Target landscape
Open Targets · retrieved 2026-09-12 · weekly12 genes recurrently implicated in endometrial cancer, triaged for whether anything can actually be aimed at them. The zeros are the informative rows.
Of 12 recurrently implicated genes, 7 carry any drug at all. That is a statement about these 12 gene targets, not about the disease: Endometrial cancer does have labelled therapy — 7 drugs, listed in the next section.
Two different questions
The table below asks what can be aimed at 12 recurrently implicated genes. That is narrower than what is approved for the disease, and narrower again than what endometrial cancer is actually treated with, which includes agents approved under broader indications. All three are on this page and they are kept apart deliberately.
| Gene | Drugs | Approval, and whether it reached this disease | Open Targets tractabilitycomputed from protein features and literature — a signal that a modality is worth trying, not evidence that it works | Cell therapy here |
|---|---|---|---|---|
| PTEN across cancers → | 0 | No drug— | antibody, protein degrader, small molecule | — |
| PIK3CA across cancers → | 31 | 3 approvedAlpelisib, Copanlisib, InavolisibApproved in breast cancer, breast neoplasm, breast carcinoma and 3 other indications. No endometrial cancer indication appears on these drugs’ labels.13 active of 32 endometrial cancer trials | antibody, protein degrader, small molecule | — |
| TP53 across cancers → | 8 | Phase 3Alrizomadlin, Cenersen, Contusugene Ladenovec, Eprenetapopt, Idasanutlin, Navtemadlin, Siremadlin, Teprasiran1 active of 1 endometrial cancer trial | other clinical modality, protein degrader, small molecule | — |
| POLE | 6 | 4 approvedClofarabine, Cytarabine, Fludarabine, GemcitabineApproved in acute lymphoblastic leukemia, myelodysplastic syndrome, acute myeloid leukemia and 10 other indications. No endometrial cancer indication appears on these drugs’ labels.11 active of 26 endometrial cancer trials | antibody, protein degrader, small molecule | — |
| MLH1 across cancers → | 0 | No drug— | protein degrader, small molecule | — |
| MSH2 across cancers → | 0 | No drug— | protein degrader, small molecule | — |
| MSH6 | 0 | No drug— | protein degrader, small molecule | — |
| ARID1A across cancers → | 0 | No drug— | protein degrader | — |
| CTNNB1 across cancers → | 1 | Phase 2Pri-724No endometrial cancer trial of any of these drugs | antibody, other clinical modality, protein degrader, small molecule | — |
| ESR1 across cancers → | 43 | 29 approvedArzoxifene, Bazedoxifene, Clomiphene, Cyclofenil, Dienestrol, Diethylstilbestrol, Diethylstilbestrol Diphosphate, Elacestrant, Estetrol, Estradiol, Estradiol Cypionate, Estradiol Valerate, Estriol, Estrogens, Conjugated, Estrogens, Conjugated Synthetic A, Estrogens, Esterified, Estrone, Estropipate, Ethinyl Estradiol, Fulvestrant, Lasofoxifene, Mestranol, Ospemifene, Polyestradiol, Quinestrol, Raloxifene, Synthetic Conjugated Estrogens, B, Tamoxifen, ToremifeneApproved in endometrial cancer: Clomiphene.63 active of 149 endometrial cancer trials | antibody, other clinical modality, protein degrader, small molecule | — |
| PGR across cancers → | 28 | 20 approvedDanazol, Desogestrel, Drospirenone, Dydrogesterone, Ethynodiol Diacetate, Etonogestrel, Hydroxyprogesterone Caproate, Levonorgestrel, Medroxyprogesterone, Megestrol, Mifepristone, Nomegestrol, Norelgestromin, Norethindrone, Norgestimate, Norgestrel, Progesterone, Segesterone, Trimegestone, UlipristalApproved in breast fibrocystic disease, endometriosis, Menorrhagia and 20 other indications. No endometrial cancer indication appears on these drugs’ labels.59 active of 136 endometrial cancer trials | antibody, protein degrader, small molecule | — |
| ERBB2 across cancers → | 45 | 17 approvedAfatinib, Afatinib Dimaleate, Dacomitinib, Lapatinib, Lapatinib Ditosylate, Margetuximab, Masoprocol, Neratinib, Pertuzumab, Trastuzumab, Trastuzumab Deruxtecan, Trastuzumab Duocarmazine, Trastuzumab Emtansine, Tucatinib, Vandetanib, Zanidatamab, ZenocutuzumabApproved in non-small cell lung carcinoma, breast cancer, breast neoplasm and 10 other indications. No endometrial cancer indication appears on these drugs’ labels.35 active of 52 endometrial cancer trials | antibody, other clinical modality, protein degrader, small molecule | — |
Dataset evidence counts studies in the 168-study ranked set whose title or abstract names the gene; the bar is scaled to PTEN. Sources: Open Targets Platform and NCBI GEO, retrieved 2026-09-12. Clinical stage is the highest reached for any indication — see the per-drug indications noted in each row. Target-prioritisation reference only; not clinical or prescribing guidance.
