Patient Characteristics Associated With Chemotherapy-Induced Peripheral Neuropathy Severity in a Phase II Clinical Trial: A Retrospective Analysis

Author:

Zhi Wanqing Iris1ORCID,Dreyfus Nechama2,Lessing Alexie3,Galantino Marylou4,Piulson Lauren5,Kot Kevin Liu6,Li Susan5,Bao Ting15ORCID

Affiliation:

1. Breast Medicine Service, Solid Tumor Division, Department of Medicine, Memorial Sloan Kettering Cancer Center , New York, NY , USA

2. Weill Department of Medicine Cornell Medicine , New York, NY , USA

3. Department of Medicine, Renaissance School of Medicine, Stony Brook University , Stony Brook, NY , USA

4. Department of Medicine, School of Health Sciences, Stockton University , Galloway, NJ , USA

5. Integrative Medicine Service, Department of Medicine, Memorial Sloan Kettering Cancer Center , New York, NY , USA

6. Department of Medicine, Albert Einstein College of Medicine , Bronx, New York, NY , USA

Abstract

Abstract Introduction Chemotherapy-induced peripheral neuropathy (CIPN) can lead to chemotherapy dose reduction, delay, and discontinuation, and has limited effective prevention strategies. Our study aimed to identify patient characteristics associated with CIPN severity during weekly paclitaxel chemotherapy in people with early-stage breast cancer. Methods We retrospectively collected baseline data including participants’ age, gender, race, body mass index (BMI), hemoglobin (regular and A1C), thyroid stimulating hormone, Vitamins (B6, B12, and D), anxiety, and depression up to 4 months prior to their first paclitaxel treatment. We also collected CIPN severity by Common Terminology Criteria for Adverse Events (CTCAE) after chemotherapy, chemotherapy relative dose density (RDI), disease recurrence, and mortality rate at the time of the analysis. Logistic regression was used for statistical analysis. Results We extracted 105 participants’ baseline characteristics from electronic medical records. Baseline BMI was associated with CIPN severity (Odds Ratio [OR] 1.08; 95% CI, 1.01-1.16, P = .024). No significant correlations were observed in other covariates. At median follow-up (61 months), there were 12 (9.5%) breast cancer recurrences and six (5.7%) breast cancer-related deaths. Higher chemotherapy RDI was associated with improved disease-free survival (DFS, OR 1.025; 95% CI, 1.00-1.05; P = .028). Conclusions and Relevance Baseline BMI may be a risk factor for CIPN and suboptimal chemotherapy delivery due to CIPN may negatively impact disease-free survival in patients with breast cancer. Further study is warranted to identify mitigating lifestyle factors to reduce incidences of CIPN during breast cancer treatment.

Funder

National Institutes of Health

National Cancer Institute

Memorial Sloan-Kettering Cancer Center

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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