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Acupuncture for Chronic Radiation-Induced Xerostomia in Head and Neck Cancer: A Multicenter Randomized Clinical Trial.

JAMA network open
January 1, 1970
Lorenzo Cohen et al. (20 authors)
Journal ArticleRandomized Controlled TrialMulticenter StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tHuman StudyClinical
Study Details

Study Goal

The researchers aimed to compare the effectiveness of true acupuncture (TA), sham acupuncture (SA), and standard oral hygiene (SOH) in treating chronic radiation-induced xerostomia in head and neck cancer patients post-radiotherapy.

Results Summary

True acupuncture (TA) significantly improved xerostomia symptoms and quality of life compared to sham acupuncture (SA) and standard oral hygiene (SOH) at weeks 4 and 12, though some differences did not remain statistically significant after multiple comparison adjustments. No significant difference was found between SA and SOH.

Population

Patients with grade 2 or 3 radiation-induced xerostomia 12+ months post-radiotherapy for head and neck cancer, recruited from US community-based cancer centers.

Effective Dosage

TA and SA were administered 2 times per week for 4 weeks, with an additional 4 weeks for minor responders.

Duration

4 weeks (up to 8 weeks for minor responders).

Interactions

None mentioned

Extracted Claims (7)
InterventionDirectionEndpointPopulationDosageImpactClaim #
true acupuncture (TA)
decrease
Xerostomia Questionnaire scores
patients reporting grade 2 or 3 radiation-induced xerostomia 12 months or more postradiotherapy for head and neck cancer
difference, -6.67; 95% CI, -11.08 to -2.27; P = .003
lower Xerostomia Questionnaire scores
#1
true acupuncture (TA)
decrease
Xerostomia Questionnaire scores
patients reporting grade 2 or 3 radiation-induced xerostomia 12 months or more postradiotherapy for head and neck cancer
difference, -4.41; 95% CI, -8.62 to -0.19; P = .04
lower Xerostomia Questionnaire scores
#2
sham acupuncture (SA)
no change
Xerostomia Questionnaire scores
patients reporting grade 2 or 3 radiation-induced xerostomia 12 months or more postradiotherapy for head and neck cancer
no significant difference
no significant difference
#3
true acupuncture (TA)
increase
Functional Assessment of Cancer Therapy-General scores
patients reporting grade 2 or 3 radiation-induced xerostomia 12 months or more postradiotherapy for head and neck cancer
difference, 3.91; 95% CI, 1.43-6.38; P = .002
higher scores
#4
true acupuncture (TA)
increase
Functional Assessment of Cancer Therapy-General scores
patients reporting grade 2 or 3 radiation-induced xerostomia 12 months or more postradiotherapy for head and neck cancer
difference, 3.64; 95% CI, 1.10-6.18; P = .005
higher scores
#5
true acupuncture (TA)
increase
Functional Assessment of Cancer Therapy-General scores
patients reporting grade 2 or 3 radiation-induced xerostomia 12 months or more postradiotherapy for head and neck cancer
difference, 4.61; 95% CI, 1.99-7.23; P = .001
higher scores
#6
true acupuncture (TA)
decrease
chronic radiation-induced xerostomia
patients 1 or more years after the end of radiotherapy for head and neck cancer
-
more effective in treating chronic radiation-induced xerostomia
#7
Abstract

IMPORTANCE: Patients with head and neck cancer who undergo radiotherapy can develop chronic radiation-induced xerostomia. Prior acupuncture studies were single center and rated as having high risk of bias, making it difficult to know the benefits of acupuncture for treating radiation-induced xerostomia. OBJECTIVE: To compare true acupuncture (TA), sham acupuncture (SA), and standard oral hygiene (SOH) for treating radiation-induced xerostomia. DESIGN, SETTING, AND PARTICIPANTS: A randomized, blinded, 3-arm, placebo-controlled trial was conducted between July 29, 2013, and June 9, 2021. Data analysis was performed from March 9, 2022, through May 17, 2023. Patients reporting grade 2 or 3 radiation-induced xerostomia 12 months or more postradiotherapy for head and neck cancer were recruited from community-based cancer centers across the US that were part of the Wake Forest National Cancer Institute Community Oncology Research Program Research Base. Participants had received bilateral radiotherapy with no history of xerostomia. INTERVENTIONS: Participants received SOH and were randomized to TA, SA, or SOH only. Participants in the TA and SA cohorts were treated 2 times per week for 4 weeks. Those experiencing a minor response received another 4 weeks of treatment. MAIN OUTCOMES AND MEASURES: Patient-reported outcomes for xerostomia (Xerostomia Questionnaire, primary outcome) and quality of life (Functional Assessment of Cancer Therapy-General) were collected at baseline, 4 (primary time point), 8, 12, and 26 weeks. All analyses were intention to treat. RESULTS: A total of 258 patients (201 men [77.9%]; mean [SD] age, 65.0 [9.16] years), participated from 33 sites across 13 states. Overall, 86 patients were assigned to each study arm. Mean (SD) years from diagnosis was 4.21 (3.74) years, 67.1% (n = 173) had stage IV disease. At week 4, Xerostomia Questionnaire scores revealed significant between-group differences, with lower Xerostomia Questionnaire scores with TA vs SOH (TA: 50.6; SOH: 57.3; difference, -6.67; 95% CI, -11.08 to -2.27; P = .003), and differences between TA and SA (TA: 50.6; SA: 55.0; difference, -4.41; 95% CI, -8.62 to -0.19; P = .04) yet did not reach statistical significance after adjustment for multiple comparisons. There was no significant difference between SA and SOH. Group differences in Functional Assessment of Cancer Therapy-General scores revealed statistically significant group differences at week 4, with higher scores with TA vs SOH (TA: 101.6; SOH: 97.7; difference, 3.91; 95% CI, 1.43-6.38; P = .002) and at week 12, with higher scores with TA vs SA (TA: 102.1; SA: 98.4; difference, 3.64; 95% CI, 1.10-6.18; P = .005) and TA vs SOH (TA: 102.1; SOH: 97.4; difference, 4.61; 95% CI, 1.99-7.23; P = .001). CONCLUSIONS AND RELEVANCE: The findings of this trial suggest that TA was more effective in treating chronic radiation-induced xerostomia 1 or more years after the end of radiotherapy than SA or SOH. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT02589938.

Medical Subject Headings (MeSH)
HumansXerostomiaMaleHead and Neck NeoplasmsFemaleMiddle AgedAgedAcupuncture TherapyRadiation InjuriesQuality of LifeTreatment OutcomeRadiotherapy
Study Links
Quality Scores
SafetyNot Assessed
Efficacy85/10
Quality90/10
Citation Metrics
Total Citations7
Citations/Year7.0
Relative Citation Ratio3.32
Research Impact Scores
APT Score0.75
Weight Score1.74
Normalized Score0.72
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