Exploring the Mechanism of Primary Resistance to Third-generation EGFR-TKIs as First-line Treatment in EGFR-positive Advanced NSCLC (PRECISE Study)
Study Details
Study Description
Brief Summary
Lung cancer is currently the world's largest malignant tumor for cancer-related deaths with non-small cell lung cancer (NSCLC) accounting for 80%-85%. Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs), especially the 3rd-generation EGFR-TKIs have demonstrated strong antitumor effects in EGFR-positive patients.
However, approximately 20% of EGFR-positive were primarily resistant to 3rd generation EGFR-TKIs, i.e., clinical non-response or disease progression in the short term.
This study aimed to clarify the molecular indicators that predict the benefits of 3-rd EGFR-TKIs as first-line therapy in NSCLCpatients with EGFR-positive. Further, to clarify their primary drug resistance mechanisms, which is of great significance for the treatment and clinical decision-making of NSCLC disease.
Condition or Disease | Intervention/Treatment | Phase |
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Study Design
Arms and Interventions
Arm | Intervention/Treatment |
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EGFR-positive lung patients recieving 3rd generation EGFR-TKIs as first-line therapy Stage III-IV EGFR-positive lung patients receiving 3rd generation EGFR-TKIs (Osimertinib 80mg/Qd or Almonertinib 110mg/Qd or Furmonertinib 80mg/Qd) as first-line therapy. |
Other: Genomic profiles detection
The Paraffin-embedded tumor tissue at diagnosis is collected and assessed by Next- generation gene sequencing
Other: circulating tumor DNA detection
The Plasma at diagnosis and at 1-month treatment are collected and assessed by Next-generation gene sequencing
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Outcome Measures
Primary Outcome Measures
- Objective Response Rate (ORR) [2 years]
The proportion of patients with a complete response or partial response to treatment according to Response Evaluation Criteria in Solid Tumors (RECIST v1.1)
- Progression-free survival (PFS) [3 years]
Time from the beginning of first-line immunotherapy to the first progression(PD) in patients with advanced NSCLC
- Differences in genomic profiles of tumor tissues and ctDNA clearance of third-generation EGFR-TKIs sensitive and primary drug-resistant NSCLC. [3 years]
The patients who don't achieve ORR or progress within 6 months are defined as the primary resistant group. The genomic profiles and ctDNA clearance detected by Next-generation gene sequencing will be compared between the primary drug-resistant group and sensitive-drug group.
Secondary Outcome Measures
- Overall survival (OS) [5 years]
Overall survival (OS) is defined as the duration from the beginning of first-line immunotherapy until death due to any cause. Subjects who are still alive at the end of the study observation period will be censored at the time of last known vital status
- Disease Control Rate (DCR) [3 years]
The proportion of patients with a complete response or partial response or stable desease to treatment according to Response Evaluation Criteria in Solid Tumors (RECIST v1.1)
Other Outcome Measures
- The correlation between tumor microenvironment signature and efficacy of 3rd EGFR-TKIs [3 years]
The baseline paraffin-embedded tissue is collected and assessed by multiplex immunohistochemistry, including T lymphocytes, B lymphocytes, NK lymphocytes, macrophagocyte, and DC cells. And explore the association between tumor microenvironment signature and primary resistance and the efficacy of 3rd EGFR-TKIs during the enrolled observation process.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Age >18 years;
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Histological or cytopathological diagnosed NSCLC;
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According to the American Joint Committee on Cancer (AJCC) eighth edition of the Lung Cancer Staging Manual, the clinical stage is unresectable IIIB-IV or recurrence and metastasis after surgery;
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At least one measurable lesion can be evaluated according to the Response Evaluation Criteria In Solid Tumours v1.1 (RECIST1.1) criteria;
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Positive EGFR mutation confirmed by tissue or cytology (pleural fluid, cerebrospinal fluid, etc.);
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Use of third-generation EGFR-TKIs approved by the NMPA for NSCLC as first-line therapy;
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Cooperate with the provision of clinicopathological data, imaging data, sample collection, and follow-up required for the research process, and agree to use the test data for subsequent research and product development;
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Agree to participate in this study and sign an informed consent form.
Exclusion Criteria:
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Patients who cannot understand the content of the experiment and cannot cooperate, and those who refuse to sign the informed consent form;
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Pregnant and lactating women;
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Other malignant neoplastic diseases within 3 years;
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Patients who have undergone other clinical drug trials;
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Received systemic anti-tumor therapy within 2 years;
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
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1 | Department of Oncology, The Second Xiangya Hospital, Central South University | Changsha | Hunan | China | 410011 |
Sponsors and Collaborators
- Fang Wu
- Xiangya Hospital of Central South University
- Shanghai Chest Hospital
- West China Hospital
- Hunan Cancer Hospital
- The Third Xiangya Hospital of Central South University
- The First Affiliated Hospital of Xiamen University
- Second Affiliated Hospital, School of Medicine, Zhejiang University
- China-Japan Friendship Hospital
- Fudan University
- Jiangxi Provincial Cancer Hospital
- The First Affiliated Hospital of Kunming Medical College
- Loudi Central Hospital
- ZhuZhou Central Hospital
- Xiangtan Central Hospital
- First People's Hospital of Chenzhou
- Yueyang Central Hospital
- Yongzhou Central Hospital
- The First Affiliated Hospital of University of South China
- Hunan Provincial People's Hospital
- Shaoyang Central Hospital
- Yiyang Central Hospital
- Changsha Central Hospital
- The first people's hospital of Guiyang
- Wuhan Union Hospital, China
- Renmin Hospital of Wuhan University
- The First People's Hospital of Changde
- Zhuzhou Second Hospital
- First Hospital of Changsha
- Hengyang Central Hospital
- Huaihua first people's Hospital
- The First People's Hospital of Xiangtan
- University of South China Affiliated Nanhua Hospital
- Xiangxi Autonomous Prefecture People's Hospital
- People's Hospital of Zhangjiajie
- Second People's Hospital Of Huaihua
- Hunan Academy of Traditional Chinese Medicine Affiliated Hospital
- The Third Hospital of Changsha
- Xiangya Changde Hospital
- Changsha County first People's Hospital
- Hunan Provincial Straight Hospital of Traditional Chinese Medicine
- Liuyang Hospital of traditional Chinese Medicine
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- XYEYY20220928