Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06877299

Low-Dose Radiation + SBRT + Tislelizumab Plus Platinum-based Chemotherapy in Stage ⅡA-ⅢB Non-small Cell Lung Cancer

Low-Dose Radiation + Stereotactic Body Radiotherapy Followed by Tislelizumab Plus Platinum-based Chemotherapy As Neoadjuvant Therapy in Patients With Resectable StageⅡA-ⅢB Non-small Cell Lung Cancer

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Sichuan University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This phase II study aims to evaluate the efficacy and safety of low-dose radiation + SBRT + Tislelizumab plus platinum-based chemotherapy as neoadjuvant therapy for stage II-III non-small cell lung cancer.

Detailed description

All eligible patients will receive LDRT combined with partial SBRT, followed by PD-1 inhibitors plus platinum-based chemotherapy, initiated within 7 days after completing radiation. PD-1 inhibitors and chemotherapy will be administered at the recommended doses according to the instruction manual every 3 weeks, with 3 cycles planned as neoadjuvant therapy. Surgery will be performed within 4 to 6 weeks (+7 days) after completing the final cycle of immunochemotherapy. Main objective and endpoint: the rate of pathological complete response (pCR) in the resected primary tumor and lymph nodes.

Conditions

Interventions

TypeNameDescription
DRUGLow-Dose Radiation(LDRT) + Stereotactic body radiotherapy (SBRT)Low-Dose Radiation(LDRT) + Stereotactic body radiotherapy (SBRT)

Timeline

Start date
2025-07-04
Primary completion
2027-06-30
Completion
2028-01-01
First posted
2025-03-14
Last updated
2026-01-02

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06877299. Inclusion in this directory is not an endorsement.