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The overall survival benefit in Chinese ALK(+) NSCLC patients received targeted therapies

BACKGROUND: Anaplastic lymphoma kinase (ALK) gene rearrangement is a series of mutations of non-small cell lung cancer (NSCLC) patients. Since 2011, multiple ALK inhibitors (ALKis) have been developed and launched for targeted therapy. In this study, we sought to investigate different strategies of...

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Autores principales: Tian, Guangming, Zhao, Xinliang, Nie, Jun, Dai, Ling, Hu, Weiheng, Zhang, Jie, Chen, Xiaoling, Han, Jindi, Ma, Xiangjuan, Wu, Di, Han, Sen, Long, Jieran, Wang, Yang, Zhang, Ziran, Fang, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9264051/
https://www.ncbi.nlm.nih.gov/pubmed/35813748
http://dx.doi.org/10.21037/jtd-22-622
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author Tian, Guangming
Zhao, Xinliang
Nie, Jun
Dai, Ling
Hu, Weiheng
Zhang, Jie
Chen, Xiaoling
Han, Jindi
Ma, Xiangjuan
Wu, Di
Han, Sen
Long, Jieran
Wang, Yang
Zhang, Ziran
Fang, Jian
author_facet Tian, Guangming
Zhao, Xinliang
Nie, Jun
Dai, Ling
Hu, Weiheng
Zhang, Jie
Chen, Xiaoling
Han, Jindi
Ma, Xiangjuan
Wu, Di
Han, Sen
Long, Jieran
Wang, Yang
Zhang, Ziran
Fang, Jian
author_sort Tian, Guangming
collection PubMed
description BACKGROUND: Anaplastic lymphoma kinase (ALK) gene rearrangement is a series of mutations of non-small cell lung cancer (NSCLC) patients. Since 2011, multiple ALK inhibitors (ALKis) have been developed and launched for targeted therapy. In this study, we sought to investigate different strategies of sequential applying the ALKis and their clinical benefits to the overall survival (OS). METHODS: A total of 176 patients with advanced NSCLC (stage IIIB–IV) harboring the ALK rearrangement were included in this cohort study. They were diagnosed between February 1, 2012 and November 19, 2019 at Peking University Cancer Hospital. Clinical characters were reviewed from patients’ records. Strategies of drugs, progression-free survival (PFS) and OS were collected during the follow-ups. The Kaplan-Meier method and multivariate Cox proportional-hazard analysis were used to conduct the analyses survival and to examine the relationship between the variables and OS. RESULTS: A significantly longer OS was observed either in patients treated with crizotinib [N=106, median OS (mOS): 32.9 months] or in patients treated with a next-generation ALKi [N=34, mOS: not reached (NR)] as the initial ALKi, compared with patients treated with conventional chemotherapy but no ALKi (N=36, mOS: 10.3 months, P<0.001). After disease progression with initial crizotinib, patients who received no ALKi had shorter OS than those who received only crizotinib beyond progressive disease (CBPD) (mOS: 9.7 vs. 20.3 months; P=0.015), only subsequent next-generation ALKis (mOS: 9.7 vs. 41.1 months; P<0.001), and CBPD followed with subsequent next-generation ALKis (mOS: 9.7 months vs. NR; P<0.001). Patients treated with 2 types of ALKi had better survival than those treated with 1 ALKi (mOS: 45.8 vs. 21.3 months, P=0.003), but no such survival benefit was observed in patients treated with ≥3 ALKis (P=0.366). CONCLUSIONS: ALKis have been shown to be clinically effective in treating NSCLC patients with ALK rearrangements. In the case of disease progression with crizotinib, either of CBPD or sequential other ALKis can extend patients’ OS. The sequential application of multiple ALKis was found to be better than it of single ALKi in prolonging OS. However, the question of which inhibitor to select as the initial inhibitor needs to be examined further in future studies.
