dc.contributor.author |
Guan, Xiaoxiang |
|
dc.contributor.author |
Yin, Ming |
|
dc.contributor.author |
Wei, Qingyi |
|
dc.contributor.author |
Zhao, Hui |
|
dc.contributor.author |
Liu, Zhensheng |
|
dc.contributor.author |
Wang, Li-E |
|
dc.contributor.author |
Yuan, Xianglin |
|
dc.contributor.author |
O'Reilly, Michael S |
|
dc.contributor.author |
Komaki, Ritsuko |
|
dc.contributor.author |
Liao, Zhongxing |
|
dc.date.accessioned |
2019-02-01T15:24:57Z |
|
dc.date.available |
2019-02-01T15:24:57Z |
|
dc.date.issued |
2010-08-16 |
|
dc.identifier |
1471-2407-10-431 |
|
dc.identifier.issn |
1471-2407 |
|
dc.identifier.issn |
1471-2407 |
|
dc.identifier.uri |
https://hdl.handle.net/10161/18014 |
|
dc.description.abstract |
Vascular endothelial growth factor (VEGF) is a major mediator of angiogenesis involving
in carcinogenesis, including lung cancer. We hypothesized that VEGF polymorphisms
may affect survival outcomes among locally advanced non-small cell lung cancer (LA-NSCLC)
patients.We genotyped three potentially functional VEGF variants [-460 T > C (rs833061),
-634 G > C (rs2010963), and +936 C > T (rs3025039)] and estimated haplotypes in 124
Caucasian patients with LA-NSCLC treated with definitive radiotherapy. We used Kaplan-Meier
log-rank tests, and Cox proportional hazard models to evaluate the association between
VEGF variants and overall survival (OS).Gender, Karnofsky's performance scores (KPS)
and clinical stage seemed to influence the OS. The variant C genotypes were independently
associated with significantly improved OS (CT+CC vs. TT: adjusted hazard ratio [HR]
= 0.58; 95% confidence interval [CI] = 0.37-0.92, P = 0.022), compared with the VEGF
-460 TT genotype.Our study suggests that VEGF -460 C genotypes may be associated with
a better survival of LA-NSCLC patients after chemoradiotherapy. Large studies are
needed to confirm our findings.
|
|
dc.language |
eng |
|
dc.publisher |
Springer Science and Business Media LLC |
|
dc.relation.ispartof |
BMC cancer |
|
dc.relation.isversionof |
10.1186/1471-2407-10-431 |
|
dc.subject |
Humans |
|
dc.subject |
Adenocarcinoma |
|
dc.subject |
Carcinoma, Large Cell |
|
dc.subject |
Carcinoma, Non-Small-Cell Lung |
|
dc.subject |
Carcinoma, Squamous Cell |
|
dc.subject |
Lung Neoplasms |
|
dc.subject |
Vascular Endothelial Growth Factor A |
|
dc.subject |
Antineoplastic Combined Chemotherapy Protocols |
|
dc.subject |
Neoplasm Staging |
|
dc.subject |
Treatment Outcome |
|
dc.subject |
Combined Modality Therapy |
|
dc.subject |
Radiotherapy Dosage |
|
dc.subject |
Survival Rate |
|
dc.subject |
Follow-Up Studies |
|
dc.subject |
Genotype |
|
dc.subject |
Haplotypes |
|
dc.subject |
Polymorphism, Single Nucleotide |
|
dc.subject |
Adult |
|
dc.subject |
Aged |
|
dc.subject |
Aged, 80 and over |
|
dc.subject |
Middle Aged |
|
dc.subject |
Female |
|
dc.subject |
Male |
|
dc.title |
Genotypes and haplotypes of the VEGF gene and survival in locally advanced non-small
cell lung cancer patients treated with chemoradiotherapy.
|
|
dc.type |
Journal article |
|
duke.contributor.id |
Wei, Qingyi|0632334 |
|
duke.contributor.id |
Liu, Zhensheng|0633329 |
|
dc.date.updated |
2019-02-01T15:24:55Z |
|
pubs.begin-page |
431 |
|
pubs.issue |
1 |
|
pubs.organisational-group |
Staff |
|
pubs.organisational-group |
Duke |
|
pubs.organisational-group |
School of Medicine |
|
pubs.organisational-group |
Duke Cancer Institute |
|
pubs.organisational-group |
Institutes and Centers |
|
pubs.organisational-group |
Population Health Sciences |
|
pubs.organisational-group |
Basic Science Departments |
|
pubs.organisational-group |
Medicine, Medical Oncology |
|
pubs.organisational-group |
Medicine |
|
pubs.organisational-group |
Clinical Science Departments |
|
pubs.publication-status |
Published |
|
pubs.volume |
10 |
|
duke.contributor.orcid |
Wei, Qingyi|0000-0002-3845-9445|0000-0003-4115-4439 |
|