A Prospective, Open-label, Randomized Controlled, Multicenter Clinical Study of MSD-HSCT Using a TBI or TMLI Conditioning Regimen for Pediatric ALL
Launched by THE FIRST AFFILIATED HOSPITAL OF ZHENGZHOU UNIVERSITY · Aug 19, 2024
Trial Information
Current as of August 21, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying how two different types of treatments, called conditioning regimens, affect children with acute lymphoblastic leukemia (ALL) who are receiving a type of stem cell transplant from a matched sibling donor. The two treatments being compared are Total Body Irradiation (TBI), which targets the entire body, and Total Marrow, Central Nervous System, and Lymphoid Irradiation (TMLI), which focuses on specific areas. Researchers believe that TMLI may be better at killing leukemia cells while causing less harm to healthy tissues, leading to fewer side effects and a better chance of recovery.
To participate in this study, children aged 1 to 17 who have been diagnosed with ALL and are in remission can be considered, as long as they have a matched sibling donor available. Participants should be able to care for themselves and have no serious health problems that would complicate their treatment. Those who join can expect close monitoring and support throughout the process, as the study aims to find the best way to improve the health and quality of life for young patients undergoing this important treatment.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Informed Consent: Participants or guardians must voluntarily sign a written informed consent form.
- • 2. Age and Gender: Participants should be male or female, aged 1-17 years, inclusive.
- • 3. Diagnosis: Participants must be diagnosed with acute lymphoblastic leukemia (ALL) according to World Health Organization (WHO) criteria, and the diagnosis must apply to pediatrics aged 1-17 years.
- • 4. Remission Status: The participant's leukemia must be in hematologic remission (complete remission, CR) prior to transplantation.
- • 5. Donor Availability: There must be a suitable matched sibling donoravailable, and the participant must consent to undergo MSD hematopoietic stem cell transplantation (MSD-HSCT).
- 6. Karnofsky Performance Status: The participant must have a Karnofsky score of 70 or higher, indicating that they are capable of caring for themselves and carrying out normal activities. Additionally, they must not have significant organ dysfunction, defined by the following:
- • Cardiac Function: New York Heart Association (NYHA) classification of class II or lower.
- • Liver Function: Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels should be no more than 2.5 times the upper limit of normal. Bilirubin levels should be no more than 2 times the upper limit of normal.
- • Renal Function: Serum creatinine levels should be no more than 1.5 times the upper limit of normal, or the creatinine clearance rate should be at least 60 ml/min. o Pulmonary Function: Participants should not experience significant dyspnea, should not require oxygen therapy, should not have interstitial lung disease, and should not have any active pulmonary infections.
- Exclusion Criteria: To be eligible for inclusion in the study, participants must not meet any of the following criteria:
- • 1. The patient has not achieved hematologic remission before transplantation. 2. The patient has chosen a non-MSD donor.
- • 3. The patient has severe cardiac, hepatic, renal, or pulmonary diseases that make them unable to tolerate the conditioning regimen.
- • 4. The patient has an active or refractory infection, or other life-threatening complications.
- • 5. The patient has a history of other malignant tumors, psychiatric disorders, or HIV infection.
- • 6. The patients or guardians refuses to sign the informed consent form, is unwilling to comply with clinical follow-up required by the study, or does not consent to the use of their data to support future research, project presentations, and clinical practices.
- • 7. The investigator deems the patient unsuitable for participation in the study for any other reason.
About The First Affiliated Hospital Of Zhengzhou University
The First Affiliated Hospital of Zhengzhou University is a leading medical institution dedicated to advancing healthcare through innovative clinical research. As a prominent teaching hospital, it combines cutting-edge medical practices with a commitment to patient-centered care. The hospital is recognized for its comprehensive array of specialties and its collaborative approach to research, fostering partnerships with academic and healthcare organizations. By engaging in rigorous clinical trials, the hospital aims to contribute to the development of new therapies and improve treatment outcomes, ultimately enhancing the quality of care for patients both locally and globally.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Zhengzhou, Henan, China
Zhengzhou, , China
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported