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注册号: Registration number: |
ChiCTR2400094179 |
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最近更新日期: Date of Last Refreshed on: |
2024-12-18 11:03:48 |
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注册时间: Date of Registration: |
2024-12-18 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
IA1期-IB期伴高危因素且MRD阳性患者接受埃克替尼三年辅助治疗药物假期的观察性研究 |
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Public title: |
An observational study on drug holidays during three years of adjuvant therapy with icotinib in patients with IA1-IB stage lung cancer with high-risk factors and positive minimal residual disease (MRD) |
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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: |
IA1期-IB期伴高危因素且MRD阳性患者接受埃克替尼三年辅助治疗药物假期的观察性研究 |
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Scientific title: |
An observational study on drug holidays during three years of adjuvant therapy with icotinib in patients with IA1-IB stage lung cancer with high-risk factors and positive minimal residual disease (MRD) |
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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: |
朱少金 |
研究负责人: |
朱少金 |
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Applicant: |
Shaojin ZHU |
Study leader: |
Shaojin ZHU |
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申请注册联系人电话: Applicant telephone: |
+86 138 0553 4126 |
研究负责人电话:
Study leader's |
+86 138 0553 4126 |
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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: |
13805534126@163.com |
研究负责人电子邮件: Study leader's E-mail: |
13805534126@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: |
安徽省芜湖市镜湖区赭山西路2号(241001) |
研究负责人通讯地址: |
安徽省芜湖市镜湖区赭山西路2号(241001) |
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Applicant address: |
No.2 Zheshan West Road, Jinghu District, Wuhu City, Anhui Province (241001) |
Study leader's address: |
No.2 Zheshan West Road, Jinghu District, Wuhu City, Anhui Province (241001) |
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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: |
皖南医学院第一附属医院弋矶山医院 |
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Applicant's institution: |
The First Affiliated Hospital of Wannan Medical College (Yijishan Hospital) |
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研究负责人所在单位: |
皖南医学院第一附属医院弋矶山医院 |
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Affiliation of the Leader: |
The First Affiliated Hospital of Wannan Medical College (Yijishan Hospital) |
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是否获伦理委员会批准: |
是 |
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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)伦理研第(81)号 |
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: |
皖南医学院弋矶山医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Yijishan Hospital, Wannan Medical College |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-09-04 00:00:00 | ||
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伦理委员会联系人: |
彭辉 |
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Contact Name of the ethic committee: |
Hui Peng |
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伦理委员会联系地址: |
安徽省芜湖市镜湖区赭山西路2号 |
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Contact Address of the ethic committee: |
No.2 Zheshan West Road, Jinghu District, Wuhu City, Anhui Province (241001) |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 151 5538 3368 |
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: |
皖南医学院第一附属医院弋矶山医院 |
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Primary sponsor: |
The First Affiliated Hospital of Wannan Medical College (Yijishan Hospital) |
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研究实施负责(组长)单位地址: |
安徽省芜湖市镜湖区赭山西路2号(241001) |
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Primary sponsor's address: |
No.2 Zheshan West Road, Jinghu District, Wuhu City, Anhui Province (241001) |
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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: |
无 |
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Source(s) of funding: |
none |
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研究疾病: |
肺癌 |
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Target disease: |
lung cancer |
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研究疾病代码: |
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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: |
非随机对照试验 |
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Study design: |
Non randomized control |
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研究目的: |
评价埃克替尼治疗IA1期-IB期术后MRD阳性且EGFR 21L858R、19Del突变的NSCLC患者3年的DFS率。 |
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Objectives of Study: |
Evaluating the 3-year Disease-Free Survival (DFS) Rate in Patients with Stage IA1-IB EGFR 21L858R and 19Del Mutation Positive Non-Small Cell Lung Cancer (NSCLC) Post-Surgery with Minimal Residual Disease (MRD) Treated with Icotinib. |
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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: |
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Inclusion criteria |
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排除标准: |
1)无EGFR 21 L858R、19Del突变或MRD阴性;有EGFR合并RB1突变; 2)不符合分期或既往接受过任何EGFR-TKI治疗的患者; 3)手术前期存在任何其他治疗方式,未签署知情同意书; 4)患者在2年内被确诊过癌症;在本研究入组前使用接受过系统性抗肿瘤治疗,包括化疗、放疗或靶向治疗; 5)患者各器官系统状况: 既往患间质性肺病、药物诱导的间质性疾病、需要激素治疗的放射性肺炎或任何具临床证据的活动性间质性肺病;基线时CT扫描发现存在间质性肺病;根据研究者判断,存在严重或不能控制的全身性疾病(如不稳定或不能代偿的呼吸、心脏,肝或肾脏疾病)的证据;任何不稳定的系统性疾病(包括活动性感染、III级高血压、不稳定心绞痛、充血性心力衰竭、肝肾或代谢性疾病); 不能接受口服给药、需要静脉内高能营养、之前进行过影响吸收的手术或有活动性消化性溃疡的患者; 任何明显眼部异常,特别是严重干眼综合征、干性角膜结膜炎、严重的暴露性角膜炎或其他可能增加上皮损害的疾病;既往有明确的神经或精神障碍史,包括癫痫或痴呆 6)已知对埃克替尼或同类药物任何成分过敏的患者; 7)怀孕或哺乳期妇女; 8)其他研究者认为不适合入组的情况。 |
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Exclusion criteria: |
1) No EGFR 21 L858R, 19Del mutations or MRD negative; presence of EGFR combined with RB1 mutations; 2) Patients who do not meet the staging criteria or have previously received any EGFR-TKI treatment; 3) Any other treatment methods existed before surgery, and informed consent was not signed; 4) Patients diagnosed with cancer within 2 years; have received systemic anti-tumor treatment, including chemotherapy, radiotherapy, or targeted therapy, before enrollment in this study; 5) Patient's organ system conditions: a. History of interstitial lung disease, drug-induced interstitial disease, radiation pneumonitis requiring steroid treatment, or any clinically evident active interstitial lung disease; interstitial lung disease found on baseline CT scan; evidence of severe or uncontrollable systemic diseases (such as unstable or uncompensated respiratory, cardiac, hepatic, or renal diseases) as judged by the investigator; any unstable systemic diseases (including active infections, grade III hypertension, unstable angina, congestive heart failure, hepatic, renal, or metabolic diseases); b. Patients who cannot receive oral medication, require intravenous high-calorie nutrition, have previously undergone surgery affecting absorption, or have active peptic ulcers; c. Any significant ocular abnormalities, especially severe dry eye syndrome, dry keratoconjunctivitis, severe exposure keratitis, or other diseases that may increase epithelial damage; history of definite neurological or psychiatric disorders, including epilepsy or dementia; 6) Patients known to be allergic to any component of Icotinib or similar drugs; 7) Pregnant or lactating women; 8) Other situations deemed unsuitable for enrollment by the investigator. |
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研究实施时间: Study execute time: |
从 From 2024-12-18 00:00:00至 To 2029-09-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2024-12-18 00:00:00 至 To 2026-09-30 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): |
无 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
None |
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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: |
无 |
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Blinding: |
none |
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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 |
否No |
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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): |
无 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
none |
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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: |
EDC |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
EDC |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |