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A single-center randomized controlled study for patients with IIIA period with unresectable non-small cell lung cancer neoadjuvant therapy strategy: targeted vs chemotherapy

A neoadjuvant therapy study of single-center randomized controlled for patients with stage IIIA unresectable non-small cell lung cancer: targeting vs chemotherapy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039906
Enrollment
Unknown
Registered
2020-11-14
Start date
2020-11-01
Completion date
Unknown
Last updated
2021-02-22

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

Conditions

Lung Cancer

Interventions

experimental group:Neoadjuvant targeting
control group:Standard AP scheme

Sponsors

Sichuan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with stage III a4-n2, III a-t4-n0 NSCLC who were consistent with AJCC eighth edition TNM staging and Robinson classification (see research background) by imaging and pathological examination, and egfrm + was detected by pathological tissue (arms method) or peripheral blood gene detection (NGS); 2. Patients with clear tumor boundary and measurable volume (measurable lesions); 3. Patients without history of lung tumor surgery; 4. Patients without previous chemoradiotherapy history; 5. Patients with KPS score >= 80; 6. Patients whose expected survival time is more than 180 days; 7. Those who sign the informed consent form will join voluntarily.

Exclusion criteria

Exclusion criteria: 1. Patients with serious uncontrolled basic medical diseases; 2. Patients with other malignant tumors; 3. Patients with liver and kidney dysfunction; 4. Patients with surgical contraindications; 5. Patients with superior sulcus type non-small cell lung cancer; 6. Patients younger than 18 years old or older than 80 years old.

Design outcomes

Primary

MeasureTime frame
Surgical resection rate, PCR rate, MPR rate;

Secondary

MeasureTime frame
QOL;overall survival;progression-free survival;

Countries

China

Contacts

Public ContactXie Ke

Sichuan Provincial People's Hospital

mei97@sina.com+86 18113003933

Outcome results

None listed

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