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Trials / Not Yet Recruiting

Not Yet RecruitingNCT07406230

Methotrexate Early Toxicity Monitoring

Methotrexate Early Toxicity Monitoring in Primary Central Nervous System Lymphomas (PCNSL)

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Assistance Publique Hopitaux De Marseille · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

High-dose methotrexate (MTX) is the main componement of first line treatment in primary central nervous system lymphoma. Renal toxicity is the main dose limiting toxicity because of major MTX elimination by the kidneys. MTX crystallizes in renal tubules, leading to a renal failure (RF) and further delaying its elimination. When RF occurs, MTX accumulates, prolonging the duration of treatment exposure. MTX prolonging exposure can cause life-threatening complications and delay further treatments in the patient. Preventive measures have been developped, such as alkaline fluid hyperhydration and folic acid administration, to try to reduce the risk of these adverse events. In suspected severe RF in link to MTX is suspected, glucarpidase can be administared. However, this is an expensive treatment and not all patients recover normal renal function despite its use. MTX is an essential treatment for the management of PCNSL which is currently a curable disease especially in patients who are able to receive a consolidation treatment as thiotepa-based intensive consolidation followed by autologous stem cell transplantation (IC-ASCT). IC-ASCT requires a normal renal function, which could be impaired by severe RF secondary to MTX. The purpose of the study is to investigate how early dosing MTX could be used to simulate late concentrations. Early monitoring of MTX elimination could be implemented to identify patients at risk of delayed elimination and thus introduce rapid mesures as early administration of glucarpidase.

Conditions

Interventions

TypeNameDescription
OTHERmethotrexate plasmatic dosingMethotrexate (MTX) dosage at 2,4,6,8,24 and 48 hours

Timeline

Start date
2026-04-01
Primary completion
2027-04-01
Completion
2027-12-01
First posted
2026-02-12
Last updated
2026-02-12

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT07406230. Inclusion in this directory is not an endorsement.