Acute Myeloid Leukemia Clinical Trial
Official title:
Randomized Prospective Phase III Clinical Trial Comparing HLA 10/10 Matched Unrelated Donor and Haploidentical Allogenic Hematopoietic Stem Cell Transplantation After Myeloablative Conditioning Regimen
The MAC-HAPLO-MUD trial is a randomized prospective phase III trial comparing HLA 10/10 matched unrelated donor and haploidentical allogeneic hematopoietic stem cell transplantation after myeloablative conditioning regimen in patients, age 15 years or older, with Acute Myeloid Leukemia (AML) or Acute Lymphoblastic Leukemia (ALL) or Myeloproliferative Syndrome (SMP) or Myelodysplastic Syndromes (SMD) and requiring allogeneic hematopoietic stem cell transplantation. Primary endpoint is the 1-year progression free survival without acute grade II-IV GvHD and without moderate and severe chronic GvHD.
An unrelated adult donor who is HLA-matched to the recipient at the allele-level (at HLA-A,
-B, -C, -DQB1 and -DRB1) is considered the best choice in the absence of an HLA-matched
sibling for patients needing hematopoietic stem cell transplantation (SCT).
However, using matched unrelated donors (MUD) is limited by (1) a prolonged time to identify
and schedule donation for some MUD allowing some patients to relapse before transplantation
can be performed, and (2) limited availability of fully HLA-MUD for the non-Caucasian
population.
Alternative donors are used for transplantation in patients without a fully-MUD including
single HLA mismatched unrelated donor, unrelated umbilical cord blood and grafts from
haploidentical related donors but are associated with higher non-relapse mortality and
delayed immune reconstitution.
A more recent strategy for haploidentical (haplo) related donor SCT (haplo-SCT) has improved
dramatically outcomes using T-cell replete grafts with administration of post-transplantation
cyclophosphamide (PTCy).
From retrospective studies, haplo-SCT with PTCy are associated with similar overall and
progression-free survivals as with MUD stem cell transplantation (MUD-SCT), but with lower
rates of toxicity and graft versus host disease (GvHD), and thus potentially better results
than MUD-SCT after reduced intensity conditioning (RIC) regimen. Haplo-SCT with PTCy is thus
highly discussed nowadays motivating prospective trials to confirm the benefit of this
procedure.
In the setting of a myeloablative conditioning (MAC) regimen in adults with high risk
hematological malignancies, few retrospective non-controlled registry studies recently
suggest that outcomes after haplo-SCT using PTCy approach might also be superior in terms of
GVHD free survival to that after MUD stem cell transplantation (MUD-SCT).
The investigators propose to address this question, in a randomized prospective phase III
clinical trial comparing HLA 10/10 MUD and haplo-SCT after MAC regimen. The stem cell source
will be bone marrow for haploidentical SCT and peripheral blood stem cell (PBSC) for
HLA-matched unrelated transplantation.
The primary endpoint is the 1-year progression free survival without acute grade II-IV GvHD
and without moderate and severe chronic GvHD.
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