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Optimizing therapy sequence to prevent patient attrition in EGFR mutation-positive advanced or metastatic NSCLC.
Roeper, Julia; Kurz, Sylke; Grohé, Christian; Griesinger, Frank.
Afiliação
  • Roeper J; Department of Hematology & Oncology, University Department Internal Medicine-Oncology, Pius-Hospital, Medical Campus University of Oldenburg, Oldenburg, Germany.
  • Kurz S; Department of Respiratory Medicine, Evangelische Lungenklinik Berlin, Berlin, Germany.
  • Grohé C; Department of Respiratory Medicine, Evangelische Lungenklinik Berlin, Berlin, Germany.
  • Griesinger F; Department of Hematology & Oncology, University Department Internal Medicine-Oncology, Pius-Hospital, Medical Campus University of Oldenburg, Oldenburg, Germany.
Future Oncol ; 17(4): 471-486, 2021 Feb.
Article em En | MEDLINE | ID: mdl-33094641
ABSTRACT
Clinical trial and real-world data in non-small-cell lung cancer indicate that 10-60% of patients that progressed on first- or second-generation EGFR-targeting tyrosine kinase inhibitors (TKI) do not receive systemic second-line therapy. In our article, we discuss efficacy, safety and treatment duration with different EGFR-TKIs and stress the need for delivery of the most efficacious therapy in the first-line. We also provide our perspective on analysis of circulating tumor DNA and the role of EGFR-TKI in combined therapies. Finally, we review new therapeutic options to overcome resistance to EGFR-TKI. We believe that overall treatment duration and access to different medications in subsequent lines of therapy should be considered when planning the optimal treatment strategy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pacientes Desistentes do Tratamento / Carcinoma Pulmonar de Células não Pequenas / Inibidores de Proteínas Quinases / Neoplasias Pulmonares / Mutação Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pacientes Desistentes do Tratamento / Carcinoma Pulmonar de Células não Pequenas / Inibidores de Proteínas Quinases / Neoplasias Pulmonares / Mutação Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article