Defining aggressive or early progressing nononcogene-addicted non-small-cell lung cancer: a separate disease entity?
Antibodies, Monoclonal
/ therapeutic use
Antibodies, Monoclonal, Humanized
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Bevacizumab
/ therapeutic use
Carcinoma, Non-Small-Cell Lung
/ drug therapy
Disease Progression
Disease-Free Survival
Docetaxel
/ therapeutic use
Humans
Indoles
/ therapeutic use
Lung
/ pathology
Lung Neoplasms
/ drug therapy
Patient Selection
Time Factors
Ramucirumab
aggressive
anti-angiogenic therapy
non-small-cell lung cancer
Journal
Future oncology (London, England)
ISSN: 1744-8301
Titre abrégé: Future Oncol
Pays: England
ID NLM: 101256629
Informations de publication
Date de publication:
Apr 2019
Apr 2019
Historique:
pubmed:
14
2
2019
medline:
20
8
2019
entrez:
14
2
2019
Statut:
ppublish
Résumé
A substantial proportion of patients with nononcogene-addicted non-small-cell lung cancer (NSCLC) has 'aggressive disease', as reflected in short time to progression or lack of disease control with initial platinum-based chemotherapy. Recently, clinical correlates of aggressive disease behavior during first-line therapy have been shown to predict greater benefit from addition of nintedanib to second-line docetaxel in adenocarcinoma NSCLC. Positive predictive effects of aggressive disease have since been reported with other anti-angiogenic agents (ramucirumab and bevacizumab), while such features may negatively impact on outcomes with nivolumab in nonsquamous NSCLC with low PD-L1 expression. Based on a review of the clinical data, we recommend aggressive nonsquamous NSCLC should be defined by progression within <6-9 months of first-line treatment initiation.
Identifiants
pubmed: 30758227
doi: 10.2217/fon-2018-0948
doi:
Substances chimiques
Antibodies, Monoclonal
0
Antibodies, Monoclonal, Humanized
0
Indoles
0
Docetaxel
15H5577CQD
Bevacizumab
2S9ZZM9Q9V
nintedanib
G6HRD2P839
Types de publication
Journal Article
Review
Langues
eng