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1.
Eur J Nucl Med Mol Imaging ; 51(7): 1955-1964, 2024 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-38351389

RESUMO

BACKGROUND: Hodgkin lymphoma (HL) in pediatric populations has a high survival rate but poses risks for long-term morbidities. Although [18F]fluoro­2­deoxy­2­d­glucose positron emission tomography ([18F]FDG PET) scans offer potential for improved risk stratification, the definitive prognostic value of quantitative [18F]FDG PET parameters remains unclear for pediatric HL. METHODS: A single-center, retrospective study included pediatric patients diagnosed with HL between 2016 and 2023 treated according to EuroNet-PHL-C1 and DAL/GPOH-HD protocols. Patients underwent baseline and interim PET/CT scans after two chemotherapy cycles. Event-free survival (EFS) was the primary endpoint, Deauville score was the secondary endpoint. Quantitative [18F]FDG PET parameters included SUVmax, metabolic tumor volume (MTV) and total lesion glycolysis (TLG) that were evaluated using two segmentation methods (SUV 2.5, 41% SUVmax). Survival outcomes were assessed using Cox regression analysis. RESULTS: A total of 115 patients (50 males, median age 14.2 years) were studied, with a median follow-up period of 35 months. During this period, 16 cases (13.9%) of relapse or progression were noted. Baseline and interim MTV 2.5, MTV 41%, TLG 2.5, and TLG 41%, along with interim SUVmax, were significantly associated with worse EFS and correlated with post-treatment Deauville scores. In multivariable analysis, interim MTV 2.5 > 0 ml (adj. hazard ratio, HR: 3.89, p = 0.009) and interim TLG 41% ≥ 30 g (adj. HR: 7.98, p = 0.006) were independent risk factors for EFS. CONCLUSION: Baseline and interim [18F]FDG PET parameters can serve as significant prognostic indicators for EFS and treatment response in pediatric HL. These quantitative measures could enhance individualized, risk-adapted treatment strategies for children and adolescents with HL.


Assuntos
Fluordesoxiglucose F18 , Doença de Hodgkin , Humanos , Doença de Hodgkin/diagnóstico por imagem , Doença de Hodgkin/metabolismo , Masculino , Feminino , Adolescente , Criança , Prognóstico , Estudos Retrospectivos , Tomografia por Emissão de Pósitrons combinada à Tomografia Computadorizada , Pré-Escolar
2.
Vestn Oftalmol ; 139(2): 84-88, 2023.
Artigo em Russo | MEDLINE | ID: mdl-37067936

RESUMO

Modern methods of treatment have significantly increased the survival rate of children with oncohematological diseases, and along with it the importance of preserving their quality of life. More than half of patients receiving long-term steroid therapy suffer from glaucoma, which reduces visual acuity. This review analyzes the literature on the patterns of glaucoma development in patients receiving steroid therapy, the results of anatomical, as well as physiological and biochemical changes in the anterior chamber angle leading to the development of glaucoma.


Assuntos
Glaucoma , Trabeculectomia , Criança , Humanos , Pressão Intraocular , Qualidade de Vida , Glaucoma/diagnóstico , Trabeculectomia/métodos , Esteroides
3.
Ter Arkh ; 89(7): 51-56, 2017.
Artigo em Russo | MEDLINE | ID: mdl-28766541

RESUMO

AIM: To evaluate the safety and efficacy of crizotinib used in pediatric patients with relapsed or refractory ALK-positive anaplastic large-cell lymphoma (ALCL). SUBJECTS AND METHODS: The paper describes the experience with crizotinib used in 8 patients with refractory ALK-ALCL before and after allogeneic hematopoietic stem cell transplantation (HSCT). RESULTS: All the 8 (100%) patients treated with crizotinib were recorded to have complete responses, including complete metabolic ones (tumor disappearance as evidenced by positron emission tomography (PET)/computed tomography. CONCLUSION: Low and manageable toxicity of crizotinib and complete PET-negative responses in patients with resistant ALK lymphomas favor the need to test the drug as first-line therapy, by possibly decreasing the intensification of chemotherapy.


Assuntos
Transplante de Células-Tronco Hematopoéticas/métodos , Linfoma Anaplásico de Células Grandes , Pirazóis , Piridinas , Receptores Proteína Tirosina Quinases/análise , Adolescente , Quinase do Linfoma Anaplásico , Criança , Crizotinibe , Monitoramento de Medicamentos/métodos , Feminino , Humanos , Imuno-Histoquímica , Linfoma Anaplásico de Células Grandes/patologia , Linfoma Anaplásico de Células Grandes/fisiopatologia , Linfoma Anaplásico de Células Grandes/terapia , Masculino , Tomografia por Emissão de Pósitrons combinada à Tomografia Computadorizada/métodos , Inibidores de Proteínas Quinases/administração & dosagem , Inibidores de Proteínas Quinases/efeitos adversos , Pirazóis/administração & dosagem , Pirazóis/efeitos adversos , Piridinas/administração & dosagem , Piridinas/efeitos adversos , Resultado do Tratamento
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