Target landscape
Open Targets · retrieved 2026-09-11 · weekly12 genes recurrently implicated in pancreatic 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: Pancreatic cancer does have labelled therapy — 5 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 pancreatic 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 |
|---|---|---|---|---|
| KRAS | 3 | 2 approvedAdagrasib, SotorasibApproved in non-small cell lung carcinoma. No pancreatic cancer indication appears on these drugs’ labels.3 active of 9 pancreatic cancer trials | antibody, protein degrader, small molecule | 3 active of 7 trials |
| TP53 | 8 | Phase 3Alrizomadlin, Cenersen, Contusugene Ladenovec, Eprenetapopt, Idasanutlin, Navtemadlin, Siremadlin, TeprasiranNo pancreatic cancer trial of any of these drugs | other clinical modality, protein degrader, small molecule | — |
| CDKN2A | 0 | No drug— | — | — |
| SMAD4 | 0 | No drug— | protein degrader, small molecule | — |
| BRCA2 | 0 | No drug— | protein degrader, small molecule | — |
| PALB2 | 0 | No drug— | protein degrader, small molecule | — |
| ATM | 0 | No drug— | protein degrader, small molecule | — |
| EGFR | 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 pancreatic cancer: Erlotinib.52 active of 223 pancreatic cancer trials | antibody, other clinical modality, protein degrader, small molecule | — |
| MSLN | 5 | Phase 2Amatuximab, Anetumab Ravtansine, Lmb-100, Rg-7600, Ss1(Dsfv)-Pe381 active of 13 pancreatic cancer trials | antibody, other clinical modality, protein degrader | 8 active of 20 trials |
| CLDN18 | 1 | 1 approvedZolbetuximabApproved in gastric cancer, neoplasm of esophagus, gastric neoplasm and 2 other indications. No pancreatic cancer indication appears on these drugs’ labels.2 active of 2 pancreatic cancer trials | antibody | 11 active of 17 trials |
| CEACAM5 | 5 | 1 approvedArcitumomabApproved in breast cancer, radiologic finding, colorectal neoplasm. No pancreatic cancer indication appears on these drugs’ labels.2 trials, none active | antibody, other clinical modality, small molecule | 6 active of 18 trials |
| MUC1 | 12 | Phase 3Ar-20.5, As-1403, Cantuzumab Mertansine, Cantuzumab Ravtansine, Cmb-401, Gatipotuzumab, Huhmfg1, M170, Nacolomab Tafenatox, Sar-566658, Sontuzumab, Tecemotide2 trials, none active | antibody, other clinical modality, small molecule | 4 active of 7 trials |
Dataset evidence counts studies in the 351-study ranked set whose title or abstract names the gene; the bar is scaled to KRAS. Sources: Open Targets Platform and NCBI GEO, retrieved 2026-09-11. 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 · weekly5 drugs carry an FDA label naming pancreatic cancer: Daraxonrasib, Erlotinib, Irinotecan, Olaparib, Zenocutuzumab. Separately, 26 of the drugs returned for the genes in the table above are approved only for other diseases and reach pancreatic cancer through trials, not through their labels.
