Targeted therapies for unresectable stage III non-small cell lung cancer.
EGFR-mutant
chemo-radiotherapy
concurrent
non-small cell lung cancer (NSCLC)
sequential
Journal
Mediastinum (Hong Kong, China)
ISSN: 2522-6711
Titre abrégé: Mediastinum
Pays: China
ID NLM: 101731833
Informations de publication
Date de publication:
2021
2021
Historique:
received:
25
01
2021
accepted:
01
05
2021
entrez:
4
2
2022
pubmed:
5
2
2022
medline:
5
2
2022
Statut:
epublish
Résumé
Until recently, the standard treatment in unresectable stage III non-small cell lung cancer was concurrent chemoradiotherapy, but often with dismal outcome. The introduction of consolidation treatment with immune checkpoint inhibitors has shifted the treatment landscape and prognosis of these patients. However, patients whose tumors harbors an epidermal growth factor receptor (EGFR) mutation derived less benefit, with an increased risk of immune-related adverse events. Moreover, current data suggested that patients with oncogenic addicted tumors, mainly
Identifiants
pubmed: 35118328
doi: 10.21037/med-21-8
pii: med-05-22
pmc: PMC8794453
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
22Informations de copyright
2021 Mediastinum. All rights reserved.
Déclaration de conflit d'intérêts
Conflicts of Interest: Both authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/med-21-8). The series “Changes in management of mediastinal tumours following the surge of COVID-19 pandemic” was commissioned by the editorial office without any funding or sponsorship. JR reports personal fees and other from MSD, other from BOEHRINGER, other from PFIZER, personal fees and other from OSE IMMUNOTHERAPEUTICS, other from BMS, other from ASTRAZENECA, other from ROCHE, outside the submitted work. LELH reports other from boehringer ingelheim, other from BMS, other from Roche Genentech, other from BMS, grants from Roche Genentech, grants from Boehringer Ingelheim, other from AstraZeneca, personal fees from Quadia, grants from Astra Zeneca, other from Eli Lilly, other from Roche Genentech, other from Pfizer, other from MSD, other from Takeda, non-financial support from AstraZeneca, non-financial support from Novartis, non-financial support from BMS, non-financial support from MSD /Merck, non-financial support from GSK, non-financial support from Takeda, non-financial support from Blueprint Medicines, non-financial support from Roche Genentech, outside the submitted work. The authors have no other conflicts of interest to declare.
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