期刊
SUPPORTIVE CARE IN CANCER
卷 27, 期 7, 页码 2471-2478出版社
SPRINGER
DOI: 10.1007/s00520-018-4531-4
关键词
Symptom reduction; Neuropathy; Chemotherapy-induced peripheral neuropathy; Exercise intervention; Physical activity
Chemotherapy-induced peripheral neuropathy (CIPN) is a prevalent and clinically relevant side effect of chemotherapy. The symptoms diminish patients' quality of life and represent a decisive limiting factor for medical therapy. To date, effective treatment options are lacking. Specific exercise interventions have proven promising to target relevant symptoms. We conducted a prospective, four-armed, randomized, controlled trial, to evaluate the effects of sensorimotor training (SMT) and whole-body vibration training (WBV) on patients with CIPN. Participants (N=40) were randomized to either one of two intervention groups (SMT N=10 or WBV N=10) or oncological control group (N=10) and matched by gender and age with a healthy control (N=10). The intervention groups exercised twice a week for 6weeks. Primary endpoint was the reduction of CIPN-related symptoms (improve peripheral deep sensitivity, Achilles tendon reflex (ASR) and patellar tendon reflex (PSR), light-touch perception, sense of position, and lower leg strength). Secondary endpoints were nerve conduction velocity and amplitude, balance control, quality of life, and CIPN-related pain. Patients exercising improved sensory and associated motor symptoms. Significant intergroup differences were found for the tendon reflexes (ASR P=.017 and PSR P=.020), peripheral deep sensitivity (P=.010), and pain (P=.043). Furthermore, tendencies were found regarding the subjective improvement of symptoms (P=.075) and two subscales of the EORTC-QLQ-C30 questionnaire: pain (P=.054) and dyspnea (P=.054). The results for the SMT group were superior regarding the tendon reflexes, and a tendency regarding the subjective report of symptoms, while WBV was superior regarding pain. SMT and WBV behold a large potential to reduce CIPN-related symptoms and can be considered feasible and safe for patients with CIPN (compliance 97.5%, no adverse events).Registration: DRKS00013027
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