Every label that names pancreatic cancer
| Drug | Role | What the label says |
|---|---|---|
| DaraxonrasibRASONQUE | Labelled here | RASONQUE is indicated for the treatment of adult patients with metastatic pancreatic adenocarcinoma who have received at least one prior systemic therapy or who are not candidates for multiagent systemic therapy. |
| ErlotinibERLOTINIB, ERLOTINIB HYDROCHLORIDE, Erlotinib | Labelled here | Pancreatic Cancer Erlotinib tablet in combination with gemcitabine is indicated for the first-line treatment of patients with locally advanced, unresectable or metastatic pancreatic cancer [see Clinical Studies |
| IrinotecanOnivyde | Labelled here | Limitations of Use: ONIVYDE is not indicated as a single agent for the treatment of patients with metastatic pancreatic adenocarcinoma. . |
| OlaparibLynparza | Labelled here | ( 1.5 , 2.1 ) Pancreatic cancer • for the maintenance treatment of adult patients with deleterious or suspected deleterious gBRCA m metastatic pancreatic adenocarcinoma whose disease has not progressed on at least 16 weeks of a first-line platinum-based chemotherapy regimen. |
| ZenocutuzumabBIZENGRI | Labelled here | Adults with advanced, unresectable or metastatic pancreatic adenocarcinoma harboring a neuregulin 1 ( NRG1 ) gene fusion with disease progression on or after prior systemic therapy.* |
| CapecitabineCAPECITABINE, Capecitabine, XELODA | Backbone | Pancreatic Cancer adjuvant treatment of adults with pancreatic adenocarcinoma as a component of a combination chemotherapy regimen. |
| FluorouracilFAVLYXA, FLUOROURACIL, Fluorouracil | Backbone | Pancreatic Adenocarcinoma |
| GemcitabineAVGEMSI, GEMCITABINE, Gemcitabine | Backbone | Pancreatic Cancer AVGEMSI is indicated as first-line treatment for patients with locally advanced (nonresectable Stage II or Stage III) or metastatic (Stage IV) adenocarcinoma of the pancreas. |
| PaclitaxelABRAXANE, PACLITAXEL, PACLITAXEL PROTEIN BOUND PARTICLES ALBUMIN BOUND | Backbone | Adenocarcinoma of the Pancreas ABRAXANE is indicated for the first-line treatment of patients with metastatic adenocarcinoma of the pancreas, in combination with gemcitabine. |
66 labels match indications_and_usage:"pancreatic cancer" OR indications_and_usage:"adenocarcinoma of the pancreas" OR indications_and_usage:"pancreatic adenocarcinoma"; they collapse to 9 distinct molecules once salt forms, biosimilars and co-formulated hyaluronidase are merged. Source: openFDA drug label API (api.fda.gov/drug/label.json), retrieved 2026-09-11. Labels change; this reflects the current label text, not the approval history. Not prescribing guidance.
Cell therapy against mesothelin
ClinicalTrials.gov · retrieved 2026-09-11 · weeklymesothelin is the busiest cell-therapy antigen in pancreatic cancer: 20 registered trials, 8 still active, 1 withdrawn before enrolling anyone. It has no gene entry of its own and is reached through MSLN: the surface glycoprotein MSLN encodes.
| Trial | Phase | Status | Title | Last update |
|---|---|---|---|---|
| NCT05779917 | 1 | Recruiting | Mesothelin/GPC3/GUCY2C-CAR-T Cells Against Cancers | 2024-06-25 |
| NCT06196294 | 1 | Recruiting | GPC3/Mesothelin-CAR-γδT Cells Against Cancers | 2024-06-26 |
| NCT07066995 | 1/2 | Recruiting | Mesothelin and Claudin 18.2 Dual-Target CAR-T Therapy in Advanced Pancreatic Cancer | 2025-07-15 |
| NCT07480928 | 1/2 | Recruiting | Dual-Targeting CAR-NK Cells Targeting Mesothelin (MSLN) and MUC1 in Advanced Pancreatic Ductal Adenocarcinoma | 2026-03-18 |
| NCT07523529 | 1/2 | Recruiting | Biomarker-Guided Dual-Target CAR-T Cells for Advanced Solid Tumors | 2026-04-13 |
