Feasibility and Challenges for Sequential Treatments in ALK-Rearranged Non-Small-Cell Lung Cancer.
ALK-rearranged non-small-cell lung cancer
chemotherapy
overall survival
sequential therapies
tyrosine kinase inhibitors
Journal
Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867
Informations de publication
Date de publication:
2021
2021
Historique:
received:
21
02
2021
accepted:
25
03
2021
entrez:
7
5
2021
pubmed:
8
5
2021
medline:
8
5
2021
Statut:
epublish
Résumé
Anaplastic lymphoma kinase-rearranged non-small-cell lung cancer (ALK We retrospectively analyzed the flow of 145 consecutive TKI-treated ALK At the time of analysis, 70/144 (49%) evaluable patients were still alive. Attrition rates related to targeted treatments were approximately 25-30% and similar for administration of a second-generation (2G) ALK inhibitor (22%, 17/79) or any subsequent systemic therapy (27%, 27/96) after crizotinib, and for the administration of lorlatinib (27%, 6/22) or any subsequent systemic therapy (25%, 15/61) after any 2G TKI. The rate of chemotherapy implementation was 67% (62/93). Both administration of additional TKI (median overall survival [mOS] 59 Despite absence of regulatory obstacles and no requirement for specific acquired mutations, 25-30% of ALK
Sections du résumé
BACKGROUND
BACKGROUND
Anaplastic lymphoma kinase-rearranged non-small-cell lung cancer (ALK
METHODS
METHODS
We retrospectively analyzed the flow of 145 consecutive TKI-treated ALK
RESULTS
RESULTS
At the time of analysis, 70/144 (49%) evaluable patients were still alive. Attrition rates related to targeted treatments were approximately 25-30% and similar for administration of a second-generation (2G) ALK inhibitor (22%, 17/79) or any subsequent systemic therapy (27%, 27/96) after crizotinib, and for the administration of lorlatinib (27%, 6/22) or any subsequent systemic therapy (25%, 15/61) after any 2G TKI. The rate of chemotherapy implementation was 67% (62/93). Both administration of additional TKI (median overall survival [mOS] 59
CONCLUSIONS
CONCLUSIONS
Despite absence of regulatory obstacles and no requirement for specific acquired mutations, 25-30% of ALK
Identifiants
pubmed: 33959513
doi: 10.3389/fonc.2021.670483
pmc: PMC8096170
doi:
Types de publication
Journal Article
Langues
eng
Pagination
670483Informations de copyright
Copyright © 2021 Elsayed, Bozorgmehr, Kazdal, Volckmar, Sültmann, Fischer, Kriegsmann, Stenzinger, Thomas and Christopoulos.
Déclaration de conflit d'intérêts
FB: research funding from BMS and travel grants from BMS and MSD. DK: advisory board and speaker’s honoraria from AstraZeneca, BMS, Pfizer. HS: advisory board and speaker’s honoraria from Roche. JF: advisory board honoraria from Boehringer, Roche, Celgene and AstraZeneca. AS: advisory board honoraria from BMS, AstraZeneca, ThermoFisher, Novartis, speaker’s honoraria from BMS, Illumina, AstraZeneca, Novartis, ThermoFisher, MSD, Roche, and research funding from Chugai. MT: advisory board honoraria from Novartis, Lilly, BMS, MSD, Roche, Celgene, Takeda, AbbVie, Boehringer, speaker’s honoraria from Lilly, MSD, Takeda, research funding from AstraZeneca, BMS, Celgene, Novartis, Roche and travel grants from BMS, MSD, Novartis, Boehringer. PC: research funding from AstraZeneca, Novartis, Roche, Takeda, and advisory board/lecture fees from AstraZeneca, Boehringer Ingelheim, Chugai, Novartis, Pfizer, Roche, Takeda. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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