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TerminatedNCT05022797Updated May 13, 2024

Reduction of MTX Levels After Glucarpidase Treatment in DLBCL Patients at Risk of CNS

A Phase 2 interventional study of Glucarpidase 1000 UNT [Voraxaze] in Diffuse Large B-Cell Lymphoma and Drug Toxicity, sponsored by Fundacion CRIS de Investigación para Vencer el Cáncer. Terminated at 2 sites in Spain. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2024-05-13.

Sponsored by Fundacion CRIS de Investigación para Vencer el Cáncer · Phase 2, Interventional, and Treatment

Why this study was terminated
closed because of low recruitment
Phase
Phase 2
Study type
Interventional
Enrollment
3
Allocation
Not applicable
Ages
18 Years to 70 Years
Sex
All
01

Study summary

Diffuse large B-cell lymphoma (DLBCL) is an aggressive subset of non-Hodgkin's lymphoma (NHL). Central nervous system (CNS) involvement in patients with NHL is a serious complication. The outcome of patients with CNS relapse is extremely poor, with a median survival of 4-6 months.

One approach to reduce CNS relapse in high-risk patients is the use of systemic high-dose intravenous (iv) methotrexate (HMTX) chemotherapy. Currently available methods of MTX clearance, including dialysis-based methods, have shown limited efficacy.

Glucarpidase hydrolyses MTX to inactive metabolites that are partially metabolised by the liver, thus providing an alternative route of limiting renal excretion.

The administration of Glucarpidase could prevent MTX toxicity as a whole as well as the following consequences. The aim of this study is to analyse the prophylactic effect of 2,000 units of glucarpidase administered after 12 hours of HDMTX on MTX clearance and on the incidence and severity of MTX-related toxicity.

Read the detailed description

Glucarpidase hydrolyzes the terminal glutamate residue from MTX to inactive metabolites [4-deoxy-4-amino-N10-methylpteroic acid (DAMPA) and glutamic acid] which are partially metabolized by the liver, thus providing an alternative route of limitation to renal excretion.

Administration of Glucarpidase cause a clinically important 99% or greater sustained MTX reduction being immediate in most patients, 87% of them experiencing a ≥ 95% reduction in serum MTX concentration at a median of 15 min post-Glucarpidase Early administration of Glucarpidase could avoid MTX toxicity as whole as well as the following consequences. The aim of this study is to analyze the prophylactic effect of 2,000 unit Glucarpidase administered after 12 hour of HDMTX on the MTX clearance and on the incidence and severity of MTX related-toxicity.

According to normal clinical practice, patients will receive for curative intent rituximab cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) by standard protocol on a 21-day cycle (a total of 6 cycles), plus 3 infusion of systemic intravenous MTX at a dose of 3 g/m2 for CNS prophylaxis (HDMTX) at cycles 1, 3 and 5.

Glucarpidase will be capped at 2,000 units per dose (in two vials of 1,000 units/vial) given as a single intravenous (IV) bolus injection over 5 minutes. Glucarpidase will be administered 12 hours following each HDMTX at cycles 1, 3 and 5.

Clinical laboratory evaluation of Hematology and Biochemistry will be conducted at each step of this study, according to the local laboratory method, to determine occurrences of adverse events (AE) or serious adverse events (SAE) following the Common Terminology Criteria for Adverse Events version 5.0 (CTCAE 5.0).

According to standard practice, the blood MTX levels will be monitored according to the local laboratory method, already in place for this purpose. In addition, blood samples for analysis of MTX levels by LC-MS/MS should be drawn at the different time-point.

Therefore, the pharmacokinetic study of MTX clearance includes a quantification of MTX plasma level before and after Glucarpidase administration, assessed by Liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis performed by Eurofins\|ADME Bioanalyses. Collection times are defined as described:

T0 is the time 12 hours after the MTX infusion starts, with reference to T0. As previously mentioned, plasma MTX levels will be measured at:

  • T0 (pre-Glucarpidase i.v. injection) It will be considered maximum plasma MTX level
  • T0+15 minutes (15 minutes after the end of Glucarpidase administration)
  • T0+6hrs (6 hours after Glucarpidase is given)
  • T0+ 12 hrs (12 hours after Glucarpidase is given)
  • T0+ 24hrs (24 hours after Glucarpidase is given Antibodies anti-Glucarpidase (ADA) will be assessed 12 hours after the MTX infusions starts before Glucarpidase administration (reference to T0) and at the follow-up visit month 3 (after the end of RCHOP treatment). In case of positively response for antibodies at any time-point, the evaluation of immune response to Glucarpidase includes a quantification of the Glucarpidase immunogenicity assessed by a neutralization assay performed by Eurofins\|ADMEBioanalyses.

Statistical analyses will be conducted based on the available data, without using techniques for inputting missing values, but describing the number of missing values for each analysis. All statistical tests will be performed at a significance level of α = 0.05, unless specifically stated otherwise.

The primary outcome will be assessed by a descriptive analysis of MTX levels: - As a categorical variable: >95% reduction of MTX (yes/no) after 6 hours after administration of 2,000 units of Glucarpidase. In addition, co-primary outcomes will be assessed by a descriptive analysis of MTX levels: - As a numerical variable: MTX in µmol/L before and after 15 minutes, 6 hours, 12 hours and 24 hours after administration of 2,000 units of Glucarpidase. - As a numerical variable: MTX change from baseline in µmol/L after 15 minutes, 6 hours, 12 hours and 24 hours after administration of 2,000 units of Glucarpidase. - As a categorical variable: >95% reduction of MTX (yes/no) after 15 minutes, 12 hours and 24 hours after administration of 2,000 units of Glucarpidase.

