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Development of Traditional Chinese Medicine Syndrome Differentiation and Typing Characteristics Model for Neoadjuvant Immunotherapy of Non Small Cell Lung Cancer

Development of Traditional Chinese Medicine Syndrome Differentiation and Typing Characteristics Model for Neoadjuvant Immunotherapy of Non Small Cell Lung Cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500105347
Enrollment
Unknown
Registered
2025-07-02
Start date
2023-09-27
Completion date
Unknown
Last updated
2025-07-07

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

Conditions

Lung cancer

Interventions

Sponsors

Zhejiang cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. According to clinical imaging evaluation, patients with stage IIA-IIIB non-small cell lung cancer who are expected to undergo complete surgical resection (based on the 8th edition AJCC TNM staging); 2. If the pathological type is adenocarcinoma and there are no EGFR/ALK sensitive mutations; 3. When signing the informed consent form, the age is equal to or greater than 18 years old and less than or equal to 75 years old; 4. The patient's ECOG score ranges from 0 to 1; 5. The functional reserve of important organs meets the requirements of chemotherapy, immunotherapy, and surgery; According to the RESIST v1.1 standard, there are target lesions that can be measured through imaging examinations.

Exclusion criteria

Exclusion criteria: 1. History of other malignant tumors; 2. Pathological diagnosis of small cell lung cancer before treatment; 3. Adenocarcinoma patients have EGFR/ALK sensitive mutations; 4. Previously received chemotherapy, radiation therapy, or other anti-tumor treatments; 5. Have received systemic immune stimulant or systemic immune suppressant treatment within 4 weeks before the first administration (excluding inhaled or locally administered steroid hormones); 6. Existence of autoimmune related diseases; 7. Known or suspected interstitial pneumonia; 8. Suffering from severe cardiovascular and cerebrovascular diseases; 9. There are significant bleeding events or arteriovenous thrombosis events within 3 months before the first administration; 10. HIV positive or active hepatitis B/C virus; 11. Other researchers believe that it is not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
Pathological remission rate;Traditional Chinese Medicine Syndrome;

Secondary

MeasureTime frame
CT;Pulmonary function;Heart function;Blood routine;Urinalysis;Fecal routine;blood biochemical;blood clotting;Blood Gas Analysis;Tumor markers;NK complete set;Infectious disease examination;

Countries

China

Contacts

Public ContactJian Zeng

Zhejiang cancer hospital

hzzengjian123@163.com+86 571 8812 8161

Outcome results

None listed

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