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Glucarpidase Effect on Severe Delayed HDM-clearance in Children Treated With High-dose Mtx in ALL (NOPHOCPG2)

Primary Purpose

Acute Lymphoblastic Leukemia (ALL)

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Glucarpidase
Sponsored by
Nordic Society for Pediatric Hematology and Oncology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Lymphoblastic Leukemia (ALL) focused on measuring Drug: Glucarpidase

Eligibility Criteria

1 Year - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Children and adolescents who experience delayed MTX-clearance and renal dysfunction during high-dose methotrexate treatment in NOPHO ALL-2008.

Exclusion Criteria:

Children and adolescents with earlier anaphylactic reaction to Glucarpidase. Pregnant patients.

Sites / Locations

  • Department of Pediatrics, Rigshospitalet
  • Helsinki University Hospital
  • University of Reykjavik
  • University Hospital of Trondheim
  • Department of Pediatrics, Drottning Sylvias Pediatric Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Glucarpidase arm

Arm Description

In the NOPHO ALL-2008 protocol patients with delayed methotrexate elimination (DME) in high-dose methotrexate treatments should be given Glucarpidase (50 ie/kg) with-in 60 hours from start of the methotrexate treatment.

Outcomes

Primary Outcome Measures

Number of Participants With Adverse Event to HD-MTX Treatment in NOPHO ALL-2008 as a Measure of Toxic Mtx Concentrations in Blood, Nephrotoxicity, Hepatotoxicity, Mucositis, MTX Elimination Time and Permanent Kidney Damage.
Glucarpidase was used in case of predefined toxic MTX values at defined time points and/or in combination with decreased renal function. A total of 47 patients of the 1286 ALL-patients included in the protocol (3.7 %) were treated with Glucarpidase.

Secondary Outcome Measures

Full Information

First Posted
February 28, 2011
Last Updated
August 31, 2018
Sponsor
Nordic Society for Pediatric Hematology and Oncology
Collaborators
Lund University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01305655
Brief Title
Glucarpidase Effect on Severe Delayed HDM-clearance in Children Treated With High-dose Mtx in ALL
Acronym
NOPHOCPG2
Official Title
Glucarpidase (CPG2) Effect on Severe Delayed Methotrexate-clearance in Children Treated With High-dose Methotrexate in Acute Lymphoblastic Leukemia (ALL)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Completed
Study Start Date
July 2008 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
December 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Nordic Society for Pediatric Hematology and Oncology
Collaborators
Lund University Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Early intervention in children and adolescents who experience delayed MTX-clearance and renal dysfunction in ALL treatments with the enzyme Glucarpidase which rapidly hydrolyses MTX to non-toxic metabolites to avoid life threatening complications.
Detailed Description
The NOPHO ALL-2008 protocol is a treatment and research protocol that aims to improve the overall outcome of Nordic children and adolescents with ALL in comparison with the ALL-2000 protocol and with the aim to reduce and prevent toxic treatment complications with high-dose methotrexate (HD-MTX). The specific and primary objectives of the randomized study is: Early intervention in children and adolescents who experience delayed MTX-clearance and renal dysfunction with the enzyme Glucarpidase which rapidly hydrolyses MTX to non-toxic metabolites and lowers the serum concentration to avoid life threatening complications. Glucarpidase should be given if the 24 hour levels of MTX is > 250 µM, 36 hour levels > 30 µM or 42 hours levels > 10 µM together with a reduced kidney function. Glucarpidase treatment should take place within 48 hours from the start of HD-MTX treatment. To evaluate if the early intervention with Glucarpidase reduce the number of days the patients have to stay at the hospital. Evaluate the reduction of health costs of early intervention in patients with delayed MTX-clearance and renal dysfunction.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Lymphoblastic Leukemia (ALL)
Keywords
Drug: Glucarpidase

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
47 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Glucarpidase arm
Arm Type
Experimental
Arm Description
In the NOPHO ALL-2008 protocol patients with delayed methotrexate elimination (DME) in high-dose methotrexate treatments should be given Glucarpidase (50 ie/kg) with-in 60 hours from start of the methotrexate treatment.
Intervention Type
Drug
Intervention Name(s)
Glucarpidase
Other Intervention Name(s)
VORAXAZE®
Intervention Description
Patients treated with Glucarpidase if the 24 hour levels of MTX is >250 µM, 36 hour levels >30 µM or 42 hours levels >10 µM together with a reduced kidney function will be compared with patients in just below the tricking values.
Primary Outcome Measure Information:
Title
Number of Participants With Adverse Event to HD-MTX Treatment in NOPHO ALL-2008 as a Measure of Toxic Mtx Concentrations in Blood, Nephrotoxicity, Hepatotoxicity, Mucositis, MTX Elimination Time and Permanent Kidney Damage.
Description
Glucarpidase was used in case of predefined toxic MTX values at defined time points and/or in combination with decreased renal function. A total of 47 patients of the 1286 ALL-patients included in the protocol (3.7 %) were treated with Glucarpidase.
Time Frame
6 years 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children and adolescents who experience delayed MTX-clearance and renal dysfunction during high-dose methotrexate treatment in NOPHO ALL-2008. Exclusion Criteria: Children and adolescents with earlier anaphylactic reaction to Glucarpidase. Pregnant patients.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jesper Heldrup, M D
Organizational Affiliation
University Childrens hospital, Lund, Sweden
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Pediatrics, Rigshospitalet
City
Copenhagen
ZIP/Postal Code
DK-2100
Country
Denmark
Facility Name
Helsinki University Hospital
City
Helsinki
Country
Finland
Facility Name
University of Reykjavik
City
Reykjavik
Country
Iceland
Facility Name
University Hospital of Trondheim
City
Trondheim
Country
Norway
Facility Name
Department of Pediatrics, Drottning Sylvias Pediatric Hospital
City
Goteborg
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Publication in preparation in Pediatric Blood and Cancer
Citations:
PubMed Identifier
27966809
Citation
Svahn T, Mellgren K, Harila-Saari A, Asberg A, Kanerva J, Jonsson O, Vaitkeviciene G, Stamm Mikkelssen T, Schmiegelow K, Heldrup J. Delayed elimination of high-dose methotrexate and use of carboxypeptidase G2 in pediatric patients during treatment for acute lymphoblastic leukemia. Pediatr Blood Cancer. 2017 Jul;64(7). doi: 10.1002/pbc.26395. Epub 2016 Dec 14.
Results Reference
derived

Learn more about this trial

Glucarpidase Effect on Severe Delayed HDM-clearance in Children Treated With High-dose Mtx in ALL

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