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NCT Number: NCT05682131

South China Children Cancer Group - Relapsed-Acute Lymphoblastic Leukemia 2022 Protocol

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.

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Key information

Age range

1 year–14 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Sun Yat-sen Memorial Hospital, Sun Yat-sen University

Guangzhou, Guangdong, 510120, China

Location status: Recruiting

Location contact

Pei J Fang, Doctoral

CONTACT

[email protected]

13682290830

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Realgar Indigo naturalis formula

Drug

Realgar Indigo naturalis formula was used in the induction, consolidation and intensive treatment of patients in intermediate or high risk

Other names: RIF

Conventional chemotherapy

Combination Product

conventional chemotherapy

Primary outcomes

  1. Complete response rate

    Time frame: from diagnosis, an average of 7 weeks

    Complete response rate after induction treatment in two groups

Study contacts

Contact information is provided by the study sponsor or research team.

Jian Wang, Master's

CONTACT

[email protected]

18588935208

Pei J Fang, Doctoral

CONTACT

[email protected]

13682290830

Sponsors and collaborators

Lead sponsor

Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

Other

Collaborators

  • First Affiliated Hospital of Guangxi Medical University
  • First Affiliated Hospital of Shantou University Medical College
  • First Affiliated Hospital, Sun Yat-Sen University
  • Guangzhou First People's Hospital
  • Hainan People's Hospital
  • Huizhou Municipal Central Hospital
  • LiuZhou People's Hospital
  • Second Xiangya Hospital of Central South University
  • The First Affiliated Hospital of Guangzhou Medical University
  • Third Affiliated Hospital, Sun Yat-Sen University
  • Zhongshan Bo Ai Hospital
  • Zhongshan People's Hospital, Guangdong, China
  • Zhujiang Hospital

Registry information

Acronym: SCCCG-R-ALL

Important dates

Study start
2022
Primary completion
2027
Study completion
2030
First posted
Jan 12, 2023
Registry last updated
Jan 12, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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