Tests acupoint electrical stimulation with immunotherapy before surgery for lung cancer
Tests electrical stimulation at the leg point ST36 with PD-1 drugs in lung cancer patients.
Key facts
- Who runs it
- West China Hospital
- Where
- Chengdu, ChinaSee the site
- Trial code
- Registry title
- Zusanli (ST36) Electroacupuncture Treatment for Neoadjuvant Immunotherapy in Non-Small Cell Lung Cancer
- Status
- Recruiting
- People taking part
- 82 people, planned
- Started
- 31 Aug 2026
- Expected to end
- 30 Jun 2028
- Type of study
- Interventional, 2 groups
- Treatments tested
- Acupuncture
- sham acupuncture
- Record updated
- 2 September 2026
Who can take part
AI summary
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for adults with non-small cell lung cancer who are getting chemotherapy plus immunotherapy before surgery. It tests electroacupuncture at the Zusanli point together with a PD-1 inhibitor.
- Age
- 18 to 80 years
- Sex
- All sexes
- Disease stage
- Non-small cell lung cancer confirmed by tissue or cell tests, with at least one measurable tumour or lymph node lesion. ECOG performance status 0-2. Life expectancy over 3 months.
- Earlier treatment
- Must be on standard chemotherapy plus immunotherapy given before surgery (neoadjuvant).
Main reasons for not taking part
- Pregnant women
- People who had an organ transplant
- People with uncontrolled diabetes, severe heart, brain or mental illness, or bleeding or clotting problems
- People with a cardiac pacemaker
- People with skin infection, wounds, ulcers or scars at the ST36 acupoint, or metal allergy or intolerance to electroacupuncture
The registry criteria, word for word
Show all 24 criteriaShow less
Who can take part
- Age ≥18 and ≤80 years at the time of written informed consent, of either sex
- Histologically or cytologically confirmed diagnosis of non-small cell lung cancer (NSCLC) receiving neoadjuvant immunotherapy
- Undergoing standard neoadjuvant treatment with chemotherapy plus immunotherapy
- ECOG performance status score of 0-2
- Life expectancy >3 months
- At least one measurable target lesion per RECIST 1.1 criteria:
- Tumor lesions with a long axis ≥10 mm on CT scan (slice thickness ≤5 mm)
- Lymph node lesions with a short axis ≥10 mm on CT scan
- Previously irradiated or locally treated lesions may be designated as target lesions if documented tumor progression post-treatment
- Adequate major organ function within 14 days prior to randomization, defined by the following laboratory parameters without blood transfusions, growth factors, albumin, or blood products:
- Hematological tests: Hemoglobin ≥80 g/L; Absolute neutrophil count >1.5×10⁹/L; Platelet count ≥90×10⁹/L
- Biochemical tests: Total bilirubin ≤1.5×ULN (upper limit of normal); ALT/AST ≤2.5×ULN; Serum creatinine ≤1.5×ULN or creatinine clearance ≥50 mL/min (Cockcroft-Gault formula)
- Coagulation tests: Prothrombin time (PT) and INR ≤1.5×ULN (unless on warfarin anticoagulation)
- Cardiac evaluation: Left ventricular ejection fraction (LVEF) ≥50% by Doppler echocardiography
- Voluntary participation with signed informed consent, good compliance, and willingness of the patient and their family to cooperate with survival follow-up
Who cannot take part
- Post-organ transplant patients
- Patients with uncontrolled diabetes mellitus, severe cardiac, central nervous system, psychiatric disorders, or coagulopathy
- Patients with implanted cardiac pacemakers
- Patients with bleeding disorders
- Patients with a history of severe allergies or anaphylaxis
- Patients with skin infections, lesions, ulcers, or scars at the ST36 (Zusanli) acupoint site
- Patients with metal allergy, severe needle phobia, or intolerance to electroacupuncture therapy
- Pregnant participants
- Patients with severe malnutrition
Check if you might fit
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 80 years old?
Where in China
- West China HospitalChengdu, ChinaContact: Nan LinTaking people
About the trial
What the trial wants to find out
This study aims to investigate the potential synergistic effects of acupuncture combined with immune checkpoint inhibitors in cancer therapy. Over the past decade, significant progress in cancer immunotherapy has been driven by breakthroughs in understanding immune checkpoint molecules; however, monotherapy with immune checkpoint inhibitors still faces challenges due to low response rates. As a traditional Chinese medical intervention, acupuncture modulates neuro-immune pathways to achieve remote regulation of organ functions, with particular anti-tumor potential observed at the Zusanli (ST36) acupoint-a site located 2 cm below the knee that can be stimulated via electroacupuncture (EA) to improve gastrointestinal function and alleviate inflammation. Preclinical evidence demonstrates that EA suppresses tumor growth in breast cancer models, reduces levels of pro-inflammatory cytokines such as IL-1β and TNF-α, enhances anti-tumor activity of CD8+ T cells and NK cells, and decreases accumulation of immunosuppressive myeloid-derived suppressor cells (MDSCs). Animal studies show that ST36 EA increases key immunomodulatory factors like serum IFN-γ, IL-2, and IL-17, thereby potentiating the efficacy of anti-tumor drugs. Guided by the traditional TCM principle of "reinforcing healthy qi to consolidate the body's resistance," modern clinical applications of EA combined with specific acupoint regimens (e.g., ST36, Sanyinjiao) have effectively alleviated cancer-related pain, chemotherapy-induced side effects, and fatigue. This study will evaluate the safety and immunosensitization effects of ST36 EA combined with PD-1 inhibitors in non-small cell lung cancer patients, employing 1 mA electroacupuncture for 3 consecutive days to activate immune responses. By leveraging acupuncture-induced immune remodeling, this approach aims to provide a novel integrative medicine strategy to overcome resistance to immunotherapy.
The 2 groups in the trial
- Electroacupuncture groupTreatment being tested
Treatment: Acupuncture
- Sham electroacupuncture groupTreatment being tested
Treatment: sham acupuncture
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- Zusanli (ST36) Electroacupuncture Treatment for Neoadjuvant Immunotherapy in Non-Small Cell Lung Cancer
- Plain-language title
- Tests acupoint electrical stimulation with immunotherapy before surgery for lung cancerGenerated from the registry record. The registry title is the official one.
- AI summary
- From the trial's eligibility criteria. Read by machine on 12 November 2026.
- Fit questions
- Built from NCT07076836, who can take part
- Record updated
- 2 September 2026