Clinical study and mechanism of spleen-strengthening traditional Chinese medicine WD-3 combined with immunotherapy for lung cancer based on the theory of "Pei Tu Shengjin"
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注册号: Registration number: |
ChiCTR2500115477 |
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最近更新日期: Date of Last Refreshed on: |
2025-12-26 11:57:01 |
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注册时间: Date of Registration: |
2025-12-26 00:00:00 |
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注册号状态: |
补注册 |
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Registration Status: |
Retrospective registration |
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注册题目: |
基于“培土生金”理论探讨健脾方 WD-3 联合免疫治疗肺癌的临床疗效与机制 |
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Public title: |
Clinical study and mechanism of spleen-strengthening traditional Chinese medicine WD-3 combined with immunotherapy for lung cancer based on the theory of "Pei Tu Shengjin" |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
基于“培土生金”理论探讨健脾方 WD-3 联合免疫治疗肺癌的临床疗效与机制 |
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Scientific title: |
Clinical study and mechanism of spleen-strengthening traditional Chinese medicine WD-3 combined with immunotherapy for lung cancer based on the theory of "Pei Tu Shengjin" |
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研究课题代号(代码): Study subject ID: |
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在二级注册机构或其它机构的注册号: The registration number of the Partner Registry or other register: |
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申请注册联系人: |
金春晖 |
研究负责人: |
金春晖 |
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Applicant: |
Chunhui Jin |
Study leader: |
Chunhui Jin |
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申请注册联系人电话: Applicant telephone: |
+86 138 6186 8628 |
研究负责人电话: Study leader's telephone: |
+86 138 6186 8628 |
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申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
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申请注册联系人电子邮件: Applicant E-mail: |
jickim@163.com |
研究负责人电子邮件: Study leader's E-mail: |
jickim@163.com |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
研究负责人网址(自愿提供): Study leader's website(voluntary supply): |
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申请注册联系人通讯地址: |
无锡市滨湖区中南西路8号 |
研究负责人通讯地址: |
无锡市滨湖区中南西路8号 |
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Applicant address: |
8 Zhongnan West Road, Binhu District, Wuxi, Jiangsu, China |
Study leader's address: |
8 Zhongnan West Road, Binhu District, Wuxi, Jiangsu, China |
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申请注册联系人邮政编码: Applicant postcode: |
研究负责人邮政编码: Study leader's postcode: |
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申请人所在单位: |
无锡市中医医院 |
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Applicant's institution: |
Wuxi Hospital of Traditional Chinese Medicine |
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研究负责人所在单位: |
无锡市中医医院 |
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Affiliation of the Leader: |
Wuxi Hospital of Traditional Chinese Medicine |
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是否获伦理委员会批准: |
是/Yes |
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Approved by ethic committee: |
Yes |
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伦理委员会批件文号: Approved No. of ethic committee: |
2024(研)-034-02;2024(研)-034-06 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
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批准本研究的伦理委员会名称: |
无锡市中医医院伦理委员会 |
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Name of the ethic committee: |
IRB of Wuxi Hospital of Traditional Chinese Medicine |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-04-25 00:00:00 |
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伦理委员会联系人: |
沈燕菊 |
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Contact Name of the ethic committee: |
Yanju Shen |
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伦理委员会联系地址: |
无锡市滨湖区中南西路8号 |
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Contact Address of the ethic committee: |
8 Zhongnan West Road, Binhu District, Wuxi, Jiangsu, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 510 8270 3775 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
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研究实施负责(组长)单位: |
无锡市中医医院 |
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Primary sponsor: |
Wuxi Hospital of Traditional Chinese Medicine |
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研究实施负责(组长)单位地址: |
无锡市滨湖区中南西路8号 |
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Primary sponsor's address: |
8 Zhongnan West Road, Binhu District, Wuxi, Jiangsu, China |
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试验主办单位(项目批准或申办者): Secondary sponsor: |
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经费或物资来源: |
省中医药重点科技发展计划项目 |
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Source(s) of funding: |
Provincial key Science and Technology Development Program of Traditional Chinese Medicine |
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Target disease: |
lung cancer |
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Target disease code: |
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研究类型: |
干预性研究 |
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Study type: |
Interventional study |
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研究所处阶段: |
其它 | ||||||||||||||||||||||