What is actually approved here
openFDA drug labels · weekly7 drugs carry an FDA label naming endometrial cancer: Choriogonadotropin Alfa, Clomiphene, Clomiphene Citrtae, Dostarlimab, Durvalumab, Lenvatinib, Pembrolizumab. Separately, 72 of the drugs returned for the genes in the table above are approved only for other diseases and reach endometrial cancer through trials, not through their labels.
Every label that names endometrial cancer
| Drug | Role | What the label says |
|---|---|---|
| Choriogonadotropin AlfaOvidrel | Labelled here | Patients in later reproductive life have a greater predisposition to endometrial carcinoma as well as a higher incidence of anovulatory disorders. |
| ClomipheneCLOMID, Clomid, Clomiphene Citrate | Labelled here | Endometriosis and Endometrial Carcinoma. |
| Clomiphene CitrtaeClomiphene Citrate | Labelled here | Endometriosis and Endometrial Carcinoma. |
| DostarlimabJemperli | Labelled here | Endometrial Cancer JEMPERLI, in combination with carboplatin and paclitaxel, followed by JEMPERLI as a single agent, is indicated for the treatment of adult patients with primary advanced or recurrent endometrial cancer (EC). |
| DurvalumabIMFINZI | Labelled here | Endometrial Cancer IMFINZI, in combination with carboplatin and paclitaxel followed by IMFINZI as a single agent, is indicated for the treatment of adult patients with primary advanced or recurrent endometrial cancer that is mismatch repair deficient (dMMR) as determined by an FDA-authorized test [see Dosage and Administration |
| LenvatinibLenvima | Labelled here | Endometrial Carcinoma (EC) In combination with pembrolizumab, for the treatment of patients with advanced endometrial carcinoma (EC) that is mismatch repair proficient (pMMR) or not microsatellite instability-high (MSI-H), as determined by an FDA-approved test, who have disease progression following prior systemic therapy in any setting and are not candidates for curative surgery or radiation. |
| PembrolizumabKEYTRUDA, KEYTRUDA QLEX | Labelled here | Endometrial Carcinoma in combination with carboplatin and paclitaxel, followed by KEYTRUDA as a single agent, for the treatment of adult patients with primary advanced or recurrent endometrial carcinoma. |
37 labels match indications_and_usage:"endometrial cancer" OR indications_and_usage:"endometrial carcinoma"; they collapse to 7 distinct molecules once salt forms, biosimilars and co-formulated hyaluronidase are merged. Source: openFDA drug label API (api.fda.gov/drug/label.json), retrieved 2026-09-12. Labels change; this reflects the current label text, not the approval history. Not prescribing guidance.