| NCT07627711 | 1/2 | Recruiting | Dual-Target CAR-NK Cells Targeting Mesothelin (MSLN) and MUC1 in Advanced Pancreatic Ductal Adenocarcinoma | 2026-06-04 |
| NCT06051695 | 1/2 | Recruiting | A Study to Evaluate the Safety and Efficacy of Mesothelin-Targeting Logic-gated CAR T, in Participants With Solid Tumors That Express MSLN and Have Lost HLA-A*02 Expression | 2026-06-12 |
| NCT06885697 | 1 | Recruiting | Anti-Mesothelin TNaive/SCM hYP218 (TNhYP218) CAR T Cells in Participants With Mesothelin-Expressing Solid Tumors Including Mesothelioma | 2026-08-26 |
| NCT02580747 | 1 | Unknown | Treatment of Relapsed and/or Chemotherapy Refractory Advanced Malignancies by CART-meso | 2015-10-20 |
| NCT02706782 | 1 | Unknown | A Study of Mesothelin Redirected Autologous T Cells for Advanced Pancreatic Carcinoma | 2016-03-11 |
10 of 20 shown, most recently active first. Other antigens searched: CEA (18), CLDN18.2 (17), MUC1 (7), KRAS G12D (7), HER2 (4), TROP2 (2), PSCA (1). Source: ClinicalTrials.gov API v2, retrieved 2026-09-11. 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 pancreatic 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 11,376 and 18,428 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 |
|---|---|---|---|---|
| Single-Cell Analysis | 0.1% | 1.0% | 9.99× | 60 papers |
| Molecular Docking Simulation | 0.08% | 0.83% | 9.99× | 50 papers |
| Extracellular Vesicles | 0.08% | 0.78% | 9.39× | 47 papers |
| Nomograms | 0.17% | 0.87% | 5.2× | 52 papers |
| Multicenter Studies as Topic | 0.08% | 0.43% | 5.19× | 26 papers |
| Ubiquitination | 0.12% | 0.6% | 5.14× | 36 papers |
| Liquid Biopsy | 0.17% | 0.77% | 4.6× | 46 papers |
| Circulating Tumor DNA | 0.17% | 0.72% | 4.3× | 43 papers |
| Pancreatic Intraductal Neoplasms | 0.63% | 2.72% | 4.29× | 163 papers |
| Cancer-Associated Fibroblasts | 0.5% | 2.08% | 4.17× | 125 papers |
Cooling
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Survival Analysis | 5.52% | 0.45% | 0.08× | 27 papers |
| Tumor Cells, Cultured | 2.43% | 0.23% | 0.1× | 14 papers |
| Tumor Burden | 3.0% | 0.33% | 0.11× | 20 papers |
| Gene Knockdown Techniques | 1.4% | 0.2% | 0.14× | 12 papers |
| Heterografts | 1.57% | 0.22% | 0.14× | 13 papers |
| Mice, SCID | 1.35% | 0.2% | 0.15× | 12 papers |
Biggest topics now
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Carcinoma, Pancreatic Ductal | 28.53% | 39.25% | 1.38× | 2355 papers |
| Prognosis | 15.27% | 16.43% | 1.08× | 986 papers |
| Tumor Microenvironment | 3.52% | 13.05% | 3.71× | 783 papers |
| Gene Expression Regulation, Neoplastic | 11.35% | 10.83% | 0.95× | 650 papers |
| Biomarkers, Tumor | 11.87% | 10.5% | 0.88× | 630 papers |
| Pancreatectomy | 12.25% | 10.22% | 0.83× | 613 papers |
| Cell Proliferation | 11.65% | 9.78% | 0.84× | 587 papers |
| Adenocarcinoma | 16.65% | 9.32% | 0.56× | 559 papers |
| Pancreas | 10.17% | 8.0% | 0.79× | 480 papers |
| Antineoplastic Combined Chemotherapy Protocols | 8.5% | 7.48% | 0.88× | 449 papers |
Publication mix
| Type | 2015–18 | 2021–25 |
|---|---|---|
| Clinical Trial | 0.0% | 0.0% |
| Randomized Controlled Trial | 2.0% | 1.0% |
| Review | 12.8% | 10.1% |
| Meta-Analysis | 2.3% | 1.9% |
| Case Reports | 0.0% | 2.3% |
Query: Pancreatic Neoplasms[MeSH Major Topic] NOT ("Neuroendocrine Tumors"[MeSH] OR "Insulinoma"[MeSH] OR "Adenoma, Islet Cell"[MeSH] OR "Carcinoma, Islet Cell"[MeSH] OR "Cholangiocarcinoma"[MeSH] OR "Bile Duct Neoplasms"[MeSH] OR "Common Bile Duct 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 2026-09-11.
