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DNA Analysis of Tumor Tissue Samples From Young Patients With Acute Lymphoblastic Leukemia

Completed
Conditions
Recurrent Childhood Acute Lymphoblastic Leukemia
Childhood Acute Lymphoblastic Leukemia in Remission
Interventions
Other: Laboratory Biomarker Analysis
Registration Number
NCT00897507
Lead Sponsor
Children's Oncology Group
Brief Summary

This laboratory study is looking at DNA in tumor tissue samples from young patients with acute lymphoblastic leukemia. DNA analysis of tumor tissue may help doctors predict how well patients will respond to treatment

Detailed Description

PRIMARY OBJECTIVE:

I. To validate significant associations between SNPs and treatment outcome and toxicity on Children's Cancer Group (CCG)-1891 on an independent sample set from a successor CCG study for standard risk acute lymphoblastic leukemia (ALL), CCG-1952.

II. To evaluate the role of SNPs in drug metabolizing enzymes and the development of veno-occlusive disease in patients on CCG-1952.

III. To evaluate interactions among genotypes and other risk factors for treatment response in a combined data set of CCG-1891 and CCG-1952 with recently developed analytic tools for high dimensional data.

IV. To develop predictive models utilizing genetic information obtained in Aim 1.1 and clinical data to predict treatment response and toxicity.

OUTLINE:

Tumor tissue samples undergo genotype assessment on the Pyrosequencing platform. Contingency tables and X\^2 test performs a univariate analysis of the risk of relapse and genotype, and multivariable analyses using logistic regression. Cox proportional hazards evaluate the risk of relapse given genotype and other confounders. Genotype patterning, classification and regression trees, and multifactor dimensionality reduction evaluates for patterns of single nucleotide polymorphisms associated with toxicity and relapse risk.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
520
Inclusion Criteria
  • Enrolled in clinical trial CCG-1891 or CCG-1952 with pediatric ALL
Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Ancillary-Correlative (genotype assessment)Laboratory Biomarker AnalysisTumor tissue samples undergo genotype assessment on the Pyrosequencing platform. Contingency tables and X\^2 test performs a univariate analysis of the risk of relapse and genotype, and multivariable analyses using logistic regression. Cox proportional hazards evaluate the risk of relapse given genotype and other confounders. Genotype patterning, classification and regression trees, and multifactor dimensionality reduction evaluates for patterns of single nucleotide polymorphisms associated with toxicity and relapse risk.
Primary Outcome Measures
NameTimeMethod
Development of veno-occlusive disease in patients on CCG-1952Day 28

Classification and Regression Trees (CART), genotype patterning, Multifactor Dimensionality Reduction (MDR) techniques will be used to identify SNP combinations associated with risk of relapse and VOD

Development of a predictive model of leukemia relapseDay 28

Predictive models will be developed utilizing genetic information obtained in Aim 1.1 and clinical data to predict treatment response

Leukemia RelapseDay 7

Contingency tables will be used to tabulate the relationship between relapse and genotype, race, leukemia cytogenetics, day 7 bone marrow status, and treatment arm

Development of a predictive model of leukemia toxicityDay 28

Predictive models will be developed utilizing genetic information obtained in Aim 1.1 and clinical data to predict treatment toxicity.

Secondary Outcome Measures
NameTimeMethod
Development of grade III/IV toxicity as defined by the CCG toxicity criteriaDay 28

Contingency tables will be used to tabulate categorical toxicities and toxicity severity grade.

Trial Locations

Locations (1)

Childrens Oncology Group

🇺🇸

Philadelphia, Pennsylvania, United States

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