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Efficacy of Paclitaxel plus TS1 against previously treated EGFR mutated non-small cell lung cancer
BACKGROUND: Later line chemotherapy (≥2nd lines) such as Docetaxel or immunotherapy is frequently used. As the life expectancy of lung cancer patients is getting longer, we need to provide more treatment options. Other treatment options are not well documented except for Doxetaxel and immunotherapy....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764356/ https://www.ncbi.nlm.nih.gov/pubmed/31579626 http://dx.doi.org/10.7717/peerj.7767 |
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author | Tseng, Yen-Han Shih, Jen-Fu Chao, Heng-Sheng Chen, Yuh-Min |
author_facet | Tseng, Yen-Han Shih, Jen-Fu Chao, Heng-Sheng Chen, Yuh-Min |
author_sort | Tseng, Yen-Han |
collection | PubMed |
description | BACKGROUND: Later line chemotherapy (≥2nd lines) such as Docetaxel or immunotherapy is frequently used. As the life expectancy of lung cancer patients is getting longer, we need to provide more treatment options. Other treatment options are not well documented except for Doxetaxel and immunotherapy. Therefore, the efficacy of paclitaxel plus TS1 (TTS1) is warranted. METHODS: We retrospectively reviewed the chart records of our non-small cell lung cancer patients who were treated between 2010 and 2013. Clinical characteristics, type of tumor, EGFR mutation status, and treatment response to first-line EGFR-TKI therapy and efficacy of TTS1, were collected. RESULTS: Twenty eight patients were enrolled in this study. No patients archived complete response and seven patients had partial response (ORR: 25%). The disease control rate was 60.7% (17/28). The progression free survival (PFS) was 4.0 months and overall survival (OS) was 15.8 months. Of them, 17 had EGFR mutations, eight EGFR wild type, and three were unknown EGFR status. After TTS1 treatment, patients with EGFR mutations had better PFS (4.9 months vs. 1.8 months) and OS (15.5 months vs. 7.2 months) compared with those of EGFR wild type. CONCLUSIONS: TTS1 are effective later line chemotherapy, especially in tumor EGFR mutated patients. Paclitaxel plus TS1 is another treatment of choice for NSCLC patients before a more effective treatment strategy is found. |
format | Online Article Text |
id | pubmed-6764356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67643562019-10-02 Efficacy of Paclitaxel plus TS1 against previously treated EGFR mutated non-small cell lung cancer Tseng, Yen-Han Shih, Jen-Fu Chao, Heng-Sheng Chen, Yuh-Min PeerJ Drugs and Devices BACKGROUND: Later line chemotherapy (≥2nd lines) such as Docetaxel or immunotherapy is frequently used. As the life expectancy of lung cancer patients is getting longer, we need to provide more treatment options. Other treatment options are not well documented except for Doxetaxel and immunotherapy. Therefore, the efficacy of paclitaxel plus TS1 (TTS1) is warranted. METHODS: We retrospectively reviewed the chart records of our non-small cell lung cancer patients who were treated between 2010 and 2013. Clinical characteristics, type of tumor, EGFR mutation status, and treatment response to first-line EGFR-TKI therapy and efficacy of TTS1, were collected. RESULTS: Twenty eight patients were enrolled in this study. No patients archived complete response and seven patients had partial response (ORR: 25%). The disease control rate was 60.7% (17/28). The progression free survival (PFS) was 4.0 months and overall survival (OS) was 15.8 months. Of them, 17 had EGFR mutations, eight EGFR wild type, and three were unknown EGFR status. After TTS1 treatment, patients with EGFR mutations had better PFS (4.9 months vs. 1.8 months) and OS (15.5 months vs. 7.2 months) compared with those of EGFR wild type. CONCLUSIONS: TTS1 are effective later line chemotherapy, especially in tumor EGFR mutated patients. Paclitaxel plus TS1 is another treatment of choice for NSCLC patients before a more effective treatment strategy is found. PeerJ Inc. 2019-09-24 /pmc/articles/PMC6764356/ /pubmed/31579626 http://dx.doi.org/10.7717/peerj.7767 Text en ©2019 Tseng et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Drugs and Devices Tseng, Yen-Han Shih, Jen-Fu Chao, Heng-Sheng Chen, Yuh-Min Efficacy of Paclitaxel plus TS1 against previously treated EGFR mutated non-small cell lung cancer |
title | Efficacy of Paclitaxel plus TS1 against previously treated EGFR mutated non-small cell lung cancer |
title_full | Efficacy of Paclitaxel plus TS1 against previously treated EGFR mutated non-small cell lung cancer |
title_fullStr | Efficacy of Paclitaxel plus TS1 against previously treated EGFR mutated non-small cell lung cancer |
title_full_unstemmed | Efficacy of Paclitaxel plus TS1 against previously treated EGFR mutated non-small cell lung cancer |
title_short | Efficacy of Paclitaxel plus TS1 against previously treated EGFR mutated non-small cell lung cancer |
title_sort | efficacy of paclitaxel plus ts1 against previously treated egfr mutated non-small cell lung cancer |
topic | Drugs and Devices |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764356/ https://www.ncbi.nlm.nih.gov/pubmed/31579626 http://dx.doi.org/10.7717/peerj.7767 |
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