CCCG Relapsed Acute Lymphoblastic Leukemia 2017 Study in Children
- Sponsor
- Chinese University of Hong Kong
- Study ID
- NCT04224571
- Phase
- PHASE2
- Status
- Completed
Conditions
- Acute Lymphoblastic Leukemia, in Relapse
Eligibility Criteria
- Sex
- ALL
- Age
- 3 Months - 21 Years
- Healthy Volunteers
- Not accepted
Interventions
- Bortezomib Injection — DRUGBortezomib: patients with BM relapsed, add for 4 doses on D1,4,7, 11 in induction; dosage 1.3 mg/m2/dose as per parenteral;
- rituximab injection — DRUGAdd rituximab in patients with CD20 positive ALL, rituximab: 6 doses of on D8,11of induction, D1,15 of consolidation1 and 2 with dosage 375 mg/m2 as parenteral (Terminated in Oct 2020)
Study Details
Relapsed acute lymphoblastic leukaemia (ALL) has a poorer outcome than newly diagnosed ALL patients with only about 40% overall survival after re-treatment. The study CCCG Relapsed ALL 2017 study will adopt the UK R3 study stratification and treatment backbone with two new agents added. There will be a 4-week induction, followed by two consolidation courses. High-risk patients will receive allogeneic stem cell transplant. While intermediate and standard risk groups will continue maintenance treatment for another 2 years or one year. New agents will be added aiming at improving survival outcome. 1. Study of adding anti-CD20 antibody (rituximab) with chemotherapy: CD20 is found to be expressed in 40-50% of B-lineage ALL, and rituximab has been studied in adult ALL with superior survival (75% vs 47%,). There is little experience of using rituximab in pediatric ALL thus a CCCG Relapsed ALL 2017 Study will perform the study assessing the remission rate and MRD response of CD20+ ALL treated with rituximab. Six doses of rituximab and will be monitored the week 5 MRD and relapse rate as study outcome. (This arm was terminated in October 2020 after interim analysis showing lack of efficacy) 2. Adding bortezomid during the induction: The very early or early bone marrow relapse has low remission rate. Previous case studies showed that Bortezomib, a proteasome inhibitor, may achieve remission in refractory ALL, 80% remission in B-ALL with combination of chemotherapy and bortezomib. Thus adding bortezomib, may improve the remission rate, thus bridging to allogeneic stem cell transplant. Adding bortezomib in the relapsed chemotherapy protocol may increase the toxicity and even treatment related mortality. In this protocol, we suggested to add during the induction therapy.
Key Dates
- Start date
- Sep 14, 2018
- Status verified
- Aug 2023
- Primary completion
- Feb 15, 2023
- Completion
- Feb 15, 2023
Study Design
- Enrollment
- 208 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: rituximab and bortezomibto test whether adding rituximab in CD20 positive patients will have improvement in remission rate. (this arm terminated in October 2020) to add bortezomib in high risk patients at Induction to improve remission rate.
Primary Outcome Measure
remission rate [ Time Frame: week 5 MRD and relapse rate ]
Related Studies
- Study of CD19 Allogeneic Memory T-cell Therapy for Relapsed/Refractory CD19+ LeukemiaPHASE1 · Recruiting · St. Jude Children's Research Hospital · Memphis, Tennessee
- Venetoclax Basket Trial for High Risk Hematologic MalignanciesPHASE1 · Recruiting · Andrew E. Place, MD · San Francisco, California
- Safety and Feasibility of CD19 CAR T Cells Using CliniMACS Prodigy for Relapsed/Refractory CD19 Positive ALL and NHLEARLY_PHASE1 · Not Yet Recruiting · Nationwide Children's Hospital · Columbus, Ohio