Impact of patient‐reported taxane‐induced peripheral neuropathy on dose reductions or worsening quality of life in Black women with breast cancer: Analysis from ECOG‐ACRIN EAZ171
BACKGROUND: Black patients with breast cancer experience higher rates of taxane-induced peripheral neuropathy (TIPN), which may compromise chemotherapy dose delivery and health-related quality of life (HRQOL). Using the prospective ECOG-ACRIN EAZ171 trial, the authors examined whether patient-reported TIPN predicts dose reductions and longer-term declines in HRQOL and physical function. METHODS: EAZ171 enrolled 249 Black patients planned for (neo)adjuvant taxane; 239 with available patient-reported outcome (PRO) data were analyzed. TIPN was assessed during treatment using the Functional Assessment of Cancer Therapy GOG Neurotoxicity scale (FACT-GOG/NTx) (4-item, 11-item, and single items) and PRO-Common Terminology Criteria for Adverse Events numbness/tingling and interference. HRQOL (FACT-G) and physical function (PROMIS PF-10a) were measured through 12 months. Multivariable mixed-effects logistic models evaluated associations between TIPN, taxane dose reduction due to neuropathy, and 12-month HRQOL or physical function decline. RESULTS: All TIPN PROs were associated with dose reduction, with the FACT-GOG/NTx 4-item subscale showing the strongest association (odds ratio [OR], 10.8; 95% CI, 4.5-25.9). Twelve-month PRO data were available for 140 patients (59%). Neuropathy reported during treatment was not associated with reduced HRQOL or physical function at 12 months; however, persistent neuropathy at 12 months was associated with worse HRQOL (OR, 5.05; 95% CI, 1.33-19.17) and physical function (OR, 5.29; 95% CI, 1.57-17.83). CONCLUSIONS: TIPN was common and strongly predicted taxane dose reduction in Black patients. The FACT-GOG/NTx 4-item subscale performed best, supporting its use in future trials. Although early TIPN did not predict long-term functional decline, persistent neuropathy adversely affected HRQOL, underscoring the importance of early identification and supportive care to improve dose delivery and equity in breast cancer outcomes.
Authors
- Guanglong Jiang (ORCID: https://orcid.org/0000-0002-9233-052X)
- Angela M. DeMichele (ORCID: https://orcid.org/0000-0003-1297-4251)
- Antonio C. Wolff (ORCID: https://orcid.org/0000-0003-3734-1063)
- Kathy D. Miller (ORCID: https://orcid.org/0000-0002-7125-883X)
- Lynne I. Wagner (ORCID: https://orcid.org/0000-0001-9685-4796)
- D Cella
- Fei Shen (ORCID: https://orcid.org/0000-0002-5494-4475)
- John D. Peipert
- Bryan P. Schneider
- Tarah J. Ballinger (ORCID: https://orcid.org/0000-0002-6797-2758)
- Fengmin Zhao (ORCID: https://orcid.org/0000-0001-9826-3703)
Institutions
- Northwestern University (US)
- University of North Carolina at Chapel Hill (US)
- Indiana University Health (US)
- Johns Hopkins University (US)
- The Edgbaston Hospital (GB)
- Dana-Farber Cancer Institute (US)
- Sidney Kimmel Comprehensive Cancer Center (US)
- Indiana University Melvin and Bren Simon Comprehensive Cancer Center
- Indiana University – Purdue University Indianapolis (US)
- University of Pennsylvania (US)
- University of Birmingham (GB)
Publication Details
- Journal
- Cancer
- Published
- 2026-05-29
- DOI
- https://doi.org/10.1002/cncr.70466
- Primary Topic
- Cancer Treatment and Pharmacology
- Type
- article
- Field-Weighted Citation Impact
- 0.00