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Clinical Trials/NCT07034326
NCT07034326RecruitingPhase 2

Observation on the Clinical Efficacy of Electroacupuncture Combined With Immune Checkpoint Inhibitors as Adjuvant Therapy After Surgery for Early-stage Non-small Cell Lung Cancer

Kong Fanming1 site in 1 country405 target enrollmentStarted: January 1, 2025Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 2
Status
Recruiting
Sponsor
Enrollment
405
Locations
1
Primary Endpoint
Disease free survival(DFS)

Study Overview

Brief Summary

Postoperative immunoadjuvant therapy has been proven to significantly reduce the risk of recurrence after resectable NSCLC, and has become a new standard of postoperative adjuvant therapy for stage II-III NSCLC. Immunotherapy faces challenges such as immune resistance, heterogeneity of biomarker expression, and limitation of immune-suitable population. How to reduce the rate of recurrence and metastasis after surgery, enhance the therapeutic effect of immunotherapy, and then prolong the survival period and improve the quality of life, has become an urgent problem facing the current clinical. Based on the standards of evidence-based medicine, this study for the first time carried out a large sample, multi-center, randomized parallel controlled clinical study to obtain high-quality clinical evidence of the effectiveness and safety of electro-acupuncture and Zilongjin tablet synergic treatment, and formed a standard treatment plan of traditional Chinese medicine.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •(1) Non-tumor patients with stage Ⅱ, ⅢA, ⅢB (N2) non-small cell lung cancer diagnosed by pathology or cytology after surgery; (2) driver mutations negative patients; (3) Postoperative adjuvant chemotherapy was received for 1 to 4 cycles;(4)conforms to two qi syndrome of traditional Chinese medicine syndrome differentiation diagnosis of patients; (5) aged 18 to 80 years old; (6) expected lifetime > 6 months; (7) ECOG 0 to 2 points; (8) patients willing to accept this solution treatment, adherence to the good.

Exclusion Criteria

  • •(1) Patients with other malignant tumors in the past or at the same time within 5 years; (2) has a serious heart, liver and kidney damage, or other serious complications; (3) the R1, R2, need after resection, postoperative adjuvant radiotherapy patients; (4) with mental disorders; (5) has a variety of drug allergy, allergic constitution; (6) in pregnancy or lactation women.

Arms & Interventions

Immunotherapy

Active Comparator

Intervention: Immunotherapy (Drug)

Electroacupuncture combined with immunotherapy

Experimental

Intervention: Electroacupuncture combined with immunotherapy (Other)

Zilongjin tablet combined with immunotherapy

Experimental

Intervention: Zilongjin tablet combined with immunotherapy (Drug)

Outcomes

Primary Outcomes

Disease free survival(DFS)

Time Frame: 2year

Time from random start to first recurrence or death.

Secondary Outcomes

  • Overall survival(3,5year)
  • DFS(3year)
  • EORTC QLQ-C30 Scale(0,2,3,6 month)
  • Immune function(0,3 month)
  • Lung cancer TCM syndrome score(0,2,3,6 month)

Investigators

Sponsor
Kong Fanming
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Kong Fanming

Director of Oncology Department

First Teaching Hospital of Tianjin University of Traditional Chinese Medicine

Study Sites (1)

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