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Risk factors and biomarkers of chemotherapy-induced peripheral neuropathy in breast cancer patients undergoing Taxane-based chemotherapy , a prospective observational study

Risk factors and biomarkers of chemotherapy-induced peripheral neuropathy in breast cancer patients undergoing Taxane-based chemotherapy , a prospective observational study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20260502001
Enrollment
204
Registered
2026-05-02
Start date
2025-08-06
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

breast cancer breast cancer , Taxane-based chemotherapy , biomarkers , peripheral neuropathy

Interventions

Breast cancer patients whom received Taxane-based regimen chemotherapy
Prevention
Breast cancer patients

Sponsors

anesthesiology department , faculty of medicine , Chiangmai university
Lead Sponsor
Cardiac Electrophysiology Research and Training Center (CERT)
Collaborator

Eligibility

Sex/Gender
All
Age
20 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Age > 20 years old 2. Breast cancer patients whom received Taxane-based regimen chemotherapy 3. Patients whom received the informed consent to participate this study 4. Ability to communicate and understand the Thai language 5. Ability to cooperate in completing the questionnaire surveys.

Exclusion criteria

Exclusion criteria: 1.Patients with a history of breast cancer recurrence and prior chemotherapy treatment for the initial diagnosis 2.Patients receiving concurrent neurotoxic medications including antiretroviral drug (stavudine, zidovudine), immunosuppressant (tacrolimus, cyclosporine), antimicrobial agent (prolong use metronidazole and linezolid, isoniazid), phenytoin, amiodarone, thalidomide and lenalidomide 3.Patients who have preexisting peripheral neuropathy such as diabetic neuropathy, Uremic neuropathy, vitamin B1,B12 deficiency, Guillain-Barre Syndrome, Idiopathic Peripheral Neuropathy, Post-Herpetic Neuralgia, HIV-Associated Neuropathy 5.Patient refusal 6.Patients with confirmed metastatic disease at the time of recruitment

Design outcomes

Primary

MeasureTime frame
Risk factors of CIPN 1 month after finish Taxane-base chemotherapy the European Organization for Research and Treatment of Cancer CIPN20 (EORTC-CIPN20) and the Common Terminology Criteria for Adverse Events (CTCAE v5.0)

Secondary

MeasureTime frame
Correlation of systemic oxidative stress, inflammatory cytokines, and metabolomic profiles with CIPN development ,Incidence of chemotherapy induced peripheral neuropathy ,Impact of CIPN 1 month after finish Taxane-base chemotherapy oxidative stress level , European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30) , Hospital anxiety and depression scale (HADS) Thai version

Countries

Thailand

Contacts

Public ContactPassakorn Sawaddirak

Chiang Mai University

passakorn.s@cmu.ac.th053935522

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026