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2.
Bone Marrow Transplant ; 58(6): 673-679, 2023 06.
Artigo em Inglês | MEDLINE | ID: mdl-36918682

RESUMO

Anti-CD19 chimeric antigen receptor T cells (CART) has rapidly been adopted as the standard third-line therapy to treat aggressive B-cell lymphomas (ABCL) after failure of second-line therapy despite the lack of direct comparisons with allogeneic hematopoietic cell transplantation (alloHCT)-based strategies. Using the Grupo Español de Trasplante y Terapia Celular (GETH-TC) registry, we selected patients with the following characteristics: CART or alloHCT performed between 2016 and 2021; ≥18 years old; ABCL diagnosis; ≥2 lines of therapy; and either anti-CD19 CART or alloHCT as therapy at relapse. The analysis included a total of 316 (CART = 215, alloHCT = 101) patients. Median follow-up was 15 and 36 months for the CART and alloHCT cohorts, respectively. In the multivariate analysis, CART was confirmed to be similar to alloHCT for the primary study endpoint (progression-free survival) (hazard ratio [HR] 0.92, CI95%:0.56-1.51, p = 0.75). Furthermore, when the analysis was limited to only patients with chemo-sensitive diseases (complete and partial response) at infusion (CART = 26, alloHCT=93), no differences were reported (progression-free survival at month +18: 65% versus 55%, p = 0.59). However, CART had lower non-relapse mortality (HR 0.34, 95% CI: 0.13-0.85, p = 0.02). Given the lower toxicity and similar survival outcomes, these results suggest the use of CART before alloHCT.


Assuntos
Transplante de Células-Tronco Hematopoéticas , Linfoma de Células B , Humanos , Adolescente , Transplante de Células-Tronco Hematopoéticas/métodos , Recidiva , Linfoma de Células B/terapia
3.
Rev. med. Risaralda ; 28(1): 71-84, ene.-jun. 2022. tab, graf
Artigo em Espanhol | LILACS-Express | LILACS | ID: biblio-1389145

RESUMO

Resumen Inetroducción: El Síndrome Respiratorio Agudo Severo (SARS-CoV-2) es la entidad patológica responsable de la actual pandemia que no solo genera un cuadro respiratorio distintivo sino que también se ha asociado con múltiples mecanismos de invasión al sistema nervioso central (SNC). Objetivo: Determinar las afecciones, manifestaciones y repercusiones neurológicas que puede generar la infección por SARS-CoV-2. Métodos: Revisión de la literatura científica de pacientes con infección por SARS-CoV-2, en quienes se evaluó desarrollo de afecciones, manifestaciones y repercusiones neurológicas, desenlace seleccionado en los estudios, presencia de afecciones micro y macroscópicas del SNC y periférico (SNP). Resultados: Se estudiaron 40 artículos que analizaban la familia y estructura del SARS-CoV-2, mecanismos fisiopatológicos, manifestaciones clínicas neurológicas y las posibles repercusiones a nivel sistema nervioso central. Conclusiones: El SARS-CoV-2 es una entidad patológica que se asocia a distintos mecanismos de intervención neurológica, por medio de infección directa al SNC, secundario a un proceso parainfeccioso y postinfeccioso, relacionado con el síndrome de tormenta de citoquinas, daño endotelial, trastornos trombóticos, adicionalmente de secundario a hipoxia, hipoxemia y fallo multiorgánico.


Abstract Introduction: Severe Acute Respiratory Syndrome (SARS-CoV-2) is the pathological entity responsible for the current pandemic that not only generates a distinctive respiratory pattern but has also been associated with multiple mechanisms of invasion of the central nervous system (CNS). Objective: To determine the affections, manifestations and neurological repercussions that SARS-CoV-2 infection can generate. Methods: Review of the scientific literature of patients with SARS-CoV-2 infection, in whom the development of conditions, manifestations and neurological repercussions, selected outcome in the studies, presence of micro and macroscopic conditions of the CNS and peripheral (PNS) were evaluated. Results: 40 articles were included where the family and structure of SARS-CoV-2, pathophysiological mechanisms, neurological clinical manifestations, and possible repercussions at the central nervous system level were analyzed. Conclusions: SARS-CoV-2 is a pathological entity that is associated with different mechanisms of neurological intervention, through direct infection to the CNS, secondary to a parainfectious and postinfectious process, related to cytokine storm syndrome, endothelial damage, thrombotic disorders, in addition to secondary to hypoxia, hypoxemia and multiple organ failure.

4.
Transfus Apher Sci ; 60(2): 103052, 2021 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-33483284

RESUMO

Plerixafor (Mozobil, Sanofi) is approved for using in patients with lymphoma and multiple myeloma when steady-state mobilization strategies fail. Although off-label use of plerixafor in healthy related donors (HRD) is known, limited data are available and no recommendations exist to guide its use in this setting. With the aim of collecting data from HRDs who received plerixafor in our country, we designed an observational case series study within the Spanish Group of Hematopoietic Transplant and Cell Therapy (GETH). Plerixafor was administered subcutaneously to 30 HRDs at a median dose of 0.24 mg/Kg (interquartile range (IQR): 0.23-0.25) because mobilization failure after using mobilization with G-CSF (mobilization failure was defined as collection of <4.0 × 106 CD34+ cells/Kg recipient). All HRDs received G-CSF at a median dose of 11 µg/Kg/day (IQR: 10-12) for 4-5 days. Leukocytapheresis after G-CSF mobilization was performed in 23 (77 %) HRDs collecting a median of 1.6 × 106 CD34+ cells/Kg recipient weight (IQR: 0.9-2.5). Addition of plerixafor allowed the collection of a higher median number of CD34 cells (4.98 × 106 CD34+ cells/Kg recipient weight (IQR: 3.5-5.8)) when compared with the collection of CD34+ cells with G-CSF alone (p < 0.01). The final median total number of CD34+ cells collected was 6.1 × 106/Kg recipient weight (IQR: 4.8-7.3). Mild adverse events related with plerixafor administration were reported in 8 (27 %) donors. In conclusion, addition of plerixafor after G-CSF mobilization failure in HRDs allowed collecting higher number of CD34+ cells in comparison with steady-state mobilization.


Assuntos
Fármacos Anti-HIV/uso terapêutico , Benzilaminas/uso terapêutico , Ciclamos/uso terapêutico , Fator Estimulador de Colônias de Granulócitos/uso terapêutico , Mobilização de Células-Tronco Hematopoéticas/métodos , Adulto , Fármacos Anti-HIV/farmacologia , Benzilaminas/farmacologia , Ciclamos/farmacologia , Feminino , Fator Estimulador de Colônias de Granulócitos/farmacologia , Voluntários Saudáveis , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Doadores de Tecidos
5.
Estilos clín ; 26(2)2021.
Artigo em Português | LILACS, Index Psicologia - Periódicos | ID: biblio-1444142

RESUMO

Este artigo propõe a discussão em torno dos atendimentos online realizados por estudantes de Psicologia de uma universidade pública, orientadas pela psicanálise, tendo em vista a pandemia COVID-19. Com o distanciamento físico imposto como medida sanitária para controle do coronavírus, foi necessário reinventar a prática com crianças e adolescentes desenvolvida em três contextos diferentes, a saber: estágio em um Centro de Atenção Psicossocial Infantojuvenil (CAPSi); extensão no projeto Atendimento Psicanalítico em Clínica Escola; e extensão no projeto Adolescência, Acolhimento Institucional e Clínica do Desamparo. Buscou-se abordar aspectos que sustentam o dispositivo analítico frente à mudança na modalidade dos atendimentos, visando sustentar uma reflexão teórica, ética e política


Este artículo propone un debate en torno a la atención psicológica en línea que prestan los estudiantes de psicología de una universidad pública, guiados por el psicoanálisis, en el contexto de la pandemia de COVID-19. Con el distanciamiento social impuesto como medida sanitaria para controlar el coronavirus, fue necesario reinventar la práctica con niños y adolescentes desarrollada en tres contextos diferentes, a saber: pasantía en un Centro de Atención Psicosocial Infantil y Juvenil (CAPSi); extensión universitaria en el proyecto "Asistencia Psicoanalítica en una escuela clínica"; y en el proyecto "Adolescencia, Acogida Institucional y Clínica del Desamparo". Se buscó abordar los aspectos que aseguran el dispositivo analítico ante el cambio en la modalidad de atención, buscando sustentar una reflexión teórica, ética y política


