Target landscape
Open Targets · retrieved 2026-09-12 · weekly12 genes recurrently implicated in cervical cancer, triaged for whether anything can actually be aimed at them. The zeros are the informative rows.
Of 12 recurrently implicated genes, 9 carry any drug at all. That is a statement about these 12 gene targets, not about the disease: Cervical cancer does have labelled therapy — 3 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 cervical 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 |
|---|---|---|---|---|
| PIK3CA across cancers → | 31 | 3 approvedAlpelisib, Copanlisib, InavolisibApproved in breast cancer, breast neoplasm, breast carcinoma and 3 other indications. No cervical cancer indication appears on these drugs’ labels.8 active of 36 cervical cancer trials | antibody, protein degrader, small molecule | — |
| TP53 across cancers → | 8 | Phase 3Alrizomadlin, Cenersen, Contusugene Ladenovec, Eprenetapopt, Idasanutlin, Navtemadlin, Siremadlin, Teprasiran7 trials, none active | other clinical modality, protein degrader, small molecule | — |
| CD274 across cancers → | 13 | 5 approvedAtezolizumab, Avelumab, Cosibelimab, Durvalumab, SugemalimabApproved in urothelial carcinoma, non-small cell lung carcinoma, breast cancer and 6 other indications. No cervical cancer indication appears on these drugs’ labels.103 active of 262 cervical cancer trials | antibody, other clinical modality, protein degrader, small molecule | 1 active of 3 trials |
| PDCD1 across cancers → | 26 | 9 approvedCemiplimab, Dostarlimab, Nivolumab, Pembrolizumab, Retifanlimab, Serplulimab, Sintilimab, Tislelizumab, ToripalimabApproved in cervical cancer: Pembrolizumab.579 active of 1124 cervical cancer trials | antibody, other clinical modality, protein degrader, small molecule | 2 active of 10 trials |
| 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 cervical cancer indication appears on these drugs’ labels.83 active of 249 cervical cancer trials | antibody, other clinical modality, protein degrader, small molecule | 1 active of 2 trials |
| KRAS across cancers → | 3 | 2 approvedAdagrasib, SotorasibApproved in non-small cell lung carcinoma. No cervical cancer indication appears on these drugs’ labels.No cervical cancer trial of any of these drugs | antibody, protein degrader, small molecule | — |
| PTEN across cancers → | 0 | No drug— | antibody, protein degrader, small molecule | — |
| FBXW7 | 0 | No drug— | protein degrader, small molecule | — |
| EGFR across cancers → | 74 | 23 approvedAfatinib, Afatinib Dimaleate, Amivantamab, Aumolertinib, Brigatinib, Cetuximab, Cetuximab Sarotalocan, Dacomitinib, Erlotinib, Gefitinib, Icotinib, Lapatinib, Lapatinib Ditosylate, Lazertinib, Mobocertinib, Necitumumab, Neratinib, Nimotuzumab, Olmutinib, Osimertinib, Panitumumab, Rociletinib, VandetanibApproved in non-small cell lung carcinoma, anaplastic large cell lymphoma, malignant tumor of neck and 14 other indications. No cervical cancer indication appears on these drugs’ labels.99 active of 596 cervical cancer trials | antibody, other clinical modality, protein degrader, small molecule | — |
| TACSTD2 across cancers → | 2 | 2 approvedDatopotamab Deruxtecan, Sacituzumab GovitecanApproved in breast cancer, breast neoplasm, non-small cell lung carcinoma and 2 other indications. No cervical cancer indication appears on these drugs’ labels.10 active of 13 cervical cancer trials | antibody, other clinical modality, protein degrader | 1 active of 1 trial |
| TERT across cancers → | 1 | 1 approvedImetelstatApproved in anemia, myelodysplastic syndrome. No cervical cancer indication appears on these drugs’ labels.2 trials, none active | antibody, other clinical modality, protein degrader, small molecule | — |
| CDKN2A across cancers → | 0 | No drug— | — | — |
Dataset evidence counts studies in the 241-study ranked set whose title or abstract names the gene; the bar is scaled to TP53. 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 · weekly3 drugs carry an FDA label naming cervical cancer: Bevacizumab, Pembrolizumab, Tisotumab Vedotin. Separately, 54 of the drugs returned for the genes in the table above are approved only for other diseases and reach cervical cancer through trials, not through their labels.