Cell therapy against PD-1
ClinicalTrials.gov · retrieved 2026-09-12 · weeklyPD-1 is the busiest cell-therapy antigen in endometrial cancer: 2 registered trials, 2 still active. It has no gene entry of its own and is reached through PDCD1: the checkpoint receptor PDCD1 encodes, on the T cell.
| Trial | Phase | Status | Title | Last update |
|---|---|---|---|---|
| NCT05410717 | 1 | Recruiting | CLDN6/GPC3/Mesothelin/AXL-CAR-NK Cell Therapy for Advanced Solid Tumors | 2024-06-25 |
| NCT01174121 | 2 | Recruiting | Immunotherapy Using Tumor Infiltrating Lymphocytes for Patients With Metastatic Cancer | 2026-09-01 |
2 of 2 shown, most recently active first. Other antigens searched: CLDN6 (2). Source: ClinicalTrials.gov API v2, retrieved 2026-09-12. Trials are matched on the antigen named in the title or intervention, so a trial stating only a product code is missed.
Research momentum
PubMed MeSH · monthlyEvery term below is a share of the endometrial cancer literature, not a count, because the field itself grew: 2015–2018 (n=3,596) against 2021–2025 (n=5,832). A topic whose papers doubled while the field doubled has not risen.
Rising, with a real baseline
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Antibodies, Monoclonal, Humanized | 0.25% | 2.57% | 10.27× | 150 papers |
| Nomograms | 0.25% | 2.04% | 8.15× | 119 papers |
| Tumor Microenvironment | 0.58% | 3.89% | 6.66× | 227 papers |
| Progression-Free Survival | 0.36% | 2.04% | 5.64× | 119 papers |
| Immunotherapy | 0.36% | 1.99% | 5.5× | 116 papers |
| Genital Neoplasms, Female | 0.17% | 0.91% | 5.44× | 53 papers |
| Programmed Cell Death 1 Receptor | 0.17% | 0.7% | 4.21× | 41 papers |
| B7-H1 Antigen | 0.36% | 1.18% | 3.27× | 69 papers |
| Conservative Treatment | 0.19% | 0.6% | 3.08× | 35 papers |
| Neoplastic Syndromes, Hereditary | 0.44% | 1.29% | 2.89× | 75 papers |
Cooling
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Neoplasms, Cystic, Mucinous, and Serous | 2.28% | 0.26% | 0.11× | 15 papers |
| Multivariate Analysis | 1.81% | 0.21% | 0.11× | 12 papers |
| Ovariectomy | 1.89% | 0.22% | 0.12× | 13 papers |
| Adenocarcinoma, Clear Cell | 6.12% | 0.93% | 0.15× | 54 papers |
| Real-Time Polymerase Chain Reaction | 1.47% | 0.24% | 0.16× | 14 papers |
| RNA, Small Interfering | 1.61% | 0.26% | 0.16× | 15 papers |
Biggest topics now
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Prognosis | 19.13% | 19.46% | 1.02× | 1135 papers |
| Neoplasm Staging | 23.67% | 16.68% | 0.7× | 973 papers |
| Biomarkers, Tumor | 13.88% | 14.06% | 1.01× | 820 papers |
| Carcinoma, Endometrioid | 19.3% | 14.01% | 0.73× | 817 papers |
| Neoplasm Recurrence, Local | 9.82% | 10.1% | 1.03× | 589 papers |
| Gene Expression Regulation, Neoplastic | 9.09% | 8.86% | 0.97× | 517 papers |
| Endometrium | 11.4% | 7.9% | 0.69× | 461 papers |
| Cell Proliferation | 8.48% | 7.25% | 0.86× | 423 papers |
| Mutation | 4.87% | 7.2% | 1.48× | 420 papers |
| Risk Factors | 10.6% | 6.91% | 0.65× | 403 papers |
Publication mix
| Type | 2015–18 | 2021–25 |
|---|---|---|
| Clinical Trial | 0.0% | 0.1% |
| Randomized Controlled Trial | 1.9% | 1.3% |
| Review | 8.1% | 7.9% |
| Meta-Analysis | 3.5% | 2.7% |
| Case Reports | 0.0% | 1.4% |
Query: Endometrial Neoplasms[MeSH Major Topic] NOT ("Leiomyosarcoma"[MeSH] OR "Sarcoma, Endometrial Stromal"[MeSH] OR "Leiomyoma"[MeSH] OR "Uterine Cervical Neoplasms"[MeSH] OR "Endometriosis"[MeSH]). Terms need at least 12 papers in the recent window and, in the rising table, at least 5 in the earlier one — a term going from 1 paper to 12 is a large fold change and no evidence of anything. Ubiquitous descriptors (Humans, Animals, age bands) and the disease’s own term are dropped. Source: PubMed MeSH, retrieved 2026-09-12.
