Impact of Pain on Symptom Burden in Chemotherapy-Induced Peripheral Neurotoxicity

被引:3
|
作者
Mahfouz, Fawaz Mayez [1 ]
Li, Tiffany [1 ]
Timmins, Hannah C. [1 ]
Horvath, Lisa G. [2 ,3 ,4 ]
Harrison, Michelle [2 ]
Grimison, Peter [2 ,3 ]
Marx, Gavin [5 ]
Goldstein, David [6 ,7 ]
Park, Susanna B. [1 ]
机构
[1] Univ Sydney, Fac Med & Hlth, Sch Med Sci, Brain & Mind Ctr, Camperdown, NSW, Australia
[2] Chris OBrien Lifehouse, Camperdown, NSW, Australia
[3] Univ Sydney, Sydney Med Sch, Camperdown, NSW, Australia
[4] Royal Prince Alfred Hosp, Camperdown, NSW, Australia
[5] Sydney Adventist Hosp, Wahroonga, Australia
[6] UNSW Sydney, Fac Med & Hlth, Prince Wales Clin Sch, Randwick, NSW, Australia
[7] Prince Wales Hosp, Dept Med Oncol, Randwick, NSW, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
QUALITY-OF-LIFE; TOTAL NEUROPATHY SCORE; CANCER SURVIVORS; OUTCOME MEASURES; OXALIPLATIN; QUESTIONNAIRE; DULOXETINE; VALIDITY; HUMANS;
D O I
10.6004/jnccn.2023.7083
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Chemotherapy -induced peripheral neurotoxicity (CIPN) affects the quality of life of cancer survivors. However, the impact of pain on symptom burden remains undefined. This study aimed to de fine differences in the clinical symptom pro file of patients with painful and nonpainful CIPN. Patients and Methods: A total of 579 participants (median age, 59 years [IQR, 19 years]; F=66%) were assessed cross sectionally 6 months posttreatment. CIPN severity was graded using multiple methods, including patient -reported outcome measures, clinically graded scale (NCI-CTCAE), and a neurologic examination score. Participants were classified into subgroups based on patient symptom report, with painful CIPN characterized by the presence of shooting/ burning pain, and nonpainful CIPN characterized by the presence numbness or tingling without shooting/burning pain. Behavioral changes were assessed via structured patient interview regarding symptom impact on sleep, exercise, and treatment -seeking. Results: Among 579 participants, 24% (n=140) reported painful CIPN, 48% (n=280) reported nonpainful CIPN, and 28% (n=159) had no CIPN. Participants with painful CIPN demonstrated higher CIPN severity than those with nonpainful CIPN across multiple measures, including NCI-CTCAE, neurologic grading, and patient report (all P <.05). Participants with painful CIPN were more likely to report that their symptoms affected their ability to exercise ( P =.007), produced sleep impairment, and increased treatment -seeking behavior due to their symptoms (both P <.001) compared with participants with nonpainful CIPN. Conclusions: Overall, participants with painful CIPN reported higher scores across all CIPN severity measures, including behavioral changes. This study underlines the need for accurate identi fication of different CIPN subgroups in hopes of informing better treatment and rehabilitation options for cancer survivors with painful CIPN.
引用
收藏
页码:108 / 116
页数:9
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