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Clinical and Molecular Characteristics of Histiocytic Disorders

Clinical and Molecular Characteristics of Histiocytic Disorders

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06331377
Enrollment
500
Registered
2024-03-26
Start date
2017-07-27
Completion date
2027-07-31
Last updated
2026-08-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Histiocytic Disorder

Brief summary

This study is being done to collect medical and personal histories as well as a samples of blood, other body fluid and/or tumor/disease tissue for current and future research studies on histiocytic disorders.

Detailed description

PRIMARY OBJECTIVES: I. Define molecular signature and genomic landscape of histiocytic disorders. II. Correlate genomic findings with transcriptional abnormalities. III. Identify promising prognostic alterations and potential therapeutic targets. OUTLINE: This is an observational study. Patients complete questionnaires and undergo blood and tissue sample collection. Patients' medical records are also reviewed.

Interventions

OTHERNon-Interventional Study

Non-interventional study

Sponsors

Mayo Clinic
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
1 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All patients diagnosed with histiocytic disorders and age ≥1 year

Exclusion criteria

* \< 1 years age

Design outcomes

Primary

MeasureTime frameDescription
Identify molecular markersBaselineBiopsy samples will be analyzed for the presence of molecular markers associated with histiocytic disorders. Potential markers include BRAF V600E, cyclinD1, PD-L1, p16, and p53.6. For any test results that are actionable, patients will be notified and the results will be available in the electronic medical record.
Change in PD-L1 and T-cell Bim expressionBaseline; post-treatment (estimated up to 2 years, potentially 4 times per year)Blood testing will be performed for soluble PD-L1 and T-cell Bim expressions before and after radiation therapy for histiocytic disease to assess change in levels and role of immunotherapy. For any test results that are actionable, patients will be notified and the results will be available in the electronic medical record.

Countries

United States

Contacts

CONTACTClinical Trials Referral Office
mayocliniccancerstudies@mayo.edu855-776-0015
PRINCIPAL_INVESTIGATORJithma P. Abeykoon, MD

Mayo Clinic in Rochester

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 5, 2026