Every label that names cervical cancer
| Drug | Role | What the label says |
|---|---|---|
| BevacizumabALYMSYS, Avastin, JOBEVNE | Labelled here | Persistent, recurrent, or metastatic cervical cancer, in combination with paclitaxel and cisplatin, or paclitaxel and topotecan. |
| PembrolizumabKEYTRUDA, KEYTRUDA QLEX | Labelled here | Cervical Cancer KEYTRUDA, in combination with chemoradiotherapy (CRT), is indicated for the treatment of patients with locally advanced cervical cancer involving the lower third of the vagina, with or without extension to pelvic sidewall, or hydronephrosis/non-functioning kidney, or spread to adjacent pelvic organs (FIGO 2014 Stage III-IVA). |
| Tisotumab VedotinTIVDAK | Labelled here | TIVDAK ® is indicated for the treatment of adult patients with recurrent or metastatic cervical cancer with disease progression on or after chemotherapy. |
| TopotecanHYCAMTIN, Topotecan, Topotecan Hydrochloride | Backbone | ( 1 ) combination therapy with cisplatin for stage IV-B, recurrent, or persistent carcinoma of the cervix which is not amenable to curative treatment with surgery and/or radiation therapy. |
13 labels match indications_and_usage:"cervical cancer" OR indications_and_usage:"carcinoma of the cervix"; they collapse to 4 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 HPV E6/E7
ClinicalTrials.gov · retrieved 2026-09-12 · weeklyHPV E6/E7 is the busiest cell-therapy antigen in cervical cancer: 11 registered trials, 5 still active, 2 withdrawn before enrolling anyone.
| Trial | Phase | Status | Title | Last update |
|---|---|---|---|---|
| NCT05639972 | 1/2 | Recruiting | E7 T-cell Receptor (TCR) -T Cell Induction Therapy for Locoregionally Advanced HPV-associated Cancers | 2026-06-12 |
| NCT05686226 | 2 | Recruiting | E7 TCR-T Cell Immunotherapy for Human Papillomavirus (HPV) Associated Cancers | 2026-06-12 |
| NCT05973487 | 1 | Active | A Basket Study of Customized Autologous TCR-T Cell Therapies in Patients With Locally Advanced (Unresectable) or Metastatic Solid Tumors | 2025-11-17 |
| NCT05582590 | 1 | Not yet recruiting | Autologous T Cells Targeting HPV16 HPV18 & Survivin in Patients With R/R HPV-related Oropharyngeal Cancers | 2024-01-16 |
| NCT06358053 | 1 | Not yet recruiting | CRTE7A2-01 TCR-T Cells for HPV-16 Positive Advanced Cancers | 2024-04-10 |
| NCT04411134 | 1 | Withdrawn | E7 TCR T Cell Immunotherapy for High-Grade Cervical Intraepithelial Neoplasia | 2020-07-15 |
| NCT04044950 | 2 | Withdrawn | A Phase II Study of Neoadjuvant E7 TCR T Cell Immunotherapy for Borderline Resectable and Unresectable Stage I HPV-Associated Oropharyngeal Cancer | 2020-09-22 |
| NCT04476251 | EARLY/1 | Terminated | E7 TCR T Cell Induction Immunotherapy for Stage IIB-IVA Cervical Cancer | 2021-12-15 |
| NCT04015336 | 2 | Terminated | E7 TCR Cell Induction Immunotherapy for Stage II and Stage III HPV-Associated Oropharyngeal Cancer | 2022-02-24 |
| NCT02858310 | 1/2 | Completed | E7 TCR T Cells for Human Papillomavirus-Associated Cancers | 2026-03-09 |
10 of 11 shown, most recently active first. Other antigens searched: PD-1 (10), PD-L1 (3), HER2 (2), TROP2 (1). 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 cervical cancer literature, not a count, because the field itself grew: 2015–2018 (n=6,000) against 2021–2025 (n=6,000). A topic whose papers doubled while the field doubled has not risen.
These are sample shares. The two windows hold 8,783 and 14,522 papers; MeSH terms were read from an evenly spaced sample of 6,000 and 6,000 of them, taken across the whole window rather than from its most recent papers. Percentages carry sampling error of roughly a percentage point and small differences between two terms are not meaningful.
