Management of cytomegalovirus infection in allogeneic hematopoietic stem cell transplants

dc.contributor.authorFatima, Allaw
dc.contributor.authorHaddad, Sara F.
dc.contributor.authorJohnny, Zakhour
dc.contributor.authorKanj, Souha S.
dc.contributor.departmentInternal Medicine
dc.contributor.departmentDivision of Infectious Diseases
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:45:21Z
dc.date.available2025-01-24T11:45:21Z
dc.date.issued2023
dc.description.abstractCytomegalovirus (CMV) is a common infection encountered in immunocompromised patients. It is associated with high morbidity and mortality, particularly in patients undergoing allogeneic (allo-) haematopoietic stem cell transplantation (HSCT). This review presents the most recent management strategies for CMV infection in allo-HSCT recipients. Pre-emptive treatment (PET) consists of frequent monitoring of CMV polymerase chain reaction (PCR) after HSCT; this has been the standard of care for prevention of CMV for many years, given the potential drug toxicity associated with the traditional drugs used as prophylaxis. However, letermovir, recently approved as a chemoprophylactic agent for prevention of CMV, has shown great efficacy in randomized clinical trials and real-world data. Treatment of CMV disease is becoming increasingly difficult, and must take into account the patient's risk profile and the potential for CMV drug resistance. Different treatment strategies exist for refractory and resistant CMV disease. Maribavir is a new drug that showed promising results in the treatment of refractory and resistant CMV disease. Other alternative treatments, such as cellular adoptive immunotherapy, artesunate and leflunomide, may play an adjunctive role in the treatment of challenging cases; however, further investigation is warranted. © 2023 Elsevier Ltd and International Society of Antimicrobial Chemotherapy
dc.identifier.doihttps://doi.org/10.1016/j.ijantimicag.2023.106860
dc.identifier.eid2-s2.0-85162235373
dc.identifier.pmid37220849
dc.identifier.urihttp://hdl.handle.net/10938/30555
dc.language.isoen
dc.publisherElsevier B.V.
dc.relation.ispartofInternational Journal of Antimicrobial Agents
dc.sourceScopus
dc.subjectCytomegalovirus
dc.subjectHaematopoietic stem cell transplantation
dc.subjectInfection
dc.subjectPre-emptive treatment
dc.subjectProphylaxis
dc.subjectAntiviral agents
dc.subjectCytomegalovirus infections
dc.subjectHematopoietic stem cell transplantation
dc.subjectHumans
dc.subjectTransplantation, homologous
dc.subjectAlemtuzumab
dc.subjectArtesunate
dc.subjectBenzimidavir
dc.subjectCidofovir
dc.subjectGanciclovir
dc.subjectLeflunomide
dc.subjectLetermovir
dc.subjectValganciclovir
dc.subjectAntivirus agent
dc.subjectAdoptive immunotherapy
dc.subjectAllogeneic hematopoietic stem cell transplantation
dc.subjectBone marrow suppression
dc.subjectCellular immunotherapy
dc.subjectChemoprophylaxis
dc.subjectCreatinine clearance
dc.subjectCytomegalovirus infection
dc.subjectDrug efficacy
dc.subjectEnzyme linked immunospot assay
dc.subjectGastrointestinal infection
dc.subjectGraft recipient
dc.subjectHuman
dc.subjectImmune reconstitution
dc.subjectInterferon gamma release assay
dc.subjectNonhuman
dc.subjectPhase 3 clinical trial (topic)
dc.subjectPneumonia
dc.subjectPolymerase chain reaction
dc.subjectRandomized controlled trial (topic)
dc.subjectRecurrent infection
dc.subjectRetinitis
dc.subjectReview
dc.subjectRisk factor
dc.subjectSensitivity and specificity
dc.subjectTreatment duration
dc.subjectTreatment response
dc.subjectVirus load
dc.subjectVirus reactivation
dc.subjectAllotransplantation
dc.subjectProcedures
dc.titleManagement of cytomegalovirus infection in allogeneic hematopoietic stem cell transplants
dc.typeReview

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
2023-669.pdf
Size:
1.16 MB
Format:
Adobe Portable Document Format