LU Chao, FENG Xukang, SHEN Qiongying, et al. Electroacupuncture with different frequencies for paclitaxel-induced peripheral neuropathy: a randomized controlled trial[J]. Chinese Acupuncture & Moxibustion, 2024, 44(10): 1139-1145.
DOI:
LU Chao, FENG Xukang, SHEN Qiongying, et al. Electroacupuncture with different frequencies for paclitaxel-induced peripheral neuropathy: a randomized controlled trial[J]. Chinese Acupuncture & Moxibustion, 2024, 44(10): 1139-1145.DOI: 10.13703/j.0255-2930.20240123-0001.
Electroacupuncture with different frequencies for paclitaxel-induced peripheral neuropathy: a randomized controlled trial
To observe the clinical efficacy of electroacupuncture (EA) at frequencies of 2 Hz
100 Hz
and 2 Hz/100 Hz for chemotherapy-induced peripheral neuropathy (CIPN).
Methods
2
One hundred and sixty female breast cancer patients with CIPN induced by paclitaxel were randomly divided into a 2 Hz EA group (40 cases
1 case dropped out)
a 100 Hz EA group (40 cases
2 cases dropped out)
a 2 Hz/100 Hz EA group (40 cases
3 cases dropped out)
and a medication group (40 cases
2 cases dropped out). The three EA groups received acupuncture at bilateral Quchi (LI 11)
Waiguan (TE 5)
Hegu (LI 4)
Zusanli (ST 36)
and Yanglingquan (GB 34). Electrodes of the HANS-200E acupoint nerve stimulator were connected to the same side Hegu (LI 4) and Waiguan (TE 5)
and Zusanli (ST 36) and Sanyinjiao (SP 6)
with EA stimulation frequencies of 2 Hz
100 Hz
and 2 Hz/100 Hz
respectively. Each session lasted 30 min
once every other day
three times a week. The medication group received oral mecobalamin tablets
0.5 mg per dose
three times a day. All groups were treated for four weeks. The functional assessment of cancer therapy/gynaecologic oncology group-neurotoxicity (FACT/GOG-Ntx)
peripheral neurotoxicity grading based on the National Cancer Institute-common terminology criteria for adverse events Version 5.0 (NCI-CTCAE V5.0)
and peripheral neuropathy pain visual analogue scale (VAS) scores were observed before and after treatment
and at follow-up after 4 weeks of treatment completion
and clinical efficacy was evaluated after theatment.
Results
2
Compared before treatment
FACT/GOG-Ntx scores in all groups were decreased after treatment and during follow-up (
P
<
0.01). The score reduction between before and after treatment in the three EA groups was greater than the medication group (
P
<
0.01
P
<
0.05)
with the 2 Hz and 2 Hz/100 Hz EA groups showing a greater reduction than the 100 Hz EA group (
P
<
0.05). The reduction of FACT/GOG-Ntx score between before treatment and follow-up in the 2 Hz and 2 Hz/100 Hz EA groups was greater than the medication group (
P
<
0.01). Peripheral neurotoxicity grading in the three EA groups were improved after treatment (
P
<
0.01). Compared before treatment
the peripheral neurotoxicity grading in the 2 Hz and 2 Hz/100 Hz EA groups was improved at follow-up (
P
<
0.01
P
<
0.05). The VAS scores for peripheral neuropathy pain in the three EA groups were decreased after treatment (
P
<
0.01
P
<
0.05). At follow-up
VAS scores in the 2 Hz
2 Hz/100 Hz
and medication groups were decreased (
P
<
0.01
P
<
0.05)
with a greater reduction in the 2 Hz/100 Hz EA group than the medication group after treatment and follow-up (
P
<
0.01
P
<
0.05). The overall effective rates for the 2 Hz
100 Hz
2 Hz/100 Hz
and medication groups were 79.5% (31/39)
68.4% (26/38)
81.1% (30/37)
and 47.4% (18/38)
respectively
with the 2 Hz and 2 Hz/100 Hz groups showing higher effective rates than the medication group (
P
<
0.05).
Conclusion
2
EA is effective in treating paclitaxel-induced CIPN. While there is no overall difference in efficacy among the different frequencies
2 Hz and 2 Hz/100 Hz EA showing potential advantages. For patients with concurrent peripheral neuropathy pain