Disease Briefing

Cervical cancer: research and therapeutic landscape

A live synthesis of what is being targeted, what is being trialled, which datasets exist, and where the actionable gaps sit — assembled from public APIs, with every figure traceable to its source.

Generated 2026-09-30Sources Open Targets · ClinicalTrials.gov · openFDA · GEO · PubMed · Europe PMC · iCite · RePORTERRanked 242 studies · 8,969 GEO samples
Page Reading as
Reorders emphasis only — nothing is hidden or loaded on demand.

Answer block

12 genes recurrently implicated in cervical cancer — PIK3CA, TP53, CD274, PDCD1, ERBB2, KRAS, PTEN, FBXW7, EGFR, TACSTD2, TERT, CDKN2A — triaged for what can actually be aimed at them, alongside the trials, public datasets, literature and funding around the disease. Every figure below carries its source and retrieval date in the section it comes from.

3
drugs carry an FDA label naming cervical cancer: Bevacizumab, Pembrolizumab, Tisotumab Vedotin. This counts labels, not treatment — the disease is also treated with agents approved under broader indications
0
of the 12 genes above carries a drug approved in cervical cancer — 217 drug entries reach them, 199 distinct once salt forms are merged, and 39 of those are approved for other indications. A statement about these gene targets, not about the disease
4
registered HPV E6/E7 cell-therapy trials in cervical cancer, 1 active and 1 withdrawn. Counted from ClinicalTrials.gov across 5 synonyms, deduplicated by NCT id, interventional studies only — the query is published in the JSON beside this page so the number can be re-derived
4
targets carry an Open Targets tractability signal and no trial in cervical cancer that the searches found (no trial naming a drug Open Targets lists for the gene, none naming it as a cell-therapy target): KRAS, PTEN, FBXW7, TERT. CD274, PDCD1 have cell-therapy trials, so they are undrugged rather than untouched
991
human GEO series match the disease; 242 survive on-topic filtering, and only 13 are patient cohorts of 100+ samples
318
Europe PMC full-text papers name GSE63514 — the highest accession-mention count in the set. A mention is not proof of reanalysis, so read it as reach rather than reuse
$75.1M
NIH obligations in FY2025, up 116% since 2013 — while distinct core projects went 72 to 127. Both more projects (+76%) and larger awards, the latter carrying more of the growth; core projects are not the same unit as laboratories

Target landscape

Open Targets · retrieved 2026-09-30 · weekly

12 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.

GeneDrugsApproval, and whether it reached this diseaseOpen Targets tractabilitycomputed from protein features and literature — a signal that a modality is worth trying, not evidence that it worksCell therapy here
PIK3CA across cancers → 31 2 approvedCopanlisib, InavolisibApproved in follicular lymphoma, non-Hodgkin lymphoma, neoplasm of mature B-cells and 1 other indications. No cervical cancer indication appears on these drugs’ labels.6 active of 8 cervical cancer trials antibody, protein degrader, small molecule —
TP53 across cancers → 8 Phase 3Alrizomadlin, Cenersen, Contusugene Ladenovec, Eprenetapopt, Idasanutlin, Navtemadlin, Siremadlin, Teprasiran1 trials, none active other clinical modality, protein degrader, small molecule —
CD274 across cancers → 13 3 approvedAvelumab, Cosibelimab, SugemalimabApproved in Merkel cell skin cancer, urothelial carcinoma, neuroendocrine neoplasm and 2 other indications. No cervical cancer indication appears on these drugs’ labels.24 active of 66 cervical cancer trials antibody, other clinical modality, protein degrader, small molecule 0 active of 1 trial
PDCD1 across cancers → 26 5 approvedCemiplimab, Retifanlimab, Serplulimab, Sintilimab, ToripalimabApproved in basal cell carcinoma, cutaneous squamous cell carcinoma, cervical cancer and 9 other indications. No cervical cancer indication appears on these drugs’ labels.101 active of 224 cervical cancer trials antibody, other clinical modality, protein degrader, small molecule 0 active of 1 trial
ERBB2 across cancers → 43 10 approvedAfatinib, Dacomitinib, Lapatinib, Margetuximab, Masoprocol, Neratinib, Trastuzumab Duocarmazine, Tucatinib, Zanidatamab, ZenocutuzumabApproved in non-small cell lung carcinoma, breast cancer, HER2 positive breast carcinoma and 6 other indications. No cervical cancer indication appears on these drugs’ labels.22 active of 33 cervical cancer trials antibody, other clinical modality, protein degrader, small molecule —
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 across cancers → 0 No drug— protein degrader, small molecule —
EGFR across cancers → 72 15 approvedAfatinib, Aumolertinib, Brigatinib, Cetuximab Sarotalocan, Dacomitinib, Erlotinib, Icotinib, Lapatinib, Lazertinib, Mobocertinib, Neratinib, Nimotuzumab, Olmutinib, Osimertinib, RociletinibApproved in non-small cell lung carcinoma, anaplastic large cell lymphoma, head and neck cancer and 3 other indications. No cervical cancer indication appears on these drugs’ labels.7 active of 35 cervical cancer trials antibody, other clinical modality, protein degrader, small molecule —
TACSTD2 across cancers → 2 1 approvedDatopotamab DeruxtecanApproved in breast cancer, breast neoplasm, non-small cell lung carcinoma. No cervical cancer indication appears on these drugs’ labels.2 active of 4 cervical cancer trials antibody, other clinical modality, protein degrader —
TERT across cancers → 1 1 approvedImetelstatApproved in myelodysplastic syndrome, anemia. No cervical cancer indication appears on these drugs’ labels.No cervical cancer trial of any of these drugs antibody, other clinical modality, protein degrader, small molecule —
CDKN2A across cancers → 0 No drug— — —

