Menu
GWAS Study

Clinical evaluation of germline polymorphisms associated with capecitabine toxicity in breast cancer: TBCRC-015.

O'Donnell PH, Trubetskoy V, Nurhussein-Patterson A et al.

32378051 PubMed ID
GWAS Study Type
147 Participants
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

OP
O'Donnell PH
TV
Trubetskoy V
NA
Nurhussein-Patterson A
HJ
Hall JP
NA
Nath A
HD
Huo D
FG
Fleming GF
IJ
Ingle JN
AV
Abramson VG
MP
Morrow PK
SA
Storniolo AM
FA
Forero A
VP
Van Poznak C
LM
Liu MC
CJ
Chang JC
MD
Merkel DE
PJ
Peppercorn JM
RH
Rugo HS
DE
Dees EC
HO
Hahn OM
HP
Hoffman PC
RG
Rosner GL
HR
Huang RS
RM
Ratain MJ
CN
Cox N
OO
Olopade OI
WA
Wolff AC
DM
Dolan ME
NR
Nanda R
Chapter II

Abstract

Summary of the research findings

Purpose: Capecitabine is important in breast cancer treatment but causes diarrhea and hand-foot syndrome (HFS), affecting adherence and quality of life. We sought to identify pharmacogenomic predictors of capecitabine toxicity using a novel monitoring tool.

147 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

147
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.