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Cytokine release syndrome and successful response to pembrolizumab therapy in a patient with EGFR ‐mutated non‐small‐cell lung cancer: A case report
A therapeutic option for advanced non‐small‐cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR)‐tyrosine kinase inhibitor (TKI) resistance is a clinical challenge. The clinical outcomes of pembrolizumab in those patients is inconclusive. Cytokine release syndrome (CRS) is...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9058301/ https://www.ncbi.nlm.nih.gov/pubmed/35384319 http://dx.doi.org/10.1111/1759-7714.14390 |
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author | Zhang, Meng Cheng, Yuan Hu, Yan Nie, Ligong |
author_facet | Zhang, Meng Cheng, Yuan Hu, Yan Nie, Ligong |
author_sort | Zhang, Meng |
collection | PubMed |
description | A therapeutic option for advanced non‐small‐cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR)‐tyrosine kinase inhibitor (TKI) resistance is a clinical challenge. The clinical outcomes of pembrolizumab in those patients is inconclusive. Cytokine release syndrome (CRS) is a rarely reported immune‐related adverse event in the field of immune checkpoint inhibitors therapy, raising challenges given the paucity of data with such presentations. We present the unique case of a 67‐year‐old female with advanced EGFR‐mutated NSCLC who successfully responded to pembrolizumab after EGFR‐TKI resistance. However, the patient developed CRS after pembrolizumab initiation and presented with fever, rash, hypotension, hypoxemia, tachycardia, and multiple organ dysfunction. Blood tests showed elevated levels of peripheral CD8+ T cells, C‐reactive protein, and tumor necrosis factor‐α. The symptoms rapidly improved after corticosteroid initiation. Based on the present case, we propose that pembrolizumab might be a potential salvage therapy for patients with advanced EGFR‐mutated NSCLC after EGFR‐TKI resistance; CRS would be a sign of the antitumor effect of PD‐1 inhibitors in those patients. However, CRS can be a fatal adverse effect and clinicians must remain vigilant for the rare toxicities to make prompt diagnosis and treatment. |
format | Online Article Text |
id | pubmed-9058301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-90583012022-05-03 Cytokine release syndrome and successful response to pembrolizumab therapy in a patient with EGFR ‐mutated non‐small‐cell lung cancer: A case report Zhang, Meng Cheng, Yuan Hu, Yan Nie, Ligong Thorac Cancer Case Reports A therapeutic option for advanced non‐small‐cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR)‐tyrosine kinase inhibitor (TKI) resistance is a clinical challenge. The clinical outcomes of pembrolizumab in those patients is inconclusive. Cytokine release syndrome (CRS) is a rarely reported immune‐related adverse event in the field of immune checkpoint inhibitors therapy, raising challenges given the paucity of data with such presentations. We present the unique case of a 67‐year‐old female with advanced EGFR‐mutated NSCLC who successfully responded to pembrolizumab after EGFR‐TKI resistance. However, the patient developed CRS after pembrolizumab initiation and presented with fever, rash, hypotension, hypoxemia, tachycardia, and multiple organ dysfunction. Blood tests showed elevated levels of peripheral CD8+ T cells, C‐reactive protein, and tumor necrosis factor‐α. The symptoms rapidly improved after corticosteroid initiation. Based on the present case, we propose that pembrolizumab might be a potential salvage therapy for patients with advanced EGFR‐mutated NSCLC after EGFR‐TKI resistance; CRS would be a sign of the antitumor effect of PD‐1 inhibitors in those patients. However, CRS can be a fatal adverse effect and clinicians must remain vigilant for the rare toxicities to make prompt diagnosis and treatment. John Wiley & Sons Australia, Ltd 2022-04-05 2022-05 /pmc/articles/PMC9058301/ /pubmed/35384319 http://dx.doi.org/10.1111/1759-7714.14390 Text en © 2022 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Reports Zhang, Meng Cheng, Yuan Hu, Yan Nie, Ligong Cytokine release syndrome and successful response to pembrolizumab therapy in a patient with EGFR ‐mutated non‐small‐cell lung cancer: A case report |
title | Cytokine release syndrome and successful response to pembrolizumab therapy in a patient with
EGFR
‐mutated non‐small‐cell lung cancer: A case report |
title_full | Cytokine release syndrome and successful response to pembrolizumab therapy in a patient with
EGFR
‐mutated non‐small‐cell lung cancer: A case report |
title_fullStr | Cytokine release syndrome and successful response to pembrolizumab therapy in a patient with
EGFR
‐mutated non‐small‐cell lung cancer: A case report |
title_full_unstemmed | Cytokine release syndrome and successful response to pembrolizumab therapy in a patient with
EGFR
‐mutated non‐small‐cell lung cancer: A case report |
title_short | Cytokine release syndrome and successful response to pembrolizumab therapy in a patient with
EGFR
‐mutated non‐small‐cell lung cancer: A case report |
title_sort | cytokine release syndrome and successful response to pembrolizumab therapy in a patient with
egfr
‐mutated non‐small‐cell lung cancer: a case report |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9058301/ https://www.ncbi.nlm.nih.gov/pubmed/35384319 http://dx.doi.org/10.1111/1759-7714.14390 |
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