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GWAS Study

Identification of novel germline polymorphisms governing capecitabine sensitivity.

O'Donnell PH, Stark AL, Gamazon ER et al.

22864933 PubMed ID
GWAS Study Type
503 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

OP
O'Donnell PH
SA
Stark AL
GE
Gamazon ER
WH
Wheeler HE
MB
McIlwee BE
GL
Gorsic L
IH
Im HK
HR
Huang RS
CN
Cox NJ
DM
Dolan ME
Chapter II

Abstract

Summary of the research findings

Capecitabine, an oral 5-fluorouracil (5-FU) prodrug, is widely used in the treatment of breast, colorectal, and gastric cancers. To guide the selection of patients with potentially the greatest benefit of experiencing antitumor efficacy, or, alternatively, of developing toxicities, identifying genomic predictors of capecitabine sensitivity could permit its more informed use.

Up to 84 East Asian ancestry lymphoblastoid cell lines, up to 164 European ancestry lymphoblastoid cell lines, up to 173 African ancestry lymphoblastoid cell lines, up to 82 African American lymphoblastoid cell lines

Chapter III

Study Statistics

Key metrics and study information

503
Total Participants
GWAS
Study Type
No
Replicated
Sub-Saharan African, East Asian, European, African American or Afro-Caribbean
Ancestry
Nigeria, Niger, China, Japan, U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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