Ovarian yolk sac tumor
diseaseOn this page
Also known as endodermal sinus neoplasm of ovaryendodermal sinus neoplasm of the ovaryendodermal sinus tumor of ovaryendodermal sinus tumor of the ovaryendodermal sinus tumour of the ovarygerm cell endodermal sinus neoplasm of ovarygerm cell endodermal sinus neoplasm of the ovarygerm cell endodermal sinus tumor of ovarygerm cell endodermal sinus tumor of the ovarygerm cell endodermal sinus tumour of ovarygerm cell endodermal sinus tumour of the ovaryovarian endodermal sinus neoplasmovarian endodermal sinus tumorovarian germ cell endodermal sinus neoplasmovarian germ cell endodermal sinus tumorovarian germ cell endodermal sinus tumourovarian yolk Sac neoplasmovary yolk sac tumorovary yolk sac tumour
Summary
Ovarian yolk sac tumor (MONDO:0006344) is a cancer and 16 clinical trials. Top therapeutic interventions include cisplatin, bleomycin sulfate, and etoposide phosphate. A subtype of yolk sac tumor — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Classification: Cancer
- Clinical trials: 16
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | ovarian yolk sac tumor |
| Mondo ID | MONDO:0006344 |
| EFO | EFO:1000437 |
| DOID | DOID:5350 |
| NCIT | C8107 |
| SNOMED CT | 254876005 |
| UMLS | C0346188 |
| MedGen | 83415 |
| GARD | 0024374 |
| Anatomy (UBERON) | UBERON:0000992 |
| Is cancer (heuristic) | yes |
Also known as: endodermal sinus neoplasm of ovary · endodermal sinus neoplasm of the ovary · endodermal sinus tumor of ovary · endodermal sinus tumor of the ovary · endodermal sinus tumour of the ovary · germ cell endodermal sinus neoplasm of ovary · germ cell endodermal sinus neoplasm of the ovary · germ cell endodermal sinus tumor of ovary · germ cell endodermal sinus tumor of the ovary · germ cell endodermal sinus tumour of ovary · germ cell endodermal sinus tumour of the ovary · ovarian endodermal sinus neoplasm · ovarian endodermal sinus tumor · ovarian germ cell endodermal sinus neoplasm · ovarian germ cell endodermal sinus tumor · ovarian germ cell endodermal sinus tumour · ovarian yolk Sac neoplasm · ovarian yolk sac tumor · ovary yolk sac tumor · ovary yolk sac tumour (+8 more)
Data availability: 10 cell lines.
Disease family
This is a subtype of yolk sac 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: human disease › disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › cancer › malignant germ cell tumor › extragonadal germ cell cancer › extragonadal nonseminomatous germ cell tumor › yolk sac tumor › ovarian yolk sac tumor
Related subtypes (6): vaginal yolk sac tumor, childhood endodermal sinus tumor, testicular yolk sac tumor, adult yolk sac tumor, yolk sac tumor of central nervous system, mediastinal yolk sac tumor
Subtypes (4): childhood ovarian yolk sac tumor, ovarian yolk sac tumor, glandular pattern, ovarian yolk sac tumor, hepatoid pattern, ovarian yolk sac tumor, polyvesicular vitelline pattern
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
Drugs indicated for this disease
0 approved, 2 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.
| Drug | Development status |
|---|---|
| Cisplatin | Phase 3 (in late-stage trials) |
| Etoposide | Phase 3 (in late-stage trials) |
Clinical trials & evidence
Clinical trials
Clinical trials: 16.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| PHASE1 | 7 |
| PHASE2 | 3 |
| Not specified | 3 |
| PHASE3 | 2 |
| PHASE2/PHASE3 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT02375204 | PHASE3 | ACTIVE_NOT_RECRUITING | Standard-Dose Combination Chemotherapy or High-Dose Combination Chemotherapy and Stem Cell Transplant in Treating Patients with Relapsed or Refractory Germ Cell Tumors |
| NCT00053352 | PHASE3 | COMPLETED | Surgery and Combination Chemotherapy in Treating Children With Extracranial Germ Cell Tumors |
| NCT06341998 | PHASE2/PHASE3 | COMPLETED | Clinical Study of Chemotherapy in the Treatment of Recurrent/Refractory Yolk Sac Tumor in Children |
| NCT06638931 | PHASE2 | RECRUITING | Agnostic Therapy in Rare Solid Tumors |
| NCT00467051 | PHASE2 | COMPLETED | Combination Chemotherapy in Treating Young Patients With Recurrent or Resistant Malignant Germ Cell Tumors |
| NCT06470464 | PHASE2 | COMPLETED | Thalidomide Combined With Chemotherapy in the Treatment of Relapsed or Refractory Yolk Sac Tumor |
| NCT04377932 | PHASE1 | ACTIVE_NOT_RECRUITING | Interleukin-15 Armored Glypican 3-specific Chimeric Antigen Receptor Expressed in T Cells for Pediatric Solid Tumors |
| NCT04715191 | PHASE1 | RECRUITING | Interleukin-15 and -21 Armored Glypican-3-specific Chimeric Antigen Receptor Expressed in T Cells for Pediatric Solid Tumors |
| NCT05103631 | PHASE1 | ACTIVE_NOT_RECRUITING | Interleukin-15 Armored Glypican 3-specific Chimeric Antigen Receptor Expressed in Autologous T Cells for Solid Tumors |
| NCT06198296 | PHASE1 | RECRUITING | Immunotherapy For Adults With GPC3-Positive Solid Tumors Using IL-15 and IL-21 Armored GPC3-CAR T Cells |
| NCT07148050 | PHASE1 | RECRUITING | Immunotherapy for Solid Tumor Malignancies in Pediatrics Using Interleukin-15 and -21 Armored Glypican-3-specific Chimeric Antigen Receptor T Cells |
| NCT07224568 | PHASE1 | NOT_YET_RECRUITING | Cytokine Armored GPC3 Specific Chimeric Antigen Receptor Expressing T-cells in Adults With Solid Tumors |
| NCT00060372 | PHASE1 | COMPLETED | Ipilimumab After Allogeneic Stem Cell Transplant in Treating Patients With Persistent or Progressive Cancer |
| NCT05564026 | Not specified | RECRUITING | Molecular Epidemiology of Pediatric Germ Cell Tumors |
| NCT01080521 | Not specified | COMPLETED | Changes in Brain Function in Patients With Stage I, Stage II, Stage III, or Stage IV Ovarian, Primary Peritoneal, or Fallopian Tube Cancer Who Are Receiving Chemotherapy |
| NCT01434355 | Not specified | COMPLETED | DNA Analysis in Samples From Younger Patients With Germ Cell Tumors and Their Parents or Siblings |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| CISPLATIN | 4 | 2 |
| BLEOMYCIN SULFATE | 4 | 1 |
| ETOPOSIDE PHOSPHATE | 4 | 1 |
| IFOSFAMIDE | 4 | 1 |
Related Atlas pages
- Drugs: Cisplatin, Bleomycin, Etoposide Phosphate, Ifosfamide