Acute Myeloid Leukemia Clinical Trial
Official title:
Chemo Sensitization Before Hematopoietic Stem Cell Transplantation With a CXCR4 Antagonist in Patients With Acute Leukemia in Complete Remission: Pilot Study
The purpose of this study is to evaluate the disease free survival and the overall survival in patients with acute leukemia in first or second complete remission after administrating a CXCR4 antagonist, as a chemo sensitization strategy, plus chemotherapy as the conditioning regimen for autologous or allogeneic hematopoietic stem cell transplantation (HSCT).
In the last decade, HSCT has become an efficient strategy for the treatment of many malignant
and non-malignant hematological diseases, being the most common, according to the European
Bone Marrow Transplantation (EBMT), acute leukemias. Both myeloid and lymphoid acute
leukemias are considered malignant clonal diseases of the hematopoietic stem cells, and
represent a therapeutic challenge due to the high relapse rate and mortality using
conventional chemotherapy regimens. HSC reside mainly within the bone marrow, protected by a
microenvironment or niche, which is perivascular, created partly by mesenchymal stromal cells
and endothelial cells. Interactions between these cells and many adhesion molecules are
considered a key factor for growing, transformation, and migration of neoplastic cells. The
main pathway involved in the cellular transit regulation is chemokine receptor 4 (CXCR4) and
its chemokine ligand 12 (CXCL12), responsible of mediating interactions between the HSC and
stromal cells, and whose blocking through other cytokines and antagonists of the CXCR4
receptor (plerixafor) favors chemotaxis and HSC output to peripheral blood. Such strategy has
become an effective technique to increase mobilization and harvesting in patients undergoing
stem cell transplantations.
On the other hand, some preclinical studies have shown that the activation of CXCL12 pathway
favors tumor growth, promoting survival and invasion of the malignant cells, recruiting
stromal cells that facilitate their proliferation and promote angiogenesis directly. In such
way, this pathway has been considered a therapeutic target to block their activity and
inhibit tumor progression.
Patients with acute leukemia in first or second complete remission undergoing autologous or
allogeneic hematopoietic stem cell transplantation (HSCT), commonly present low response
rates and low survival due to persistent minimal residual disease, despite conventional high
dose chemotherapy regimens. It is necessary to create strategies to increase the destruction
rate of neoplastic cells in patients with acute leukemia candidates to HSCT. Our hypothesis
is that the administration of a CXCR4 antagonist as part of the conditioning regimen in
patients with acute leukemia candidates to HSCT will allow the mobilization and sensitization
of leukemia blast cells, eradicating efficiently the minimal residual disease, responsible of
posterior relapse, and will achieve a higher response rate and survival of patients
undergoing this procedure.
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