Randomized sham-controlled pilot trial of weekly electro-acupuncture for the prevention of taxane-induced peripheral neuropathy in women with early stage breast cancer

被引:0
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作者
Heather Greenlee
Katherine D. Crew
Jillian Capodice
Danielle Awad
Donna Buono
Zaixing Shi
Anne Jeffres
Sharon Wyse
Wendy Whitman
Meghna S. Trivedi
Kevin Kalinsky
Dawn L. Hershman
机构
[1] Columbia University,Mailman School of Public Health
[2] Columbia University,Herbert Irving Comprehensive Cancer Center
[3] Columbia University,College of Physicians and Surgeons
[4] Mount Sinai School of Medicine,undefined
[5] Columbia University,undefined
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关键词
Acupuncture; Electro-acupuncture; Breast cancer; Chemotherapy-induced peripheral neuropathy; Taxane;
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摘要
To investigate the effect of electro-acupuncture (EA) as a non-pharmacological intervention to prevent or reduce chemotherapy-induced peripheral neuropathy (CIPN) in breast cancer patients undergoing chemotherapy of taxane. Women with stage I-III breast cancer scheduled to receive taxane therapy were randomized to receive a standardized protocol of 12 true or sham EA (SEA) weekly treatments concurrent with taxane treatment. Subjects completed the Brief Pain Inventory-Short Form (BPI-SF), Functional Assessment of Cancer Therapy-Taxane neurotoxicity subscale (FACT-NTX), and other assessments at baseline and weeks 6, 12, and 16. A total of 180 subjects were screened, 63 enrolled and 48 completed week 16 assessments. Mean age was 50 with 25 % white, 25 % black, and 43 % Hispanic; 52 % had no prior chemotherapy. At week 12, both groups reported an increase in mean BPI-SF worst pain score, but no mean differences were found between groups (SEA 2.8 vs. EA 2.6, P = .86). By week 16, the SEA group returned to baseline, while the EA group continued to worsen (SEA 1.7 vs. EA 3.4, P = .03). The increase in BPI-SF worst pain score was 1.62 points higher in the EA group than in the SEA group at week 16 (P = .04). In a randomized, sham-controlled trial of EA for prevention of taxane-induced CIPN, there were no differences in pain or neuropathy between groups at week 12. Of concern, subjects on EA had a slower recovery than SEA subjects. Future studies should focus on EA for treatment as opposed to prevention of CIPN.
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页码:453 / 464
页数:11
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