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
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.
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 →King's College Hospital NHS Trust is the lead sponsor of 171 studies on the registry; 56 are open to participants now.
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DISEASE INCLUSION CRITERIA:
In general this encompasses all haematological disorders where a volunteer unrelated donor transplant is clinically indicated.
Acute, chronic leukaemia or myelodysplastic syndrome for which allogeneic transplantation is considered as the best treatment option.
Acute myeloid leukaemia (AML) in first complete remission (CR1) with one of the following characteristics:
Myelodysplastic syndromes
i. In first chronic phase if refractory and/or intolerance to tyrosine kinase inhibitors is clearly demonstrated ii. In second chronic phase
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
Non-Hodgkin's lymphoma
Hodgkin's disease
a. in second or subsequent complete or partial remission
Chronic lymphocytic leukaemia.
PATIENT SELECTION
Inclusion criteria: myeloablative conditioning regimen
Exclusion criteria: myeloablative conditioning regimen
Inclusion criteria: reduced-intensity conditioning regimen (For both FluMel \& FluCyTBI regimens):
Exclusion Criteria: reduced-intensity conditioning regimen (For both FluMel \& FluCyTBI regimens):
Drug: Thiotepa · Drug: Fludarabine · Drug: Intravenous busulphan · Drug: Thymoglobulin · Drug: Ciclosporin · Drug: Mycophenolate mofetil (MMF)
Drug: Fludarabine · Drug: Cyclophosphamide · Radiation: Radiotherapy · Drug: Thymoglobulin · Drug: Ciclosporin · Drug: Mycophenolate mofetil (MMF)
Drug: Fludarabine · Drug: Melphalan · Drug: Thymoglobulin · Drug: Ciclosporin · Drug: Mycophenolate mofetil (MMF)
Also known as: Busilvex
Treatment related mortality at day 100
Time frame: Day 100
Disease free survival at one year post-transplant for each cohort
Time frame: 1 year
Chimerism
Time frame: Days 14 (myeloblative conditioning only), 28, 56, 100 and months 6 and 12
Incidence of neutrophil engraftment by day 42
Time frame: Days 14, 28 and 42
Incidence of platelet engraftment by 6 months
Time frame: Days 14, 28, 56, 100 and month 6
Incidence of grade II-IV and III-IV acute GVHD
Time frame: Days 28, 56, 100 and months 6, 9, 12, 18 and 24
Incidence of chronic GVHD during the first year
Time frame: Day 100 and months 6 and 12
One year overall survival for each treatment cohort
Time frame: 1 year
Incidence of systemic infections
Time frame: Twice a week pre-transplant to day 100 then weekly or as clinically indicated
Incidence of CMV, adenovirus and EBV activation
Time frame: Twice a week pre-transplant to day 100 then weekly or as clinically indicated
Immune reconstitution
Time frame: Days 14, 28, 56, 100 and months 6, 9, 12, 18 and 24
Dynamics of EBV infection and immunity following cord blood transplantation
Time frame: Days 14, 28, 56, 100 and months 6, 9 and 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
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
Quality of life
Time frame: Pre-transplant and months 6, 12, 18 and 24
Incidence of one year relapse or disease progression for each treatment cohort
Time frame: 1 year
This study is terminated, as verified in Mar 2012. You cannot join it, but the record below documents what was studied.
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Studies of the drugs tested here: Thiotepa · Busulfan · Cyclophosphamide · Melphalan
King's College Hospital NHS Trust →