Blinatumomab for First-Line Treatment of Children and Young Persons With B-ALL
dc.contributor.author | Hodder, Angus | |
dc.contributor.author | Mishra, Avijeet K | |
dc.contributor.author | Enshaei, Amir | |
dc.contributor.author | Baird, Susan | |
dc.contributor.author | Elbeshlawi, Ismail | |
dc.contributor.author | Bonney, Denise | |
dc.contributor.author | Clesham, Katherine | |
dc.contributor.author | Cummins, Michelle | |
dc.contributor.author | Vedi, Aditi | |
dc.contributor.author | Gibson, Brenda | |
dc.contributor.author | George, Lindsay | |
dc.contributor.author | Ingham, Danielle | |
dc.contributor.author | Jigoulina, Galina | |
dc.contributor.author | Lancaster, Donna | |
dc.contributor.author | Lindsay, Katherine | |
dc.contributor.author | Madni, Majid | |
dc.contributor.author | Malone, Andrea | |
dc.contributor.author | Mitchell, Bethany | |
dc.contributor.author | Moppett, John | |
dc.contributor.author | Motwani, Jayashree | |
dc.contributor.author | Moorman, Anthony V | |
dc.contributor.author | Patrick, Katharine | |
dc.contributor.author | Samrin, Lamia | |
dc.contributor.author | Tewari, Sanjay | |
dc.contributor.author | Thakur, Indu | |
dc.contributor.author | O'Connor, David | |
dc.contributor.author | Samarasinghe, Sujith | |
dc.contributor.author | Vora, Ajay | |
dc.date.accessioned | 2023-12-04T17:28:15Z | |
dc.date.available | 2023-12-04T17:28:15Z | |
dc.date.issued | 2023-11-15 | |
dc.identifier.citation | Hodder 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.issn | 0732-183X | |
dc.identifier.eissn | 1527-7755 | |
dc.identifier.doi | 10.1200/JCO.23.01392 | |
dc.identifier.pmid | 37967307 | |
dc.identifier.uri | http://hdl.handle.net/20.500.14200/3119 | |
dc.description.abstract | From 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.iso | en | en_US |
dc.publisher | American Society of Clinical Oncology | en_US |
dc.subject | Oncology. Pathology. | en_US |
dc.title | Blinatumomab for First-Line Treatment of Children and Young Persons With B-ALL | en_US |
dc.type | Article | |
dc.source.journaltitle | Journal of Clinical Oncology | |
dc.source.beginpage | JCO2301392 | |
dc.source.endpage | ||
dc.source.country | United States | |
rioxxterms.version | NA | en_US |
dc.contributor.trustauthor | GEorge, Lindsay | |
dc.contributor.department | Haematology | en_US |
dc.contributor.role | Medical and Dental | en_US |
oa.grant.openaccess | na | en_US |