following characteristics:

      • High risk cytogenetic or molecular alterations (e.g. t(9;22), deletion 7/7q-, monosomy 5 or del(5q), 3q26 alterations, complex karyotype [3 or more anomalies], p53 alterations, 11q23 especially t(6;11) abnormalities, FLT-3 ITD)
      • Leukocytes at diagnosis > 50 x109/l (except in cases with good prognosis molecular rearrangements for which leukocytes should be > 100 x 109/l)
    2. Myelodysplastic syndromes

      • International Prognosis Index (IPSS) above 1 (intermediate group 2 or high risk)
      • IPSS 0 or 0.5 in the presence of cytopenias requiring treatment.
    3. Therapy related AML or MDS in first CR
    4. AML or MDS in second (CR2) or subsequent CR
    5. Ph'-positive chronic myeloid leukaemia

    i. In first chronic phase if refractory and/or intolerance to tyrosine kinase inhibitors is clearly demonstrated ii. In second chronic phase

  2. Acute lymphoblastic leukaemia (ALL)

    a. In CR1 with one of the following characteristics: i. Very high risk chromosome or molecular alterations (e.g. t(9;22), t(4;11), complex karyotype in adults, bcr/abl rearrangements, MLL rearrangements) ii. Slow response to induction treatment defined as the presence of >10% blasts in bone marrow at day 14 of induction treatment iii. Adults aged > 30 years iv. Adults with B ALL cell line with a number of leukocytes at diagnosis >25 x 109/L or T ALL cell line with a number of leukocytes at diagnosis >100X109/L

    b. In CR2 or subsequent CR

  3. Non-Hodgkin's lymphoma

    1. Follicular NHL: in second or subsequent complete or partial remission
    2. Mantle cell NHL: in second or subsequent complete or partial remission
    3. High grade NHL: in second complete or very good partial remission
  4. Hodgkin's disease

    a. in second or subsequent complete or partial remission

  5. Chronic lymphocytic leukaemia.

    1. in second or subsequent remission
    2. with adverse risk prognostic features in first remission
  6. Acquired bone marrow failure syndromes
  7. Other haematological malignancies for which UD bone marrow transplantation is indicated

PATIENT SELECTION

Inclusion criteria: myeloablative conditioning regimen

  1. Aged under 35 years and greater than 18 years
  2. Absence of HLA compatible related donor.
  3. Need for an urgent transplantation or absence of HLA-compatible VUD after searching the international registries.
  4. Patients with a HLA-compatible VUD but whose donor is considered by the transplantation centre as unsuitable will also be eligible.
  5. Availability of suitable UD-UCB unit/s.
  6. Informed consent.

Exclusion criteria: myeloablative conditioning regimen

  1. Patients with an available 5-6/6 HLA-A, -B, -DRB1 matched sibling donor or 10/10 unrelated bone marrow donor
  2. ECOG performance status worse than 2
  3. Cardiac insufficiency requiring treatment, symptomatic coronary artery disease or LVEF less than 40%.
  4. Hepatic disease, with total bilirubin above 20umol/l or AST > 3 times upper limit of normal.
  5. Severe hypoxaemia, pO2 \< 70 mm Hg, with decreased DLCO \< 70% of predicted; or mild hypoxemia, pO2 \< 80 mm Hg with severely decreased DLCO \< 60% of predicted.
  6. Impaired renal function (creatinine > 2 times upper limit of normal or creatinine clearance \< 50% for age, gender, weight).
  7. Patients who have received previous treatment with Thymoglobulin®
  8. HIV or HTLV positive patients.
  9. Female patients who are pregnant or breast feeding due to risks to foetus from conditioning regimen and potential risks to nursing infants.
  10. Life expectancy severely limited by diseases other than the disease indication for transplant
  11. Serious concurrent untreated infection e.g. active tuberculosis, mycoses or viral infection
  12. Serious psychiatric/ psychological disorders
  13. Absence of /inability to provide informed consent
  14. Serious diseases that prevent treatments with chemotherapy
  15. Myelofibrosis

Inclusion criteria: reduced-intensity conditioning regimen (For both FluMel \& FluCyTBI regimens):

  1. Age under 70 years and older than 18 years
  2. Absence of HLA compatible related donor.
  3. Need for an urgent transplantation or absence of HLA-compatible VUD after searching the international registries.
  4. Patients with a HLA-compatible VUD but whose donor is considered by the transplantation centre as unsuitable will also be eligible.
  5. Availability of suitable UD-UCB unit/s.
  6. Informed consent.

