Chemotherapy Plus Immunotherapy Combined With SBRT as Neoadjuvant Therapy for Patients With Resectable NSCLC

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorFirst People's Hospital of Hangzhou

About this trial

In this study, patients with EGFR/ALK wild-type, resectable locally advanced NSCLC are expected to receive 1 cycle of chemoimmunotherapy as neoadjuvant therapy, followed by SBRT to the primary lung lesion, and chemoimmunotherapy for 2 cycles. Surgical treatment will be given within 4-6 weeks after the last cycle of chemoimmunotherapy, then immunotherapy maintenance for 1 year.

Eligibility criteria

Qualifiers

Histologically or pathologically confirmed, newly diagnosed non-small cell lung cancer patients;

Age ≥18 years;

(Eastern Cooperative Oncology Group, ECOG) (Performance Status, PS) score 0-1;

According to the 8th-9th edition of (American Joint Committee on Cancer, AJCC) (stage II-IIIA, for stage IIIB included T3-4N2, T4 only included tumor > 7cm);

Disqualifiers

Patients with severe dysfunctions of the heart, lungs and other organs who are not suitable for surgery;

Patients with severe autoimmune diseases: active inflammatory bowel disease (including Crohn's disease, ulcerative colitis), rheumatoid arthritis, scleroderma, systemic lupus erythematosus, autoimmune vasculitis (such as Wegener's granuloma), etc;

Other malignancies within 5 years (excluding non-melanoma skin cancer and cervical cancer);

Patient with active infection, heart failure, heart attack, unstable angina pectoris or unstable arrhythmia within the last 6 months;

Trial design

Treatments tested in this trial

  • Chemotherapy
  • Immunotherapy
  • Radical resection of lung cancer
  • SBRT

Treatment groups

40 Participants
are divided into 1 treatment group