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Efficacy and Safety of Neoadjuvant Reduced-dose Chemotherapy Combined with Tislelizumab in the Treatment of Resectable Non - Small Cell Lung Cancer: A Single - Center, Prospective, Single - Arm Study

Efficacy and Safety of Neoadjuvant Reduced-dose Chemotherapy Combined with Tislelizumab in the Treatment of Resectable Non - Small Cell Lung Cancer: A Single - Center, Prospective, Single - Arm Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097822
Enrollment
Unknown
Registered
2025-02-26
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-small cell lung cancer

Interventions

Reduced-dose Chemotherapy group:Reduced chemotherapy combined with immunotherapy

Sponsors

The Third Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) 60=1.5L, blood gas analysis PaO2>=70mmHg; (7) Have not received any anti-tumor therapy; (8) Well-controlled underlying diseases such as hypertension, diabetes, hyperthyroidism, and hypothyroidism; (9) Blood system: absolute neutrophil value (ANC) >=2.0×10^9/L, platelet >=100×10^9/L, hemoglobin >=9g/dl; (10) Liver: bilirubin = 60ml/min.

Exclusion criteria

Exclusion criteria: (1) Patients with stage IA or IIIB (T1-2N3) /IIIC or IV NSCLC; (2) Patients with ECOG PS score >=3, who could not tolerate surgery; (3) There are contraindications of chemotherapy, immunotherapy and surgery: active tuberculosis, hepatitis, immune diseases (HIV infection), fungal and bacterial infections, severe coronary artery stenosis, etc. (4) Large cell neuroendocrine carcinoma tumor, carcinosarcoma, carcinoid rare histology; (5) pregnancy or breastfeeding; (6) There are other malignant tumor lesions; (7) The investigator believes that the subject may not be able to complete the study or may not be able to meet the requirements of the study (for administrative reasons or otherwise).

Design outcomes

Primary

MeasureTime frame
Complete pathological response;

Secondary

MeasureTime frame
Major pathological response;Disease-free Survival;Overall survival;

Countries

China

Contacts

Public ContactChen Huiguo

The Third Affiliated Hospital of Sun Yat-sen University

chen_sysu@qq.com+86 135 6000 8207

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026