This article aims to discuss online consultations performed by Psychology students at a public university, guided by Psychoanalysis, in view of COVID-19 pandemic. Social distancing was imposed as a sanitary measure for the control of the coronavirus and this regulation compelled us to reinvent the psychological practices with children and adolescents. The practices are developed in three different contexts, namely: a traineeship at a Psychosocial Care Center for Children and Adolescents (CAPSi); an university extension project "Psychoanalytic practices at training clinic"; and the project "Adolescence, Institutional Care and Clinic of Helplessness". The article seeks to discuss aspects that maintain the analytical device in the face of changes in psychological care, in order to support a theoretical, ethical and political reflection


Cet article porte sur l'assistance en ligne proposée par des étudiants de Psychologie d'une université publique, guidée par la psychanalyse, en raison de la pandémie de la COVID-19. Avec la distanciation sociale imposée comme mesure sanitaire pour contrôler le coronavirus, il a fallu réinventer la pratique avec des enfants et des adolescents. Des pratiques sont développées en trois contextes différents, à savoir : un centre de soins psychosociaux pour enfants et adolescents (CAPSi); le projet d'extension universitaire "Consultations psychanalytiques dans la clinique publique"; et le projet "Adolescence, Accueil institutionnell et Clinique de la Détresse". Le but est d'aborder les aspects qui soutiennent le dispositif analytique face aux changements de type d'assistance, servant d'appui à une réflexion théorique, éthique et politique


Assuntos
Humanos , Criança , Adolescente , Terapia Psicanalítica , Orientação Infantil , Intervenção Baseada em Internet , COVID-19/psicologia , Transferência Psicológica , Criança , Adolescente
6.
Biol Blood Marrow Transplant ; 26(4): 651-658, 2020 04.
Artigo em Inglês | MEDLINE | ID: mdl-31917270

RESUMO

Extracorporeal photopheresis (ECP) is an established treatment strategy in steroid-refractory graft-versus-host disease (GVHD). This study's main objective was to analyze the clinical response and impact of ECP therapy in steroid dose reduction. A retrospective observational series of 113 patients from 7 transplantation centers was analyzed. Sixty-five patients (58%) had acute GVHD (aGVHD), and 48 (42%) had chronic GVHD (cGVHD). All ECP procedures were performed with the off-line system. The median number of procedures until achievement of initial response was 3 for both patients with aGVHD and those with cGVHD. ECP was the second-line therapy in 48% of the aGVHD cases and in 50% of the cGVHD cases. 71% of the cases of aGVHD were grade III-IV, and 69% of the cases of cGVHD were severe. The overall response rate on day 28 was 53% (complete response [CR] rate, 45%) in the patients with aGVHD and 67% (CR, 23%) in those with cGVHD. Skin was the most frequently involved organ, with a response rate of 58% (CR, 49%) in the patients with aGVHD and 69% (CR 29%) in those with cGVHD. At the end of ECP treatment, 60% of patients treated for aGVHD who responded were able to stop steroid therapy, with a median dose reduction of 100%. Significant differences in overall survival were observed for patients responding to ECP with aGVHD (hazard ratio [HR], 4.3; P < .001) and with cGVHD (HR, 4.8; P = .003). Our data indicate that ECP is a valid therapeutic alternative in patients with steroid-refractory aGVHD and cGVHD, permitting significant steroid dosage reductions.


