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dc.contributor.authorHodder, Angus
dc.contributor.authorMishra, Avijeet K
dc.contributor.authorEnshaei, Amir
dc.contributor.authorBaird, Susan
dc.contributor.authorElbeshlawi, Ismail
dc.contributor.authorBonney, Denise
dc.contributor.authorClesham, Katherine
dc.contributor.authorCummins, Michelle
dc.contributor.authorVedi, Aditi
dc.contributor.authorGibson, Brenda
dc.contributor.authorGeorge, Lindsay
dc.contributor.authorIngham, Danielle
dc.contributor.authorJigoulina, Galina
dc.contributor.authorLancaster, Donna
dc.contributor.authorLindsay, Katherine
dc.contributor.authorMadni, Majid
dc.contributor.authorMalone, Andrea
dc.contributor.authorMitchell, Bethany
dc.contributor.authorMoppett, John
dc.contributor.authorMotwani, Jayashree
dc.contributor.authorMoorman, Anthony V
dc.contributor.authorPatrick, Katharine
dc.contributor.authorSamrin, Lamia
dc.contributor.authorTewari, Sanjay
dc.contributor.authorThakur, Indu
dc.contributor.authorO'Connor, David
dc.contributor.authorSamarasinghe, Sujith
dc.contributor.authorVora, Ajay
dc.date.accessioned2023-12-04T17:28:15Z
dc.date.available2023-12-04T17:28:15Z
dc.date.issued2023-11-15
dc.identifier.citationHodder A, Mishra AK, Enshaei A, Baird S, Elbeshlawi I, Bonney D, Clesham K, Cummins M, Vedi A, Gibson B, George L, Ingham D, Jigoulina G, Lancaster D, Lindsay K, Madni M, Malone A, Mitchell B, Moppett J, Motwani J, Moorman AV, Patrick K, Samrin L, Tewari S, Thakur I, O'Connor D, Samarasinghe S, Vora A. Blinatumomab for First-Line Treatment of Children and Young Persons With B-ALL. J Clin Oncol. 2024 Mar 10;42(8):907-914. doi: 10.1200/JCO.23.01392. Epub 2023 Nov 15.en_US
dc.identifier.issn0732-183X
dc.identifier.eissn1527-7755
dc.identifier.doi10.1200/JCO.23.01392
dc.identifier.pmid37967307
dc.identifier.urihttp://hdl.handle.net/20.500.14200/3119
dc.description.abstractFrom February 2018 to February 2023, 105 patients were treated, of whom 85 were in the Blin-CT group and 20 were in the Blin-HSCT group. A majority of Blin-CT patients received Blina for chemotherapy intolerance (70 of 85, 82%), and the group had a higher-risk profile than unselected patients with B-ALL. Blina was well tolerated with only one patient having a grade 3/4-related toxicity event, and of the 60 patients who were minimal residual disease-positive pre-Blina, 58 of 60 (97%) responded. At a median follow-up of 22 months, the 2-year outcomes of the 80 matched Blin-CT group patients were similar to those of 192 controls (EFS, 95% [95% CI, 85 to 98] v 90% [95% CI, 65 to 93] and OS, 97% [95% CI, 86 to 99] v 94% [95% CI, 89 to 96]). Of the 20 in the HSCT group, three died because of transplant complications and two relapsed.en_US
dc.language.isoenen_US
dc.publisherAmerican Society of Clinical Oncologyen_US
dc.subjectOncology. Pathology.en_US
dc.titleBlinatumomab for First-Line Treatment of Children and Young Persons With B-ALLen_US
dc.typeArticle
dc.source.journaltitleJournal of Clinical Oncology
dc.source.beginpageJCO2301392
dc.source.endpage
dc.source.countryUnited States
rioxxterms.versionNAen_US
dc.contributor.trustauthorGEorge, Lindsay
dc.contributor.departmentHaematologyen_US
dc.contributor.roleMedical and Dentalen_US
oa.grant.openaccessnaen_US


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