Induction therapy prior to autologous stem cell transplantation (ASCT) in newly diagnosed multiple myeloma: an update

dc.contributor.authorBazarbachi, Abdul Hamid
dc.contributor.authorAl-Hamed, Rama
dc.contributor.authorMalard, Florent
dc.contributor.authorBazarbachi, Ali Abdul Hamid
dc.contributor.authorHarousseau, Jean Luc
dc.contributor.authorMohty, Mohamad
dc.contributor.departmentInternal Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:43:44Z
dc.date.available2025-01-24T11:43:44Z
dc.date.issued2022
dc.description.abstractThe current standard of care model for newly diagnosed fit multiple myeloma (NDMM) patients is the sequential treatment of induction, high dose melphalan, autologous stem cell transplantation (ASCT), and maintenance. Adequate induction is required to achieve good disease control and induce deep response rates while minimizing toxicity as a bridge to transplant. Doublet induction regimens have greatly fallen out of favor, with current international guidelines favoring triplet or quadruplet induction regimens built around the backbone of the proteasome inhibitor bortezomib and dexamethasone (Vd). In fact, the updated 2021 European Haematology Association (EHA) and European Society for Medical Oncology (ESMO) clinical practice guidelines recommend the use of either lenalidomide-Vd (VRd), or daratumumab-thalidomide-Vd (Dara-VTd) as first-line options for transplant-eligible NDMM patients, and when not available, thalidomide-Vd (VTd) or cyclophosphamide-Vd (VCd) as acceptable alternatives. Quadruplet regimens featuring anti-CD38 monoclonal antibodies are extremely promising and remain heavily investigated, as is the incorporation of more recent proteasome inhibitors such as carfilzomib. This review will focus on induction therapies prior to ASCT examining the latest data and guidelines on triplet and quadruplet regimens. © 2022, The Author(s).
dc.identifier.doihttps://doi.org/10.1038/s41408-022-00645-1
dc.identifier.eid2-s2.0-85127261727
dc.identifier.pmid35347107
dc.identifier.urihttp://hdl.handle.net/10938/30344
dc.language.isoen
dc.publisherSpringer Nature
dc.relation.ispartofBlood Cancer Journal
dc.sourceScopus
dc.subjectAntineoplastic combined chemotherapy protocols
dc.subjectBortezomib
dc.subjectDexamethasone
dc.subjectHematopoietic stem cell transplantation
dc.subjectHumans
dc.subjectInduction chemotherapy
dc.subjectMultiple myeloma
dc.subjectProteasome inhibitors
dc.subjectStem cell transplantation
dc.subjectThalidomide
dc.subjectTransplantation, autologous
dc.subjectAntineoplastic agent
dc.subjectCarfilzomib
dc.subjectCyclophosphamide
dc.subjectDaratumumab
dc.subjectElotuzumab
dc.subjectIsatuximab
dc.subjectIxazomib
dc.subjectLenalidomide
dc.subjectProteasome inhibitor
dc.subjectAdverse drug reaction
dc.subjectAutologous stem cell transplantation
dc.subjectBone marrow suppression
dc.subjectCancer diagnosis
dc.subjectComparative study
dc.subjectConsolidation chemotherapy
dc.subjectDrug safety
dc.subjectHuman
dc.subjectIntention to treat analysis
dc.subjectMinimal residual disease
dc.subjectNeutropenia
dc.subjectOverall response rate
dc.subjectPeripheral neuropathy
dc.subjectPractice guideline
dc.subjectQuadruple chemotherapy
dc.subjectReview
dc.subjectThrombocytopenia
dc.subjectTriplet chemotherapy
dc.subjectAutotransplantation
dc.titleInduction therapy prior to autologous stem cell transplantation (ASCT) in newly diagnosed multiple myeloma: an update
dc.typeReview

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