| Literature DB >> 28205327 |
Biljana Horn1, Justin T Wahlstrom1, Alexis Melton1, Angela Liou1, Marie Ouachee-Chardin2, Gauri Sunkersett1, Jennifer Willert1, Jimmy Hwang3, Jueleah Expose-Spencer1, Mort C Cowan1, Janelle Facchino1, Christopher C Dvorak1.
Abstract
This retrospective analysis comprises 10-year experience with early posttransplant mixed chimerism-based preemptive intervention. Out of 104 patients, 51 received preemptive immunotherapy. Their outcomes were similar to patients achieving full donor chimerism spontaneously. Among patients receiving intervention, 5-year event-free survival was identical in patients with and without pretransplant residual disease, respectively (68% [95% confidence interval (CI) 38-98%] vs. 69% [95% CI 54-85%] log-rank = 0.4). In patients who received preemptive immunotherapy, chimerism status and residual disease prior to transplant were no longer predictors of poor outcome; however, 41% of the patients with residual disease prior to transplant relapsed early and did not benefit from this strategy.Entities:
Keywords: allogeneic stem cell transplant; immunotherapy; pediatric leukemia
Mesh:
Year: 2017 PMID: 28205327 PMCID: PMC9254698 DOI: 10.1002/pbc.26464
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.838