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晚期肺腺癌靶向耐药后小细胞癌转化2例并文献复习

Treatment of advanced non-small cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR) mutation with EGFR-tyrosine kinase inhibitors (EGFR-TKIs) can achieve good disease control, but it will inevitably produce drug resistance. About 3%-10% of the resistance mechanism is small...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720681/
https://www.ncbi.nlm.nih.gov/pubmed/36419397
http://dx.doi.org/10.3779/j.issn.1009-3419.2022.102.41
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collection PubMed
description Treatment of advanced non-small cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR) mutation with EGFR-tyrosine kinase inhibitors (EGFR-TKIs) can achieve good disease control, but it will inevitably produce drug resistance. About 3%-10% of the resistance mechanism is small cell transformation. Two cases of stage IV lung adenocarcinoma with EGFR mutation were reported and the disease was controlled after EGFR-TKIs treatment. In case 1, progression-free survival (PFS) before small cell carcinoma transformation was 16 months, and in case 2, PFS before small cell carcinoma transformation was 24 months. Subsequent biopsy after disease progression indicated a shift to small cell lung cancer. Case 1 PFS after small cell carcinoma transformation was 6 months, and case 2 PFS after small cell carcinoma transformation was 8 months, and overall survival (OS) was 36 months, which significantly prolonged the patient's survival. At the same time, the literature of such drug resistance mutations was reviewed. For patients with advanced NSCLC with sensitive mutations, it is necessary to conduct secondary histopathological tests after TKIs treatment resistance, and select subsequent treatment according to different resistance mechanisms for the whole course of disease management.
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spelling pubmed-97206812022-12-22 晚期肺腺癌靶向耐药后小细胞癌转化2例并文献复习 Zhongguo Fei Ai Za Zhi 病例报道 Treatment of advanced non-small cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR) mutation with EGFR-tyrosine kinase inhibitors (EGFR-TKIs) can achieve good disease control, but it will inevitably produce drug resistance. About 3%-10% of the resistance mechanism is small cell transformation. Two cases of stage IV lung adenocarcinoma with EGFR mutation were reported and the disease was controlled after EGFR-TKIs treatment. In case 1, progression-free survival (PFS) before small cell carcinoma transformation was 16 months, and in case 2, PFS before small cell carcinoma transformation was 24 months. Subsequent biopsy after disease progression indicated a shift to small cell lung cancer. Case 1 PFS after small cell carcinoma transformation was 6 months, and case 2 PFS after small cell carcinoma transformation was 8 months, and overall survival (OS) was 36 months, which significantly prolonged the patient's survival. At the same time, the literature of such drug resistance mutations was reviewed. For patients with advanced NSCLC with sensitive mutations, it is necessary to conduct secondary histopathological tests after TKIs treatment resistance, and select subsequent treatment according to different resistance mechanisms for the whole course of disease management. 中国肺癌杂志编辑部 2022-11-20 /pmc/articles/PMC9720681/ /pubmed/36419397 http://dx.doi.org/10.3779/j.issn.1009-3419.2022.102.41 Text en 版权所有©《中国肺癌杂志》编辑部2022 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
晚期肺腺癌靶向耐药后小细胞癌转化2例并文献复习
title 晚期肺腺癌靶向耐药后小细胞癌转化2例并文献复习
title_full 晚期肺腺癌靶向耐药后小细胞癌转化2例并文献复习
title_fullStr 晚期肺腺癌靶向耐药后小细胞癌转化2例并文献复习
title_full_unstemmed 晚期肺腺癌靶向耐药后小细胞癌转化2例并文献复习
title_short 晚期肺腺癌靶向耐药后小细胞癌转化2例并文献复习
title_sort 晚期肺腺癌靶向耐药后小细胞癌转化2例并文献复习
topic 病例报道
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720681/
https://www.ncbi.nlm.nih.gov/pubmed/36419397
http://dx.doi.org/10.3779/j.issn.1009-3419.2022.102.41
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