Germline testing for inherited risk of myeloid blood cancers
Official title: MyeloGen: Germline Testing for Predisposition to Myeloid Malignancies
Run by Dana-Farber Cancer Institute · NCT07112287 · Data updated 2026-11-12
This research will test whether a germline genetic test (MyeloGen Gene Panel) can find inherited changes linked to myeloid blood cancers in adults who have been diagnosed.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | Dana-Farber Cancer Institute Academic / other |
| Locations | 1 site (Boston, Massachusetts) |
| Status | Recruiting |
| Started | November 10, 2025 |
| Main results expected | April 1, 2030 |
| Study ends | April 1, 2033 |
| Registry record updated | April 24, 2026 |
| Trial ID | NCT07112287 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18 years or older with a confirmed myeloid malignancy or bone marrow failure within the prior 6 months who can provide consent in English and can safely undergo a skin biopsy are the intended participants.
✕Probably not a fit
People who have already had germline genetic testing for myeloid predisposition or who cannot safely undergo a skin biopsy are unlikely to receive additional benefit from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This prospective, single-arm study will enroll about 200 adults with histologically confirmed myeloid malignancies or recent bone marrow failure to undergo germline testing using the investigational MyeloGen Gene Panel. Study procedures include eligibility screening, in‑clinic visits, questionnaires, and a punch skin biopsy to obtain germline DNA. The protocol aims to determine how feasible it is to incorporate routine germline testing into clinical care for people with blood cancers regardless of their personal or family history. The Broad Clinical Laboratory sponsors the testing and the trial is conducted at Dana‑Farber Cancer Institute.
Why it matters
Potential benefit: If successful, routine germline testing could identify inherited risk factors that help guide treatment decisions, transplant donor selection, and cascade testing of family members.
How similar studies have gone: Previous targeted germline panels have identified hereditary predisposition in subsets of patients with myeloid malignancies, though broad routine implementation is still being studied.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age of 18 years or older * Participants must have histologically confirmed myeloid malignancy OR bone marrow failure within the last 6 months prior to screening. * Ability to understand and provide a signed and completed consent document in English. Exclusion Criteria: * Participants who cannot safely undergo clinically indicated skin biopsy as adjudicated by the study team. * Participants who have previously undergone germline genetic testing for predisposition to myeloid malignancies
Where it's running
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Dana-Farber Cancer Institute
Boston, Massachusetts, United States Recruiting
Study contacts
- Principal investigator: Christopher R Reilly, MD — Dana-Farber Cancer Institute
- Study coordinator: Christopher R Reilly, MD
- Email: Christopherr_reilly@dfci.harvard.edu
- Phone: 407-443-6243
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.