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1.
Hematol., Transfus. Cell Ther. (Impr.) ; 42(4): 348-355, Oct.-Dec. 2020. tab, graf
Article Dans Anglais | LILACS | ID: biblio-1142973

Résumé

ABSTRACT Background: The minimal residual disease (MRD) is the most important prognostic factor for acute lymphoblastic leukemia (ALL) in children. This study aimed to investigate the influence of detecting the MRD by the multiparametric flow cytometry (MFC) at day 15 (D15) of the induction on the analysis of the risk group classifications of the different childhood ALL treatment protocols used in a referral hospital in southern Brazil. Method: We retrospectively reviewed the medical records of patients with B-cell ALL, aged 1 to 18 years, treated at a hospital from January 2013 to April 2017. Main results: Seventy-five patients were analyzed. Regarding the MRD by the MFC at D15, the analyses showed statistical significance when the MRD was grouped into three categories, < 0.1%, 0.1-10%, and > 10%, with the following distribution: 30.7%, 52.0%, and 17.3%, respectively. There was a significant association between D15 MRD-MFC < 0.1% and the likelihood of dying or relapsing and between D15 MRD-MFC > 10% and the likelihood of dying or relapsing. The cumulative hazard ratio for the relapse of patients with D15 MRD-MFC < 0.1%, 0.1-10%, and > 10% was 19.2%, 59.8%, and 80.1%, respectively. Conclusion: Our analysis suggests D15 MRD-MFC < 0.1% as a cut-off point for patients with more favorable outcomes and that the MRD at D15 in risk classifications is particularly useful for the stratification of patients with a more favorable prognosis.


Sujets)
Humains , Mâle , Femelle , Nourrisson , Enfant d'âge préscolaire , Enfant , Adolescent , Pronostic , Orientation vers un spécialiste , Leucémie aigüe biphénotypique/thérapie , Facteurs de risque , Maladie résiduelle , Leucémie-lymphome lymphoblastique à précurseurs B et T
2.
Braz. j. med. biol. res ; 48(10): 871-876, Oct. 2015. tab, ilus
Article Dans Anglais | LILACS | ID: lil-761603

Résumé

Treatments for patients with hematologic malignancies not in remission are limited, but a few clinical studies have investigated the effects of salvaged unrelated cord blood transplantation (CBT). We retrospectively studied 19 patients with acute leukemia, 5 with myelodysplastic syndrome (MDS with refractory anemia with excess blasts [RAEB]), and 2 with non-Hodgkin's lymphoma who received 1 CBT unit ≤2 loci human leukocyte antigen (HLA)-mismatched after undergoing myeloablative conditioning regimens between July 2005 and July 2014. All of them were in non-remission before transplantation. The infused total nucleated cell (TNC) dose was 4.07 (range 2.76-6.02)×107/kg and that of CD34+ stem cells was 2.08 (range 0.99-8.65)×105/kg. All patients were engrafted with neutrophils that exceeded 0.5×109/L on median day +17 (range 14-37 days) and had platelet counts of >20×109/L on median day +35 (range 17-70 days). Sixteen patients (61.5%) experienced pre-engraftment syndrome (PES), and six (23.1%) patients progressed to acute graft-versus-host disease (GVHD). The cumulative incidence rates of II-IV acute GVHD and chronic GVHD were 50% and 26.9%, respectively. After a median follow-up of 27 months (range 5-74), 14 patients survived and 3 relapsed. The estimated 2-year overall survival (OS), disease-free survival (DFS), and non-relapse mortality (NRM) rates were 50.5%, 40.3%, and 35.2%, respectively. Salvaged CBT might be a promising modality for treating hematologic malignancies, even in patients with a high leukemia burden.


Sujets)
Adolescent , Adulte , Enfant , Femelle , Humains , Mâle , Jeune adulte , Allogreffes , Anémie réfractaire avec excès de blastes/thérapie , Transplantation de cellules souches de sang du cordon , Maladie du greffon contre l'hôte , Leucémie aigüe biphénotypique/thérapie , Lymphome malin non hodgkinien/thérapie , Anémie réfractaire avec excès de blastes/mortalité , Transplantation de cellules souches de sang du cordon/mortalité , Survie sans rechute , Études de suivi , Maladie du greffon contre l'hôte/mortalité , Tumeurs hématologiques/mortalité , Tumeurs hématologiques/thérapie , Leucémie aigüe biphénotypique/mortalité , Leucémie lymphoïde/mortalité , Leucémie lymphoïde/thérapie , Leucémie myéloïde/mortalité , Leucémie myéloïde/thérapie , Leucémies/mortalité , Leucémies/thérapie , Lymphome malin non hodgkinien/mortalité , Syndromes myélodysplasiques/mortalité , Syndromes myélodysplasiques/thérapie , Études rétrospectives , Induction de rémission/méthodes , Résultat thérapeutique
4.
Medicina (B.Aires) ; 56(4): 339-45, 1996. tab
Article Dans Espagnol | LILACS | ID: lil-186254

Résumé

Se registra la sinonimia entre leucemia mixta, bilineal, biclonal e híbrida, diferenciándola de leucemia bifenotípica. Se define leucemia aguda mixta (LA mixta) como aquella en la que coexistem 1) dos caracteres citoquímicos de línea diferente, o 2) uno de ellos y más de uno inmunológico opuesto, o 3) más de uno inmunológico opuesto a otra línea inmune. Se aportan 7 casos (5 de LA mixta común y 2 de viraje postratamiento). Se concluye que el carácter mixto de una leucemia aguda empeora el pronóstico y se discute la selección de la terapêutica.


Sujets)
Humains , Mâle , Femelle , Enfant d'âge préscolaire , Enfant , Adolescent , Adulte , Sujet âgé , Immunohistochimie , Immunophénotypage , Leucémies/immunologie , Maladie aigüe , Lignée cellulaire , Leucémie aigüe biphénotypique/immunologie , Leucémie aigüe biphénotypique/thérapie , Leucémies/thérapie , Marqueurs biologiques , Myeloperoxidase , Pronostic
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