Exclusion Criteria: reduced-intensity conditioning regimen (For both FluMel \& FluCyTBI regimens):

  1. Patients with an available 5-6/6 HLA-A, -B, -DRB1 matched sibling donor or 10/10 unrelated bone marrow donor
  2. ECOG performance status worse than 2
  3. Cardiac insufficiency requiring treatment, symptomatic coronary artery disease or LVEF less than 35%.
  4. Hepatic disease, with total bilirubin greater than 2 times upper limit of normal or AST > 5 times upper limit of normal.
  5. Severe hypoxaemia, pO2 \< 70 mm Hg, with decreased DLCO \< 50% of predicted; or mild hypoxemia, pO2 \< 80 mm Hg with severely decreased DLCO \< 50% of predicted.
  6. Impaired renal function (creatinine > 2 times upper limit of normal or creatinine clearance \< 50% for age, gender, weight).
  7. Previous irradiation that precludes the safe administration of an additional dose of 200 cGy of total body irradiation (TBI).
  8. Patients who have received previous treatment with Thymoglobulin®
  9. HIV or HTLV positive patients.
  10. Female patients who are pregnant or breast feeding due to risks to foetus from conditioning regimen and potential risks to nursing infants.
  11. Life expectancy severely limited by diseases other than the disease indication for transplant
  12. Serious concurrent uncontrolled infection e.g. active tuberculosis, mycoses or viral infection
  13. Serious psychiatric/ psychological disorders
  14. Absence of /inability to provide informed consent
  15. Within 6 months of prior myeloablative transplant.
  16. Patients with acute leukaemia in morphological relapse/ persistent/ progressive disease
  17. Intermediate or high grade NHL, mantle cell NHL and Hodgkin's disease that is refractory or progressive on salvage therapy.
  18. Myelofibrosis
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
40 participants (estimated)

Study arms

  • Other
    Myeloblative conditioning regimen

    Drug: Thiotepa · Drug: Fludarabine · Drug: Intravenous busulphan · Drug: Thymoglobulin · Drug: Ciclosporin · Drug: Mycophenolate mofetil (MMF)

  • Other
    Reduced intensity conditioning regimen - FluCyTBI

    Drug: Fludarabine · Drug: Cyclophosphamide · Radiation: Radiotherapy · Drug: Thymoglobulin · Drug: Ciclosporin · Drug: Mycophenolate mofetil (MMF)

  • Other
    Reduced intensity conditioning regimen - FluMel

    Drug: Fludarabine · Drug: Melphalan · Drug: Thymoglobulin · Drug: Ciclosporin · Drug: Mycophenolate mofetil (MMF)

06

What researchers measure

Primary outcomes

  1. Treatment related mortality at day 100

    Time frame: Day 100

Secondary outcomes

  1. Disease free survival at one year post-transplant for each cohort

    Time frame: 1 year

  2. Chimerism

    Time frame: Days 14 (myeloblative conditioning only), 28, 56, 100 and months 6 and 12

  3. Incidence of neutrophil engraftment by day 42

    Time frame: Days 14, 28 and 42

  4. Incidence of platelet engraftment by 6 months

    Time frame: Days 14, 28, 56, 100 and month 6

  5. Incidence of grade II-IV and III-IV acute GVHD

    Time frame: Days 28, 56, 100 and months 6, 9, 12, 18 and 24

  6. Incidence of chronic GVHD during the first year

    Time frame: Day 100 and months 6 and 12

  7. One year overall survival for each treatment cohort

    Time frame: 1 year

  8. Incidence of systemic infections

    Time frame: Twice a week pre-transplant to day 100 then weekly or as clinically indicated

  9. Incidence of CMV, adenovirus and EBV activation

    Time frame: Twice a week pre-transplant to day 100 then weekly or as clinically indicated

  10. Immune reconstitution

    Time frame: Days 14, 28, 56, 100 and months 6, 9, 12, 18 and 24

  11. Dynamics of EBV infection and immunity following cord blood transplantation

    Time frame: Days 14, 28, 56, 100 and months 6, 9 and 12

  12. The development (if any) of transplant associated post transplant lymphoproliferative disease (PTLD)

    Time frame: Days 14, 28, 56, 100 and months 6, 9 and 12

  13. Identify any possible predictive markers for patients most at risk of PTLD development

    Time frame: Days 14, 28, 56, 100 and months 6, 9 and 12

  14. Quality of life

    Time frame: Pre-transplant and months 6, 12, 18 and 24

  15. Incidence of one year relapse or disease progression for each treatment cohort

    Time frame: 1 year

07

Study locations

1 site
  • King's College Hosptial NHS Foundation Trust
    London, SE5 9RS, United Kingdom
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 11, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00916045
First posted
Jun 8, 2009
Start date
Sep 2009
Primary completion
Mar 2012
Completion
Mar 2012
Last update
Feb 11, 2015

Study contacts

Antonio Pagliuca, MBBS, MA, FRCP, FRCPath
principal investigator · King's College Hospital NHS Trust

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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Studies of the drugs tested here: Thiotepa · Busulfan · Cyclophosphamide · Melphalan

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