Clinical trial · Interventional
Study of 6-Thioguanine in Combination With 6-Mercaptopurine During Maintenance Therapy of Childhood Lymphoma
A Phase 1-2 Study of 6-Thioguanine in Combination With Methotrexate and 6-Mercaptopurine During Maintenance Therapy of Childhood Non-Hodgkin's Lymphoma
NCT02141100CI-TRIAL-00024180withdrawnPhase 1 / Phase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose of this phase 1-2 study is to explore the applicability of supplementing standard methotrexate/6-mercaptopurine (MTX/6MP) maintenance therapy of children with non-Hodgkin lymphoma with 6-thioguanine (6TG). The investigators hypothesize that addition of 6TG to 6MP-based maintenance therapy of patients with high TPMT activity will mimic the more favourable thiopurine metabolism of patients with low TPMT activity and ultimately reduce relapse rates.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Non-Hodgkin Lymphoma | Non-Hodgkin Lymphoma | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| 6-thioguanine | Drug | Thioguanine | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- 6-thioguanine, 6-mercaptopurine and methotrexate
- description
- This is the only treatment arm; all eligible patients will receive standard methotrexate/6-mercaptopurine (6MP/MTX) maintenance therapy supplemented with 6-thioguanine (6TG). Patients are enrolled when they have 12 to 3.5 months remaining of their maintenance therapy. After dose reduction in 6MP to 2/3 of the current dose 6TG therapy is initiated with a starting dose of 2.5 mg/m2/day. The 6TG dose will hereafter be increased at 2.5 mg/m2/day every 14 days until a max. of 12.5 mg/m2/day is reached or until the thiopurine metabolite profile (Ery-TGN/Ery-MeMP) has been increased by at least a factor 5.
- interventionNames
- Drug: 6-thioguanine
Primary outcomes (1)
- measure
- Change in median thiopurine metabolite index
- timeFrame
- Every 2 weeks up to the max. trial period of 12 months
- description
- Change in Ery-TGN/Ery-MeMP after addition of 6-thioguanine to therapy. The thiopurine metabolites will be measured every 2 weeks during the trial period. The trial period is max. 12 months.
Secondary outcomes (2)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 2 Years
- Maximum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Confirmed histomorphological or cytomorphological diagnosis of NHL or ALL. * Meets just one of the following: 1. Patient with NHL treated after the EURO-LB 02 protocol with at least 3.5 months of 6MP/MTX maintenance therapy remaining or 2. Patient with ALL or NHL not achieving the target WBC (patients with a WBC \> 3.0 x10\^9/L) and/or experience elevated liver enzymes (ALAT \> UNL) attributed to a simultaneous high Ery-MeMP level on standard MTX/6MP maintenance therapy. * TPMT wild-type genotype or TPMT high activity phenotype (TPMT activity above 14 IU/mL or during maintenance therapy TPMT above 8 IU/mL measured in erythrocytes). * Bilirubin \< 35 micromol/L, factor 2-7-10 \> 0.5 or INR \< 1.5 and normal hepatic blood flow (verified by ultrasound) within 1 week prior to inclusion. * WBC \> 1.5 x10\^9/L, ANC \> 0.5 x10\^9/L and TBC \> 50 x10\^9/L within 1 week prior to inclusion. * Pubertal females, Tanner stage B3/PH3 or higher, must present with a negative pregnancy test. * Sexually active females must use accepted safe contraception (OCPs, IUD, transdermal hormonal patch, vaginal hormonal ring or subdermal hormonal implants) during therapy and until a month after completion of therapy. * Absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule. * Oral and written informed consent to participate have been provided by both the parents (and when appropriate by the patient) according to the ICH/GCP guidelines and the Helsinki II Declaration. * Patients with acute lymphoblastic lymphoma (0-17.9 yrs) not achieving the target WBC (patients with a WBC \> 3.0 x10\^9/L) and/or experience elevated liver enzymes (ALAT \> UNL) attributed to a simultaneous high Ery-MeMP level on standard MTX/6MP maintenance therapy. Exclusion Criteria: * Any clinical suspicion of relapse or disease progression on routine imaging or in laboratory results. * Previous veno-occlusive disease (VOD). * Allergy towards any of the ingredients in the three medicinal products used in the study.
References
Publications (0)
Data not yet available
No reference posted for this study.