Borderline epithelial tumor of ovary
diseaseOn this page
Also known as borderline epithelial neoplasm of ovaryborderline epithelial neoplasm of the ovaryborderline epithelial tumor of the ovaryborderline epithelial tumour of the ovaryborderline ovarian epithelial neoplasmborderline ovarian epithelial tumorborderline ovarian epithelial tumourborderline ovarian surface epithelial-stromal tumorborderline ovarian surface epithelial-stromal tumourepithelial neoplasm of ovary of borderline malignancyepithelial neoplasm of the ovary of borderline malignancyepithelial ovarian neoplasm of borderline malignancyepithelial ovarian tumor of borderline malignancyepithelial ovarian tumour of borderline malignancyepithelial tumor of ovary of borderline malignancyepithelial tumor of the ovary of borderline malignancyepithelial tumour of ovary of borderline malignancyepithelial tumour of the ovary of borderline malignancylow malignant potential ovarian tumor
Summary
Borderline epithelial tumor of ovary (MONDO:0016093) is a cancer and 6 clinical trials. Top therapeutic interventions include selumetinib, belinostat, and ucn-01. A subtype of ovarian epithelial tumor — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Classification: Cancer
- Clinical trials: 6
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | borderline epithelial tumor of ovary |
| Mondo ID | MONDO:0016093 |
| EFO | EFO:1000140 |
| Orphanet | 206473 |
| NCIT | C4783 |
| SNOMED CT | 764791008 |
| UMLS | C3665489 |
| MedGen | 777110 |
| GARD | 0009363 |
| Is cancer (heuristic) | yes |
Also known as: borderline epithelial neoplasm of ovary · borderline epithelial neoplasm of the ovary · borderline epithelial tumor of ovary · borderline epithelial tumor of the ovary · borderline epithelial tumour of the ovary · borderline ovarian epithelial neoplasm · borderline ovarian epithelial tumor · borderline ovarian epithelial tumour · borderline ovarian surface epithelial-stromal tumor · borderline ovarian surface epithelial-stromal tumour · epithelial neoplasm of ovary of borderline malignancy · epithelial neoplasm of the ovary of borderline malignancy · epithelial ovarian neoplasm of borderline malignancy · epithelial ovarian tumor of borderline malignancy · epithelial ovarian tumour of borderline malignancy · epithelial tumor of ovary of borderline malignancy · epithelial tumor of the ovary of borderline malignancy · epithelial tumour of ovary of borderline malignancy · epithelial tumour of the ovary of borderline malignancy · low malignant potential ovarian tumor (+10 more)
Disease family
This is a subtype of ovarian epithelial tumor. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.
Classification path: disease › human disease › disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › epithelial neoplasm › ovarian epithelial tumor › borderline epithelial tumor of ovary
Related subtypes (10): ovarian Brenner tumor, ovarian squamous cell neoplasm, ovarian mucinous neoplasm, ovarian seromucinous tumor, ovarian papillary tumor, ovarian mucinous adenofibroma, ovarian adenoma benign, malignant epithelial tumor of ovary, ovarian clear cell tumor, ovarian serous tumor
Subtypes (1): borderline ovarian serous tumor
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 6.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| PHASE2 | 2 |
| PHASE1 | 2 |
| Not specified | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00301756 | PHASE2 | COMPLETED | Belinostat in Treating Patients With Advanced Ovarian Epithelial Cancer, Primary Peritoneal Cancer, or Fallopian Tube Cancer or Ovarian Low Malignant Potential Tumors |
| NCT00551070 | PHASE2 | COMPLETED | Selumetinib Sulfate in Treating Woman With Recurrent Low-Grade Ovarian Cancer or Peritoneum Cancer |
| NCT00031681 | PHASE1 | COMPLETED | 7-Hydroxystaurosporine and Irinotecan Hydrochloride in Treating Patients With Metastatic or Unresectable Solid Tumors or Triple Negative Breast Cancer (Currently Accruing Only Triple-negative Breast Cancer Patients Since 6/8/2007) |
| NCT02520115 | PHASE1 | COMPLETED | Folate Receptor in Diagnosing Ovarian Cancer Using Serum Samples From Patients With Newly Diagnosed Pelvic Mass or Previously Diagnosed Ovarian Cancer |
| NCT00897442 | Not specified | COMPLETED | Collecting Tumor Samples From Patients With Gynecological Tumors |
| NCT03742388 | Not specified | UNKNOWN | A Genomic Analysis of Evolution of Epithelia Ovarian Tumors |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| SELUMETINIB | 4 | 2 |
| BELINOSTAT | 4 | 1 |
| UCN-01 | 2 | 1 |
| CHEMBL4463209 | 0 | 1 |
| CHEMBL1236539 | 0 | 1 |
Related Atlas pages
- Drugs: Selumetinib, Belinostat