South China Children Cancer Group - Relapsed-Acute Lymphoblastic Leukemia 2022 Protocol (SCCCG-R-ALL)
Primary Purpose
Arsenic Trioxide, Childhood ALL
Status
Recruiting
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Realgar Indigo naturalis formula
Conventional chemotherapy
Sponsored by
About this trial
This is an interventional treatment trial for Arsenic Trioxide
Eligibility Criteria
Inclusion Criteria: B or T cell type; the first recurrence; the risk stratification was medium or high risk. Exclusion Criteria: mature B cell leukemia; acute mixed phenotype leukemia; patients with positive BCR/ABL fusion gene; the second tumor definite CML blast crisis; ALL with Down's syndrome.
Sites / Locations
- Sun Yat-sen Memorial Hospital, Sun Yat-sen UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
Control group
Experimental Group
Arm Description
Oral placebo was added to conventional chemotherapy
Oral RIF was added to conventional chemotherapy
Outcomes
Primary Outcome Measures
Complete response rate
Complete response rate after induction treatment in two groups
Secondary Outcome Measures
Full Information
NCT ID
NCT05682131
First Posted
January 2, 2023
Last Updated
January 10, 2023
Sponsor
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Collaborators
First Affiliated Hospital, Sun Yat-Sen University, Third Affiliated Hospital, Sun Yat-Sen University, Zhujiang Hospital, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou First People's Hospital, Huizhou Municipal Central Hospital, First Affiliated Hospital of Shantou University Medical College, Zhongshan People's Hospital, Guangdong, China, Zhongshan Bo Ai Hospital, First Affiliated Hospital of Guangxi Medical University, LiuZhou People's Hospital, Second Xiangya Hospital of Central South University, Hainan People's Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05682131
Brief Title
South China Children Cancer Group - Relapsed-Acute Lymphoblastic Leukemia 2022 Protocol
Acronym
SCCCG-R-ALL
Official Title
South China Children Cancer Group - Relapsed-Acute Lymphoblastic Leukemia 2022 Protocol
Study Type
Interventional
2. Study Status
Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 27, 2022 (Actual)
Primary Completion Date
September 27, 2027 (Anticipated)
Study Completion Date
September 27, 2030 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Collaborators
First Affiliated Hospital, Sun Yat-Sen University, Third Affiliated Hospital, Sun Yat-Sen University, Zhujiang Hospital, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou First People's Hospital, Huizhou Municipal Central Hospital, First Affiliated Hospital of Shantou University Medical College, Zhongshan People's Hospital, Guangdong, China, Zhongshan Bo Ai Hospital, First Affiliated Hospital of Guangxi Medical University, LiuZhou People's Hospital, Second Xiangya Hospital of Central South University, Hainan People's Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
In recent years, the prognosis of pediatric relapsed ALL patients has improved, but the 5-year OS of patients with first recurrence is still less than 50%. A number of in vitro studies have shown that arsenic trioxide (ATO) can selectively inhibit the growth and induce apoptosis in a variety of leukemia cell lines, suggesting that ATO as a synergist combined with other common chemotherapy drugs may provide a new target for the treatment of relapsed ALL. Realgar Indigo naturalis formula is a compound traditional Chinese medicine preparation developed in China. The main component of realgar is arsenic tetrasulfide (As4S4), which can produce similar pharmacological effects to ATO. Based on the R3 protocol, this study plans to perform a double-blind randomized controlled trial, and to randomly combine compound Huangdai tablets with compound Huangdai tablets in the treatment of intermediate and high risk ALL children, in order to improve the MRD negative rate after induction therapy in this group of children, which may provide a new method for the clinical treatment of relapsed ALL.
Detailed Description
In recent years, the prognosis of pediatric relapsed ALL patients has improved, but the 5-year OS of patients with first recurrence is still less than 50%, and the prognosis of children with intermediate and high risk is even worse, so there is an urgent need to explore new and effective treatment methods. A number of in vitro studies have shown that arsenic trioxide (ATO), which is safe and effective in the treatment of APL, can selectively inhibit the growth and induce apoptosis in a variety of leukemia cell lines, suggesting that ATO as a synergist combined with other common chemotherapy drugs may provide a new target for the treatment of relapsed ALL. Realgar Indigo naturalis formula is a compound traditional Chinese medicine preparation developed in China. The main component of realgar is arsenic tetrasulfide (As4S4), which can produce similar pharmacological effects to ATO. The UK ALL R3 protocol is an advanced and mature clinical trial. The results showed that the MRD negative rate after induction chemotherapy and the 2-year DFS of traditional chemotherapy ±HSCT in children with intermediate and high risk did not reach 50%. Based on the R3 protocol, this study plans to perform a double-blind randomized controlled trial, and to randomly combine compound Huangdai tablets with compound Huangdai tablets in the treatment of intermediate and high risk ALL children, in order to improve the MRD negative rate after induction therapy in this group of children, which may provide a new method for the clinical treatment of relapsed ALL.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Arsenic Trioxide, Childhood ALL
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
210 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
Oral placebo was added to conventional chemotherapy
Arm Title
Experimental Group
Arm Type
Experimental
Arm Description
Oral RIF was added to conventional chemotherapy
Intervention Type
Drug
Intervention Name(s)
Realgar Indigo naturalis formula
Other Intervention Name(s)
RIF
Intervention Description
Realgar Indigo naturalis formula was used in the induction, consolidation and intensive treatment of patients in intermediate or high risk
Intervention Type
Combination Product
Intervention Name(s)
Conventional chemotherapy
Intervention Description
conventional chemotherapy
Primary Outcome Measure Information:
Title
Complete response rate
Description
Complete response rate after induction treatment in two groups
Time Frame
from diagnosis, an average of 7 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
B or T cell type;
the first recurrence;
the risk stratification was medium or high risk.
Exclusion Criteria:
mature B cell leukemia;
acute mixed phenotype leukemia;
patients with positive BCR/ABL fusion gene;
the second tumor
definite CML blast crisis;
ALL with Down's syndrome.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Pei J Fang, Doctoral
Phone
13682290830
Email
jpfang2005@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Jian Wang, Master's
Phone
18588935208
Email
459283765@qq.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xin Y Chen, Doctoral
Organizational Affiliation
Medical Ethics Committee of Sun Yat-sen Memorial Hospital of Sun Yat-sen University
Official's Role
Study Chair
Facility Information:
Facility Name
Sun Yat-sen Memorial Hospital, Sun Yat-sen University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510120
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pei J Fang, Doctoral
Phone
13682290830
Email
jpfang2005@163.com
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
South China Children Cancer Group - Relapsed-Acute Lymphoblastic Leukemia 2022 Protocol
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