Dataset evidence counts studies in the 242-study ranked set whose title or abstract names the gene; the bar is scaled to TP53. Sources: Open Targets Platform and NCBI GEO, retrieved 2026-09-30. 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 · weekly

3 drugs carry an FDA label naming cervical cancer: Bevacizumab, Pembrolizumab, Tisotumab Vedotin. Separately, 35 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.

3Labelled for cervical cancerFDA INDICATIONS AND USAGE names the disease
35Approved, but for another diseasereturned for the genes in the table above
1Backbone agents listing itbroad cytotoxics whose labels name many tumours
1Active cell-therapy trials naming HPV E6/E7of 4 registered

Every label that names cervical cancer

DrugRoleWhat the label says
BevacizumabALYMSYS, Avastin, JOBEVNELabelled herePersistent, recurrent, or metastatic cervical cancer, in combination with paclitaxel and cisplatin, or paclitaxel and topotecan.
PembrolizumabKEYTRUDA, KEYTRUDA QLEXLabelled hereCervical 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 VedotinTIVDAKLabelled hereTIVDAK ® is indicated for the treatment of adult patients with recurrent or metastatic cervical cancer with disease progression on or after chemotherapy.
TopotecanHYCAMTIN, Topotecan, Topotecan HydrochlorideBackbone( 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.

16 labels carry a positive indication naming the disease under 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 2026-09-18. Labels change; this reflects the current label text, not the approval history. Not prescribing guidance.

Cell therapy against HPV E6/E7

ClinicalTrials.gov · retrieved 2026-09-18 · weekly

HPV E6/E7 is the busiest cell-therapy target among those this briefing searched in cervical cancer: 4 registered trials naming it, 1 still active, 1 withdrawn before enrolling anyone.

TrialPhaseStatusTitleLast update
NCT056862262RecruitingE7 TCR-T Cell Immunotherapy for Human Papillomavirus (HPV) Associated Cancers2026-06-12
NCT044111341WithdrawnE7 TCR T Cell Immunotherapy for High-Grade Cervical Intraepithelial Neoplasia2020-07-15
NCT04476251EARLY/1TerminatedE7 TCR T Cell Induction Immunotherapy for Stage IIB-IVA Cervical Cancer2021-12-15
NCT028583101/2CompletedE7 TCR T Cells for Human Papillomavirus-Associated Cancers2026-03-09

4 of 4 shown, most recently active first. Other targets searched: PD-1 (1), PD-L1 (1). Source: ClinicalTrials.gov API v2, retrieved 2026-09-18. A trial counts here when its registered conditions name cervical cancer or a tumour-agnostic basket, its title names an administered cell product, and the title names this target: a HER2 CAR-T trial that adds a PD-1 antibody is a HER2 trial. A trial stating only a product code is missed.

Research momentum

PubMed MeSH · monthly

Every 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 term2015–182021–25ChangeShare now
Nomograms0.08%1.22%14.6×73 papers
Microbiota0.1%1.02%10.17×61 papers
Machine Learning0.1%0.98%9.83×59 papers
Tumor Microenvironment0.47%3.38%7.25×203 papers
Photosensitizing Agents0.1%0.67%6.67×40 papers
Antibodies, Monoclonal, Humanized0.25%1.55%6.2×93 papers
Neural Networks, Computer0.13%0.75%5.62×45 papers
Ethiopia0.27%1.45%5.44×87 papers
Progression-Free Survival0.17%0.83%5.0×50 papers
Genital Neoplasms, Female0.2%0.95%4.75×57 papers