Assuntos
Doença Enxerto-Hospedeiro , Fotoferese , Doença Aguda , Doença Crônica , Doença Enxerto-Hospedeiro/tratamento farmacológico , Humanos , Estudos Retrospectivos , Esteroides/uso terapêutico
7.
Eur J Epidemiol ; 27(10): 781-90, 2012 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22892901

RESUMO

Benzene, a recognized occupational leukemogen in adults, has been hypothesized to also increase the risk of childhood leukemia. We carried out a population-based case-control study in a northern Italy community involving 83 cases with acute childhood leukemia diagnosed in the years 1998-2009 and 332 matched controls. We assessed residential exposure to benzene and to particulate matter ≤10 µm (PM10) from motorized traffic using geocoded residences and detailed emission and dispersion modeling. Exposure to benzene, and to a lesser extent to PM10, appeared to be independently associated with an excess leukemia risk. When we stratified the study population by age and by leukemia subtype, the relative risk associated with benzene exposure was higher among children aged less than 5 years, and despite small numbers this relation appeared to be considerably stronger for acute myeloid leukemia than for acute lymphoblastic leukemia. Overall, these findings suggest that exposure to low levels of benzene released from motorized traffic may increase the risk of childhood leukemia, and suggest a possible independent effect of PM10, although unmeasured confounding due to other pollutants cannot be ruled out.


Assuntos
Benzeno/toxicidade , Leucemia/induzido quimicamente , Material Particulado/toxicidade , Poluentes Atmosféricos/análise , Benzeno/análise , Estudos de Casos e Controles , Criança , Pré-Escolar , Exposição Ambiental/efeitos adversos , Exposição Ambiental/estatística & dados numéricos , Feminino , Humanos , Itália/epidemiologia , Leucemia/epidemiologia , Leucemia Mieloide Aguda/induzido quimicamente , Leucemia Mieloide Aguda/epidemiologia , Modelos Logísticos , Masculino , Veículos Automotores , Material Particulado/análise , Leucemia-Linfoma Linfoblástico de Células Precursoras/induzido quimicamente , Leucemia-Linfoma Linfoblástico de Células Precursoras/epidemiologia , Risco , Fatores de Risco
8.
Belo Horizonte; s.n; 2012. 66 p.
Tese em Português | LILACS, BBO - Odontologia | ID: lil-715965

RESUMO

A satisfação do paciente no consultório odontológico é almejada através de procedimentos nenos traumáticos, com tempo cirúrgico reduzido, ocazionando melhor pós-oeratório e longevidade dos trabalhos realizados...


Assuntos
Humanos , Masculino , Feminino , Cirurgia Assistida por Computador , Implantes Dentários/tendências , Protocolos Clínicos
9.
Leuk Lymphoma ; 43(12): 2377-81, 2002 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-12613527

RESUMO

It has been demonstrated that some myeloid blasts express renin, but normal bone marrow (BM) does not display this expression. The aim of the present work was to analyze the renin expression in different hematological malignancies and different myeloid cell lines. We investigated the expression of renin by RT-PCR in BM from patients with hematological malignancies (106 patients), in nine normal BM from healthy donors and in leukemic cell lines (K562, KU812, MEG-01, U-937 and HL60), as well in K562 cell line subjected to differentiation treatments. We have observed renin expression in cells from acute myeloid leukemia (AML), chronic myelogenous leukemia (CML) and acute lymphoblastic leukemia (ALL) cases. The highest frequency was observed in AML-non acute promyelocytic leukemia(APL) cases (47.2% of the cases). The disappearance of this expression was associated with the status of complete remission of AML. Renin is expressed in some myeloid human leukemia cell lines such as K562, KU812 and MEG-01. However, when K562 cells were treated with inducers of growth inhibition and/or differentiation, the expression did not disappear, indicating that renin expression is associated with a blastic phenotype rather than with cell proliferation. The obtained findings suggest that the renin expression could have a role on the disease development and could be used as an aberrant marker of leukemia.


Assuntos
Hematopoese , Leucemia/patologia , Renina/análise , Renina/fisiologia , Antineoplásicos/farmacologia , Medula Óssea/patologia , Diferenciação Celular/efeitos dos fármacos , Hematopoese/efeitos dos fármacos , Humanos , Células K562 , Leucócitos Mononucleares/efeitos dos fármacos , Leucócitos Mononucleares/patologia , Proteínas de Neoplasias/análise , RNA Mensageiro/análise , RNA Mensageiro/efeitos dos fármacos , Indução de Remissão , Renina/efeitos dos fármacos , Renina/genética
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