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GWAS Study

Pharmacogenetic Discovery in CALGB (Alliance) 90401 and Mechanistic Validation of a VAC14 Polymorphism that Increases Risk of Docetaxel-Induced Neuropathy.

Hertz DL, Owzar K, Lessans S et al.

27143689 PubMed ID
GWAS Study Type
623 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

HD
Hertz DL
OK
Owzar K
LS
Lessans S
WC
Wing C
JC
Jiang C
KW
Kelly WK
PJ
Patel J
HS
Halabi S
FY
Furukawa Y
WH
Wheeler HE
SA
Sibley AB
LC
Lassiter C
WL
Weisman L
WD
Watson D
KS
Krens SD
MF
Mulkey F
RC
Renn CL
SE
Small EJ
FP
Febbo PG
SI
Shterev I
KD
Kroetz DL
FP
Friedman PN
MJ
Mahoney JF
CM
Carducci MA
KM
Kelley MJ
NY
Nakamura Y
KM
Kubo M
DS
Dorsey SG
DM
Dolan ME
MM
Morris MJ
RM
Ratain MJ
MH
McLeod HL
Chapter II

Abstract

Summary of the research findings

Purpose: Discovery of SNPs that predict a patient's risk of docetaxel-induced neuropathy would enable treatment individualization to maximize efficacy and avoid unnecessary toxicity. The objectives of this analysis were to discover SNPs associated with docetaxel-induced neuropathy and mechanistically validate these associations in preclinical models of drug-induced neuropathy.

50 European ancestry cases with neuropathy, 573 European ancestry cases without neuropathy

Chapter III

Study Statistics

Key metrics and study information

623
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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