EGFR-TKIs Plus PD-1 in EGFR-Mutant Advanced NSCLC
2026年6月4日 更新者:Nanfang Hospital, Southern Medical University
A Clinical Study Evaluating the Preliminary Antitumor Activity and Safety of EGFR-TKIs Combined With PD-1 Monoclonal Antibody as First-Line Therapy in Patients With EGFR-Mutant Advanced Non-Small Cell Lung Cancer
This study is an open-label, multicenter, single-arm clinical study.
研究概览
地位
招聘中
详细说明
This open-label, multicenter, single-arm exploratory clinical trial plans to enroll a total of 32 patients: 6 in a safety lead-in phase and the remaining 26 in an expansion phase.
Eligible subjects are treatment-naïve patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) harboring EGFR 19del or L858R mutations.
All patients receive first-line oral therapy with standard-dose third-generation EGFR-TKIs (osimertinib, aumolertinib, or furmonertinib).
Once stable disease is confirmed by two consecutive radiological assessments, sintilimab (200 mg intravenously every three weeks) is added as maintenance treatment until disease progression, unacceptable toxicity, or a maximum treatment duration of two years.
The primary endpoint is progression-free survival (PFS).
Secondary endpoints include objective response rate (ORR), disease control rate (DCR), overall survival (OS), and adverse events occurring throughout treatment.
Exploratory analyses focus on the correlation of serum lipid profiles and the tumor immune microenvironment with the safe treatment window and mechanisms of drug resistance.
The trial consists of screening, treatment, safety follow-up, and survival follow-up periods.
Tumor imaging evaluations are performed every six weeks during the first 24 weeks of treatment and every nine weeks thereafter.
研究类型
介入性
注册 (估计的)
32
阶段
- 阶段2
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
-
-
Guangdong
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Guangzhou、Guangdong、中国
- 招聘中
- Southern Medical University Nanfang Hospital Department of Oncology
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接触:
- Professor Wang
- 电话号码:+86 20 87150
- 邮箱:doc_wang@163.com
-
-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria:
- Patients with histologically or cytologically confirmed, previously untreated EGFR-mutant (19del/L858R) locally advanced or metastatic (stage IIIB/IIIC or IV) non-small cell lung cancer (NSCLC), according to the 9th edition of the TNM staging system for lung cancer jointly issued by the International Association for the Study of Lung Cancer (IASLC) and the American Joint Committee on Cancer (AJCC);
- Male or female patients aged ≥ 18 years;
- Patients who are willing to receive third-generation EGFR-TKI targeted therapy, followed by maintenance therapy with a PD-1 antibody during the stable phase of the disease (defined as no further tumor shrinkage for at least two consecutive assessments based on RECIST v1.1 criteria);
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1;
- At least one measurable or non-measurable but evaluable lesion according to RECIST version 1.1;
- Adequate organ function;
- Female or male patients of childbearing potential must agree to use highly effective contraceptive measures throughout the study period;
- Willing and able to comply with scheduled visits, treatment plans, laboratory tests, and other study requirements as specified in the visit schedule.
