Needles vs. cancer: acupuncture may supercharge immunotherapy
NCT ID NCT06461338
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether adding acupuncture to standard immunotherapy and chemotherapy helps people with advanced non-small cell lung cancer. Sixty participants will receive either real or sham acupuncture alongside their first four treatment cycles. The goal is to see if acupuncture can improve how well the cancer responds and extend survival.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2024
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Has a histologically-confirmed or cytologically confirmed diagnosis of stage IIIB or IV NSCLC. 2. PD-L1 TPS\<50% 3. EGFR/ALK wild-type 4. Has not received prior systemic treatment for advanced NSCLC. For patients who received preoperative neoadjuvant chemotherapy or postoperative adjuvant chemotherapy or radical chemoradiotherapy, if the disease progresses occurred one six months after the last treatment, they can be enrolled. Patients who received targeted therapy or immunotherapy can not be enrolled. 5. Has a performance status of 0-2 on the Eastern Cooperative Oncology Group (ECOG) Performance Status. 6. Age≥18 years 7. Has a life expectancy of at least 3 months 8. Has measurable disease 9. Has adequate organ function 10. Voluntarily enrolled into the study, sign the informed consent form and have good compliance Exclusion Criteria: 1. Unable to complete baseline assessments 2. Expected to receive radiotherapy within the next 4 cycles 3. With a combination of serious primary diseases of the heart, cerebrovascular, hepatic, renal, and hematopoietic systems 4. With dementia, neurological disorders, mental retardation, or language impairment, and pregnant or breastfeeding women 5. Combined autoimmune diseases, hematologic disorders, or long-term use of hormones or immunosuppressive drugs 6. Combined with a primary tumor from other sites 7. Had participated in any other clinical trial within the prior 3 months 8. Has known history of Human Immunodeficiency Virus (HIV) or solid organ transplantation 9. With legal incapacity 10. With skin breakdown at the acupuncture point that interferes with treatment 11. With a pacemaker 12. With a fear of acupuncture 13. Had received acupuncture treatment within 6 weeks 14. Has known active Hepatitis B 15. Has interstitial lung disease or a history of pneumonitis that required oral of IV glucocorticoids to assist with management 16. Has fever (\>38°C) or clinically significant infection within 1 week prior to enrolment 17. Has active tuberculosis or indications of severe or uncontrolled systemic diseases 18. With a bleeding tendency, and receiving thrombolytics or anticoagulants
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Guangdong Provincial Hospital of Chinese Medicine
Guangzhou, Guangdong, 510120, China
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Jiangsu Provincial Hospital of Chinese Medicine
Nanjing, Jiangsu, 210000, China
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The First Affiliated Hospital of Guangzhou University of Chinese Medicine.
Guangzhou, Guangdong, 510000, China
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Other studies related to the condition(s) this trial covers.
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