Symptoms: Chemotherapy-Induced Peripheral Neuropathy

被引:35
作者
Schneider, Bryan P. [1 ]
Hershman, Dawn L. [2 ]
Loprinzi, Charles [3 ]
机构
[1] Indiana Univ, Simon Canc Ctr, Med & Med Mol Genet, Indianapolis, IN 46204 USA
[2] Columbia Univ, Herbert Irving Comprehens Canc Ctr, Med & Epidemiol, New York, NY 10168 USA
[3] Div Med Oncol, Breast Canc Res, Rochester, MN USA
来源
IMPROVING OUTCOMES FOR BREAST CANCER SURVIVORS: PERSPECTIVES ON RESEARCH CHALLENGES AND OPPORTUNITIES | 2015年 / 862卷
关键词
Neuropathy; CIPN (Chemotherapy-induced peripheral neuropathy); Taxanes; Breast cancer; Toxicity; Pharmacogenetics; PRO (Patient reported outcomes); TAXANE-CONTAINING REGIMENS; DORSAL-ROOT GANGLIA; DOUBLE-BLIND; PACLITAXEL; MANAGEMENT; ADJUVANT; TRIAL; THERAPY; TAXOL; NEUROTOXICITY;
D O I
10.1007/978-3-319-16366-6_6
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Chemotherapy-induced peripheral neuropathy (CIPN) is a problematic, treatment-induced toxicity that has the potential to impact quality of life and limit the doses of curative intent therapy. This therapy-induced side effect is one of the most troublesome in oncology clinical practices, considering the morbidity, the frequency, and the potential irreversibility of this problem. Patients with breast cancer are particularly impacted by this side effect as multiple agents commonly used for this disease can cause neuropathy. In this chapter, we provide an overview of CIPN, including: clinical predictors, frequency, and its impact on quality of life. Further, we highlight the pathophysiology and review the literature to date for agents designed to prevent or treat CIPN. We also highlight the most important ongoing clinical and translational research questions that hope to help better predict and prevent this toxicity. This includes optimizing the methods of assessment, using host specific factors (Race and genetics) to predict those more likely to experience CIPN, and determining how CIPN might impact clinical decisions toward therapy.
引用
收藏
页码:77 / 87
页数:11
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