Rising, with a real baseline
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Nomograms | 0.08% | 1.22% | 14.58× | 73 papers |
| Microbiota | 0.1% | 1.02% | 10.16× | 61 papers |
| Machine Learning | 0.1% | 0.98% | 9.82× | 59 papers |
| Tumor Microenvironment | 0.47% | 3.38% | 7.25× | 203 papers |
| Photosensitizing Agents | 0.1% | 0.67% | 6.66× | 40 papers |
| Antibodies, Monoclonal, Humanized | 0.25% | 1.55% | 6.2× | 93 papers |
| Neural Networks, Computer | 0.13% | 0.75% | 5.62× | 45 papers |
| Ethiopia | 0.27% | 1.45% | 5.44× | 87 papers |
| Progression-Free Survival | 0.17% | 0.83% | 5.0× | 50 papers |
| Genital Neoplasms, Female | 0.2% | 0.95% | 4.75× | 57 papers |
Cooling
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Survival Analysis | 2.03% | 0.23% | 0.11× | 14 papers |
| Time Factors | 2.7% | 0.32% | 0.12× | 19 papers |
| Tumor Burden | 2.0% | 0.23% | 0.12× | 14 papers |
| Up-Regulation | 2.18% | 0.28% | 0.13× | 17 papers |
| Down-Regulation | 2.1% | 0.37% | 0.17× | 22 papers |
| RNA, Small Interfering | 1.43% | 0.25% | 0.17× | 15 papers |
Biggest topics now
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Papillomavirus Infections | 24.48% | 31.67% | 1.29× | 1900 papers |
| Early Detection of Cancer | 18.57% | 25.43% | 1.37× | 1526 papers |
| Papillomaviridae | 13.62% | 14.5% | 1.06× | 870 papers |
| Uterine Cervical Dysplasia | 15.03% | 13.33% | 0.89× | 800 papers |
| Human Papillomavirus Viruses | 0.0% | 9.45% | 94501.0× | 567 papers |
| Mass Screening | 9.95% | 9.12% | 0.92× | 547 papers |
| Prognosis | 11.37% | 8.77% | 0.77× | 526 papers |
| Papillomavirus Vaccines | 7.63% | 8.47% | 1.11× | 508 papers |
| Cross-Sectional Studies | 6.0% | 7.98% | 1.33× | 479 papers |
| Neoplasm Staging | 12.85% | 7.8% | 0.61× | 468 papers |
Publication mix
| Type | 2015–18 | 2021–25 |
|---|---|---|
| Clinical Trial | 0.0% | 0.1% |
| Randomized Controlled Trial | 2.7% | 2.0% |
| Review | 7.2% | 6.9% |
| Meta-Analysis | 2.1% | 1.9% |
| Case Reports | 0.0% | 1.1% |
Query: Uterine Cervical Neoplasms[MeSH Major Topic] NOT ("Vulvar Neoplasms"[MeSH] OR "Vaginal Neoplasms"[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. Windows are read whole where they fit and sampled where they do not; the totals and the sample sizes are both in the JSON beside this page. 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 | 13,490 cases/year | direct | 2026 SEER Cancer Stat Facts, Cervical Cancer, retrieved 2026-09-12 |
| Deaths each year | 4,200 deaths/year | direct | 2026 SEER Cancer Stat Facts, Cervical Cancer, retrieved 2026-09-12 |
| Incidence rate | 7.7 cases per 100,000 women per year | direct | 2019-2023 SEER Cancer Stat Facts, Cervical Cancer, retrieved 2026-09-12 |
| Death rate | 2.1 deaths per 100,000 women per year | direct | 2020-2024 SEER Cancer Stat Facts, Cervical Cancer, retrieved 2026-09-12 |
| People living with it | 305,284 women living with the disease | direct | 2023 SEER Cancer Stat Facts, Cervical Cancer, retrieved 2026-09-12 |
| Median age at diagnosis | 50.0 years | direct | 2019-2023 SEER Cancer Stat Facts, Cervical Cancer, retrieved 2026-09-12 |
| median age at death | 60 years | direct | 2020-2024 SEER Cancer Stat Facts, Cervical Cancer, retrieved 2026-09-12 |
| Five-year relative survival | 68.8% | direct | 2016-2022 SEER Cancer Stat Facts, Cervical Cancer, retrieved 2026-09-12 |
Years of life lost
8.9 years per case, 119,532 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 cervical cancer, after removing the 5,273 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 | $41.1M | 105 | 82 | 373 |
| FY2014 | $47.0M | 111 | 86 | 394 |
| FY2015 | $39.4M | 87 | 68 | 357 |
| FY2016 | $37.2M | 79 | 64 | 339 |
| FY2017 | $27.8M | 71 | 57 | 355 |
| FY2018 | $30.3M | 69 | 52 | 444 |
| FY2019 | $39.3M | 84 | 66 | 377 |
| FY2020 | $41.4M | 97 | 71 | 409 |
| FY2021 | $49.2M | 105 | 74 | 405 |
| FY2022 | $64.0M | 125 | 94 | 447 |
| FY2023 | $84.6M | 172 | 129 | 456 |
| FY2024 | $80.4M | 170 | 136 | 458 |
| FY2025 | $75.1M | 203 | 127 | 459 |
Where FY2025 money went
| Institution | Obligations | Awards |
|---|---|---|
| Washington University | $5.2M | 13 |
| Johns Hopkins University | $4.0M | 7 |
| Division Of Cancer Epidemiology And Genetics | $3.7M | 0 |
| University Of Tx Md Anderson Can Ctr | $3.7M | 11 |
| Tufts Medical Center | $3.3M | 0 |
| Emory University | $3.1M | 16 |
| University Of Miami School Of Medicine | $2.9M | 0 |
| University Of California, San Diego | $2.5M | 6 |
| Columbia University Health Sciences | $2.4M | 9 |
| Fred Hutchinson Cancer Center | $2.0M | 8 |
Text search cervical 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 119,532 years of life lost a year, FY2025 obligations are $628 per life-year — $5,566 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 6 and account for 203 of 203.
