Evaluating Myelodysplastic Syndrome Risks in NET Patients Planned for Peptide Radionuclide Therapy

RecruitingOBSERVATIONAL
Enrollment

45

Participants

Timeline

Start Date

August 1, 2024

Primary Completion Date

April 1, 2028

Study Completion Date

June 30, 2029

Conditions
Myelodysplastic SyndromeAcute Myeloid Leukemia
Interventions
RADIATION

Peptide receptor radionuclide therapy (PRRT)

Specialized type of radionuclide therapy used to treat neuroendocrine tumors.

DIAGNOSTIC_TEST

Blood collection

Patients will have approximately 5 ml of blood drawn 6,12,24,36,48, 60 months and at the time of MDS/AML diagnosis on follow up. Genomic DNA will be extracted from serum sample using the Qiagen QIAamp DNA Mini Kit. Single-molecule molecular inversion probes (smMIPs) will be used to detect mutations. Single nucleotide variants (SNVs), short insertions and deletions (indels), and mutated myeloid genes will be captured (e.g PPM1D, DNMT3A, TET2, TP53).

Trial Locations (1)

M5G 2M9

RECRUITING

Princess Margaret Cancer Centre, Toronto

All Listed Sponsors
lead

University Health Network, Toronto

OTHER