2018
DOI: 10.1200/po.18.00194
|View full text |Cite
|
Sign up to set email alerts
|

Characterization of the Epidermal Growth Factor Receptor T790M Mutation in Colorectal Cancer

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

1
1
0

Year Published

2020
2020
2023
2023

Publication Types

Select...
2

Relationship

1
1

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 11 publications
1
1
0
Order By: Relevance
“…No significant adverse events were seen. Finally, as previously described, 16-159 PDX was sensitive to irinotecan and resistant to oxaliplatin [14]. Together, these studies indicated that our screening and validation platform enabled rapid analysis of sensitivity and resistance to standard-of-care agents.…”
Section: High-throughput Drug Screening In Vitro and In Vivo Validatisupporting
confidence: 69%
“…No significant adverse events were seen. Finally, as previously described, 16-159 PDX was sensitive to irinotecan and resistant to oxaliplatin [14]. Together, these studies indicated that our screening and validation platform enabled rapid analysis of sensitivity and resistance to standard-of-care agents.…”
Section: High-throughput Drug Screening In Vitro and In Vivo Validatisupporting
confidence: 69%
“…While both approaches lead to the inhibition of EGFR autophosphorylation, TKI efficacy is restricted to cancers that carry EGFR mutations in the TK domain (exons 18-21). Still, these mutations are rarely seen in colorectal cancer[ 8 ]. Available TKIs against EGFR TK mutations are approved for non-small cell lung cancer and include first-generation agents gefitinib and erlotinib and second-generation agents afatinib and dacomitinib[ 9 ].…”
Section: Discussionmentioning
confidence: 99%