Disease Briefing

Pancreatic 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 2026-09-11Sources Open Targets · ClinicalTrials.gov · openFDA · GEO · PubMed · Europe PMC · iCite · RePORTERRanked 351 studies · 24,011 GEO samples
Reading as
Reorders emphasis only — nothing is hidden or loaded on demand.

Answer block

12 genes recurrently implicated in pancreatic cancer — KRAS, TP53, CDKN2A, SMAD4, BRCA2, PALB2, ATM, EGFR, MSLN, CLDN18, CEACAM5, MUC1 — 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.

5
drugs carry an FDA label naming pancreatic cancer: Daraxonrasib, Erlotinib, Irinotecan, Olaparib, Zenocutuzumab. This counts labels, not treatment — the disease is also treated with agents approved under broader indications
1
of the 12 genes above carry a drug that is approved in pancreatic cancer itself — EGFR. Across all of them 117 drug entries reach these genes, 108 distinct once salt forms are merged
20
registered mesothelin cell-therapy trials in pancreatic cancer, 8 active and 1 withdrawn. Counted from ClinicalTrials.gov across 6 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
5
targets carry an Open Targets tractability signal and have no clinical programme of any kind: TP53, SMAD4, BRCA2, PALB2, ATM. KRAS, MSLN, CLDN18, CEACAM5, MUC1 all have cell-therapy trials, so they are undrugged rather than untouched
1,930
human GEO series match the disease; 351 survive on-topic filtering, and only 25 are patient cohorts of 100+ samples
635
Europe PMC full-text papers name GSE62452 — the highest accession-mention count in the set. A mention is not proof of reanalysis, so read it as reach rather than reuse
$229.9M
NIH obligations in FY2025, up 195% since 2013 — while distinct core projects went 238 to 419. 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 2026-09-11 · weekly

12 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.

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
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 · weekly

5 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.

5Labelled for pancreatic cancerFDA INDICATIONS AND USAGE names the disease
26Approved, but for another diseasereturned for the genes in the table above
4Backbone agents listing itbroad cytotoxics whose labels name many tumours
8Active mesothelin cell-therapy trialsof 20 registered

Every label that names pancreatic cancer

DrugRoleWhat the label says
DaraxonrasibRASONQUELabelled hereRASONQUE 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, ErlotinibLabelled herePancreatic 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
IrinotecanOnivydeLabelled hereLimitations of Use: ONIVYDE is not indicated as a single agent for the treatment of patients with metastatic pancreatic adenocarcinoma. .
OlaparibLynparzaLabelled 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.
ZenocutuzumabBIZENGRILabelled hereAdults 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, XELODABackbonePancreatic Cancer adjuvant treatment of adults with pancreatic adenocarcinoma as a component of a combination chemotherapy regimen.
FluorouracilFAVLYXA, FLUOROURACIL, FluorouracilBackbonePancreatic Adenocarcinoma
GemcitabineAVGEMSI, GEMCITABINE, GemcitabineBackbonePancreatic 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 BOUNDBackboneAdenocarcinoma 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 · weekly

mesothelin 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.

TrialPhaseStatusTitleLast update
NCT057799171RecruitingMesothelin/GPC3/GUCY2C-CAR-T Cells Against Cancers2024-06-25
NCT061962941RecruitingGPC3/Mesothelin-CAR-γδT Cells Against Cancers2024-06-26
NCT070669951/2RecruitingMesothelin and Claudin 18.2 Dual-Target CAR-T Therapy in Advanced Pancreatic Cancer2025-07-15
NCT074809281/2RecruitingDual-Targeting CAR-NK Cells Targeting Mesothelin (MSLN) and MUC1 in Advanced Pancreatic Ductal Adenocarcinoma2026-03-18
NCT075235291/2RecruitingBiomarker-Guided Dual-Target CAR-T Cells for Advanced Solid Tumors2026-04-13
NCT076277111/2RecruitingDual-Target CAR-NK Cells Targeting Mesothelin (MSLN) and MUC1 in Advanced Pancreatic Ductal Adenocarcinoma2026-06-04
NCT060516951/2RecruitingA 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 Expression2026-06-12
NCT068856971RecruitingAnti-Mesothelin TNaive/SCM hYP218 (TNhYP218) CAR T Cells in Participants With Mesothelin-Expressing Solid Tumors Including Mesothelioma2026-08-26
NCT025807471UnknownTreatment of Relapsed and/or Chemotherapy Refractory Advanced Malignancies by CART-meso2015-10-20
NCT027067821UnknownA Study of Mesothelin Redirected Autologous T Cells for Advanced Pancreatic Carcinoma2016-03-11

