Clinical trial · Interventional
Acupuncture Combined With PD-1/PD-L1 Inhibitors for Advanced Lung Cancer
Effectiveness of Acupuncture Combined With PD-1/PD-L1 Inhibitors for Advanced Lung Cancer：A Randomized Controlled Clinical Study
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This study will be an evaluation of the efficacy and safety of acupuncture to enhance the response rate of immunotherapy in advanced lung cancer. The main questions it aims to answer are 1. Does acupuncture heighten the response rate of immunotherapy in advanced lung cancer? 2. Does acupuncture heighten the safety of immunotherapy in advanced lung cancer? Researchers will compare acupuncture to sham acupuncture to see if acupuncture could enhance the response rate of immunotherapy in advanced lung cancer. Both groups will receive a standard anti-tumor Western medical treatment regimen (PD-1/PD-L1 inhibitor combined with chemotherapy), and the experimental and control groups will be treated with 4 cycles of acupuncture or sham-acupuncture on top of the anti-tumor treatment regimen, respectively. Patients were followed up every three weeks for the first three months and every three months thereafter to record any disease progression, adverse events, survival or mortality status, and so on.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Lung Cancers | Malignant Lung Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Acupuncture | Device | — | UNRESOLVED |
| Sham Comparator | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Acupuncture
- interventionNames
- Device: Acupuncture
- type
- SHAM_COMPARATOR
- label
- sham acupuncture
- interventionNames
- Device: Sham Comparator
Primary outcomes (1)
- measure
- Objective Response Rate
- timeFrame
- At 0,4,7,10,13 weeks,6,9,12,15,18,21,24 months from randomization, until progression occurred
Secondary outcomes (11)
- measure
- Disease Control Rate
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion criteria: * Age 18-75 years; * ECOG/PS score of grade 0-1 and expected survival ≥ 3 months; * Non-small cell lung cancer AJCC lung cancer staging of stage IIIB-IV, or small cell lung cancer staging of extensive stage; * PD-L1 immunohistochemistry detection of tumor cell positive proportion score (TPS) \<50%; * Non-small cell lung cancer adenocarcinoma patients do not have EGFR-sensitive mutations, ALK fusions, ROS1 fusions, BRAFV600 mutations, NTRK fusions, RET fusions, MET14 skipping mutations, and amplified gene-driven mutations by genetic testing; * Patients with no previous systemic therapy/first-line treatment; * Patients suitable for chemotherapy combined with immunotherapy; * Traditional Chinese Medicine (TCM) diagnosis of Qi Depression; * Having at least 1 measurable tumor lesion (diameter \> 1cm) or lymph node short diameter ≥ 1.5cm; * Sign the informed consent form and voluntarily participate in this study. Exclusion criteria: * Combined with other primary malignant tumors; * Those who have contraindications to immunotherapy after basic assessment of immunotherapy; * Those with autoimmune diseases or those who need long-term treatment with systemic steroids or immunosuppressants; * Those with combined serious and uncontrolled primary diseases of heart, cerebrovascular, liver, kidney, hematopoietic system and so on; * Those with metal allergy or severe fear of needles; * Those who are pregnant or breastfeeding; * Those who are unable to cooperate to complete the assessment due to mental disorder, intellectual or language impairment; * Those with active severe infectious or inflammatory diseases; * Those who have received acupuncture treatment or other clinical trials within 1 month prior to randomization; * In the judgment of the investigator, persons who have a concomitant medical condition that seriously jeopardizes the safety of the participant or interferes with the completion of the study, or who are deemed to have other reasons for not being suitable for enrollment.
References
Publications (0)
Data not yet available