Neoadjuvant Chemoimmunotherapy in Stage IIIA- N2IIIB Non-small Cell Lung Cancer
- Conditions
- Non-small Cell Lung Cancer Stage ⅢANon-small Cell Lung Cancer Stage IIIB
- Interventions
- Other: cycles of neoadjuvant therapy and duration of waiting for surgery
- Registration Number
- NCT06394427
- Lead Sponsor
- West China Hospital
- Brief Summary
to explore the impact of preoperative neoadjuvant immunotherapy on perioperative outcomes and long-term prognosis of locally advanced NSCLC in the real world
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 250
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Confirmed as primary lung cancer through cytology or histological examination;
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ECOG score of 0 or 1; ③ 18 years old or above;
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Received imaging examination, with a preliminary clinical staging of stage III;
- Received genetic testing and tested negative for EGFR mutations, ALK or ROS-1 fusion; ⑥ Accepting preoperative neoadjuvant immunotherapy combined with chemotherapy; ⑦ Receive surgical treatment after completion of neoadjuvant therapy; ⑧ The postoperative specimens were sent to the pathology department of our hospital for pathological testing, and a complete pathological report is available.
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Patients with combined small cell lung cancer; ② Patients with severe liver/kidney dysfunction, cardiovascular disease, or systemic immune disorders;
- Accept other neoadjuvant treatments; ④ Patients participating in any clinical trial.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description chemoimmunotherapy group 2 cycles of neoadjuvant therapy and duration of waiting for surgery the duration of before patients received surgery after neoadjuvant chemoimmunotherapy chemoimmunotherapy group 1 cycles of neoadjuvant therapy and duration of waiting for surgery patients received different cycles of neoadjuvant chemoimmunotherapy
- Primary Outcome Measures
Name Time Method major pathological remission one month proportion of patients with no more than 10% residual viable tumor cells; patients who showed no viable tumor in the lung primary setting but lymph nodes show viable metastatic carcinoma were also classified as MPR
survival time 5 years time since diagnosed with NSCLC
pathological complete remission one month proportion of patients without residual viable tumor cell on evaluation of resected lung cancer specimens including all sampled regional lymph nodes
- Secondary Outcome Measures
Name Time Method