Efficacy and Biomarkers of the Second-line Treatment of Adebelizumab Combined With Irinotecan Liposome in Advanced Small Cell Lung Cancer
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 46
- 试验地点
- 1
- 主要终点
- Progression Free Survival (PFS)
研究概览
简要总结
This study is an open, single-arm, single-center phase II clinical study, which aims to evaluate the efficacy and safety of adebelizumab combined with irinotecan liposome in the second-line treatment of advanced small cell lung cancer, explore biomarkers to predict the efficacy, and further select the dominant population in immunotherapy.
In this study, 46 patients with extensive SCLC who had previously received immunotherapy combined with chemotherapy were enrolled. Subjects who met the enrollment conditions will be given adebelizumab combined with irinotecan liposome at the same time. After 4-6 cycles of treatment, if their condition has not progressed, they will be treated with adebelizumab until the disease progresses, toxicity can not be tolerated or other reasons specified in the scheme can be terminated. Subjects who finish the treatment will enter the follow-up period for safety follow-up and survival follow-up.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age: 18-75 years old;
- •Small cell lung cancer diagnosed by histology; Compound small cell lung cancer is not allowed;
- •Progress in receiving first-line chemotherapy combined with immunotherapy (including PD-1 inhibitor and PD-L1 inhibitor);
- •According to RECIST 1.1 standard, there is at least one measurable objective lesion; 5.ECOG score 0-1;
- •The functions of important organs meet the following requirements:Bone marrow function: neutrophils ≥1.5×109/L, platelets ≥100×109/L, hemoglobin concentration ≥ 90g/L;Liver function: bilirubin ≤ 1.5× ULN; Aspartate aminotransferase and glutamate aminotransferase ≤2.5×ULN, and AST and ALT ≤ 5× ULN in case of liver metastasis; Total bilirubin ≤1.5 times the upper limit of normal value;Renal function: serum creatinine ≤1.5×ULN, or creatinine clearance rate (CCR) ≥ 60 ml/min;
- •Expected survival > 12 weeks;Patients have good compliance with the planned treatment, can understand the research process of this study and sign a written informed consent.
排除标准
- •Irinotecan liposome or Irinotecan has been used before;
- •Severe heart and lung diseases, new york Heart Association (NYHA) scores that patients with heart diseases above Grade II (including Grade II);
- •Patients with severe systemic infection or other serious diseases;
- •Patients who are known to be allergic or intolerant to chemotherapy drugs or their accessories;
- •Other malignant tumors have appeared in the past 5 years, except cured cervical carcinoma in situ and non-melanoma skin cancer;
- •Patients of childbearing age during pregnancy or lactation, and those who refused to take appropriate contraceptive measures during this experiment;
- •Have participated in clinical studies of other drugs within 21 days before the first dose of the study drug is given;
- •Combined with active autoimmune diseases and inflammatory diseases;
- •Grade 3-4 immune-related adverse reactions occurred during previous immunotherapy;
- •Symptomatic brain metastasis and meningeal metastasis;
- •Before the first administration, you are receiving long-term systemic corticosteroid therapy with prednisone > 10mg/d or equivalent anti-inflammatory active drugs or any form of immunosuppressive therapy. Subjects who need bronchodilators, inhaled or topical steroids or local steroid injections can be included in this study;
- •Patients with a large amount of serous cavity effusion, or serous cavity effusion with symptoms, or poor control of serous cavity effusion (poor control is defined as: puncture and drainage are needed twice or more in one month);The researcher judges the patients who are not suitable to participate in this study.
研究组 & 干预措施
experimental arm
adebelizumab and irinotecan liposome
干预措施: Adebelizumab combined with irinotecan liposome as second-line therapy (Drug)
结局指标
主要结局
Progression Free Survival (PFS)
时间窗: 0-12months
It refers to the time from the date when the subjects enter the group to the time when the disease progresses or dies, whichever comes first.
次要结局
- Percentage of Participants Who Had an Objective Response Rate(ORR) Based on Response Evaluation Criteria In Solid Tumors (RECIST) Criteria.(through study completion, an average of 1 year)
- Overall Survival (OS)(0-5years)
- Safety: Number of participants with treatment-related adverse events as assessed by CTCAE v5.0(through study completion, an average of 2 year)
- Biomarker("Baseline" and "after 2 cycles of treatment")
研究者
Yang Wang
Associate Professor of Medicine
Peking University Cancer Hospital & Institute