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阿帕替尼用于小细胞肺癌多线治疗后的挽救治疗

Small cell lung cancer (SCLC) was highly malignant and lack effective treatment after the failure of radiotherapy and chemotherapy. Antiangiogenic therapy had shown a certain effect in advanced SCLC. Apatinib, a new potent oral small-molecule tyrosine kinase inhibitor targeting the intracellular dom...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058660/
https://www.ncbi.nlm.nih.gov/pubmed/30037379
http://dx.doi.org/10.3779/j.issn.1009-3419.2018.07.11
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description Small cell lung cancer (SCLC) was highly malignant and lack effective treatment after the failure of radiotherapy and chemotherapy. Antiangiogenic therapy had shown a certain effect in advanced SCLC. Apatinib, a new potent oral small-molecule tyrosine kinase inhibitor targeting the intracellular domain of vascular endothelial growth factor receptor 2 (VEGFR-2), showed the effect of anti-angiogenesis. However, the efficacy in SCLC was rarely reported. We reported 1 case of advanced SCLC with Gilbert syndrome, the patient received Apatinib after the failure of 4 lines of chemotherapy, and achieved a partial response according to the Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 standard after one month. The progression-free survival (PFS) was 5 months. Apatinib was well tolerated except recurrent grade 3 hyperbilirubinemia because of the metabolic disorder of Bilirubin. Salvage treatment with Apatinib for advanced SCLC deserved further exploration.
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spelling pubmed-60586602018-08-23 阿帕替尼用于小细胞肺癌多线治疗后的挽救治疗 Zhongguo Fei Ai Za Zhi 病例报道 Small cell lung cancer (SCLC) was highly malignant and lack effective treatment after the failure of radiotherapy and chemotherapy. Antiangiogenic therapy had shown a certain effect in advanced SCLC. Apatinib, a new potent oral small-molecule tyrosine kinase inhibitor targeting the intracellular domain of vascular endothelial growth factor receptor 2 (VEGFR-2), showed the effect of anti-angiogenesis. However, the efficacy in SCLC was rarely reported. We reported 1 case of advanced SCLC with Gilbert syndrome, the patient received Apatinib after the failure of 4 lines of chemotherapy, and achieved a partial response according to the Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 standard after one month. The progression-free survival (PFS) was 5 months. Apatinib was well tolerated except recurrent grade 3 hyperbilirubinemia because of the metabolic disorder of Bilirubin. Salvage treatment with Apatinib for advanced SCLC deserved further exploration. 中国肺癌杂志编辑部 2018-07-20 /pmc/articles/PMC6058660/ /pubmed/30037379 http://dx.doi.org/10.3779/j.issn.1009-3419.2018.07.11 Text en 版权所有©《中国肺癌杂志》编辑部2018 https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/
spellingShingle 病例报道
阿帕替尼用于小细胞肺癌多线治疗后的挽救治疗
title 阿帕替尼用于小细胞肺癌多线治疗后的挽救治疗
title_full 阿帕替尼用于小细胞肺癌多线治疗后的挽救治疗
title_fullStr 阿帕替尼用于小细胞肺癌多线治疗后的挽救治疗
title_full_unstemmed 阿帕替尼用于小细胞肺癌多线治疗后的挽救治疗
title_short 阿帕替尼用于小细胞肺癌多线治疗后的挽救治疗
title_sort 阿帕替尼用于小细胞肺癌多线治疗后的挽救治疗
topic 病例报道
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058660/
https://www.ncbi.nlm.nih.gov/pubmed/30037379
http://dx.doi.org/10.3779/j.issn.1009-3419.2018.07.11
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