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A phase II clinical study using NGS combined with mIHC technology to explore the efficacy of terellizumab combined with neoadjuvantchemotherapy in operable non-small cell lung cancer

A phase II clinical study using NGS combined with mIHC technology to explore the efficacy of terellizumab combined with neoadjuvantchemotherapy in operable non-small cell lung cancer

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063855
Enrollment
Unknown
Registered
2022-09-19
Start date
2022-09-19
Completion date
Unknown
Last updated
2023-04-17

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

Conditions

nonsmall-cell lung cancer

Interventions

A:terellizumab combined with neoadjuvantchemotherapy

Sponsors

The Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 79 Years

Inclusion criteria

Inclusion criteria: 1.Older than 18 years old 2.Histologically confirmed stage II-IIIA NSCLC patients (Classification IASLC classification) 3.The evaluation by the thoracic surgeon confirmed compliance with the requirements for R0 resection for the purpose of radical treatment 4.The driver gene EGFR / ALK was negative 5.Patient compliance was good, and the screening period was able to provide complete tissue and blood samples 6.The patient had good liver and kidney, bone marrow function and other general indicators, and met the conditions for enrollment in general clinical trials 7.Subjects read and fully understood the patient instructions and signed the informed consent form

Exclusion criteria

Exclusion criteria: 1.Immunocompromised patients, or those currently undergoing systemic immunosuppressive therapy 2.Patients taking immunosuppressive drugs within two weeks prior to enrollment 3.Seriously infected patients with infectious disease that requires treatment with antimicrobial agents 4.Blood transfusion was performed within two weeks before surgery 5.The patient had a history of alcoholism or substance abuse 6.Pregnant or lactating female patient 7.Patients with incomplete samples during the screening period for various reasons 8.The investigator thinks it is not suitable for enrollment

Design outcomes

Primary

MeasureTime frame
pCR;

Countries

China

Contacts

Public ContactHao Zhang
haozhang-xz@163.com17798835177

Outcome results

None listed

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