Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Mais filtros










Filtros aplicados
Base de dados
Intervalo de ano de publicação
1.
Clin. transl. oncol. (Print) ; 18(1): 33-39, ene. 2016. tab, ilus
Artigo em Inglês | IBECS | ID: ibc-148049

RESUMO

Purpose. Second-line chemotherapy of advanced non-small cell lung cancer (NSCLC) with docetaxel or pemetrexed allows to achieve objective response rate only in 5-10 % of patients. Recent studies have shown that single nucleotide polymorphisms (SNPs) in genes encoding proteins which regulate dynamics of microtubules may be considered as predictive factors of response to taxane-based chemotherapy. STMN1 gene encodes stathmin 1, which plays role in cell division by regulation of microtubules epolarisation, and this process may be associated with taxanes’ effectiveness. Materials and methods. Using HRM-PCR technique, we evaluated the −2166C>T SNP of STMN1 gene in DNA from peripheral blood leucocytes of 54 advanced NSCLC patients treated in second-line monotherapy with docetaxel or paclitaxel. Results. Patients with TT genotype of STMN1 gene demonstrated significantly longer progression-free survival (PFS) and the lower risk of early disease progression after second-line treatment compared to patients with other STMN1 genotypes (median PFS: 7 and 2 months; p = 0.0154; HR = 0.371; 95 % CI 0.184-0.743). Early disease progression during second-line chemotherapy was significantly more frequently observed in patients with CC genotype of STMN1 in contrast to patients with presence of T allele (median PFS: 2 and 4 months; p = 0.0385; HR = 1.776; 95 % CI 0.905-3.445). Conclusion. Only selected NSCLC patients could benefit from second-line chemotherapy. Therefore, investigations of novel predictive molecular factors for proper qualification of patients to second-line taxane-based chemotherapy are justified. Studied SNP of STMN1 gene may have potential predictive role in such therapy (AU)


No disponible


Assuntos
Humanos , Masculino , Feminino , Neoplasias Pulmonares/metabolismo , Neoplasias Pulmonares/patologia , Análise do Polimorfismo de Comprimento de Fragmentos Amplificados/métodos , Nucleotídeos/administração & dosagem , Nucleotídeos/metabolismo , Buffy Coat/citologia , Buffy Coat/metabolismo , Neoplasias da Mama/genética , Neoplasias da Mama/patologia , Sobrevivência/fisiologia , Neoplasias Pulmonares/tratamento farmacológico , Neoplasias Pulmonares/radioterapia , Análise do Polimorfismo de Comprimento de Fragmentos Amplificados/classificação , Nucleotídeos/farmacologia , Buffy Coat/classificação , Buffy Coat/fisiologia , Neoplasias da Mama/tratamento farmacológico , Neoplasias da Mama/terapia , Sobrevivência/psicologia , Estudos Retrospectivos
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...