Prediction and Prevention of PEG-Asparaginase Associated Pancreatitis, Hepatotoxicity and Hyperlipidemia in Children With Acute Lymphoblastic Leukemia

The recruitment status of this study is unknown because the information has not been verified recently.
Verified March 2011 by Rigshospitalet, Denmark.
Recruitment status was  Recruiting
Sponsor:
Collaborator:
Technical University of Denmark
Information provided by:
Rigshospitalet, Denmark
ClinicalTrials.gov Identifier:
NCT01393249
First received: July 12, 2011
Last updated: NA
Last verified: March 2011
History: No changes posted
  Purpose

The purpose of this study is to create a model enabling us to predict pancreatitis, hyperlipidemia and hepatotoxicity during treatment with PEG-Asparaginase in children with Acute Lymphoblastic Leukemia.


Condition
Acute Lymphoblastic Leukemia
Pancreatitis
Asparaginase

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Prediction and Prevention of PEG-Asparaginase Associated Pancreatitis, Hepatotoxicity and Hyperlipidemia in Children With Acute Lymphoblastic Leukemia

Resource links provided by NLM:


Further study details as provided by Rigshospitalet, Denmark:

Estimated Enrollment: 40
Study Start Date: July 2011
Estimated Study Completion Date: September 2012
Estimated Primary Completion Date: August 2012 (Final data collection date for primary outcome measure)
Groups/Cohorts
ALL, Asparaginase, pancreatitis
Patients that have been scanned and have had blood tests

Detailed Description:

Leukemia is the leading cause of cancer in children in Europe and the U.S. with an annual incidence of appoximately 3,5 cases per 100.000 children 0-14,9 years.

Although the rate of cure has increased significantly, treatment is still unsuccesfull in appoximately 20 % of the patients. There is great variation in the how the individual patient processes the different chemotherapeutic agents. Furthermore there is a signifikant difference regarding the severity of sideeffects and toxicities. So far it has not been possible to predict which patients are at speciel risk of developing toxicities.

Acute pancreatitis is a severe sideffect/toxicity when treating ALL. Patients are at risk of developing pancreatitis, because of the drug Asparaginase. The condition can not be prevented and in severe cases, e.g. hemorhaggic pancreatitis the only solution is to discontinue the drug, in spite of the fact that Asparaginase is on of the most important drugs when treating leukemia.

In the current study we will map the occurence of pancreatitis, hepatotoxicity and hyperlipidemia among approximately 1000 children and adolescents with leukemia. This study is unique because it is the largest study of its kind regarding Asparaginase associated pancreatitis. Among other things it will involve extensive genetic analysis.

We believe that this study will improve the possibilities, not only, for individualized treatmentVi mener at dette studie vil forbedre mulighederne for individ orienteret behandling, but also for other studies like this regarding other toxicities in patients with cancer.

  Eligibility

Ages Eligible for Study:   1 Year to 18 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

Children aged 1-17.9, diagnosed with ALL and undergoing treatment with Peg-Asparaginase.

Criteria

Inclusion Criteria:

  • IR- or SR- type ALL, and treatment with Peg-Asparaginase

Exclusion Criteria:

  • HR ALL, and changing subgroup from IR or SR to HR
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01393249

Contacts
Contact: Raheel Raja, M.D. +45 26137089 raja_sahib@yahoo.com
Contact: Kjeld Schmiegelow, Professor +35451357 kjeld.schmiegelow@rh.dk

Locations
Denmark
Rigshospitalet Recruiting
Copenhagen, Denmark, 2100
Contact: Raheel Raja, M.D.     +4526137089     raja_sahib@yahoo.com    
Contact: Kjeld Schmiegelow, Professor     +453545131357     kjeld.schmiegelow@rh.dk    
Principal Investigator: Raheel Raja, M.D.            
Sponsors and Collaborators
Rigshospitalet, Denmark
Technical University of Denmark
  More Information

No publications provided

Responsible Party: Raheel Altaf Raja, M.D., PhD student, University Hospital, Rigshospitalet, Blegdamsvej 9, 2100, Copenhagen
ClinicalTrials.gov Identifier: NCT01393249     History of Changes
Other Study ID Numbers: RR240778PEGASP, PEGASPALL240778
Study First Received: July 12, 2011
Last Updated: July 12, 2011
Health Authority: Denmark: The Regional Committee on Biomedical Research Ethics

Keywords provided by Rigshospitalet, Denmark:
Acute Lymphoblastic Leukemia
Pediatric
Asparaginase
Pancreatitis

Additional relevant MeSH terms:
Hyperlipidemias
Leukemia
Leukemia, Lymphoid
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Pancreatitis
Dyslipidemias
Lipid Metabolism Disorders
Metabolic Diseases
Neoplasms by Histologic Type
Neoplasms
Lymphoproliferative Disorders
Lymphatic Diseases
Immunoproliferative Disorders
Immune System Diseases
Pancreatic Diseases
Digestive System Diseases
Pegaspargase
Asparaginase
Antineoplastic Agents
Therapeutic Uses
Pharmacologic Actions

ClinicalTrials.gov processed this record on May 19, 2013