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Clonal Hematopoiesis and Therapy-Emergent Myeloid Neoplasms in Patients With Cancers, CHANCES Study

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University of Washington

Status

Enrolling

Conditions

Myeloid Neoplasm Post Cytotoxic Therapy
Recurrent Primary Peritoneal Carcinoma
Recurrent Malignant Solid Neoplasm
Clonal Cytopenia of Undetermined Significance
Recurrent Fallopian Tube Carcinoma
Non-Neoplastic Hematopoietic and Lymphoid Cell Disorder
Ovarian Carcinoma
Idiopathic Cytopenia of Undetermined Significance
Recurrent Ovarian Carcinoma
Clonal Hematopoiesis

Treatments

Other: Non-Interventional Study

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT06295965
FHIRB0020162 (Other Identifier)
R01CA272594 (U.S. NIH Grant/Contract)
NCI-2023-10315 (Registry Identifier)
RG1123813

Details and patient eligibility

About

This study is being done to investigate clonal hematopoiesis and therapy-emergent myeloid neoplasms in patients with ovarian or other solid cancers. Researchers want to identify risk factors for developing these blood cancers as well as if there is/are a genetic/environmental component(s) to developing blood cancer.

Full description

OUTLINE: This is an observational study.

Patients undergo blood sample collection and complete surveys on study. Patients' medical records are also reviewed.

Enrollment

2,000 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subjects who have or have had ovarian, peritoneal, or fallopian tube carcinoma who have a life expectancy of greater than 6 months and:

    • Have completed or plan to complete at least 5 cycles of platinum-based chemotherapy

OR

  • Subjects who have or have had a solid tumor diagnosis and any of the following:

    • At least 4 months of exposure to a PARP inhibitor
    • Diagnosis of a blood disorder including, but not limited to, clonal hematopoiesis of indeterminate potential, cytopenia of unknown significance, or therapy-related myeloid neoplasm

Exclusion criteria

  • Individuals with a life expectancy of less than 6 months

Trial design

2,000 participants in 1 patient group

Observational
Description:
Patients undergo blood sample collection and complete surveys on study. Patients' medical records are also reviewed.
Treatment:
Other: Non-Interventional Study

Trial contacts and locations

1

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Central trial contact

Swisher Lab Research Coordinators

Data sourced from clinicaltrials.gov

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