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ALK Rearrangement in Small-Cell Lung Cancer and Durable Response to Alectinib: A Case Report
BACKGROUND: With the development of next-generation sequencing (NGS), several anaplastic lymphoma kinase (ALK) fusion partner genes have been identified. However, ALK fusion is extremely rare in small cell lung cancer (SCLC), and there is no standard treatment option. Here, we report a patient with...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8554320/ https://www.ncbi.nlm.nih.gov/pubmed/34729013 http://dx.doi.org/10.2147/OTT.S323700 |
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author | Sun, Ning Zhuang, Yan Zhang, Junling Chen, Shiqing Dai, Yuwen Guo, Renhong |
author_facet | Sun, Ning Zhuang, Yan Zhang, Junling Chen, Shiqing Dai, Yuwen Guo, Renhong |
author_sort | Sun, Ning |
collection | PubMed |
description | BACKGROUND: With the development of next-generation sequencing (NGS), several anaplastic lymphoma kinase (ALK) fusion partner genes have been identified. However, ALK fusion is extremely rare in small cell lung cancer (SCLC), and there is no standard treatment option. Here, we report a patient with SCLC who carried an ALK- Intergenic Region (IR) rearrangement and responded to Alectinib. CASE PRESENTATION: A 26-year-old man was pathologically diagnosed with extensive-stage SCLC. After 2 cycles of first-line chemotherapy, CT showed a large soft tissue mass in the middle lobe of the right lung and increased liver nodules, left kidney lesions and right kidney lesions. To seek potential therapeutic regimens, ALK rearrangement was identified. The patient achieved a rapid and durable partial response with Alectinib (600 mg BID). The patient experienced a significant clinical response with a progression-free survival of more than 6 months. There were no grade 3 or more adverse events reported, and there was no dose reduction during treatment. Following Alectinib treatment, the allele frequency of ALK rearrangement and RB1 and TP53 mutations in plasma circulating tumor DNA decreased with the reduction in tumor size. CONCLUSION: This case provides a meaningful reference for the treatment of SCLC patients with ALK rearrangement. This case also provides valuable information on the response to ALK inhibitors in patients with ALK-IR rearrangement and better understanding of ALK-TKI applications in the future. |
format | Online Article Text |
id | pubmed-8554320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-85543202021-11-01 ALK Rearrangement in Small-Cell Lung Cancer and Durable Response to Alectinib: A Case Report Sun, Ning Zhuang, Yan Zhang, Junling Chen, Shiqing Dai, Yuwen Guo, Renhong Onco Targets Ther Case Report BACKGROUND: With the development of next-generation sequencing (NGS), several anaplastic lymphoma kinase (ALK) fusion partner genes have been identified. However, ALK fusion is extremely rare in small cell lung cancer (SCLC), and there is no standard treatment option. Here, we report a patient with SCLC who carried an ALK- Intergenic Region (IR) rearrangement and responded to Alectinib. CASE PRESENTATION: A 26-year-old man was pathologically diagnosed with extensive-stage SCLC. After 2 cycles of first-line chemotherapy, CT showed a large soft tissue mass in the middle lobe of the right lung and increased liver nodules, left kidney lesions and right kidney lesions. To seek potential therapeutic regimens, ALK rearrangement was identified. The patient achieved a rapid and durable partial response with Alectinib (600 mg BID). The patient experienced a significant clinical response with a progression-free survival of more than 6 months. There were no grade 3 or more adverse events reported, and there was no dose reduction during treatment. Following Alectinib treatment, the allele frequency of ALK rearrangement and RB1 and TP53 mutations in plasma circulating tumor DNA decreased with the reduction in tumor size. CONCLUSION: This case provides a meaningful reference for the treatment of SCLC patients with ALK rearrangement. This case also provides valuable information on the response to ALK inhibitors in patients with ALK-IR rearrangement and better understanding of ALK-TKI applications in the future. Dove 2021-10-24 /pmc/articles/PMC8554320/ /pubmed/34729013 http://dx.doi.org/10.2147/OTT.S323700 Text en © 2021 Sun et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Case Report Sun, Ning Zhuang, Yan Zhang, Junling Chen, Shiqing Dai, Yuwen Guo, Renhong ALK Rearrangement in Small-Cell Lung Cancer and Durable Response to Alectinib: A Case Report |
title | ALK Rearrangement in Small-Cell Lung Cancer and Durable Response to Alectinib: A Case Report |
title_full | ALK Rearrangement in Small-Cell Lung Cancer and Durable Response to Alectinib: A Case Report |
title_fullStr | ALK Rearrangement in Small-Cell Lung Cancer and Durable Response to Alectinib: A Case Report |
title_full_unstemmed | ALK Rearrangement in Small-Cell Lung Cancer and Durable Response to Alectinib: A Case Report |
title_short | ALK Rearrangement in Small-Cell Lung Cancer and Durable Response to Alectinib: A Case Report |
title_sort | alk rearrangement in small-cell lung cancer and durable response to alectinib: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8554320/ https://www.ncbi.nlm.nih.gov/pubmed/34729013 http://dx.doi.org/10.2147/OTT.S323700 |
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