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spelling pubmed-92640512022-07-09 The overall survival benefit in Chinese ALK(+) NSCLC patients received targeted therapies Tian, Guangming Zhao, Xinliang Nie, Jun Dai, Ling Hu, Weiheng Zhang, Jie Chen, Xiaoling Han, Jindi Ma, Xiangjuan Wu, Di Han, Sen Long, Jieran Wang, Yang Zhang, Ziran Fang, Jian J Thorac Dis Original Article BACKGROUND: Anaplastic lymphoma kinase (ALK) gene rearrangement is a series of mutations of non-small cell lung cancer (NSCLC) patients. Since 2011, multiple ALK inhibitors (ALKis) have been developed and launched for targeted therapy. In this study, we sought to investigate different strategies of sequential applying the ALKis and their clinical benefits to the overall survival (OS). METHODS: A total of 176 patients with advanced NSCLC (stage IIIB–IV) harboring the ALK rearrangement were included in this cohort study. They were diagnosed between February 1, 2012 and November 19, 2019 at Peking University Cancer Hospital. Clinical characters were reviewed from patients’ records. Strategies of drugs, progression-free survival (PFS) and OS were collected during the follow-ups. The Kaplan-Meier method and multivariate Cox proportional-hazard analysis were used to conduct the analyses survival and to examine the relationship between the variables and OS. RESULTS: A significantly longer OS was observed either in patients treated with crizotinib [N=106, median OS (mOS): 32.9 months] or in patients treated with a next-generation ALKi [N=34, mOS: not reached (NR)] as the initial ALKi, compared with patients treated with conventional chemotherapy but no ALKi (N=36, mOS: 10.3 months, P<0.001). After disease progression with initial crizotinib, patients who received no ALKi had shorter OS than those who received only crizotinib beyond progressive disease (CBPD) (mOS: 9.7 vs. 20.3 months; P=0.015), only subsequent next-generation ALKis (mOS: 9.7 vs. 41.1 months; P<0.001), and CBPD followed with subsequent next-generation ALKis (mOS: 9.7 months vs. NR; P<0.001). Patients treated with 2 types of ALKi had better survival than those treated with 1 ALKi (mOS: 45.8 vs. 21.3 months, P=0.003), but no such survival benefit was observed in patients treated with ≥3 ALKis (P=0.366). CONCLUSIONS: ALKis have been shown to be clinically effective in treating NSCLC patients with ALK rearrangements. In the case of disease progression with crizotinib, either of CBPD or sequential other ALKis can extend patients’ OS. The sequential application of multiple ALKis was found to be better than it of single ALKi in prolonging OS. However, the question of which inhibitor to select as the initial inhibitor needs to be examined further in future studies. AME Publishing Company 2022-06 /pmc/articles/PMC9264051/ /pubmed/35813748 http://dx.doi.org/10.21037/jtd-22-622 Text en 2022 Journal of Thoracic Disease. 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 Original Article
Tian, Guangming
Zhao, Xinliang
Nie, Jun
Dai, Ling
Hu, Weiheng
Zhang, Jie
Chen, Xiaoling
Han, Jindi
Ma, Xiangjuan
Wu, Di
Han, Sen
Long, Jieran
Wang, Yang
Zhang, Ziran
Fang, Jian
The overall survival benefit in Chinese ALK(+) NSCLC patients received targeted therapies
title The overall survival benefit in Chinese ALK(+) NSCLC patients received targeted therapies
title_full The overall survival benefit in Chinese ALK(+) NSCLC patients received targeted therapies
title_fullStr The overall survival benefit in Chinese ALK(+) NSCLC patients received targeted therapies
title_full_unstemmed The overall survival benefit in Chinese ALK(+) NSCLC patients received targeted therapies
title_short The overall survival benefit in Chinese ALK(+) NSCLC patients received targeted therapies
title_sort overall survival benefit in chinese alk(+) nsclc patients received targeted therapies
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9264051/
https://www.ncbi.nlm.nih.gov/pubmed/35813748
http://dx.doi.org/10.21037/jtd-22-622
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