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1.
Mol Cancer Ther ; 20(11): 2189-2197, 2021 11.
Artículo en Inglés | MEDLINE | ID: mdl-34482287

RESUMEN

Limited clinical data are available regarding the utility of multikinase inhibition in neuroblastoma. Repotrectinib (TPX-0005) is a multikinase inhibitor that targets ALK, TRK, JAK2/STAT, and Src/FAK, which have all been implicated in the pathogenesis of neuroblastoma. We evaluated the preclinical activity of repotrectinib monotherapy and in combination with chemotherapy as a potential therapeutic approach for relapsed/refractory neuroblastoma. In vitro sensitivity to repotrectinib, ensartinib, and cytotoxic chemotherapy was evaluated in neuroblastoma cell lines. In vivo antitumor effect of repotrectinib monotherapy, and in combination with chemotherapy, was evaluated using a genotypically diverse cohort of patient-derived xenograft (PDX) models of neuroblastoma. Repotrectinib had comparable cytotoxic activity across cell lines irrespective of ALK mutational status. Combination with chemotherapy demonstrated increased antiproliferative activity across several cell lines. Repotrectinib monotherapy had notable antitumor activity and prolonged event-free survival compared with vehicle and ensartinib in PDX models (P < 0.05). Repotrectinib plus chemotherapy was superior to chemotherapy alone in ALK-mutant and ALK wild-type PDX models. These results demonstrate that repotrectinib has antitumor activity in genotypically diverse neuroblastoma models, and that combination of a multikinase inhibitor with chemotherapy may be a promising treatment paradigm for translation to the clinic.


Asunto(s)
Compuestos Macrocíclicos/uso terapéutico , Neuroblastoma/tratamiento farmacológico , Pirazoles/uso terapéutico , Animales , Humanos , Compuestos Macrocíclicos/farmacología , Ratones , Neuroblastoma/patología , Pirazoles/farmacología
2.
Rev Assoc Med Bras (1992) ; 62 Suppl 1: 25-28, 2016 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-27982317

RESUMEN

The hematopoietic stem cell transplantation (HSCT) is the only curative alternative for Myelodysplastic Syndrome (MDS), but many patients are not eligible for this treatment, as there are several limiting factors, especially in the case of patients with low-risk MDS. The aim of this study is to discuss the factors that can guide the decision-making on referring or not a patient to HSCT. Three cases of MDS, two of which were submitted to HSCT are presented. We intend to report the difficulties in referring patients with MDS to transplant and the prognostic factors that contribute to define eligibility.


Asunto(s)
Trasplante de Células Madre Hematopoyéticas/métodos , Síndromes Mielodisplásicos/cirugía , Anciano , Toma de Decisiones , Resultado Fatal , Humanos , Masculino , Persona de Mediana Edad , Síndromes Mielodisplásicos/patología , Pronóstico , Medición de Riesgo
3.
Rev. Assoc. Med. Bras. (1992, Impr.) ; Rev. Assoc. Med. Bras. (1992, Impr.);62(supl.1): 25-28, Oct. 2016. graf
Artículo en Inglés | LILACS | ID: biblio-829563

RESUMEN

ABSTRACT The hematopoietic stem cell transplantation (HSCT) is the only curative alternative for Myelodysplastic Syndrome (MDS), but many patients are not eligible for this treatment, as there are several limiting factors, especially in the case of patients with low-risk MDS. The aim of this study is to discuss the factors that can guide the decision-making on referring or not a patient to HSCT. Three cases of MDS, two of which were submitted to HSCT are presented. We intend to report the difficulties in referring patients with MDS to transplant and the prognostic factors that contribute to define eligibility.


RESUMO O transplante de células-tronco hematopoéticas (TCTH) é a única alternativa curativa para Síndrome Mielodisplásica (SMD), porém muitos pacientes não são elegíveis para esta opção, pois existem diversos fatores limitantes, principalmente no caso de pacientes com SMD de baixo risco. O objetivo do estudo é discutir os fatores que podem orientar a decisão no encaminhamento ou não para o TCTH. São apresentados três casos de SMD, dos quais dois foram submetidos ao TCTH. Nos propomos a relatar as dificuldades no encaminhamento dos pacientes com SMD ao transplante e os fatores prognósticos que contribuem para definir a elegibilidade.


Asunto(s)
Humanos , Masculino , Femenino , Daño del ADN/fisiología , Estrés Oxidativo/fisiología , Trasplante de Células Madre Hematopoyéticas/métodos , Linfoma/cirugía , Mieloma Múltiple/cirugía , Valores de Referencia , Factores de Tiempo , Trasplante Autólogo/métodos , Biomarcadores , Estudios de Casos y Controles , Análisis de Varianza , Resultado del Tratamiento , Linfoma/genética , Linfoma/mortalidad , Malondialdehído/análisis , Mieloma Múltiple/genética , Mieloma Múltiple/metabolismo
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