Serplulimab Monotherapy in Elderly Patients With NSCLC and PD-L1 TPS ≥ 50%
Multicenter, Single-arm, Phase II Exploratory Study of Serplulimab Monotherapy in Elderly Patients With NSCLC and PD-L1 TPS ≥ 50%
This prospective clinical study aims to evaluate and observe the efficacy and safety of Serplulimab Monotherapy in Elderly Patients with NSCLC and PD-L1 TPS ≥ 50% using a multicenter, single-arm, phase II design.
The study is planned to be conducted in Shaanxi Province, China, with an initial target enrollment of 60 patients. The study commenced in May 2026, and recruitment is expected to conclude around May 2026, with the trial anticipated to end by May 2027.
Assuming no occurrences such as withdrawal of informed consent by subjects, intolerable adverse drug reactions, or investigator-assessed unsuitability for further participation, each participant's estimated duration of study treatment will continue until radiographically confirmed tumor progression.
研究概览
研究类型
注册 (估计的)
阶段
- 阶段2
联系人和位置
学习联系方式
- 姓名:Lei Pan, Dr
- 电话号码:13991161903
- 邮箱:panlei@fmmu.edu.cn
学习地点
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Shannxi
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Xi'an、Shannxi、中国、710000
- 招聘中
- Tangdu Hospital Affiliated to the Fourth Military Medical University
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接触:
- Lei Pan, Dr
- 电话号码:13991161903
- 邮箱:panlei@fmmu.edu.cn
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参与标准
资格标准
适合学习的年龄
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
1.Voluntary participation and informed consent: Subjects must voluntarily join the study, sign the written informed consent form (ICF), and demonstrate good compliance.
2.Age and Gender: Aged ≥65 years at the time of signing the ICF, regardless of gender.
3.Diagnosis and Staging: Histologically or cytologically confirmed Stage IIIB (ineligible for definitive chemoradiotherapy), Stage IIIC, or Stage IV NSCLC according to the AJCC 8th edition staging system.
4.PD-L1 Expression: Tumor tissue confirmed as PD-L1 TPS≥50% by a central laboratory or a validated local laboratory, using SP263 or 22C3 assays (a formal test report must be provided).
5.Driver Gene Status: Known absence of actionable driver mutations, including but not limited to EGFR sensitive mutations, ALK fusions, and ROS1 fusions.
6.Measurable Disease: At least one measurable target lesion per RECIST v1.1 criteria (lesions must not have received prior radiotherapy).
7.Prior Treatment History: No prior systemic therapy for advanced or metastatic disease. For patients who received adjuvant or neoadjuvant chemotherapy, inclusion is permitted if disease recurrence occurred ≥6 months after the completion of the last dose.
8.Performance Status: Eastern Cooperative Oncology Group (ECOG) performance status (PS) score of 0-2.
9.Adequate organ and bone marrow function (no blood transfusions or hematopoietic stimulating factor therapy within 14 days prior to the first dose):
- Absolute Neutrophil Count (ANC)≥1.5 x 10^9//L
- Platelet Count (PLT)≥100 x 10^9//L
- Hemoglobin (Hb)≥90 g/L
- Serum Creatinine (Cr) ≤ 1.5 x Limit of Normal (ULN) or Creatinine Clearance ≥ 50mL/min
- Total Bilirubin (TBIL) ≤ 1.5 x ULN
- Aspartate Aminotransferase (AST) and Alanine Aminotransferase (ALT)≤ 2.5 x ULN(≤ 5 x ULN for patients with liver metastases)
Exclusion Criteria:
1. Hypersensitivity: Known hypersensitivity to serplulimab or any of its excipients.
2. Prior Immunotherapy: Prior treatment with any anti-PD-1, anti-PD-L1, anti-CTLA-4, or other immune checkpoint inhibitors (ICIs).
3. Autoimmune Disease: Active autoimmune disease requiring systemic treatment (e.g., corticosteroids or immunosuppressants) within the past 2 years. Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement for adrenal or pituitary insufficiency) is permitted.
4. Lung Disease/Pneumonitis: Active interstitial lung disease (ILD) or pneumonitis, or a history of (non-infectious) pneumonitis requiring steroid treatment.
5. Infections: Active infection requiring systemic therapy. 6. CNS Metastases: Known active central nervous system (CNS) metastases and/or carcinomatous meningitis. However, patients with treated (via surgery or radiotherapy) and stable brain metastases are eligible, provided they are radiographically stable for at least 4 weeks prior to the first dose, have no evidence of new or enlarged brain lesions, and have discontinued glucocorticoids for at least 14 days.
7. Pregnancy and Breastfeeding: Pregnant or breastfeeding women. 8. Investigator Discretion: Any other condition that, in the investigator's opinion, may interfere with the evaluation of the study drug, jeopardize subject safety, or confound the interpretation of study results.
学习计划
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 |
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实验性的:Serplulimab Monotherapy
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The treatment follows a 21-day (3-week) cycle.
Serplulimab is administered intravenously at a fixed dose of 300 mg on Day 1 of each cycle (Q3W).
Prior to each administration, subjects shall undergo comprehensive clinical assessments-including vital signs, anthropometric measurements, physical examinations, laboratory monitoring, and ECOG performance status (PS)-to confirm safety and tolerability for continued treatment.
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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 |
|---|---|---|
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无进展生存期
大体时间:无进展生存期 (PFS) 分析基于研究者根据 RECIST 1.1 进行的评估,评估期限长达 2 年
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无进展生存期(PFS)是指研究人员评估的从记录第一次化疗到疾病进展之日的时间。
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无进展生存期 (PFS) 分析基于研究者根据 RECIST 1.1 进行的评估,评估期限长达 2 年
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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客观响应率
大体时间:获得的数据直到进展或在没有进展的情况下进行最后的可评估评估,最多将评估长达1年。
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使用研究者评估的实体瘤版本1.1(RECIST 1.1)中的每个响应评估标准定义为具有完全反应或部分反应反应的患者人数(%),最多将评估长达1年。
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获得的数据直到进展或在没有进展的情况下进行最后的可评估评估,最多将评估长达1年。
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Overall Survival
大体时间:The maximum time from receiving treatment to dying for any reason is 4 years.
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Overall survival (OS) refers to the time that researchers evaluate from recording the first chemotherapy to death (of any cause)
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The maximum time from receiving treatment to dying for any reason is 4 years.
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Disease Control Rate
大体时间:Disease Control Rate (DCR) is analysis based on investigator assessment per RECIST 1.1, and will be assessed up to 2 years.
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Disease Control Rate (DCR) is defined as the percentage of participants who achieved a Best Overall Response (BOR) of Complete Response (CR), Partial Response (PR), or Stable Disease (SD) according to Response Evaluation Criteria in Solid Tumors (RECIST)
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Disease Control Rate (DCR) is analysis based on investigator assessment per RECIST 1.1, and will be assessed up to 2 years.
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合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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