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dc.contributor.authorCesaro, Simone
dc.contributor.authorCrocchiolo, Roberto
dc.contributor.authorTridello, Gloria
dc.contributor.authorKnelange, Nina
dc.contributor.authorVan Lint, Maria Teresa
dc.contributor.authorKoc, Yener
dc.contributor.authorCiceri, Fabio
dc.contributor.authorGulbas, Zafer
dc.contributor.authorTischer, Johanna
dc.contributor.authorAfanasyev, Boris
dc.contributor.authorBruno, Benedetto
dc.contributor.authorCastagna, Luca
dc.contributor.authorBlaise, Didier
dc.contributor.authorMohty, Mohamad
dc.contributor.authorIrrera, Giuseppe
dc.contributor.authorDiez-Martin, J. L.
dc.contributor.authorPierelli, Luca
dc.contributor.authorPioltelli, Pietro
dc.contributor.authorArat, Mutlu
dc.contributor.authorDelia, Mario
dc.contributor.authorFagioli, Franca
dc.contributor.authorEhninger, Gerhard
dc.contributor.authorAljurf, Mahmoud
dc.contributor.authorCarella, Angelo Michele
dc.contributor.authorOzdogu, Hakan
dc.contributor.authorMikulska, Malgorzata
dc.contributor.authorLjungman, Per
dc.contributor.authorNagler, Arnon
dc.contributor.authorStyczynski, Jan
dc.date.accessioned2023-04-18T08:00:55Z
dc.date.available2023-04-18T08:00:55Z
dc.date.issued2018
dc.identifier.issn0268-3369en_US
dc.identifier.urihttp://hdl.handle.net/11727/8816
dc.description.abstractThe role of donor CMV serostatus in the setting of non T-cell depleted haplo-HSCT with post-transplant cyclophosphamide (PT-Cy) has not been specifically addressed so far. Here we analyzed the impact of the donor CMV serological status on the outcome of 983 CMV seropositive (CMV+), acute leukemia patients receiving a first, non T-cell depleted haplo-HSCT registered in the EBMT database. The 1-year NRM was 21.3% (95% CI: 18.4-24.8) and 18.8% (95% CI: 13.8-25.5) in the CMV D+P/R+ and D-/R+ pairs, respectively (p = 0.40). Similarly, 1-year OS was 55.1% (95% CI: 50.1-58.0) and 55.7% (95% CI: 48.0-62.8) in the same groups (p = 0.50). The other main outcomes were comparable. No difference in NRM nor OS was observed after stratification for the intensity of conditioning and multivariate anaysis confirmed the lack of significant association with NRM or OS. In conclusion, the choice of a CMV-seronegative donor did not impair early survival of CMV-seropositive patients with acute leukemia after a first, non T-cell depleted haploidentical HSCT and PT-Cy among this series of 983 consecutive patients. Future research may focus on the assessment of the hierarchy of all the donor variables.en_US
dc.language.isoengen_US
dc.relation.isversionof10.1038/s41409-017-0016-1en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectSTEM-CELL TRANSPLANTATIONen_US
dc.subjectVERSUS-HOST-DISEASEen_US
dc.subjectACUTE MYELOID-LEUKEMIAen_US
dc.subjectHIGH-DOSE CYCLOPHOSPHAMIDEen_US
dc.subjectBONE-MARROW-TRANSPLANTATIONANTI-THYMOCYTE GLOBULINPOSTTRANSPLANTATION CYCLOPHOSPHAMIDEHAPLOIDENTICAL TRANSPLANTATIONCYTOMEGALOVIRUS SEROPOSITIVITYUNRELATED DONORSen_US
dc.titleComparable Survival Using A CMV-Matched Or A Mismatched Donor For CMV Plus Patients Undergoing T-Replete Haplo-HSCT With PT-Cy For Acute Leukemia: A Study Of Behalf Of The Infectious Diseases And Acute Leukemia Working Parties Of The EBMTen_US
dc.typearticleen_US
dc.relation.journalBONE MARROW TRANSPLANTATIONen_US
dc.identifier.volume53en_US
dc.identifier.issue4en_US
dc.identifier.startpage422en_US
dc.identifier.endpage430en_US
dc.identifier.wos000429913700007en_US
dc.identifier.scopus2-s2.0-85040373844en_US
dc.contributor.pubmedID29330396en_US
dc.contributor.orcIDhttps://orcid.org/0000-0002-8902-1283en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.contributor.researcherIDAAD-5542-2021en_US


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