Disease burden
What the public sources count, and how closely each category matches this disease.
| Measure | Value | Match | What it counts |
|---|---|---|---|
| New cases each year | 67,530 cases/year | direct | 2026 SEER Cancer Stat Facts, Pancreatic Cancer, retrieved 2026-09-11 |
| Deaths each year | 52,740 deaths/year | direct | 2026 SEER Cancer Stat Facts, Pancreatic Cancer, retrieved 2026-09-11 |
| Incidence rate | 13.9 cases per 100,000 per year | direct | 2019-2023 SEER Cancer Stat Facts, Pancreatic Cancer, retrieved 2026-09-11 |
| Death rate | 11.3 deaths per 100,000 per year | direct | 2020-2024 SEER Cancer Stat Facts, Pancreatic Cancer, retrieved 2026-09-11 |
| People living with it | 113,931 people living with the disease | direct | 2023 SEER Cancer Stat Facts, Pancreatic Cancer, retrieved 2026-09-11 |
| Median age at diagnosis | 71.0 years | direct | 2019-2023 SEER Cancer Stat Facts, Pancreatic Cancer, retrieved 2026-09-11 |
| median age at death | 73 years | direct | 2020-2024 SEER Cancer Stat Facts, Pancreatic Cancer, retrieved 2026-09-11 |
| Five-year relative survival | 13.7% | direct | 2016-2022 SEER Cancer Stat Facts, Pancreatic Cancer, retrieved 2026-09-11 |
Years of life lost
6.4 years per case, 431,260 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 pancreatic cancer, after removing the 10,678 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 | $77.8M | 287 | 238 | 684 |
| FY2014 | $94.8M | 305 | 252 | 646 |
| FY2015 | $96.1M | 320 | 274 | 678 |
| FY2016 | $124.3M | 366 | 296 | 728 |
| FY2017 | $146.4M | 366 | 308 | 757 |
| FY2018 | $159.4M | 417 | 332 | 974 |
| FY2019 | $165.3M | 439 | 357 | 895 |
| FY2020 | $172.4M | 424 | 359 | 886 |
| FY2021 | $184.6M | 440 | 386 | 849 |
| FY2022 | $209.8M | 503 | 414 | 895 |
| FY2023 | $222.1M | 537 | 447 | 943 |
| FY2024 | $229.9M | 563 | 467 | 914 |
| FY2025 | $229.9M | 493 | 419 | 829 |
Where FY2025 money went
| Institution | Obligations | Awards |
|---|---|---|
| University Of Tx Md Anderson Can Ctr | $15.2M | 23 |
| Johns Hopkins University | $12.5M | 20 |
| Sloan-Kettering Inst Can Research | $10.8M | 20 |
| University Of Michigan At Ann Arbor | $8.4M | 23 |
| Washington University | $7.1M | 15 |
| Stanford University | $7.1M | 12 |
| Univ Of North Carolina Chapel Hill | $7.0M | 11 |
| Oregon Health & Science University | $6.0M | 0 |
| Division Of Basic Sciences - Nci | $5.7M | 0 |
| Salk Institute For Biological Studies | $5.5M | 0 |
Text search pancreatic 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 2026-09-11.
What that buys
Against 431,260 years of life lost a year, FY2025 obligations are $533 per life-year — $3,404 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 10 and account for 491 of 493.
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 428 of 493.
Where it lands
Share of $229.9M in FY2025. The top three hold 17%.