Disease burden
What the public sources count, and how closely each category matches this disease. The same figures for every disease on the site are on one table.
| Measure | Value | Match | What it counts |
|---|---|---|---|
| New cases each year | 68,270 cases/year | direct | 2026 SEER Cancer Stat Facts, Uterine Cancer, retrieved 2026-09-12 |
| Deaths each year | 14,450 deaths/year | direct | 2026 SEER Cancer Stat Facts, Uterine Cancer, retrieved 2026-09-12 |
| Incidence rate | 28.7 cases per 100,000 women per year | direct | 2019-2023 SEER Cancer Stat Facts, Uterine Cancer, retrieved 2026-09-12 |
| Death rate | 5.4 deaths per 100,000 women per year | direct | 2020-2024 SEER Cancer Stat Facts, Uterine Cancer, retrieved 2026-09-12 |
| People living with it | 890,295 women living with the disease | direct | 2023 SEER Cancer Stat Facts, Uterine Cancer, retrieved 2026-09-12 |
| Median age at diagnosis | 64.0 years | direct | 2019-2023 SEER Cancer Stat Facts, Uterine Cancer, retrieved 2026-09-12 |
| median age at death | 71 years | direct | 2020-2024 SEER Cancer Stat Facts, Uterine Cancer, retrieved 2026-09-12 |
| Five-year relative survival | 80.9% | direct | 2016-2022 SEER Cancer Stat Facts, Uterine Cancer, retrieved 2026-09-12 |
Years of life lost
2.8 years per case, 187,770 a year, from survival and age at diagnosis rather than from a death count. derived proxy What this costs to fund is in Funding.
3 assumptions behind this estimate
- Five-year relative survival stands in for cure; a death after five years is not counted.
- The median age at diagnosis stands in for the whole age distribution.
- Life expectancy at birth (78.4 years) is the reference, rather than remaining expectancy at the age of death from a life table.
- Each assumption moves the result by more than the difference between the two diseases currently on this site, so this figure separates a disease from one ten times its size, not from a close neighbour.
Funding
NIH RePORTER · quarterlyNIH obligations naming endometrial cancer, after removing the 2,256 records across all years that matched the search but are about something else. That filter is not cosmetic: without it this section reports another field’s funding as this disease’s.
