| dc.contributor.author | Ormazabal Vélez, Irati | es_ES |
| dc.contributor.author | Galbete Jiménez, Arkaitz | es_ES |
| dc.contributor.author | Sánchez Escamilla, Miriam | es_ES |
| dc.contributor.author | Marcos Jiménez, Ana | es_ES |
| dc.contributor.author | Fernández Ruiz, Elena | es_ES |
| dc.contributor.author | Salmanton García, Jon | es_ES |
| dc.contributor.author | Bermúdez Rodríguez, María Aranzazu | es_ES |
| dc.contributor.author | Figuera Álvarez, Ángela | es_ES |
| dc.contributor.other | Universidad de Cantabria | es_ES |
| dc.date.accessioned | 2025-12-12T12:10:49Z | |
| dc.date.available | 2025-12-12T12:10:49Z | |
| dc.date.issued | 2025 | es_ES |
| dc.identifier.issn | 0025-7753 | es_ES |
| dc.identifier.issn | 1578-8989 | es_ES |
| dc.identifier.issn | 2387-0206 | es_ES |
| dc.identifier.uri | https://hdl.handle.net/10902/38506 | |
| dc.description.abstract | Introduction: Inthis retrospective study, withprolongedfollow-up, we analyze the outcomes of allogeneic
hematopoietic stem cell transplantation (allo-HSCT) in adult acute lymphoblastic leukemia (ALL) and the
impact of pre-transplantation measurable residual disease (pre-HSCT MRD).
Methods: Detection of MRD was performed by multiparametric flow cytometry (MFC) for Philadelphia
chromosome-negative ALL (Ph-neg ALL) and by classic genetic tests for Ph-pos ALL.
Results: Among 46 patients in first complete remission (CR1) who had available MRD data, 1- and 3-year cumulative incidences of relapse (CIR) for patients with positive and negative MRD were 47.1% and 52.9% vs. 3.4% and 6.9%, respectively (p < 0.001). Disease free survival (DFS) at 1 and 3 years was 82.8% (95% CI 70.1–97.7) and 79.3% (95% CI 65.9–95.5) in the negative MRD group and 35.3% (95% CI 18.5–67.2) and 29.4% (95% CI 14.1–61.4) in the positive MRD group (p < 0.001). With a median follow up of 29 months in the entire cohort and 177.6 months (14.8 years) in survivors, 1- and 3-year overall survival (OS) for the pre-HSCT negative MRD group was 82.8% (95% CI 70.1–97.7) and 79.2% (95% CI 65.6–95.5), respectively, compared to 64.7% (95% CI 45.5–91.9) and 41.2% (95% CI 23.3–72.7) in the positive MRD group (p = 0.001). In a multivariate model, positive pre-HSCT MRD is associated with increased CIR and poorer DFS and OS. Conclusion: These results support that pre-HSCT MRD should be eradicated to improve survival of adult ALL patients who undergo allo-HSCT. | es_ES |
| dc.publisher | Elsevier | es_ES |
| dc.rights | © 2024 The Author(s). Published by Elsevier España, S.L.U. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/) | * |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
| dc.source | Medicina clínica | es_ES |
| dc.subject.other | Acute lymphoblastic leukemia | es_ES |
| dc.subject.other | Allogeneic hematopoietic stem cell transplantation | es_ES |
| dc.subject.other | Measurable residual disease | es_ES |
| dc.subject.other | Multiparametric flow cytometry | es_ES |
| dc.subject.other | Quantitative polymerase chain reaction | es_ES |
| dc.subject.other | Graft versus host disease | es_ES |
| dc.title | Importance of measurable residual disease in the outcome of adults with acute lymphoblastic leukemia after allogeneic stem cell transplantation: long follow-up analysis from a single transplant center | es_ES |
| dc.type | info:eu-repo/semantics/article | es_ES |
| dc.rights.accessRights | openAccess | es_ES |
| dc.identifier.DOI | 10.1016/j.medcli.2024.09.023 | es_ES |
| dc.type.version | publishedVersion | es_ES |