Public datasets, ranked
NCBI GEO + Europe PMC + iCite · weekly1,930 human GEO series match pancreatic cancer. Keyword relevance cannot tell a 1,403-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 351-study ranked set
Established
high reuse, older| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE71729 | Virtual Microdissection of Pancreatic Ductal Adenocarcinoma Reveals Tumor and Stroma Subtypes.2015 · array | 357 | 359 | 49.1 | APT 0.95survival1,736 cites |
| GSE62452 | Microarray gene-expression profiles of 69 pancreatic tumors and 61 adjacent non-tumor tissue from patients with pancreatic ductal adenocarcinoma2016 · array | 130 | 635 | 8.5 | patient cohortAPT 0.75275 cites |
| GSE21501 | A six-gene signature predicts survival of patients with localized pancreatic ductal adenocarcinoma2010 · array | 132 | 187 | 4.2 | patient cohortAPT 0.75survivalmolecular194 cites |
| GSE155698 | Multimodal Mapping of the Tumor and Peripheral Blood Immune Landscape in Human Pancreatic Cancer2020 · sequencing | 41 | 176 | 16.5 | patient cohortAPT 0.75464 cites |
| GSE49149 | Genome-wide DNA methylation patterns in pancreatic ductal adenocarcinoma (PDAC)2014 · methylation | 196 | 25 | 91.7 | patient cohortAPT 0.952,903 cites |
| GSE62165 | Prognostic relevance of molecular subtypes and master regulators in pancreatic ductal adenocarcinoma2016 · array | 131 | 193 | 3.4 | patient cohortAPT 0.75survival114 cites |
| GSE179351 | Radiation Therapy Inhances Immunotherapy Response in Microsatellite-stable Colorectal and Pancreatic Adenocarcinoma in a Phase II Trial2021 · sequencing | 54 | 36 | 12.0 | patient cohortAPT 0.95246 cites |
| GSE93326 | Gene expression from laser capture microdissected pancreatic cancer epithelium and stroma2018 · sequencing | 204 | 37 | 14.1 | APT 0.75432 cites |
Recent
2022 onward, by score| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE183795 | Microarray gene-expression profiles of 139 pancreatic tumor,102 adjacent non-tumor tissue from patients with pancreatic ductal adenocarcinoma and 3 normal pancreas from donors.2022 · array | 244 | 102 | 3.2 | patient cohortAPT 0.5survival47 cites |
| GSE199102 | Spatial transcriptome profiling of pancreatic cancer identifies multicellular dynamics associated with neoadjuvant treatment2022 · spatial | 608 | 4 | 20.1 | patient cohortAPT 0.75survivalmolecular341 cites |
| GSE263733 | Single-cell transcriptome analysis reveals subtype-specific clonal evolution and microenvironmental changes in liver metastasis of pancreatic adenocarcinoma and their clinical implications2024 · single-cell | 218 | 10 | 3.7 | patient cohortAPT 0.5survivalmolecularKRAS36 cites |
| GSE217847 | IL-1b+ tumor-associated macrophages fuel pathogenic inflammation in pancreatic cancer2023 · single-cell | 136 | 3 | 26.2 | patient cohortAPT 0.75survival333 cites |
| GSE240078 | Neoadjuvant-induced Complement Upregulation in Tumor Microenvironment is Associated with Immunomodulation and Improved Survival in Pancreatic Ductal Adenocarcinoma: Insights from Spatially Resolved Transcriptomics2024 · spatial | 242 | 2 | 4.0 | patient cohortAPT 0.5survivalmolecular15 cites |
| GSE261159 | Gene expression dynamics of branching morphogenesis in pancreatic cancer organoids (2)2024 · sequencing | 181 | 1 | 9.7 | mixedAPT 0.75molecular40 cites |
Sources: NCBI GEO + Europe PMC + iCite, retrieved 2026-09-11. SubSeries are collapsed to one row per study by linked PMID. Of 606 series retrieved, 15 were dropped by the profile’s exclusion rules and 166 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.
CDKN2A
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
SMAD4
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
BRCA2
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
PALB2
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
ATM
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
MSLN
20 cell-therapy trials against mesothelin, 8 active, and no approved product. The clinical activity is real and none of it has reached a label.
MUC1
7 cell-therapy trials against MUC1, 4 active, and no approved product. The clinical activity is real and none of it has reached a label.
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 (2026-09-11), ClinicalTrials.gov (2026-09-11), openFDA (2026-09-11), NCBI GEO (2026-09-11), PubMed (2026-09-11), NIH RePORTER (2026-09-11).
Negatives stated explicitly
Where nothing exists for pancreatic 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
5 exclusion patterns are applied to free text before anything is ranked, because PANC-1, MIA PaCa-2 and BxPC-3 is used as a model system in nanoparticle delivery, EMT and hypoxia models, multi-line compound screens. What was removed and why is stated in each section rather than silently applied.
{
"disease": "Pancreatic cancer",
"mesh": "Pancreatic Neoplasms",
"facts": "https://usebiotransfer.org/disease/pancreatic-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."
}