Li-Fraumeni Syndrome/TP53 Biobank

Last updated: July 18, 2024
Sponsor: Abramson Cancer Center at Penn Medicine
Overall Status: Active - Recruiting

Phase

N/A

Condition

Precancerous Condition

Treatment

No Intervention

Clinical Study ID

NCT04367246
UPCC 24919
IRB 834147
IRB 18-015810
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

Li-Fraumeni Syndrome (LFS) and Li-Fraumeni-like (LFL) Syndrome are cancer predisposition syndromes due to germline aberrations in the TP53 gene. Patients with classical LFS have a lifetime malignancy risk between 80-90%, with 21% of those cancers occurring by the age of 15 years. There are established guidelines for screening patients with LFS that have led to earlier detection and treatment of cancer in this population. There are a number of important issues facing patients identified to have germline TP53 variations. First, with the advent of massively parallel sequencing, increasing numbers of patients are now being identified with a wide range of clinical phenotypes associated with germline TP53 mutations, and the natural history of these patients is less well understood. Second, surveillance for malignancy in LFS and other TP53-associated syndromes involves frequent laboratory and radiologic studies that are imperfect measures of disease onset; therefore, more specific, less invasive biomarker-driven screening methods are needed. Finally, studies to date have not yet identified whether tumors which form in LFS or other germline TP53-associated tumors have unique aberrations or signatures that could be exploited in precision medicine treatment of these patients. In order to study these important issues in LFS, this protocol will establish a TP53 Clinical Database and Biobank. The Investigator plans to use this biobank to study genotype-phenotype correlations in patients with LFS and other germline TP53-associated syndromes, mechanisms of tumor formation, and novel methods of cancer screening in this high risk population.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Affected Patient (Group 1)

  1. Males or females aged 0 and above.

  2. Confirmed germline TP53 mutation or variant. OR Family history of LFS and clinicallymanaged as a LFS patient. OR Meet LFS diagnostic criteria including Classic,Chompret, and LFL (Birch and Eeles) criteria.

  3. Informed consent for capable participants. OR Parental/legally authorizedrepresentative permission (informed consent) for pediatric participants or subjectswith diminished capacity, and if appropriate, assent.

Unaffected Family Member (Group 2)

  1. Males or females aged 0 and above.

  2. Biological relative of subjects with germline TP53 mutation or variant (LFS),including first degree (siblings, parents) and second degree (grandparents, aunts,uncles) relatives.

  3. Negative for germline TP53 mutation or variant.

  4. Informed consent for capable participants. OR Parental/legally authorizedrepresentative permission (informed consent) for pediatric participants or subjectswith diminished capacity, and if appropriate, assent.

Household Member (Group 3)

  1. Males or females aged 0 and above.

  2. Household member of subjects with germline TP53 mutation or variant (LFS), sharing aliving space (apartment or free-standing home) for at least 6 months prior to studyenrollment.

  3. Informed consent for capable participants. OR Parental/legally authorizedrepresentative (LAR) permission (informed consent) for pediatric participants orsubjects with diminished capacity, and if appropriate, assent.

Exclusion

Exclusion Criteria:

  1. Parents/LAR or subjects who, in the opinion of the Investigator, may benon-compliant with study schedules or procedures.

  2. Known pregnancy at the time of study enrollment.

Subjects that do not meet all of the enrollment criteria may not be enrolled. Pregnant women will not be actively enrolled, but if a woman becomes pregnant she will not be removed from the study; sample collection will be held during known pregnancy.

Study Design

Total Participants: 300
Treatment Group(s): 1
Primary Treatment: No Intervention
Phase:
Study Start date:
September 24, 2019
Estimated Completion Date:
September 24, 2029

Study Description

Context: Li-Fraumeni Syndrome (LFS) and Li-Fraumeni-like (LFL) Syndrome are cancer predisposition syndromes due to germline aberrations in the TP53 gene. Patients with classical LFS have a lifetime malignancy risk between 80-90%. There are guidelines for screening patients with LFS that have led to earlier detection and treatment of cancer in this population. There are a number of important issues facing patients identified to have germline TP53 variations, including study of genotype-phenotype correlations, enhanced cancer screening modalities, and novel treatment strategies for cancers that develop.

Objectives: In order to study important clinical issues in LFS, the primary objective of this biobank is to gather and store ongoing clinical data and biospecimens from patients with LFS and other potential germline TP53-associated syndromes. The investigators plan to use this biobank to study genotype-phenotype correlations in patients with inherited TP53 mutations, mechanisms of tumor formation, and methods of cancer screening.

Study Design: This study is a retrospective/prospective biobank containing clinical data and data and biospecimen. Patients for inclusion will be identified by query of our clinical electronic medical record from the Children's Hospital of Philadelphia (CHOP) and Penn Medicine (PENN) for patients followed in our respective clinics. In addition, patients will be recruited by ongoing prospective collection in clinic. Data collection, data entry and biobank maintenance, will be conducted by the investigators listed on this protocol at CHOP and at PENN through the Master Reliance Agreement. Future investigators and collaborators at other institutions will have access to samples and limited data by executing a written Data User Agreement and/or Materials Transfer Agreement with the biobank.

Setting/Participants: The biobank will be conducted at CHOP and PENN. Any infant, child, or adult with a germline TP53 mutation will be invited to participate. In addition, individuals with a diagnosis of LFS or LFL, who have been seen by a physician at Penn/CHOP or referred from outside physicians will be contacted for participation. To provide control group samples, unaffected family members and/or household members will also be recruited. Prospective enrollment into the biobank is planned to be an ongoing effort, without a fixed end date or target subject number. At minimum, however, the estimated number of recruitment is approximately 300 affected individuals and their family/household members along with their data and specimens.

Data/Specimen Collection Procedures and Frequency: The only required study procedure is the review of medical records. Optional study procedures include collection of germline DNA (via blood, saliva, urine, or hair), plasma collection, stool collection, and skin biopsies. Clinical data will be updated every 6 months. Subjects can opt-out of this follow-up process.

Connect with a study center

  • Children's Hospital of Philadelphia

    Philadelphia, Pennsylvania 19104
    United States

    Active - Recruiting

  • University of Pennsylvania

    Philadelphia, Pennsylvania 19104
    United States

    Active - Recruiting

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