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 189 of 203.
Where it lands
Share of $75.1M in FY2025. The top three hold 17%.
Public datasets, ranked
NCBI GEO + Europe PMC + iCite · weekly989 human GEO series match cervical cancer. Keyword relevance cannot tell a 576-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 241-study ranked set
Established
high reuse, older| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE6791 | Gene Expression Profiles of HPV-Positive and -Negative Head/Neck and Cervical Cancers2007 · array | 84 | 186 | 8.1 | patient cohortAPT 0.75372 cites |
| GSE63514 | Gene expression analysis of cervical cancer progression2015 · array | 128 | 318 | 8.0 | APT 0.75243 cites |
| GSE44001 | Genetic profiling to predict recurrence of early cervical cancer2013 · array | 300 | 182 | 1.6 | patient cohortAPT 0.5survival66 cites |
| GSE39001 | Mitosis is the main pathway altered in cervical cancer and is a source of potential markers for screening and survival, and therapeutic targets.2013 · array | 79 | 74 | 2.2 | patient cohortAPT 0.5survivalstagemolecularCDKN2A76 cites |
| GSE7803 | Human pre-invasive and invasive cervical squamous cell carcinomas and normal cervical epithelia2007 · array | 41 | 163 | 4.3 | APT 0.75stage209 cites |
| GSE26511 | Involvement of the TGF-β and β-catenin pathways in pelvic lymph node metastasis in early stage cervical cancer2011 · array | 39 | 40 | 2.6 | patient cohortAPT 0.5survivalstage110 cites |
| GSE5787 | Survey of Intra- and Inter-Tumour Heterogeneity of Gene Expression in Cervical Cancer2006 · array | 33 | 32 | 2.4 | patient cohortAPT 0.75molecular127 cites |
| GSE67522 | Genome-wide analysis of gene expression to identify the probably functionally relevant pathways in cervical cancer progression2015 · array | 42 | 53 | 3.4 | patient cohortAPT 0.5103 cites |
Recent
2022 onward, by score| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE208653 | Spatiotemporally Deciphering the Unknown Role of Persistent HPV Infection in Precancer to Cervical Cancer Progression: Integrating Single-Cell RNA-Sequencing Landscape and Spatial Transcriptomics Atlas [scRNA-seq]2023 · single-cell | 9 | 52 | 9.2 | APT 0.75survival101 cites |
| GSE197461 | Decipher heterogeneity of cervical squamous cell carcinoma and adenocarcinoma with different HPV status: combining scRNA and TCR-seq with 3D organoid2023 · single-cell | 16 | 26 | 5.8 | APT 0.75survival74 cites |
| GSE192897 | Identifying molecular changes in early cervical cancer samples of patients that developed metastasis2022 · other | 48 | 11 | 1.6 | patient cohortAPT 0.5survivalstage18 cites |
| GSE190075 | Adoptively transferred tumor-infiltrating lymphocyte immunotherapy following concurrent chemoradiotherapy in patients with advanced cervical cancer: a phase 1 trial2022 · single-cell | 8 | 3 | 3.0 | patient cohortAPT 0.75survivalstage53 cites |
| GSE279998 | Proteogenomic analysis reveals a compendium of therapeutic targets for treatment-resistant subtypes of locally advanced cervical cancers2025 · sequencing | 16 | 4 | 3.8 | APT 0.25survivalstagemolecularTP5316 cites |
| GSE178629 | miRNA expression profiling of locally advancer cervical cancer2022 · sequencing | 200 | 3 | 1.2 | patient cohortAPT 0.25survival11 cites |
Sources: NCBI GEO + Europe PMC + iCite, retrieved 2026-09-12. SubSeries are collapsed to one row per study by linked PMID. Of 989 series retrieved, 17 were dropped by the profile’s exclusion rules and 702 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.
KRAS
2 approved drugs (Adagrasib, Sotorasib) and no registered trial in cervical cancer. The molecules exist; nobody has tested them here.
PTEN
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
FBXW7
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
CDKN2A
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 cervical 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 HeLa is used as a model system in everything: HeLa is the default human cell for cell biology. What was removed and why is stated in each section rather than silently applied.
{
"disease": "Cervical cancer",
"mesh": "Uterine Cervical Neoplasms",
"facts": "https://usebiotransfer.org/disease/cervical-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."
}