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审核状态: Project audit state: |
通过审核 Successful |
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注册号: Registration number: |
ChiCTR2300075242 |
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最近更新日期: Date of Last Refreshed on: |
2023-08-30 16:45:20 |
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注册时间: Date of Registration: |
2023-08-30 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: |
华南地区儿童癌症协作组——急性淋巴细胞白血病2023方案的多中心前瞻性队列研究 |
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Public title: |
A multicenter prospective cohort study of the acute lymphoblastic leukemia 2023 protocol of the South China Children’s Cancer Group |
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注册题目简写: |
SCCCG-ALL-2023 |
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English Acronym: |
SCCCG-ALL-2023 |
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研究课题的正式科学名称: |
华南地区儿童癌症协作组——急性淋巴细胞白血病2023方案的多中心前瞻性队列研究 |
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Scientific title: |
A multicenter prospective cohort study of the acute lymphoblastic leukemia 2023 protocol of the South China Children’s Cancer Group |
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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: |
李欣瑜 |
研究负责人: |
方建培 |
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Applicant: |
Xinyu Li |
Study leader: |
Jianpei Fang |
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申请注册联系人电话: Applicant telephone: |
+86 159 1438 8992 |
研究负责人电话: Study leader's telephone: |
+86 136 8229 0830 |
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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: |
lixy228@mail.sysu.edu.cn |
研究负责人电子邮件: Study leader's E-mail: |
jpfang2005@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: |
广东省广州市越秀区沿江西路107号 |
研究负责人通讯地址: |
广东省广州市越秀区沿江西路107号 |
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Applicant address: |
107 West Yanjiang Road, Yuexiu District, Guangzhou, Guangdong, China |
Study leader's address: |
107 West Yanjiang Road, Yuexiu District, Guangzhou, Guangdong, China |
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申请注册联系人邮政编码: Applicant postcode: |
510120 |
研究负责人邮政编码: Study leader's postcode: |
510120 |
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申请人所在单位: |
中山大学孙逸仙纪念医院 |
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Applicant's institution: |
Sun Yat-Sen Memorial Hosipital of Sun Yat-Sen University |
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研究负责人所在单位: |
中山大学孙逸仙纪念医院 |
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Affiliation of the Leader: |
Sun Yat-Sen Memorial Hosipital of Sun Yat-Sen University |
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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: |
SYSKY-2023-474-02 |
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: |
中山大学孙逸仙纪念医院医学伦理委员会 |
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Name of the ethic committee: |
The Ethic Commitee of Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-07-11 00:00:00 |
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伦理委员会联系人: |
区柳珊 |
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Contact Name of the ethic committee: |
Ou Liushan |
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伦理委员会联系地址: |
广东省广州市越秀区沿江西路107号 |
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Contact Address of the ethic committee: |
107 West Yanjiang Road, Yuexiu District, Guangzhou, Guangdong, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 20 8133 2587 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
sys_iit@163.com |
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研究实施负责(组长)单位: |
中山大学孙逸仙纪念医院 |
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Primary sponsor: |
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University |
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研究实施负责(组长)单位地址: |
广东省广州市越秀区沿江西路107号 |
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Primary sponsor's address: |
107 West Yanjiang Road, Yuexiu District, Guangzhou, Guangdong, 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: |
无 |
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Source(s) of funding: |
No |
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Target disease: |
Childhood acute lymphoblastic leukemia |
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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: |
上市后药物 | ||||||||||||||||||||||
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Study phase: |
4 |
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研究设计: |
单臂 |
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Study design: |
Single arm |
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研究目的: |
主要研究目标:SCCCG-ALL-2023方案治疗儿童急性淋巴细胞白血病(ALL)的有效性及安全性。 次要研究目标:SCCCG-ALL-2023方案治疗儿童急性淋巴细胞白血病(ALL)的对患者生活质量的影响。 探索性目标: (1)MRD水平对中危儿童ALL预后的作用; (2)不同融合基因在中危组儿童ALL预后中的作用。 |
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Objectives of Study: |
The primary purpose: To study the efficacy and safety of SSCCCG-ALL-2023 regimen in the treatment of children ALL. The secondary purpose: To study the impact of the SCCC-ALL-2023 treatment plan on the quality of life of children ALL. The exploratory Objectives: (1) The effect of MRD levels on the prognosis of children ALL in intermediate-risk group; (2) The effect of different fusion genes in the prognosis of children ALL in intermediate-risk group. |
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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.年龄为1~18岁; 2.确诊为急性淋巴细胞白血病(ALL); 3.新发患者; 4.受试者及监护人签署知情同意书。 |
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Inclusion criteria |
1. Aged between 1 and 18 years; 2. Patients diagnosed with acute lymphoblastic leukemia (all); 3. First diagnosed patients; 4. Who will participate research and guardian to sign the informed consent form. |
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排除标准: |
1.急性混合表型白血病(诊断标准见研究者手册附件一); 2.继发于免疫缺陷病; 3.为第二肿瘤; 4.明确的CML 急变; 5.伴Down’S 综合征的ALL; 6.入组前一个月内使用糖皮质激素超过一周; 7.入组前一个月内使用蒽环类药物; 8.重度肝功能不全(肝酶(ALT或AST) ≥3xULN); 9.重度肾功能损伤(eGFR < 30 ml/min/1.73m3或终末期肾病患者); 10.心脏病,纽约心脏协会(NYHA)分级为3级或以上的心力衰竭,或需要治疗的严重心律失常,或随机分组后6个月内的近期心肌梗死; 11.入组前24周内有深静脉血栓形成或卒中病史的患者; 12.入组前24周内有急、慢性胰腺炎病史的患者; 13.生命垂危,预期寿命不足6个月者; 14.任何重大的其他医疗状况、实验室异常或精神疾病,研究者认为不适合纳入者。 |
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Exclusion criteria: |
1.With acute mixed-phenotypic leukemia (see annex I of the researcher's manual for diagnostic criteria); 2. With secondary immunodeficiency; 3. Patients with leukemia which is the second tumor; 4. With definite CML abrupt change; 5.ALL with Down's syndrome; 6. Patients who used glucocorticoids for more than one week in the month before enrollment; 7. Patients who used anthracyclines within one month before enrollment. 8.Severe hepatic insufficiency(ALT or AST ≥3xULN). 9.Severe renal impairment (eGFR < 30 ml/min/1.73m3 or end-stage renal disease patients). 10.Heart disease, New York Heart Association (NYHA) classification of grade 3 or above heart failure, or severe arrhythmia requiring treatment, or recent myocardial infarction within 6 months after randomization. 11.Patients with a history of deep vein thrombosis or stroke within 24 weeks prior to enrollment. 12.Patients with a history of acute or chronic pancreatitis within 24 weeks prior to enrollment. 13.Those whose lives are in danger and have a life expectancy of less than 6 months. 14.Any significant other medical condition, laboratory abnormality, or psychiatric illness that the investigators consider unsuitable for inclusion. |
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研究实施时间: Study execute time: |
从 From 2023-09-01 00:00:00至 To 2033-08-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2023-09-01 00:00:00 至 To 2028-08-31 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: |
尚未开始 Not yet 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): |
非随机分组 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
no randomization procedure |
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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: |
不公开/Private |
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盲法: |
开放 |
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Blinding: |
open label |
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是否共享原始数据: IPD sharing |
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): |
Https://redcap.syshospital.org:8082/ |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Https://redcap.syshospital.org:8082/ |
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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: |
病例记录表及电子采集和管理系统 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Standard data collection and management system |
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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 |