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NOT YET RECRUITING
NCT07231575
PHASE2

Neoadjuvant SBRT and Tislelizumab (Immunotherapy) Plus Anlotinib for Resectable EGFR Wild-type NSCLC

Sponsor: Sun Yat-sen University

View on ClinicalTrials.gov

Summary

The neoadjuvant strategy of immunotherapy combined with chemotherapy has been recommended for resectable or potentially resectable tumors without driver-gene alterations.However, the AE of chemotherapy is more than 40%,which bring fear to the patients,especially for those who cannot tolerate or refuse chemotherapy.Several studies indicated that the strategies of chemo-free ,such as the combination of immunotherapy with antiangiogenic therapy or with SBRT, were safe and well tolerated, without increasing adverse reactions. Both of them have a promising efficacy with a manageable toxicity profile in patients with resectable NSCLC. The investigators aim to assess the activity and safety of neoadjuvant SBRT and immunotherapy plus antiangiogenic therapy in patients with resectable NSCLC.

Official title: Preoperative Stereotactic Body Radiotherapy and Tislelizumab (Immunotherapy) Plus Anlotinib for Operable Stage IB to III EGFR Wild-type Non-small Cell Lung Cancer(STATION)

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

39

Start Date

2025-11-10

Completion Date

2032-05-30

Last Updated

2025-11-18

Healthy Volunteers

No

Interventions

RADIATION

SBRT

SBRT 8Gy\*3

DRUG

Immunotherapy

Tislelizumab (immunotherapy) 200mg Q3W

DRUG

antiangiogenesis therapy

Anlotinib 8mg D1-D14 Q3W