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ALK‐rearranged squamous cell carcinoma of the lung

BACKGROUND: ALK rearrangement is a very rare subset of squamous cell carcinoma (SCC) and one of the clinical features in patients is lack of data. Here, we report eight patients diagnosed with SCC of the lung harboring ALK rearrangement. METHODS: We collected primary NSCLC samples at the Beijing Che...

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Autores principales: Meng, Qiyi, Dong, Yujie, Tao, Hong, Shi, Liang, Tong, Li, Tang, Junfang, Zhang, Shucai, Liu, Zhe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8017260/
https://www.ncbi.nlm.nih.gov/pubmed/33565277
http://dx.doi.org/10.1111/1759-7714.13818
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author Meng, Qiyi
Dong, Yujie
Tao, Hong
Shi, Liang
Tong, Li
Tang, Junfang
Zhang, Shucai
Liu, Zhe
author_facet Meng, Qiyi
Dong, Yujie
Tao, Hong
Shi, Liang
Tong, Li
Tang, Junfang
Zhang, Shucai
Liu, Zhe
author_sort Meng, Qiyi
collection PubMed
description BACKGROUND: ALK rearrangement is a very rare subset of squamous cell carcinoma (SCC) and one of the clinical features in patients is lack of data. Here, we report eight patients diagnosed with SCC of the lung harboring ALK rearrangement. METHODS: We collected primary NSCLC samples at the Beijing Chest Hospital between January 2012 and December 2018 for Ventana (D5F3) immunohistochemical detection. Among the 148 patients was diagnosed ALK‐rearranged non small cell lung cancer (NSCLC), only eight cases was SCC. We collected patients information from electronic patent records (EPRs). RESULTS: The eight cases of SCC were diagnosed by immunohistochemistry (IHC). Two were given crizotinib as second‐line therapy. One patient had stable disease (SD) and progression‐free survival (PFS) of six months. The other patient had progressive disease (PD) but PFS was only one month. The side effects were tolerable. This report identified 31 cases of ALK rearrangement in SCC patients from a literature search (including the eight patients in this study). These fusion genes are often seen in a younger age group (mean age: 55.6 years) and non‐smokers (18/31, 58.1%). A total of 20 cases received an ALK inhibitor as first‐ or second‐line treatment which included 11 with a partial response (PR), four with SD, and five with PD. The DCR and ORR was 75.0% (15/20) and 55.0% (11/20), respectively. The median duration time of therapy was 6.4 ± 4.4 months. CONCLUSIONS: Patients with ALK‐rearranged SCC obtained clinical benefit from ALK‐inhibitor therapy, especially those who were non‐smokers and whose tumors had been identified by IHC+/FISH+.
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spelling pubmed-80172602021-04-02 ALK‐rearranged squamous cell carcinoma of the lung Meng, Qiyi Dong, Yujie Tao, Hong Shi, Liang Tong, Li Tang, Junfang Zhang, Shucai Liu, Zhe Thorac Cancer Case Reports BACKGROUND: ALK rearrangement is a very rare subset of squamous cell carcinoma (SCC) and one of the clinical features in patients is lack of data. Here, we report eight patients diagnosed with SCC of the lung harboring ALK rearrangement. METHODS: We collected primary NSCLC samples at the Beijing Chest Hospital between January 2012 and December 2018 for Ventana (D5F3) immunohistochemical detection. Among the 148 patients was diagnosed ALK‐rearranged non small cell lung cancer (NSCLC), only eight cases was SCC. We collected patients information from electronic patent records (EPRs). RESULTS: The eight cases of SCC were diagnosed by immunohistochemistry (IHC). Two were given crizotinib as second‐line therapy. One patient had stable disease (SD) and progression‐free survival (PFS) of six months. The other patient had progressive disease (PD) but PFS was only one month. The side effects were tolerable. This report identified 31 cases of ALK rearrangement in SCC patients from a literature search (including the eight patients in this study). These fusion genes are often seen in a younger age group (mean age: 55.6 years) and non‐smokers (18/31, 58.1%). A total of 20 cases received an ALK inhibitor as first‐ or second‐line treatment which included 11 with a partial response (PR), four with SD, and five with PD. The DCR and ORR was 75.0% (15/20) and 55.0% (11/20), respectively. The median duration time of therapy was 6.4 ± 4.4 months. CONCLUSIONS: Patients with ALK‐rearranged SCC obtained clinical benefit from ALK‐inhibitor therapy, especially those who were non‐smokers and whose tumors had been identified by IHC+/FISH+. John Wiley & Sons Australia, Ltd 2021-02-09 2021-04 /pmc/articles/PMC8017260/ /pubmed/33565277 http://dx.doi.org/10.1111/1759-7714.13818 Text en © 2021 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Meng, Qiyi
Dong, Yujie
Tao, Hong
Shi, Liang
Tong, Li
Tang, Junfang
Zhang, Shucai
Liu, Zhe
ALK‐rearranged squamous cell carcinoma of the lung
title ALK‐rearranged squamous cell carcinoma of the lung
title_full ALK‐rearranged squamous cell carcinoma of the lung
title_fullStr ALK‐rearranged squamous cell carcinoma of the lung
title_full_unstemmed ALK‐rearranged squamous cell carcinoma of the lung
title_short ALK‐rearranged squamous cell carcinoma of the lung
title_sort alk‐rearranged squamous cell carcinoma of the lung
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8017260/
https://www.ncbi.nlm.nih.gov/pubmed/33565277
http://dx.doi.org/10.1111/1759-7714.13818
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