The Elephant in The Room: AML Relapse Post Allogeneic Hematopoietic Cell Transplantation

dc.contributor.authorAbou Dalle, Iman
dc.contributor.authorAtoui, Ali
dc.contributor.authorBazarbachi, Ali Abdul Hamid
dc.contributor.departmentInternal Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:43:36Z
dc.date.available2025-01-24T11:43:36Z
dc.date.issued2022
dc.description.abstractRelapsed acute myeloid leukemia (AML) following allogeneic hematopoietic cell transplantation (allo-HCT) is an unfavorable event associated with a poor prognosis, particularly for patients with early relapses. It usually arises from resistant leukemic blasts that escaped both preparative chemotherapy regimen and the graft-versus-leukemia (GVL) effect. Independent from the choice of salvage treatment, only minority of patients can achieve durable remissions. In recent years, better understanding of the disease relapse biology post allo-HCT allowed the application of newer strategies that could induce higher rates of remission, and potential longer survival. Those strategies aim at optimizing drugs that have a direct anti-leukemia activity by targeting different oncogenic mutations, metabolism pathways or surface antigens, and concurrently enhancing the immune microenvironment to promote GVL effect. This review discusses the current treatment landscape of AML relapse post allo-HCT. Copyright © 2022 Abou Dalle, Atoui and Bazarbachi.
dc.identifier.doihttps://doi.org/10.3389/fonc.2021.793274
dc.identifier.eid2-s2.0-85123065433
dc.identifier.urihttp://hdl.handle.net/10938/30320
dc.language.isoen
dc.publisherFrontiers Media S.A.
dc.relation.ispartofFrontiers in Oncology
dc.sourceScopus
dc.subjectAllotransplant
dc.subjectAml
dc.subjectGraft versus leukaemia (gvl)
dc.subjectImmunotherapy
dc.subjectRelapse
dc.subjectCd135 antigen
dc.subjectCd33 antigen
dc.subjectChimeric antigen receptor
dc.subjectCytotoxic t lymphocyte antigen 4
dc.subjectHla dqb1 antigen
dc.subjectHla drb1 antigen
dc.subjectImmune checkpoint inhibitor
dc.subjectInterleukin 15
dc.subjectIsocitrate dehydrogenase 1
dc.subjectMembrane antigen
dc.subjectProgrammed death 1 receptor
dc.subjectProtein bcl 2
dc.subjectStat5 protein
dc.subjectThymocyte antibody
dc.subjectTranscription factor ezh2
dc.subjectAcute lymphoblastic leukemia
dc.subjectAcute myeloid leukemia
dc.subjectAdoptive immunotherapy
dc.subjectAllogeneic hematopoietic stem cell transplantation
dc.subjectAllograft
dc.subjectAntigen presenting cell
dc.subjectAntileukemic activity
dc.subjectApoptosis
dc.subjectAutologous stem cell transplantation
dc.subjectCancer chemotherapy
dc.subjectCancer immunotherapy
dc.subjectCancer prognosis
dc.subjectCancer recurrence
dc.subjectCancer survival
dc.subjectCd8+ t lymphocyte
dc.subjectCell nucleus inclusion body
dc.subjectChemotherapy
dc.subjectCopy number variation
dc.subjectCytogenetics
dc.subjectCytotoxicity
dc.subjectDonor lymphocyte infusion
dc.subjectDown regulation
dc.subjectFlow cytometry
dc.subjectGraft versus leukemia effect
dc.subjectHaplotype
dc.subjectHematopoietic stem cell
dc.subjectHematopoietic stem cell transplantation
dc.subjectHuman
dc.subjectInnate immunity
dc.subjectKaryotype
dc.subjectLymphoblastoma
dc.subjectMetabolism
dc.subjectMicroenvironment
dc.subjectMutation
dc.subjectMyelodysplastic syndrome
dc.subjectNatural killer cell
dc.subjectNonhuman
dc.subjectOverall survival
dc.subjectProgression free survival
dc.subjectPromyelocytic leukemia
dc.subjectQuality of life
dc.subjectRecurrence free survival
dc.subjectRecurrent disease
dc.subjectRegulatory t lymphocyte
dc.subjectRetrospective study
dc.subjectReview
dc.subjectSalvage therapy
dc.subjectSignal transduction
dc.subjectTumor microenvironment
dc.subjectTumor volume
dc.subjectUpregulation
dc.titleThe Elephant in The Room: AML Relapse Post Allogeneic Hematopoietic Cell Transplantation
dc.typeReview

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