注册号: Registration number: |
ChiCTR-IPR-14005706 |
最近更新日期: Date of Last Refreshed on: |
2019-02-24 |
注册时间: Date of Registration: |
2014-06-04 |
注册号状态: |
预注册 |
Registration Status: |
Prospective registration |
注册题目: |
中国儿童肿瘤协作组急性淋巴细胞白血病2015方案多中心临床研究 |
Public title: |
CCCG-ALL-2015 protocol based multi-center trial of acute lymphoblastic leukemia |
注册题目简写: |
CCCG-ALL-2015 多中心研究 |
English Acronym: |
CCCG-ALL-2015 multi-center trial |
研究课题的正式科学名称: |
中国儿童肿瘤协作组急性淋巴细胞白血病2015方案多中心临床研究 |
Scientific title: |
CCCG-ALL-2015 protocol based multi-center trial of acute lymphoblastic leukemia |
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: |
申请注册联系人: |
蔡娇阳 |
研究负责人: |
沈树红 |
Applicant: |
Cai Jiaoyang |
Study leader: |
Shen Shuhong |
申请注册联系人电话: Applicant telephone: |
+86 021 38626297 |
研究负责人电话: Study leader's telephone: |
+86 021 38626161-82055 |
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: |
caijiaoyang@scmc.com.cn |
研究负责人电子邮件: Study leader's E-mail: |
shenshuhong@scmc.com.cn |
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: |
上海浦东新区东方路1678号上海儿童医学中心血液肿瘤大楼 |
研究负责人通讯地址: |
上海浦东新区东方路1678号上海儿童医学中心血液肿瘤大楼 |
Applicant address: |
1678 Dongfang Road, Shanghai, China |
Study leader's address: |
1678 Dongfang Road, Shanghai, China |
申请注册联系人邮政编码: Applicant postcode: |
200127 |
研究负责人邮政编码: Study leader's postcode: |
200127 |
申请人所在单位: |
上海儿童医学中心 |
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Applicant's institution: |
Shanghai Children's Medical Center |
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: |
SCMCIRB-K2014060 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
批准本研究的伦理委员会名称: |
上海交通大学医学院附属上海儿童医学中心伦理委员会 |
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Name of the ethic committee: |
IRB of Shanghai Children's Medical Center Affiliated Shanghai Jiao Tong University School of Meicine |
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伦理委员会批准日期: Date of approved by ethic committee: |
2014-12-31 | ||
伦理委员会联系人: |
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Contact Name of the ethic committee: |
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伦理委员会联系地址: |
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Contact Address of the ethic committee: |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
研究实施负责(组长)单位: |
上海儿童医学中心 |
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Primary sponsor: |
Shanghai Children's Medical Center |
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研究实施负责(组长)单位地址: |
上海浦东新区东方路1678号上海儿童医学中心血液肿瘤大楼 |
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Primary sponsor's address: |
1678 Dongfang Road, Shanghai, 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: |
社会捐款 新加坡Viva基金会 |
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Source(s) of funding: |
Social donation, Singapore Viva foundation |
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研究疾病: |
急性淋巴细胞性白血病 |
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Target disease: |
acute lymphoblastic leukemia |
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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: |
IV期临床试验 | ||||||||||||||||||||||||||||||||||||||||||||
Study phase: |
4 |
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研究目的: |
CCCG-ALL-2015方案在美国St. Jude儿童研究医院的Total-XV方案基础之上结合我国国情以及最近的国内外研究进展形成。希望提高我国急性淋巴细胞白血病患儿的预后,并为将来的方案修正提供可靠的临床资料依据。 入组病人随机对照,了解疗效:1)低危组:在再诱导治疗结束后开始随机分分为LR-A(有VCR+Dex)和LR-B(无VCR+Dex)。2)中、高危组:在再诱导治疗结束后开始随机分分为I/HR-C(MTX25mg/m2)和I/HR-D(MTX40mg/m2)。3)Ph+ALL或对伊马替尼和达沙替尼敏感的Ph-Like-ALL一经确诊即随机分为Ph-I 和Ph-D。 |
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Objectives of Study: |
CCCG-ALL-2015 protocol was modified from St. Jude children's research hospital Total-XV for newly diagnosed patients with acute lymphoblastic leukemia. The goal of this study are to evaluate the survival fuction of this risk-directed protocol and to provide reliable data for further improvment. By randomized stuty we try to clarify if the VCR+ Dex puls is necessary for low risk patients; to compare MTX 25mg/m2 Vs MTX 40mg/m2 in intermediate and high risk patients; to compare imatinib Vs dasatinib as a TKI to treat Ph+ ALL. |
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药物成份或治疗方案详述: |
强的松,地塞米松,长春新碱,柔红霉素,门冬酰胺酶,甲氨蝶呤,阿糖胞苷,6-巯基嘌呤,环磷酰胺,伊马替尼,达沙替尼 |
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Description for medicine or protocol of treatment in detail: |
Prednison, Vincristine, Donorubincine, Asparaginase, Methorexate, Cytarabin, dexamethason, thiopurine, Cyclophosphomide |
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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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纳入标准: |
1.急性淋巴细胞白血病; 2.年龄在1月~18岁; 3.签署知情同意书。 |
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Inclusion criteria |
1. Diagnosis of precursor B-cell or precursor T-cell ALL by immunophenotyping; 2. Younger than 18 years of age; 3. Signing the informed consent. |
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排除标准: |
1.成熟B-ALL、混合表型白血病(不包括ALL伴有髓系抗原表达); 2.为第二肿瘤者; 3.继发于免疫缺陷病者; 4.入组前1月到1周期间使用糖皮质激素大于等于7天,或前3个月内有任何化疗、放疗史者(为解除压迫症状而采取的紧急放疗不在除外之列)。 |
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Exclusion criteria: |
1. Mature B-ALL, mixed phenotypic leukemia; 2. secondary neoplasmia; 3. Leukemia secondary to immunodeficiency disease; 4. Participants with prior therapy (emergency radiation to the mediastinum not included. |
研究实施时间: Study execute time: |
从From2015-01-01至To 2034-12-31 |
征募观察对象时间: Recruiting time: |
从From2015-01-01至To 2034-12-31 |
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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