NIH obligations by fiscal year
| Year | Obligations | Awards | Distinct projects | Dropped as off-topic |
|---|---|---|---|---|
| FY2013 | $8.8M | 31 | 21 | 150 |
| FY2014 | $11.0M | 33 | 25 | 139 |
| FY2015 | $6.8M | 21 | 19 | 132 |
| FY2016 | $11.7M | 32 | 23 | 136 |
| FY2017 | $13.4M | 36 | 25 | 139 |
| FY2018 | $12.7M | 43 | 25 | 198 |
| FY2019 | $13.0M | 33 | 25 | 170 |
| FY2020 | $23.2M | 39 | 26 | 180 |
| FY2021 | $9.2M | 21 | 19 | 192 |
| FY2022 | $11.6M | 27 | 25 | 215 |
| FY2023 | $14.9M | 29 | 23 | 213 |
| FY2024 | $21.2M | 43 | 29 | 201 |
| FY2025 | $29.8M | 47 | 30 | 191 |
Where FY2025 money went
| Institution | Obligations | Awards |
|---|---|---|
| Washington University | $5.0M | 8 |
| Dana-Farber Cancer Inst | $4.5M | 4 |
| Univ Of North Carolina Chapel Hill | $4.3M | 8 |
| University Of New Mexico Health Scis Ctr | $4.0M | 3 |
| Henry Ford Health + Michigan State University Health Sciences | $1.4M | 2 |
| National Human Genome Research Institute | $1.4M | 0 |
| University Of Texas Hlth Science Center | $1.1M | 2 |
| University Of Missouri-Columbia | $1.0M | 2 |
| Brigham And Women'S Hospital | $0.8M | 0 |
| Ohio State University | $0.7M | 2 |
Text search endometrial cancer over project title, terms and abstract, per fiscal year. Awards are individual funding actions; distinct projects collapse them by core project number, so a multi-year grant counts once. The most recent year may be incomplete. Source: NIH RePORTER, retrieved 2026-09-12.
What that buys
Against 187,770 years of life lost a year, FY2025 obligations are $159 per life-year — $436 per case. The estimate and its assumptions are in Disease burden.
Who funds it, FY2025
The total says how much. These say who from, through what kind of award, and to whom — which a dollar figure cannot.
NIH institutes
Projects by administering institute. The rows above are the top 4 and account for 47 of 47.
Award mechanisms
R01 is an investigator-initiated grant; ZIA is NIH intramural, meaning the work happens inside NIH rather than being funded outside it. The rows above are the top 15 and account for 47 of 47.
Where it lands
Share of $29.8M in FY2025. The top three hold 46%.
Public datasets, ranked
NCBI GEO + Europe PMC + iCite · weekly437 human GEO series match endometrial cancer. Keyword relevance cannot tell a 189-sample patient cohort from a six-well cell-line experiment, so this ranking scores four things GEO does not expose: how often the accession is named in full-text papers, field-normalised citation impact, clinical annotation, and cohort type.
Composition of the 168-study ranked set
Established
high reuse, older| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE14860 | Integrated genomic profiling of endometrial carcinoma2009 · array | 291 | 7 | 5.3 | mixedAPT 0.95survivalstagemolecularPIK3CAPTEN239 cites |
| GSE17025 | Gene Expression Analysis of Stage I Endometrial Cancers2011 · array | 103 | 208 | 1.6 | APT 0.5stage72 cites |
| GSE63678 | Expression data from Vulvar, Cervical, Endometrial Carcinoma tissue2015 · array | 35 | 118 | 1.7 | APT 0.555 cites |
| GSE93911 | Aberrant mRNA m6A methylation promotes the progression of endometrial cancer by altering Akt activity2018 · sequencing | 32 | 6 | 21.4 | cell lineAPT 0.75657 cites |
| GSE67116 | Genome wide DNA methylation profiling of hyperplasias, primary endometrial cancer and metastases2015 · methylation | 96 | 7 | 4.9 | cell lineAPT 0.95167 cites |
| GSE115810 | Expression profiling of endometrial cancer of different grades2018 · array | 27 | 42 | 1.4 | APT 0.25stage32 cites |
| GSE56026 | Gene expression in human endometrial cancer tissues and serous papillary endometrial cancer cell line, SPAC-1L, treated by STAT1-siRNA and/or IFN-gamma2014 · array | 75 | 6 | 1.8 | mixedAPT 0.25survivalstage69 cites |
| GSE146889 | RNA-seq Reveals Differences in Expressed Tumor Mutation Burden in Colorectal and Endometrial Cancer With and Without Defective DNA Mismatch Repair2020 · sequencing | 176 | 17 | — | patient cohortmolecularMLH1 |
Recent