Cooling

MeSH term2015–182021–25ChangeShare now
Survival Analysis2.03%0.23%0.11×14 papers
Time Factors2.7%0.32%0.12×19 papers
Tumor Burden2.0%0.23%0.12×14 papers
Up-Regulation2.18%0.28%0.13×17 papers
Down-Regulation2.1%0.37%0.17×22 papers
RNA, Small Interfering1.43%0.25%0.17×15 papers

Biggest topics now

MeSH term2015–182021–25ChangeShare now
Papillomavirus Infections24.48%31.67%1.29×1900 papers
Early Detection of Cancer18.57%25.43%1.37×1526 papers
Papillomaviridae13.62%14.5%1.06×870 papers
Uterine Cervical Dysplasia15.03%13.33%0.89×800 papers
Human Papillomavirus Viruses0.0%9.45%new567 papers
Mass Screening9.95%9.12%0.92×547 papers
Prognosis11.37%8.77%0.77×526 papers
Papillomavirus Vaccines7.63%8.47%1.11×508 papers
Cross-Sectional Studies6.0%7.98%1.33×479 papers
Neoplasm Staging12.85%7.8%0.61×468 papers

Publication mix

Type2015–182021–25
Clinical Trial0.0%0.1%
Randomized Controlled Trial2.7%2.0%
Review7.2%6.9%
Meta-Analysis2.1%1.9%
Case Reports0.0%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.

MeasureValueMatchWhat it counts
New cases each year13,490 cases/yeardirect2026
Deaths each year4,200 deaths/yeardirect2026
Incidence rate7.7 cases per 100,000 women per yeardirect2019-2023
Death rate2.1 deaths per 100,000 women per yeardirect2020-2024
People living with it305,284 women living with the diseasedirect2023
Median age at diagnosis50.0 yearsdirect2019-2023
median age at death60 yearsdirect2020-2024
Five-year relative survival68.8%direct2016-2022

Years of life lost (proxy)

8.9 years per case, 119,532 a year, from survival and age at diagnosis rather than from a death count. derived proxy Not the WHO/GBD measure, which uses age at death and a life table; comparable across these briefings, not with published YLL figures. 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 · quarterly

NIH obligations naming cervical cancer, after removing the 5,188 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.

$75.1MNIH obligations, FY2025from $34.8M in FY2013 · +116%
127distinct projects funded72 in FY2013
$82.4Mpeak year was FY2023obligations, all institutes
93%of FY2025 awards from NCI189 of 203

NIH obligations by fiscal year

$21M$41M$62M$82M13151719212325
YearObligationsAwardsDistinct projectsDropped as off-topic
FY2013$34.8M9372361
FY2014$42.1M10378387
FY2015$30.9M7861351
FY2016$29.2M7360333
FY2017$26.4M7056352
FY2018$29.3M6851439
FY2019$39.1M8264376
FY2020$41.3M9569403
FY2021$49.0M10473399
FY2022$64.0M12594439
FY2023$82.4M171128448
FY2024$80.4M170136447
FY2025$75.1M203127453

Where FY2025 money went

InstitutionObligationsAwards
Washington University$5.2M13
Johns Hopkins University$4.0M7
Division Of Cancer Epidemiology And Genetics$3.7M0
University Of Tx Md Anderson Can Ctr$3.7M11
Tufts Medical Center$3.3M0
Emory University$3.1M16
University Of Miami School Of Medicine$2.9M0
University Of California, San Diego$2.5M6
Columbia University Health Sciences$2.4M9
Fred Hutchinson Cancer Center$2.0M8

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 2026-09-19.

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

NCI189 · 93%
NIMHD8 · 4%
FIC3 · 1%
NIGMS1 · 0%
NIAID1 · 0%
NCATS1 · 0%

Projects by administering institute. The rows above are the top 6 and account for 203 of 203.

Award mechanisms

R0148 · 24%
U0139 · 19%
U5434 · 17%
R3715 · 7%
UG113 · 6%
R217 · 3%

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

Washington University$5.2M · 7.0%
Johns Hopkins University$4.0M · 5.3%
Division Of Cancer Epidemiology And Gene$3.7M · 5.0%
University Of Tx Md Anderson Can Ctr$3.7M · 5.0%
Tufts Medical Center$3.3M · 4.4%
Emory University$3.1M · 4.1%

Share of $75.1M in FY2025. The top three hold 17%.

