Condition: Acute Myeloid Leukemia (AML) · Myelodysplastic Syndrome (MDS)/AML · Proton Therapy · Sponsor: Institute of Hematology and Blood Transfusion, Czech Republic
This is an open-label, single-center, non-randomized phase I/II pilot study evaluating proton-based Total Marrow Irradiation (TMI) as part of the conditioning regimen prior to allogeneic hematopoietic stem cell transplantation (allo-HSCT) in adult patients with high-risk or relapsed/refractory acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS). These patients have an unfavorable prognosis with standard conditioning approaches. Participants will receive a standard conditioning regimen consisting of either myeloablative or reduced-intensity chemotherapy, selected according to age and comorbidities, combined with proton TMI delivered at a total dose of 12 Gy in three fractions. Graft-versus-host disease (GvHD) prophylaxis will be administered according to institutional standards, preferentially using post-transplant cyclophosphamide. Patients will subsequently undergo standard allo-HSCT and will be followed for at least 24 months after transplantation. The primary objective of the study is to assess the safety and tolerability of proton TMI added to standard conditioning, as measured by non-relapse mortality and treatment-related toxicity within the first 100 days after transplantation. Secondary objectives include evaluation of engraftment kinetics, incidence of relapse, overall and relapse-free survival, GvHD outcomes, and quality of life. Study outcomes will be analyzed descriptively and compared with a matched historical cohort.
This description comes directly from the study's public registry record.
Veronika Valkova, Assoc. Prof., MD, PhD · +420 221 977 301 · Veronika.Valkova@uhkt.cz
Jan Vydra, MD, PhD. · +420 221 977 290 · Jan.Vydra@uhkt.cz
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| Institute of Hematology and Blood Transfusion | Prague, Czechia | Recruiting |
| Proton Therapy Center Czech | Prague, Czechia | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07532824