[Translation] A randomized, double-blind, parallel-controlled, multicenter phase III clinical trial on the efficacy and safety of recombinant human tumor necrosis factor for injection (rmhTNF-NC, Tianenfu®) combined with cisplatin versus intracavitary cisplatin perfusion in the treatment of malignant pleural and peritoneal effusions
主要有效性目的:
以无穿刺生存期(Puncture-Free Survival,PuFS)和客观缓解率(ORR)作为主要疗效指标,评价rmhTNF-NC+顺铂相较于顺铂单药腔内灌注治疗恶性胸、腹腔积液的有效性。
次要有效性目的:
基于以下次要疗效指标,评价rmhTNF-NC+顺铂相较于顺铂单药腔内灌注治疗恶性胸、腹腔积液的有效性:
1)6个月生存率(6m-OS);
2)疾病控制率(DCR);
3)总生存期(OS);
4)患者报告结局(PRO):生活质量评分(QLQ评分)相对于基线的变化。
安全性目的:
基于以下指标评估各治疗组的安全性:
1)不良事件的发生率和严重程度;
2)生命体征、体格检查、实验室检查(包括血常规、尿常规、血生化、凝血功能)以及心电图相对于基线的变化;
特别关注不良事件(AESI)发生率。
[Translation] Primary efficacy objective:
Using puncture-free survival (PuFS) and objective response rate (ORR) as the primary efficacy indicators, evaluate the effectiveness of rmhTNF-NC + cisplatin compared with cisplatin monotherapy in the treatment of malignant pleural and peritoneal effusions.
Secondary efficacy objective:
Based on the following secondary efficacy indicators, evaluate the effectiveness of rmhTNF-NC + cisplatin compared with cisplatin monotherapy in the treatment of malignant pleural and peritoneal effusions:
1) 6-month survival rate (6m-OS);
2) disease control rate (DCR);
3) overall survival (OS);
4) patient-reported outcomes (PRO): changes in quality of life score (QLQ score) relative to baseline.
Safety objective:
The safety of each treatment group was evaluated based on the following indicators:
1) the incidence and severity of adverse events;
2) changes in vital signs, physical examination, laboratory tests (including blood routine, urine routine, blood biochemistry, coagulation function) and electrocardiogram relative to baseline;
Special attention was paid to the incidence of adverse events (AESI).