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A pathological complete response to neoadjuvant chemotherapy and immunotherapy in a non-small cell lung cancer patient

Lung cancer is the leading cause of cancer-related mortality worldwide. Patients with locally advanced non-small cell lung cancer (NSCLC) have lower overall survival. Studies have shown that some patients with unresectable stage III NSCLC develop disease progression after initial chemoradiotherapy,...

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Autores principales: Gao, Pengqiang, Chen, Hao, Zeng, Taidui, Wu, Weidong, Xu, Guobing, Xu, Chi, Zheng, Bin, Zhu, Yong, Zheng, Wei, Chen, Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7653127/
https://www.ncbi.nlm.nih.gov/pubmed/33209635
http://dx.doi.org/10.21037/tlcr-20-770
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author Gao, Pengqiang
Chen, Hao
Zeng, Taidui
Wu, Weidong
Xu, Guobing
Xu, Chi
Zheng, Bin
Zhu, Yong
Zheng, Wei
Chen, Chun
author_facet Gao, Pengqiang
Chen, Hao
Zeng, Taidui
Wu, Weidong
Xu, Guobing
Xu, Chi
Zheng, Bin
Zhu, Yong
Zheng, Wei
Chen, Chun
author_sort Gao, Pengqiang
collection PubMed
description Lung cancer is the leading cause of cancer-related mortality worldwide. Patients with locally advanced non-small cell lung cancer (NSCLC) have lower overall survival. Studies have shown that some patients with unresectable stage III NSCLC develop disease progression after initial chemoradiotherapy, and new treatment is needed to improve the prognosis of these patients. The rapid development of therapy has greatly changed and continued to renew the treatment strategy of advanced NSCLC. However, the clinical treatment for patients with the wild-type gene remains problematic, and chemotherapy with platinum are not yet considered satisfactory. Herein, we are reporting a case of a patient with wild-type gene mutation locally advanced NSCLC who was treated with neoadjuvant therapy by using combined targeted anti-PD-1 immunotherapy and chemotherapy. The percentage of tumor cells with membranous PD-L1 staining (tumor proportion score) was 90% or greater. After receiving all three cycles of treatment, the patient underwent video-assisted right upper lung lobectomy and wedge resection plus radical mediastinal lymph node dissection. Pathological section samples showed a pathological complete response. This experience has led us to believe that the subgroup of patients with unresectable advanced NSCLC may benefit from this strategy and may have an opportunity for radical surgery.
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spelling pubmed-76531272020-11-17 A pathological complete response to neoadjuvant chemotherapy and immunotherapy in a non-small cell lung cancer patient Gao, Pengqiang Chen, Hao Zeng, Taidui Wu, Weidong Xu, Guobing Xu, Chi Zheng, Bin Zhu, Yong Zheng, Wei Chen, Chun Transl Lung Cancer Res Case Report Lung cancer is the leading cause of cancer-related mortality worldwide. Patients with locally advanced non-small cell lung cancer (NSCLC) have lower overall survival. Studies have shown that some patients with unresectable stage III NSCLC develop disease progression after initial chemoradiotherapy, and new treatment is needed to improve the prognosis of these patients. The rapid development of therapy has greatly changed and continued to renew the treatment strategy of advanced NSCLC. However, the clinical treatment for patients with the wild-type gene remains problematic, and chemotherapy with platinum are not yet considered satisfactory. Herein, we are reporting a case of a patient with wild-type gene mutation locally advanced NSCLC who was treated with neoadjuvant therapy by using combined targeted anti-PD-1 immunotherapy and chemotherapy. The percentage of tumor cells with membranous PD-L1 staining (tumor proportion score) was 90% or greater. After receiving all three cycles of treatment, the patient underwent video-assisted right upper lung lobectomy and wedge resection plus radical mediastinal lymph node dissection. Pathological section samples showed a pathological complete response. This experience has led us to believe that the subgroup of patients with unresectable advanced NSCLC may benefit from this strategy and may have an opportunity for radical surgery. AME Publishing Company 2020-10 /pmc/articles/PMC7653127/ /pubmed/33209635 http://dx.doi.org/10.21037/tlcr-20-770 Text en 2020 Translational Lung Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Case Report
Gao, Pengqiang
Chen, Hao
Zeng, Taidui
Wu, Weidong
Xu, Guobing
Xu, Chi
Zheng, Bin
Zhu, Yong
Zheng, Wei
Chen, Chun
A pathological complete response to neoadjuvant chemotherapy and immunotherapy in a non-small cell lung cancer patient
title A pathological complete response to neoadjuvant chemotherapy and immunotherapy in a non-small cell lung cancer patient
title_full A pathological complete response to neoadjuvant chemotherapy and immunotherapy in a non-small cell lung cancer patient
title_fullStr A pathological complete response to neoadjuvant chemotherapy and immunotherapy in a non-small cell lung cancer patient
title_full_unstemmed A pathological complete response to neoadjuvant chemotherapy and immunotherapy in a non-small cell lung cancer patient
title_short A pathological complete response to neoadjuvant chemotherapy and immunotherapy in a non-small cell lung cancer patient
title_sort pathological complete response to neoadjuvant chemotherapy and immunotherapy in a non-small cell lung cancer patient
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7653127/
https://www.ncbi.nlm.nih.gov/pubmed/33209635
http://dx.doi.org/10.21037/tlcr-20-770
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