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 · monthly

Every 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 term2015–182021–25ChangeShare now
Single-Cell Analysis0.1%1.0%9.99×60 papers
Molecular Docking Simulation0.08%0.83%9.99×50 papers
Extracellular Vesicles0.08%0.78%9.39×47 papers
Nomograms0.17%0.87%5.2×52 papers
Multicenter Studies as Topic0.08%0.43%5.19×26 papers
Ubiquitination0.12%0.6%5.14×36 papers
Liquid Biopsy0.17%0.77%4.6×46 papers
Circulating Tumor DNA0.17%0.72%4.3×43 papers
Pancreatic Intraductal Neoplasms0.63%2.72%4.29×163 papers
Cancer-Associated Fibroblasts0.5%2.08%4.17×125 papers

Cooling

MeSH term2015–182021–25ChangeShare now
Survival Analysis5.52%0.45%0.08×27 papers
Tumor Cells, Cultured2.43%0.23%0.1×14 papers
Tumor Burden3.0%0.33%0.11×20 papers
Gene Knockdown Techniques1.4%0.2%0.14×12 papers
Heterografts1.57%0.22%0.14×13 papers
Mice, SCID1.35%0.2%0.15×12 papers

Biggest topics now

MeSH term2015–182021–25ChangeShare now
Carcinoma, Pancreatic Ductal28.53%39.25%1.38×2355 papers
Prognosis15.27%16.43%1.08×986 papers
Tumor Microenvironment3.52%13.05%3.71×783 papers
Gene Expression Regulation, Neoplastic11.35%10.83%0.95×650 papers
Biomarkers, Tumor11.87%10.5%0.88×630 papers
Pancreatectomy12.25%10.22%0.83×613 papers
Cell Proliferation11.65%9.78%0.84×587 papers
Adenocarcinoma16.65%9.32%0.56×559 papers
Pancreas10.17%8.0%0.79×480 papers
Antineoplastic Combined Chemotherapy Protocols8.5%7.48%0.88×449 papers

Publication mix

Type2015–182021–25
Clinical Trial0.0%0.0%
Randomized Controlled Trial2.0%1.0%
Review12.8%10.1%
Meta-Analysis2.3%1.9%
Case Reports0.0%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.

MeasureValueMatchWhat it counts
New cases each year67,530 cases/yeardirect2026
Deaths each year52,740 deaths/yeardirect2026
Incidence rate13.9 cases per 100,000 per yeardirect2019-2023
Death rate11.3 deaths per 100,000 per yeardirect2020-2024
People living with it113,931 people living with the diseasedirect2023
Median age at diagnosis71.0 yearsdirect2019-2023
median age at death73 yearsdirect2020-2024
Five-year relative survival13.7%direct2016-2022

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 · quarterly

NIH 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.

$229.9MNIH obligations, FY2025from $77.8M in FY2013 · +195%
419distinct projects funded238 in FY2013
$229.9Mpeak year was FY2024obligations, all institutes
92%of FY2025 awards from NCI451 of 491

NIH obligations by fiscal year

$57M$115M$172M$230M13151719212325
YearObligationsAwardsDistinct projectsDropped as off-topic
FY2013$77.8M287238684
FY2014$94.8M305252646
FY2015$96.1M320274678
FY2016$124.3M366296728
FY2017$146.4M366308757
FY2018$159.4M417332974
FY2019$165.3M439357895
FY2020$172.4M424359886
FY2021$184.6M440386849
FY2022$209.8M503414895
FY2023$222.1M537447943
FY2024$229.9M563467914
FY2025$229.9M493419829

Where FY2025 money went

InstitutionObligationsAwards
University Of Tx Md Anderson Can Ctr$15.2M23
Johns Hopkins University$12.5M20
Sloan-Kettering Inst Can Research$10.8M20
University Of Michigan At Ann Arbor$8.4M23
Washington University$7.1M15
Stanford University$7.1M12
Univ Of North Carolina Chapel Hill$7.0M11
Oregon Health & Science University$6.0M0
Division Of Basic Sciences - Nci$5.7M0
Salk Institute For Biological Studies$5.5M0

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

NCI451 · 91%
VA13 · 3%
NIGMS12 · 2%
NIBIB6 · 1%
OD2 · 0%
NHLBI2 · 0%

Projects by administering institute. The rows above are the top 10 and account for 491 of 493.