Exclusion Criteria:
- Patients who are ineligible for standard anti-tumor therapy according to routine clinical practice;
- Prior treatment with anti-PD-1/PD-L1 immunotherapy;
- Concurrent enrollment in another clinical study;
- Known history of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation;
- Receipt of systemic corticosteroids or other immunosuppressive therapy within 2 weeks prior to the first dose of study drug;
- Receipt of any live vaccine within 4 weeks prior to the first dose of study drug, or planned receipt of live vaccine during the study period;
- Presence of brainstem, leptomeningeal, spinal cord metastasis, or spinal cord compression;
- Presence of uncontrolled concomitant diseases, including but not limited to decompensated cirrhosis, nephrotic syndrome, uncontrolled metabolic disorders, etc.;
- History of severe gastrointestinal ulcer, gastrointestinal perforation, fistula or obstruction, intra-abdominal abscess, or acute gastrointestinal bleeding within 6 months prior to the first dose, or other gastrointestinal diseases that, in the investigator's opinion, may predispose to bleeding or perforation;
- Presence of severe uncontrolled cardiovascular disease;
- Interstitial lung disease (ILD) (including pulmonary fibrosis or radiation pneumonitis) requiring corticosteroid therapy, or current ILD/non-infectious pneumonitis;
- Concomitant pulmonary disease resulting in clinically severe impairment of respiratory function;
- Chronic autoimmune disease or inflammatory disease requiring systemic therapy or receiving systemic therapy within 2 years prior to the first dose;
- Active or history of documented inflammatory bowel disease (e.g., Crohn's disease, ulcerative colitis, or chronic diarrhea), intestinal obstruction, or extensive bowel resection;
- Diagnosis of Gilbert's syndrome;
- Severe infection within 4 weeks prior to the first dose, including but not limited to complications requiring hospitalization, sepsis, or severe pneumonia;
- Known active pulmonary tuberculosis;
- Known active syphilis infection;
- Known history of immunodeficiency, or positive test for human immunodeficiency virus (HIV) antibody;
- Presence of active hepatitis B virus (HBV) or hepatitis C virus (HCV) infection;
- Known allergy to any component of any study drug, history of severe allergic reactions (e.g., anaphylactic shock), history of severe hypersensitivity to other monoclonal antibodies or recombinant protein-based substances, or history of severe infusion reactions;
- Women who are pregnant, breastfeeding, or planning to become pregnant or breastfeed during the study period;
- Any disease, medical condition, organ system dysfunction, or social circumstance (including but not limited to psychiatric illness, substance/alcohol abuse, history of drug abuse, etc.) that, in the investigator's opinion, may interfere with the subject's ability to provide informed consent, adversely affect the subject's cooperation and participation in the study, or confound the interpretation of study results.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:EGFR-TKIs Combined with PD-1 Monoclonal Antibody
All patients receive first-line oral therapy with standard-dose third-generation EGFR-TKIs (osimertinib, aumolertinib, or furmonertinib).
Once stable disease is confirmed by two consecutive radiological assessments, sintilimab (200 mg intravenously every three weeks) is added as maintenance treatment until disease progression, unacceptable toxicity, or a maximum treatment duration of two years.
|
EGFR-TKIs Combined with PD-1 Monoclonal Antibody
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Median Progression-free survival
大体时间:From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months
|
from randomization (or initiation of treatment) to the first occurrence of disease progression or death from any cause.
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From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
objective response rate
大体时间:through study completion, an average of 3 years.
|
The proportion of patients whose tumor volume reduction meets predefined criteria (Complete Response or Partial Response) and is maintained for a certain period of time.
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through study completion, an average of 3 years.
|
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Disease Control Rate
大体时间:through study completion, an average of 3 years.
|
The DCR is the percentage of patients achieving CR, PR or SD per RECIST criteria at the first tumor assessment.
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through study completion, an average of 3 years.
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Median Overall Survival
大体时间:From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months
|
the time from randomization (or initiation of treatment) at which 50% of patients have died.
|
From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months
|
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The incidence and severity of treatment-related adverse events (AEs) and serious adverse events (SAEs) assessed according to NCI CTCAE v5.0, as well as laboratory abnormalities.
大体时间:through study completion, an average of 3 years.
|
Adverse events were graded according to NCI CTCAE v5.0 and collected from the first dose to 30 days after the last dose.
Serious adverse events were collected from the signing of informed consent through the end of the study.
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through study completion, an average of 3 years.
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2026年5月21日
初级完成 (估计的)
2029年3月1日
研究完成 (估计的)
2030年3月1日
研究注册日期
首次提交
2026年5月28日
首先提交符合 QC 标准的
2026年6月4日
首次发布 (实际的)
2026年6月9日
研究记录更新
最后更新发布 (实际的)
2026年6月9日
上次提交的符合 QC 标准的更新
2026年6月4日
最后验证
2026年6月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.