Somatic Mosaicism in Twins Discordant for Childhood Cancer

Sponsor
Children's Oncology Group (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06054295
Collaborator
National Cancer Institute (NCI) (NIH)
50
35.8

Study Details

Study Description

Brief Summary

Somatic mosaicism in cancer associated genes is one potential explanation for discordance in childhood cancer that has not been fully explored to date. This pilot study will focus on twins with central nervous system (CNS) tumors who are identified through the Children's Oncology Group's Project: EveryChild (PEC) registry or volunteer.

Condition or Disease Intervention/Treatment Phase
  • Other: Biospecimen collection
  • Other: Questionnaire Administration

Detailed Description

PRIMARY OBJECTIVES:
  1. To conduct a descriptive study of same sex twins (MZ and DZ) discordant for childhood CNS tumors identified through the Children's Oncology Group Project:EveryChild registry.

  2. To compare the prevalence of somatic mosaicism in classic cancer-associated genes in monozygotic (MZ) twins discordant for childhood brain tumors. In our pilot study, we will sequence blood and saliva DNA samples from 25 MZ twin pairs using a panel of 94 known cancer associated genes.

SECONDARY OBJECTIVES:
  1. To compare the profile of mutations detected in DNA extracted from pre- and post-treatment blood samples from a subset of CNS tumor patients. The purpose of this aim is to ensure that differences in somatic mosaicism detected in twin pairs are not caused by cancer therapy.
Outline:

Twins with CNS tumors will undergo blood and saliva DNA samples with the goal is to learn more about genetic differences that may lead to CNS tumor development.

Study Design

Study Type:
Observational
Anticipated Enrollment :
50 participants
Observational Model:
Family-Based
Time Perspective:
Prospective
Official Title:
Somatic Mosaicism in Twins Discordant for Childhood Cancer: a Pilot Study
Anticipated Study Start Date :
Oct 6, 2023
Anticipated Primary Completion Date :
Sep 30, 2026
Anticipated Study Completion Date :
Sep 30, 2026

Arms and Interventions

Arm Intervention/Treatment
Ancillary-Correlative

Twins with CNS tumors, identified through the Children's Oncology Group's Project:EveryChild (PEC) registry, will have both blood and saliva samples collected at the time of study enrollment.

Other: Biospecimen collection
Collection of both blood and saliva samples from participants at the time of study enrollment

Other: Questionnaire Administration
The brief questionnaire will assess health history, demographics, environmental exposures, family history of cancer, and birth characteristics.

Outcome Measures

Primary Outcome Measures

  1. Compare the prevalence of somatic mosaicism in classic cancer-associated genes in monozygotic (MZ) twins discordant for childhood brain tumors. [Up to 18 months]

    Sequence blood and saliva DNA samples from 25 MZ twin pairs using a panel of 94 known cancer associated genes.

Secondary Outcome Measures

  1. Compare the profile of mutations detected in DNA extracted from pre- and post-treatment blood samples from a subset of CNS tumor patients. [Up to 18 months]

    Determine the frequency of somatic mosaicism in twins discordant for CNS tumors. Will use an exact test of proportions to determine whether the affected twin is more likely to have a mosaic mutation. The comparison of pre-treatment and post-treatment samples in the CNS tumor cases will include a descriptive comparison of the mutations identified in each sample

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Newly diagnosed patient with CNS tumor or have recurrent disease and enrolled on APEC14B1.

  • Patient must have same sex twin. Note: (history of) treatment on a COG therapeutic trial is not required.

  • Patients must be diagnosed at < 19 years of age at the time of diagnosis.

  • A family is eligible to participate if the twin with the CNS tumor is deceased but has a blood sample banked through APEC14B1.

  • All patients and/or their parents or legal guardians must provide informed consent. Assent will be obtained for participants between the ages of 8-17 years.

  • All institutional, FDA, and NCI requirements for human studies must be met.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Children's Oncology Group
  • National Cancer Institute (NCI)

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Children's Oncology Group
ClinicalTrials.gov Identifier:
NCT06054295
Other Study ID Numbers:
  • AEPI22N2
First Posted:
Sep 26, 2023
Last Update Posted:
Sep 26, 2023
Last Verified:
Sep 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 26, 2023