Public datasets, ranked

NCBI GEO + Europe PMC + iCite · weekly

991 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 242-study ranked set

unspecified 83cell line 73patient 67mixed 19
83 unspecified73 cell line67 patient19 mixed100 carry clinical annotation65 carry survival13 patient cohorts ≥100 GEO samples8,969 GEO samples totalin 10 single-cell series the GEO sample count is the submitter’s unit (cells, libraries or pools), not patients

Established

high reuse, older
AccessionStudySamplesMentionsEurope PMCRCREvidence
GSE6791Gene Expression Profiles of HPV-Positive and -Negative Head/Neck and Cervical Cancers2007 · array841868.1
patient cohortAPT 0.75372 cites
GSE63514Gene expression analysis of cervical cancer progression2015 · array1283188.0
APT 0.75243 cites
GSE44001Genetic profiling to predict recurrence of early cervical cancer2013 · array3001821.6
patient cohortAPT 0.5survival66 cites
GSE39001Mitosis is the main pathway altered in cervical cancer and is a source of potential markers for screening and survival, and therapeutic targets.2013 · array79742.2
patient cohortAPT 0.5survivalstagemolecularCDKN2A76 cites
GSE7803Human pre-invasive and invasive cervical squamous cell carcinomas and normal cervical epithelia2007 · array411634.3
APT 0.75stage209 cites
GSE26511Involvement of the TGF-β and β-catenin pathways in pelvic lymph node metastasis in early stage cervical cancer2011 · array39402.6
patient cohortAPT 0.5survivalstage110 cites
GSE5787Survey of Intra- and Inter-Tumour Heterogeneity of Gene Expression in Cervical Cancer2006 · array33322.4
patient cohortAPT 0.75molecular127 cites
GSE67522Genome-wide analysis of gene expression to identify the probably functionally relevant pathways in cervical cancer progression2015 · array42533.4
patient cohortAPT 0.5103 cites

Recent

2022 onward, by score
AccessionStudySamplesMentionsEurope PMCRCREvidence
GSE208653Spatiotemporally 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-cell9529.2
APT 0.75survival101 cites
GSE197461Decipher heterogeneity of cervical squamous cell carcinoma and adenocarcinoma with different HPV status: combining scRNA and TCR-seq with 3D organoid2023 · single-cell16265.8
APT 0.75survival74 cites
GSE192897Identifying molecular changes in early cervical cancer samples of patients that developed metastasis2022 · other48111.6
patient cohortAPT 0.5survivalstage18 cites
GSE190075Adoptively transferred tumor-infiltrating lymphocyte immunotherapy following concurrent chemoradiotherapy in patients with advanced cervical cancer: a phase 1 trial2022 · single-cell833.0
patient cohortAPT 0.75survivalstage53 cites
GSE279998Proteogenomic analysis reveals a compendium of therapeutic targets for treatment-resistant subtypes of locally advanced cervical cancers2025 · sequencing1643.8
APT 0.25survivalstagemolecularTP5316 cites
GSE178629miRNA expression profiling of locally advancer cervical cancer2022 · sequencing20031.2
patient cohortAPT 0.25survival11 cites

Sources: NCBI GEO + Europe PMC + iCite, retrieved 2026-09-19. SubSeries are collapsed to one row per study by linked PMID. Of 991 series retrieved, 17 were dropped by the profile’s exclusion rules and 703 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 refresh

Each 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 naming any of them on ClinicalTrials.gov. The molecules exist; the search finds no test of them here.

PTEN

Open Targets lists no drug against it and no trial in cervical cancer names it. A bounded negative: the sources and search terms are in the JSON beside this page.

FBXW7

Open Targets lists no drug against it and no trial in cervical cancer names it. A bounded negative: the sources and search terms are in the JSON beside this page.

TERT

1 approved drug (Imetelstat) and no registered trial in cervical cancer naming any of them on ClinicalTrials.gov. The molecules exist; the search finds no test of them here.

CDKN2A

Open Targets lists no drug against it and no trial in cervical cancer names it. A bounded negative: the sources and search terms are in the JSON beside this page.

How a machine reads this page

Static

This 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. The cross-disease layer — burden, genes, drugs and antigens across every briefing — is described at /disease/api.json.

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 (2026-09-30), ClinicalTrials.gov (2026-09-18), openFDA (2026-09-18), NCBI GEO (2026-09-19), PubMed (2026-09-12), NIH RePORTER (2026-09-19).

Negatives stated explicitly

Where the searches find nothing for cervical cancer — no drug, no trial, no approval — the page says so in those words rather than omitting the row, and names the source searched. An absent row is unquotable; a bounded 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/",
  "all_diseases": "https://usebiotransfer.org/disease/api.json",
  "note": "Every figure on the page is in that JSON with its source and retrieval date. Quote from it rather than from the HTML."
}