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Pilot Study of Hematopoietic Stem Cell Transplantation From Two Matched Sibling Donors in Treating Patients With Poor Prognosis Acute Leukemia and Advanced Lymphoproliferative Malignancies

Pilot Study of Hematopoietic Stem Cell Transplantation From Two Matched Sibling Donors in Treating Patients With Poor Prognosis Acute Leukemia and Advanced Lymphoproliferative Malignancies

Status
UNKNOWN
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01385072
Enrollment
10
Registered
2011-06-29
Start date
2011-08-31
Completion date
2015-04-30
Last updated
2011-11-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Relapsed and Refractory Acute Leukemia

Keywords

acute leukemia, relapse, induction failure, allogeneic transplantation, graft versus leukemia effect

Brief summary

Patients with active acute leukemia have dismal prognoses even with allogeneic transplantation.Thus,new measures to enhance graft versus leukemia effect and reduce relapse rates are needed. Relapse risk after double umbilical cord transplantations have been shown to be significantly lower compared to matched sibling and matched unrelated donor transplantations due to better graft versus leukemia effect. The investigators hypothesize, that concomitant transplantation from 2 matched siblings may improve GVL effect and reduce relapse rate in patients with high risk acute leukemias and other high risk hematological malignancies.

Interventions

BIOLOGICALDouble matched sibling transplantation

Patients with poor risk active acute leukemia and who have 2 matched sibling donors can be included. Patients' conditioning may be myeloablative or non-myeloablative. Both matched donors will be mobilized with G-CSF and their peripheral blood stem cells will be collected on day 0.Equal numbers of CD34+ cells from both donors will be transfused to the patient. Patients will be followed for engraftment kinetics, chimerism, GVHD rate, severity and response to treatment, relapse rates, DFS and OS.

Sponsors

Rabin Medical Center
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age 18 years or older 2. Patients with refractory or relapsed acute leukemia unable to receive myeloablative conditioning. 3. Patients with refractory or relapsed acute leukemia able to receive myeloablative conditioning but with the following factors: AML- 2 or more of the following: duration of CR1 \< 6 months, poor cytogenetics, circulating blasts, karnofsky \< 90. ALL- age \> 40 or second and additional relapse, or 2 or more of the following: BM blasts \> 25%, age 18-39,first refractory relapse, donor CMV positive. 4. Patients with 2 matched siblings and donor age \> 18 years old. 5. Patients with advanced multiple myeloma with life expectancy of less than 6 months with standard therapy or transplantation. 6. Patients with advanced lymphoma with life expectancy of less than 6 months with standard therapy or transplantation.

Exclusion criteria

1. Patient age \< 18 years. 2. Donor age \< 18 years. 3. Patients in remission or not fulfilling above disease criteria -

Design outcomes

Primary

MeasureTime frame
Acute graft versus host disease rate,severity and response to treatment100 days

Secondary

MeasureTime frame
relapse rate12 months

Countries

Israel

Contacts

Primary ContactMoshe Yeshurun, MD
moshey@clalit.org.il972-9378127
Backup ContactRon Ram, MD
RonRa@clalit.org.il972-9378116

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026