2022 onward, by score| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE212217 | Distinct Mechanisms of Mismatch-Repair Deficiency Delineate Two Modes of Response to Anti–PD-1 Immunotherapy in Endometrial Carcinoma2022 · single-cell | 104 | 5 | 4.4 | patient cohortAPT 0.95survivalmolecularPD-1PEMBROLIZUMAB66 cites |
| GSE268903 | Neoadjuvant immune checkpoint blockade in women with mismatch repair deficient endometrial cancer: a phase I study2024 · sequencing | 10 | 1 | 3.0 | patient cohortAPT 0.75survivalstagemolecularPEMBROLIZUMAB29 cites |
| GSE225691 | Netrin-1 blockade induces tumor growth inhibition and EMT reversion in endometrial cancer.2023 · sequencing | 36 | 5 | 11.0 | APT 0.75140 cites |
| GSE193430 | The clinicopathological characteristics, prognosis and immune microenvironment mapping in MSI-H/MMR-D endometrial carcinomas2022 · single-cell | 1 | 3 | 1.5 | patient cohortAPT 0.5survivalstagemolecularPD-1POLE22 cites |
| GSE251923 | Integrated single-cell RNA sequencing and spatial transcriptomics analysis reveals the tumor microenvironment in patients with endometrial cancer responding to anti-PD-1 treatment2023 · single-cell | 4 | 7 | 1.5 | patient cohortAPT 0.5molecularPD-113 cites |
| GSE205209 | PLK3 amplification and tumor immune microenvironment of metastatic tumors are linked to adjuvant treatment outcomes in uterine serous cancer2022 · array | 60 | 3 | 0.3 | patient cohortAPT 0.25survivalstagemolecularTP535 cites |
Sources: NCBI GEO + Europe PMC + iCite, retrieved 2026-09-12. SubSeries are collapsed to one row per study by linked PMID. Of 437 series retrieved, 62 were dropped by the profile’s exclusion rules and 163 named the disease only in passing. The ranked set is a relevance-ranked sample, not a census, so the composition figures describe the sample only.
Where the gaps are
Derived from the sections above · recomputed on every refreshEach card below is a disagreement between two of the tables on this page — a drug that exists but was never tried here, a target that looks tested and was not, a gene with no drug whose product has a busy clinical programme. They are computed from the same facts as the tables, so they cannot contradict them.
PTEN
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
MLH1
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
MSH2
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
MSH6
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
ARID1A
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
How a machine reads this page
StaticThis page is written to be quoted correctly by a model as much as read by a person. The same facts are available as JSON at the sibling URL below, which is what to cite.
Fully server-rendered
Every figure is in the HTML at first byte. No JavaScript runs, no figure is fetched after load, and nothing on this page requires a renderer to see.
Every number carries a source
Each section names the API it came from and the date it was retrieved: Open Targets (2026-09-12), ClinicalTrials.gov (2026-09-12), openFDA (2026-09-12), NCBI GEO (2026-09-12), PubMed (2026-09-12), NIH RePORTER (2026-09-12).
Negatives stated explicitly
Where nothing exists for endometrial cancer — no drug, no trial, no approval — the page says so in those words rather than omitting the row. An absent row is unquotable; a stated negative is the finding.
Denominators, not just percentages
Every share is printed with the count and the total it came from, so a figure can be checked rather than taken.
The filters are published
3 exclusion patterns are applied to free text before anything is ranked, because HEC-1A, AN3CA is used as a model system in endometrial receptivity and implantation biology, where the tumour lines stand in for endometrium. What was removed and why is stated in each section rather than silently applied.
{
"disease": "Endometrial cancer",
"mesh": "Endometrial Neoplasms",
"facts": "https://usebiotransfer.org/disease/endometrial-cancer.json",
"methods": "https://usebiotransfer.org/methods/",
"note": "Every figure on the page is in that JSON with its source and retrieval date. Quote from it rather than from the HTML."
}