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
| Type | Name | Description |
|---|---|---|
| DRUG | Low-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.