Award mechanisms

R01190 · 39%
U0135 · 7%
U5429 · 6%
P0125 · 5%
R3724 · 5%
F3122 · 4%

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

University Of Tx Md Anderson Can Ctr$15.2M · 6.6%
Johns Hopkins University$12.5M · 5.5%
Sloan-Kettering Inst Can Research$10.8M · 4.7%
University Of Michigan At Ann Arbor$8.4M · 3.6%
Washington University$7.1M · 3.1%
Stanford University$7.1M · 3.1%

Share of $229.9M in FY2025. The top three hold 17%.

Public datasets, ranked

NCBI GEO + Europe PMC + iCite · weekly

1,930 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

patient 118unspecified 100cell line 81mixed 43xenograft 9
118 patient100 unspecified81 cell line43 mixed9 xenograft218 carry clinical annotation139 carry survival25 patient cohorts ≥100 GEO samples24,011 GEO samples totalin 28 single-cell series a GEO sample is one cell, not one patient

Established

high reuse, older
AccessionStudySamplesMentionsEurope PMCRCREvidence
GSE71729Virtual Microdissection of Pancreatic Ductal Adenocarcinoma Reveals Tumor and Stroma Subtypes.2015 · array35735949.1
APT 0.95survival1,736 cites
GSE62452Microarray gene-expression profiles of 69 pancreatic tumors and 61 adjacent non-tumor tissue from patients with pancreatic ductal adenocarcinoma2016 · array1306358.5
patient cohortAPT 0.75275 cites
GSE21501A six-gene signature predicts survival of patients with localized pancreatic ductal adenocarcinoma2010 · array1321874.2
patient cohortAPT 0.75survivalmolecular194 cites
GSE155698Multimodal Mapping of the Tumor and Peripheral Blood Immune Landscape in Human Pancreatic Cancer2020 · sequencing4117616.5
patient cohortAPT 0.75464 cites
GSE49149Genome-wide DNA methylation patterns in pancreatic ductal adenocarcinoma (PDAC)2014 · methylation1962591.7
patient cohortAPT 0.952,903 cites
GSE62165Prognostic relevance of molecular subtypes and master regulators in pancreatic ductal adenocarcinoma2016 · array1311933.4
patient cohortAPT 0.75survival114 cites
GSE179351Radiation Therapy Inhances Immunotherapy Response in Microsatellite-stable Colorectal and Pancreatic Adenocarcinoma in a Phase II Trial2021 · sequencing543612.0
patient cohortAPT 0.95246 cites
GSE93326Gene expression from laser capture microdissected pancreatic cancer epithelium and stroma2018 · sequencing2043714.1
APT 0.75432 cites

Recent

2022 onward, by score
AccessionStudySamplesMentionsEurope PMCRCREvidence
GSE183795Microarray 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 · array2441023.2
patient cohortAPT 0.5survival47 cites
GSE199102Spatial transcriptome profiling of pancreatic cancer identifies multicellular dynamics associated with neoadjuvant treatment2022 · spatial608420.1
patient cohortAPT 0.75survivalmolecular341 cites
GSE263733Single-cell transcriptome analysis reveals subtype-specific clonal evolution and microenvironmental changes in liver metastasis of pancreatic adenocarcinoma and their clinical implications2024 · single-cell218103.7
patient cohortAPT 0.5survivalmolecularKRAS36 cites
GSE217847IL-1b+ tumor-associated macrophages fuel pathogenic inflammation in pancreatic cancer2023 · single-cell136326.2
patient cohortAPT 0.75survival333 cites
GSE240078Neoadjuvant-induced Complement Upregulation in Tumor Microenvironment is Associated with Immunomodulation and Improved Survival in Pancreatic Ductal Adenocarcinoma: Insights from Spatially Resolved Transcriptomics2024 · spatial24224.0
patient cohortAPT 0.5survivalmolecular15 cites
GSE261159Gene expression dynamics of branching morphogenesis in pancreatic cancer organoids (2)2024 · sequencing18119.7
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 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.

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

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.

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."
}