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Study phase: |
N/A |
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研究设计: |
随机平行对照 |
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Study design: |
Parallel |
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研究目的: |
(1)评价中药 WD-3 联合 PD-1/PD-L1 抑制剂+化疗对 IIIb-IV 期非小细胞肺癌(NSCLC)患者的有效性。 (2)评价中药 WD-3 联合 PD-1/PD-L1 抑制剂+化疗对 IIIb-IV 期非小细胞肺癌(NSCLC)患者的安全性。 |
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Objectives of Study: |
(1)To evaluate the effectiveness of traditional Chinese medicine WD-3 in combination with PD-1/PD-L1 inhibitors + chemotherapy in patients with stage IIIb-IV non-small cell lung cancer (NSCLC). (2)To evaluate the safety of traditional Chinese medicine WD-3 in combination with PD-1/PD-L1 inhibitors + chemotherapy in patients with stage IIIb-IV non-small cell lung cancer (NSCLC). |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
1)符合西医诊断标准,确诊为肺腺癌或鳞癌,TNM分期为IIIb-IV期的患者;无EGFR/ALK/ROS-1/c-MET驱动基因突变,且明确PDL1免疫组化检测结果; 2)中医辨证诊断为肺脾气虚证型:久咳痰稀、胸闷气短、神疲乏力、腹胀纳呆、浮肿便溏、舌质淡苔薄,边有齿痕,脉沉细。 3)有可测量的靶病灶; 4)体力状况评分(Eastern Cooperative Oncology Group,ECOG)≤1 分 5)年龄≥18 岁 6)自愿参加并签署知情同意书。 |
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Inclusion criteria |
1. Patients who meet the diagnostic criteria of Western medicine and are diagnosed as lung adenocarcinoma or squamous cell carcinoma with TNM stage IIIb-IV; EGFR/ALK/ROS-1/c-MET driver gene mutation was not detected, and PDL1 immunohistochemical test results were clear; 2. TCM syndrome differentiation diagnosis is lung qi deficiency syndrome type: long cough thin sputum, chest stuffy short breath, fatigue, abdominal distension and lethargy, bloated loose stool, tongue light moss thin, tooth marks on the edge, and thin pulse; 3. Measurable target lesions; 4. Physical strength score (Eastern Cooperative Oncology Group (ECOG)) <=1 score; 5. Age >=18 years old; 6.Volunteer to participate and sign the informed consent. |
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排除标准: |
1)一个月内接受过任何针对肿瘤的放疗、化疗、靶向或免疫治疗的患者; 2)病理组织、血液、体液标本基因检测提示EGFR、ALK、ROS-1等基因突变阳性,适宜服用相应靶向药物的患者; 3)有症状的脑转移的患者; 4)有严重出血倾向、血小板小于50×109/L和凝血功能严重紊乱的患者; 5)孕妇和哺乳期妇女;或肝、肾、心、肺、脑功能严重不全者;或严重贫血、脱水及营养代谢严重紊乱,无法在短期内纠正或改善者;或严重全身感染、高热(T>38.5℃)的患者; 6)HIV抗体阳性,或患有其它获得性、先天性免疫缺陷疾病的患者; 7)有器官移植史的患者; 8)三个月内参加其他临床试验的患者。 9)正在接受具有抗肿瘤作用的其他中药治疗的患者。 |
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Exclusion criteria: |
1.Patients who have received any tumor specific radiotherapy, chemotherapy, targeted or immunotherapy within one month; 2.Gene detection of pathological tissue, blood and body fluid samples showed positive mutations of EGFR, ALK, ROS-1 and other genes, which was suitable for patients taking corresponding targeted drugs. 3. Patients with symptomatic brain metastases; 4. Patients with severe bleeding tendency, platelet less than 50×10^9/L and severe coagulation disorder; 5. Pregnant and lactating women; Or liver, kidney, heart, lung, brain serious insufficiency; Or severe anemia, dehydration and severe disorder of nutrient metabolism, which cannot be corrected or improved in a short time; Or severe systemic infection, high fever (T>38.5℃); 6.HIV antibody positive, or suffering from other acquired, congenital immunodeficiency disease patients; 7. Patients with a history of organ transplantation; 8. Patients enrolled in other clinical trials within three months. 9. Patients who are receiving other Chinese medicines with antitumor effects. |
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研究实施时间: Study execute time: |
从 From 2024-06-03 00:00:00至 To 2026-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2024-06-03 00:00:00 至 To 2025-12-31 00:00:00 |
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干预措施: Interventions: |
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研究实施地点: Countries of recruitment and research settings: |
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测量指标: Outcomes: |
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采集人体标本:
Collecting sample(s)
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征募研究对象情况: Recruiting status: |
正在进行 Recruiting |
年龄范围: Participant age: |
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性别: |
男女均可 |
Gender: |
Both |
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随机方法(请说明由何人用什么方法产生随机序列): |
由无锡市中医医院中研所redcap系统,电脑生产随机数字表。自动分配受试者编号 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
The random number table is produced by the redcap system of the Central Research Institute of Wuxi Hospital of traditional Chinese medicine. Automatic assignment of subject number |
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是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
公开/Public |
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盲法: |
医生、受试者、统计专家皆处于盲法 |
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Blinding: |
Doctors, subjects, statisticians are blinded |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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是否共享原始数据: IPD sharing |
Yes |
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共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址): |
发表文章后,经研究者同意后可邮箱获取; |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
After the article is published, it can be obtained by email with the consent of the researcher; |
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数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC: |
CRF随访软件 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
CRF follow-up software |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |