2018
DOI: 10.1016/j.jtho.2018.08.655
|View full text |Cite
|
Sign up to set email alerts
|

P1.01-99 Detecting HER2 Alterations by Next Generation Sequencing (NGS) in Patients with Advanced NSCLC from the United States and China

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2020
2020
2021
2021

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 0 publications
0
2
0
Order By: Relevance
“…The co-occurring genomic spectrum of ERBB2ex20ins in our cohort of Chinese people had an overall strong concordance with the MSKCC cohort from the United States (R 2 = 0.74, p < 0.01). In a retrospective study collated two cohorts of patients with ERBB2 alteration from the MSKCC and Guangdong General Hospital, they also found great consistency with each other in the aspect of the prevalence and baseline clinical parameters of patients possessing ERBB2 mutation (34). These findings, on the one hand, can be supporting evidence for U.S.-China collaborations in clinical trials to accelerate new drug development for this infrequent mutation; on the one hand, highlight the robustness of our results.…”
Section: Discussionmentioning
confidence: 76%
“…The co-occurring genomic spectrum of ERBB2ex20ins in our cohort of Chinese people had an overall strong concordance with the MSKCC cohort from the United States (R 2 = 0.74, p < 0.01). In a retrospective study collated two cohorts of patients with ERBB2 alteration from the MSKCC and Guangdong General Hospital, they also found great consistency with each other in the aspect of the prevalence and baseline clinical parameters of patients possessing ERBB2 mutation (34). These findings, on the one hand, can be supporting evidence for U.S.-China collaborations in clinical trials to accelerate new drug development for this infrequent mutation; on the one hand, highlight the robustness of our results.…”
Section: Discussionmentioning
confidence: 76%
“…However, whether this technique could detect the amplification of HER2 in NSCLC by plasma genotyping had not been discussed previously. Besides dPCR, next-generation sequencing (NGS) is also used to reveal HER2 alterations in NSCLC patients (16). However, compared with NGS, the validity of dPCR, and the feasibility of detecting in blood samples in NSCLC patients are still unclear.…”
Section: Introductionmentioning
confidence: 99%