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The optimal neoadjuvant regimen for nonsmall cell lung cancer: A meta-analysis

To compare the efficacy and complications of different neoadjuvant to determine the optimal regimens for nonsmall cell lung cancer (NSCLC) patients. METHODS: A systematic search of the Web of Science, and PubMed databases was conducted through June 3, 2021, reporting a comparison of chemotherapy, ch...

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Autores principales: Liu, Yi, Zhao, Chong, Lu, Qiuliang, Hu, Yirong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410656/
https://www.ncbi.nlm.nih.gov/pubmed/36042672
http://dx.doi.org/10.1097/MD.0000000000030159
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author Liu, Yi
Zhao, Chong
Lu, Qiuliang
Hu, Yirong
author_facet Liu, Yi
Zhao, Chong
Lu, Qiuliang
Hu, Yirong
author_sort Liu, Yi
collection PubMed
description To compare the efficacy and complications of different neoadjuvant to determine the optimal regimens for nonsmall cell lung cancer (NSCLC) patients. METHODS: A systematic search of the Web of Science, and PubMed databases was conducted through June 3, 2021, reporting a comparison of chemotherapy, chemoradiotherapy, and immunotherapy. RESULTS: Of 3462 studies, 25 were considered for evidence synthesis. 1035 patients who received chemotherapy or radiotherapy before surgery did not prolong the overall survival (OS) compared with 1038 patients who received surgery alone (hazard ratio [HR] 1.13, 95% CI 1·00–1·28, P = 0·05). 1192 patients received chemoradiotherapy and 864 patients received chemotherapy or radiotherapy; chemoradiotherapy prolonged the OS compared with chemotherapy (HR 0.52, 95% CI 0·29 to 0.95, P = .03). Compared with 110 patients who received other therapy, 93 patients who received immunotherapy had prolonged the OS (HR 1.56, 95% CI 1·08–2·25, P = .02). Chemoradiotherapy increased the pathological response rate (HR 1.68, 95% CI 1·33–2·12, P < .0001), and grade 3 and 4 adverse effects were not increased (HR 5.90, 95% CI 0.88 to 39.60, P = .007). Immunotherapy increased the pathological response (HR 2.79, 95% CI 1·71–4·54, P < .0001), with no significant effects on grades 3 and 4 adverse(HR 0.71, 95% CI 0·19–2·64, P = .61). CONCLUSION: Our data showed that chemotherapy may prolong OS and PFS, but not statistically significant; however, the combination of chemotherapy and radiation did show an advantage, and immunotherapy may be also the choice for neoadjuvant therapy.
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spelling pubmed-94106562022-08-26 The optimal neoadjuvant regimen for nonsmall cell lung cancer: A meta-analysis Liu, Yi Zhao, Chong Lu, Qiuliang Hu, Yirong Medicine (Baltimore) Research Article To compare the efficacy and complications of different neoadjuvant to determine the optimal regimens for nonsmall cell lung cancer (NSCLC) patients. METHODS: A systematic search of the Web of Science, and PubMed databases was conducted through June 3, 2021, reporting a comparison of chemotherapy, chemoradiotherapy, and immunotherapy. RESULTS: Of 3462 studies, 25 were considered for evidence synthesis. 1035 patients who received chemotherapy or radiotherapy before surgery did not prolong the overall survival (OS) compared with 1038 patients who received surgery alone (hazard ratio [HR] 1.13, 95% CI 1·00–1·28, P = 0·05). 1192 patients received chemoradiotherapy and 864 patients received chemotherapy or radiotherapy; chemoradiotherapy prolonged the OS compared with chemotherapy (HR 0.52, 95% CI 0·29 to 0.95, P = .03). Compared with 110 patients who received other therapy, 93 patients who received immunotherapy had prolonged the OS (HR 1.56, 95% CI 1·08–2·25, P = .02). Chemoradiotherapy increased the pathological response rate (HR 1.68, 95% CI 1·33–2·12, P < .0001), and grade 3 and 4 adverse effects were not increased (HR 5.90, 95% CI 0.88 to 39.60, P = .007). Immunotherapy increased the pathological response (HR 2.79, 95% CI 1·71–4·54, P < .0001), with no significant effects on grades 3 and 4 adverse(HR 0.71, 95% CI 0·19–2·64, P = .61). CONCLUSION: Our data showed that chemotherapy may prolong OS and PFS, but not statistically significant; however, the combination of chemotherapy and radiation did show an advantage, and immunotherapy may be also the choice for neoadjuvant therapy. Lippincott Williams & Wilkins 2022-08-26 /pmc/articles/PMC9410656/ /pubmed/36042672 http://dx.doi.org/10.1097/MD.0000000000030159 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal.
spellingShingle Research Article
Liu, Yi
Zhao, Chong
Lu, Qiuliang
Hu, Yirong
The optimal neoadjuvant regimen for nonsmall cell lung cancer: A meta-analysis
title The optimal neoadjuvant regimen for nonsmall cell lung cancer: A meta-analysis
title_full The optimal neoadjuvant regimen for nonsmall cell lung cancer: A meta-analysis
title_fullStr The optimal neoadjuvant regimen for nonsmall cell lung cancer: A meta-analysis
title_full_unstemmed The optimal neoadjuvant regimen for nonsmall cell lung cancer: A meta-analysis
title_short The optimal neoadjuvant regimen for nonsmall cell lung cancer: A meta-analysis
title_sort optimal neoadjuvant regimen for nonsmall cell lung cancer: a meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410656/
https://www.ncbi.nlm.nih.gov/pubmed/36042672
http://dx.doi.org/10.1097/MD.0000000000030159
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