02

Conditions studied

  • Diffuse Large B-Cell Lymphoma
  • Drug Toxicity
03

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Subjects aged 18-70 years
  2. Patients with diagnosis of diffuse large B-cell lymphoma
  3. Patients at high risk of CNS involvement (>2 extranodal sites plus an elevated LDH or /and involvement of high-risk extranodal sites including testes, paranasal sinuses, breast, liver, adrenal and renal)
  4. Patients who will receive HDMTX (three cycles) into R-CHOP regimen (6 cycles) prescribed according to normal clinical practice
  5. Absence of focal neurological signs
  6. Absence of CNS involvement determined by cerebrospinal fluid (CSF) cytometry flow test prior to start treatment
  7. Eastern Cooperative Oncology Group (ECOG) performance status 0-2
  8. Absolute neutrophil count 1800-7500/µL, platelet count 130.000- 450.000/ µL, hemoglobin 13,5-18 g/dL,
  9. Serum creatinine ≤1.5 x the upper limit of normal (ULN) or glomerular filtration rate (GFR) ≥60ml/min/1.73m\^2
  10. Total serum bilirubin ≤2 x ULN. Serum aspartate transaminase (AST) and/or alanine transaminase (ALT) ≤2.5 x ULN
  11. Ability to understand and the willingness to sign a written informed consent document
  12. In women of childbearing potential (from menarche and until becoming post-menopausal [i.e., no menses for 12 months with an alternative medical cause], unless permanently sterile) and men, use of highly effective measure of contraception (abstinence, hormonal contraception, intra-uterine device [IUD], intrauterine hormone-releasing system, [IUS], or anatomical sterility in self or partner) committed during 3 months after the last IMP administration.

Exclusion criteria

Exclusion Criteria:

  1. Malignant disease, other than those being treated in this study. Exceptions to this exclusion include malignancies that were treated curatively and have not recurred within 2 years after completion of treatment.
  2. Patients suffered from cardiovascular diseases (arrhythmias, previous heart failure, thromboembolic disease)
  3. Previous treatment with Glucarpidase
  4. Pregnant or breastfeeding women
  5. Concomitant treatment with agents which interact with methotrexate metabolism or excretion
  6. Known intolerance/hypersensitivity to Glucarpidase or any of its excipients.
04

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
3 participants (actual)

Study arms

  • Experimental
    Glucarpidase, methotrexate, R-CHOP

    Glucarpidase 2000Units per dose. IV. Bolus injection over 5 minutes. Administered 12 hours following after each HDMTX cycle, for a maximum of 3 cycles.

    Drug: Glucarpidase 1000 UNT [Voraxaze]

Interventions

  • DrugGlucarpidase 1000 UNT [Voraxaze]

    2 vials of 1000 units per vial

    Also known as: VORAXAZE®, P21011D

05

What researchers measure

Primary outcomes

  1. Proportion of patients who achieve significant change blood MTX levels (more than 95% reduction of blood MTX levels) at 6 hours after administration of Glucarpidase

    As a categorical variable: \>95% reduction of MTX (yes/no) after 6 hours after administration of 2,000 units of Glucarpidase.

    Time frame: 6 hours

Secondary outcomes

  1. Change blood MTX levels achieved at 15 minutes, 6 hours, 12 hours and 24 hours after administration of Glucarpidase

    As a numerical variable: MTX in µmol/L before and after 15 minutes, 6 hours, 12 hours and 24 hours after administration of 2,000 units of Glucarpidase.

    Time frame: 15min, 6 hours, 12 hours, 24 hours

  2. Proportion of patients with more than 95% reduction of blood MTX levels after administration of Glucarpidase

    As a numerical variable: MTX change from baseline in µmol/L after 15 minutes, 6 hours, 12 hours and 24 hours after administration of 2,000 units of Glucarpidase.

    Time frame: 15min, 6 hours, 12 hours, 24 hours

  3. Proportion of patients who achieve clinically important reduction (CIR) in blood MTX level at 15 minutes, 6 hours, 12 hours and 24 hours after administration of Glucarpidase.

    CIR is defined as a reduction in blood MTX concentration to ≤ 1 µmol/L in post-Glucarpidase time points. As a categorical variable: reduction in blood MTX concentration to ≤ 1 µmol/L (yes/no) after 15 minutes, 6 hours, 12 hours and 24 hours after administration of 2,000 units of Glucarpidase.

    Time frame: 15min, 6 hours, 12 hours, 24 hours

06

Study locations

2 sites
  • MD Anderson
    Madrid, 28033, Spain
  • Hospital Universitario Ramón y Cajal
    Madrid, 28034, Spain
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT05022797
Lead sponsor
Fundacion CRIS de Investigación para Vencer el Cáncer
Collaborators
BioClever 2005 S.L., Eurofins ADME, S.L., NTShub, S.L., BTG International Inc.
Responsible party
Sponsor
First posted
Aug 26, 2021
Start date
Jul 19, 2021
Primary completion
Nov 22, 2022
Completion
Nov 22, 2022
Last update
May 13, 2024

Study contacts

Adolfo De la Fuente, PD
principal investigator · MD Anderson

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
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