Efficacy of second-line targeted agents in kras wild metastatic colorectal cancer patients who received prior targeted agent: First anti-epidermal growth factor receptor or vascular endothelial growth factor in right and left colon?
Adult
Aged
Aged, 80 and over
Bevacizumab
/ administration & dosage
Colorectal Neoplasms
/ drug therapy
Disease-Free Survival
ErbB Receptors
/ antagonists & inhibitors
Female
Humans
Male
Middle Aged
Proto-Oncogene Proteins p21(ras)
/ genetics
Retrospective Studies
Vascular Endothelial Growth Factor A
/ antagonists & inhibitors
Metastatic colon cancer
anti-EGFR
anti-VEGF
Journal
Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners
ISSN: 1477-092X
Titre abrégé: J Oncol Pharm Pract
Pays: England
ID NLM: 9511372
Informations de publication
Date de publication:
Jun 2020
Jun 2020
Historique:
pubmed:
27
6
2019
medline:
29
9
2020
entrez:
27
6
2019
Statut:
ppublish
Résumé
We aimed to investigate the impact of first biological agents on second-line biological agents in kras wild-type metastatic colon patients in right and left colon. The patients received anti-EGFR compared with anti-VEGF in right and left colon separately according to progression-free survival and overall survival in second line. A total of 84 patients were included in the study. In left colon, progression-free survival and overall survival were 9 and 14 months for anti-EGFR and 9 and 16 months for anti-VEGF in the second line. In right colon, progression-free survival and overall survival were 5 and 9 months for anti-EGFR and 4 and 6 months for anti-VEGF in the second line. Progression-free survival was higher in patients who received bevacizumab first followed by anti-EGFR than reverse sequencing in right colon. Overall survival was similar between two groups.
Identifiants
pubmed: 31238809
doi: 10.1177/1078155219856682
doi:
Substances chimiques
KRAS protein, human
0
Vascular Endothelial Growth Factor A
0
Bevacizumab
2S9ZZM9Q9V
ErbB Receptors
EC 2.7.10.1
Proto-Oncogene Proteins p21(ras)
EC 3.6.5.2
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM