RecruitingNCT02610439

Whole Exome Sequencing in Finding Causative Variants in Germline DNA Samples From Patients With Peripheral Neuropathy Receiving Paclitaxel for Breast Cancer

Exploratory Next Generation Sequencing to Identify Causative Variants for Taxane-Induced Peripheral Neuropathy From Breast Cancer Study E5103 Germline DNA Samples


Sponsor

National Cancer Institute (NCI)

Enrollment

575 participants

Start Date

Mar 25, 2014

Study Type

OBSERVATIONAL

Conditions

Summary

This research trial studies whole exome sequencing in finding causative variants in germline deoxyribonucleic acid (DNA) samples from patients with peripheral neuropathy receiving chemotherapy for breast cancer. Studying samples of germline DNA in the laboratory from patients with peripheral neuropathy receiving paclitaxel for breast cancer may help doctors learn more about changes that occur in DNA and identify biomarkers related to peripheral neuropathy.


Eligibility

Inclusion Criteria3

  • European American patients with DNA available and designated case or control
  • African American patients with DNA available and designated case or control status
  • Patients who developed grade 2-4 for African American (AA) and grade 3-4 for European American (EA) peripheral neuropathy during their treatment with paclitaxel and who did not develop peripheral neuropathy following a full course of treatment with paclitaxel

Interventions

OTHERLaboratory Biomarker Analysis

Correlative studies


Locations(1)

Eastern Cooperative Oncology Group

Boston, Massachusetts, United States

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NCT02610439


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