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

被引:0
|
作者
Zhi, Wanqing Iris [1 ]
Dreyfus, Nechama [2 ]
Lessing, Alexie [3 ]
Galantino, Marylou [4 ]
Piulson, Lauren [5 ]
Kot, Kevin Liu [6 ]
Li, Susan [5 ]
Bao, Ting [1 ,5 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, Solid Tumor Div, Breast Med Serv, 650 Commack Rd, New York, NY 11725 USA
[2] Cornell Med, Weill Dept Med, New York, NY USA
[3] SUNY Stony Brook, Dept Med, Renaissance Sch Med, Stony Brook, NY 11794 USA
[4] Stockton Univ, Sch Hlth Sci, Dept Med, Galloway, NJ USA
[5] Mem Sloan Kettering Canc Ctr, Dept Med, Integrat Med Serv, 1275 York Ave, New York, NY 10021 USA
[6] Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
来源
ONCOLOGIST | 2023年 / 28卷 / 07期
基金
美国国家卫生研究院;
关键词
breast cancer; paclitaxel; peripheral neuropathy; body mass index; QUALITY-OF-LIFE; BREAST-CANCER; NEOADJUVANT CHEMOTHERAPY; PACLITAXEL; PREVALENCE; DISABILITY; SYMPTOMS; PLATINUM; ADJUVANT; TAXANE;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:604 / 608
页数:5
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