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Hematopoietic stem cell allografting for chronic lymphocytic leukemia: A focus on reduced-intensity conditioning regimens

Show simple item record Kharfan-Dabaja M.A. Bazarbachi A.
dc.contributor.editor Jan-2012 2017-10-05T15:43:29Z 2017-10-05T15:43:29Z 2012
dc.identifier.issn 10732748
dc.description.abstract Background: Allogeneic hematopoietic cell transplantation (allo-HCT) remains the only known treatment modality that currently offers a potential cure to patients with chronic lymphocytic leukemia (CLL). A better understanding of the role of adoptive immunotherapy and its consequent bona fide graft-vs-leukemia (GVL) effect has resulted in a reduction of the ablative intensity and toxicity of preparative allo-HCT regimens. Methods: The authors review the published data of reduced-intensity conditioning (RIC) allo-HCT in patients with CLL. Results: RIC allo-HCT has reduced the transplant associated morbidity and mortality of the procedure and has consequently broadened applicability of allo-HCT to patients with CLL who are generally of more advanced age ( 60 years) and who often have associated comorbidities. Conclusions: Published literature supports the use of RIC allo-HCT for these patients once a suitable donor is identified, provided they fulfill acceptable consensus criteria for hematopoietic stem cell allografting. Several studies have shown that T-cell-replete RIC allo-HCT is also capable of overcoming the adverse effect of poor prognostic factors in CLL such as del(17p), unmutated IgVH, or ZAP-70 expression. Continued clinical trials to identify the optimal regimen for RIC allo-HCT for patients with CLL are warranted.
dc.format.extent Pages: (68-75)
dc.language English
dc.publisher TAMPA
dc.relation.ispartof Publication Name: Cancer Control; Publication Year: 2012; Volume: 19; no. 1; Pages: (68-75);
dc.source Scopus
dc.title Hematopoietic stem cell allografting for chronic lymphocytic leukemia: A focus on reduced-intensity conditioning regimens
dc.type Review
dc.contributor.affiliation Kharfan-Dabaja, M.A., Department of Internal Medicine, Division of Hematology-Oncology, Naef K. Basile Cancer Institute, American University of Beirut, Beirut, Lebanon
dc.contributor.affiliation Bazarbachi, A., Department of Internal Medicine, Division of Hematology-Oncology, Naef K. Basile Cancer Institute, American University of Beirut, Beirut, Lebanon
dc.contributor.authorAddress Kharfan-Dabaja, M. A.; Division of Hematology-Oncology and Bone Marrow Transplantation, Department of Internal Medicine, American University of Beirut, P.O. Box 11-0236, Beirut, Lebanon; email:
dc.contributor.authorCorporate University: American University of Beirut Medical Center; Faculty: Faculty of Medicine; Department: Naef K. Basile Cancer Institute (NKBCI);
dc.contributor.authorDepartment Naef K. Basile Cancer Institute (NKBCI)
dc.contributor.authorFaculty Faculty of Medicine
dc.contributor.authorInitials Kharfan-Dabaja, MA
dc.contributor.authorInitials Bazarbachi, A
dc.contributor.authorReprintAddress Kharfan-Dabaja, MA (reprint author), Amer Univ Beirut, Dept Internal Med, Div Hematol Oncol and Bone Marrow Transplantat, POB 11-0236, Beirut, Lebanon.
dc.contributor.authorUniversity American University of Beirut Medical Center
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dc.description.citedCount 8
dc.description.citedTotWOSCount 12
dc.description.citedWOSCount 12
dc.format.extentCount 8
dc.identifier.coden CACOF
dc.identifier.pubmedID 22143063
dc.identifier.scopusID 83255164801
dc.publisher.address 12902 MAGNOLIA DR, TAMPA, FL 33612 USA
dc.relation.ispartOfISOAbbr Cancer Control
dc.relation.ispartOfIssue 1
dc.relation.ispartofPubTitle Cancer Control
dc.relation.ispartofPubTitleAbbr Cancer Control
dc.relation.ispartOfVolume 19
dc.source.ID WOS:000307968300007
dc.type.publication Journal
dc.subject.otherChemCAS alemtuzumab, 216503-57-0
dc.subject.otherChemCAS busulfan, 55-98-1
dc.subject.otherChemCAS cyclophosphamide, 50-18-0
dc.subject.otherChemCAS fludarabine, 21679-14-1
dc.subject.otherChemCAS melphalan, 148-82-3
dc.subject.otherChemCAS protein kinase ZAP 70, 148047-34-1
dc.subject.otherChemCAS rituximab, 174722-31-7
dc.subject.otherIndex alemtuzumab
dc.subject.otherIndex busulfan
dc.subject.otherIndex cyclophosphamide
dc.subject.otherIndex fludarabine
dc.subject.otherIndex immunoglobulin heavy chain
dc.subject.otherIndex melphalan
dc.subject.otherIndex protein kinase ZAP 70
dc.subject.otherIndex rituximab
dc.subject.otherIndex allogeneic hematopoietic stem cell transplantation
dc.subject.otherIndex cancer patient
dc.subject.otherIndex cancer risk
dc.subject.otherIndex chemoradiotherapy
dc.subject.otherIndex chronic lymphatic leukemia
dc.subject.otherIndex comorbidity
dc.subject.otherIndex disease association
dc.subject.otherIndex graft versus host reaction
dc.subject.otherIndex graft versus leukemia effect
dc.subject.otherIndex human
dc.subject.otherIndex morbidity
dc.subject.otherIndex mortality
dc.subject.otherIndex prognosis
dc.subject.otherIndex protein expression
dc.subject.otherIndex reduced intensity conditioning
dc.subject.otherIndex review
dc.subject.otherIndex treatment outcome
dc.subject.otherIndex Hematopoietic Stem Cell Transplantation
dc.subject.otherIndex Humans
dc.subject.otherIndex Leukemia, Lymphocytic, Chronic, B-Cell
dc.subject.otherIndex Prognosis
dc.subject.otherIndex Survival Analysis
dc.subject.otherIndex Transplantation Conditioning
dc.subject.otherIndex Treatment Outcome
dc.subject.otherKeywordPlus BONE-MARROW-TRANSPLANTATION
dc.subject.otherKeywordPlus TREATMENT-RELATED MORTALITY
dc.subject.otherKeywordPlus VARIABLE-REGION MUTATIONS
dc.subject.otherKeywordPlus VERSUS-HOST-DISEASE
dc.subject.otherKeywordPlus HEAVY-CHAIN GENE
dc.subject.otherKeywordPlus ALLOGENEIC TRANSPLANTATION
dc.subject.otherKeywordPlus POOR-PROGNOSIS
dc.subject.otherKeywordPlus CLL3X TRIAL
dc.subject.otherKeywordPlus CYCLOPHOSPHAMIDE
dc.subject.otherKeywordPlus RITUXIMAB
dc.subject.otherWOS Oncology

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