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Study identifier: NCT06785077 Synced from ClinicalTrials.gov · July 28, 2026
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Genetic Landscape in Women with Metastatic Ovarian Cancer Before and During Treatment with PARP Inhibitors

Condition: Leukemia, Myeloid, Acute · Myeloid Dysplasia · Ovarian Epithelial Cancer  ·  Sponsor: European Institute of Oncology

PhaseNA
Planned participants157
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

Therapy related acute myeloid leukemia and myelodysplasia (t-MN) is a potential late complication of cytotoxic therapy, and it is of particular concern in the treatment of patients with epithelial ovarian carcinoma (EOC) exposed to multiple cycles of platinum-based chemotherapy during the course of their disease. An epidemiological analysis published in 2011 (Gynecologic Oncology) showed that the overall incidence of t-AML is 0.17%, with a median latency to development of leukemia of 4 years (range 0-27 years). Inhibition of PARP is a potential synthetic lethal therapeutic strategy for the treatment of cancers characterized by specific DNA repair defects, such as those that harbor a BRCA1 or BRCA2 (BRCA1/2) mutation and are therefore deficient in homologous recombination repair. In homologous recombination-deficient tumors, PARP inhibition eliminates an alternative DNA repair pathway essential for maintaining viability, leading to tumor cell death. The estimated prevalence of BRCA1/2 mutations in V2 03/06/2021 2 patients with newly diagnosed high-grade serous ovarian cancer is 20-25% and it might be higher in patients with platinum-sensitive, relapsed ovarian cancer. Early studies have shown significant efficacy for PARP inhibitors in patients with germline BRCA1/2 mutations. Our hypothesis is that these patients are carriers of clonal hematopoiesis of indeterminate potential (CHIP) before treatment with PARPi. CHIP refers to the presence of clonal population(s) of hematopo…

This description comes directly from the study's public registry record.

Talk to the study team

Federica Gigli  ·  +390257489538  ·  federica.gigli@ieo.it

Fulvia Fusar  ·  +390257489538  ·  fulvia.fusarimperatore@ieo.it

Always discuss trial participation with your own doctor first.

Locations (1)

Istituto Europeo di OncologiaMilan, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT06785077