Disease Briefing

Colorectal 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 2072 studies · 91,851 GEO samples
Page Reading as
Reorders emphasis only — nothing is hidden or loaded on demand.

Answer block

12 genes recurrently implicated in colorectal cancer — APC, KRAS, TP53, SMAD4, BRAF, EGFR, ERBB2, PIK3CA, MLH1, MSH2, NTRK1, CEACAM5 — 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.

15
drugs carry an FDA label naming colorectal cancer: Adagrasib, Bevacizumab, Cetuximab, Encorafenib, Fruquintinib, Ipilimumab and 9 more. This counts labels, not treatment — the disease is also treated with agents approved under broader indications
2
of the 12 genes above carry a drug that is approved in colorectal cancer itself — ERBB2, KRAS. Across all of them 214 drug entries reach these genes, 194 distinct once salt forms are merged
18
registered CEA cell-therapy trials in colorectal cancer, 8 active and 2 withdrawn.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
4
targets carry an Open Targets tractability signal and no trial in colorectal cancer that the searches found (no trial naming a drug Open Targets lists for the gene, none naming it as a cell-therapy target): APC, SMAD4, MLH1, MSH2. EGFR, ERBB2, CEACAM5 all have cell-therapy trials, so they are undrugged rather than untouched
5,232
human GEO series match the disease; 2,072 survive on-topic filtering, and only 141 are patient cohorts of 100+ samples
1,738
Europe PMC full-text papers name GSE40967 — the highest accession-mention count in the set. A mention is not proof of reanalysis, so read it as reach rather than reuse
$211.7M
NIH obligations in FY2025, up 40% since 2013 — while distinct core projects went 326 to 370. Larger awards rather than more distinct core projects; core projects are not the same unit as laboratories

Target landscape

Open Targets · retrieved 2026-09-30 · weekly

12 genes recurrently implicated in colorectal cancer, triaged for whether anything can actually be aimed at them. The zeros are the informative rows.

Of 12 recurrently implicated genes, 8 carry any drug at all. That is a statement about these 12 gene targets, not about the disease: Colorectal cancer does have labelled therapy — 15 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 colorectal 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
APC across cancers → 0 No drug— antibody, protein degrader, small molecule —
KRAS across cancers → 3 2 approvedAdagrasib, SotorasibApproved in colorectal cancer: Adagrasib, Sotorasib.12 active of 18 colorectal cancer trials antibody, protein degrader, small molecule —
TP53 across cancers → 8 Phase 3Alrizomadlin, Cenersen, Contusugene Ladenovec, Eprenetapopt, Idasanutlin, Navtemadlin, Siremadlin, Teprasiran3 trials, none active other clinical modality, protein degrader, small molecule —
SMAD4 across cancers → 0 No drug— protein degrader, small molecule —
BRAF across cancers → 16 3 approvedDabrafenib, Sorafenib, TovorafenibApproved in metastatic melanoma, low grade glioma, renal cell carcinoma and 1 other indications. No colorectal cancer indication appears on these drugs’ labels.72 active of 226 colorectal cancer trials antibody, 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 colorectal cancer indication appears on these drugs’ labels.100 active of 460 colorectal cancer trials antibody, other clinical modality, protein degrader, small molecule 1 active of 3 trials
ERBB2 across cancers → 43 10 approvedAfatinib, Dacomitinib, Lapatinib, Margetuximab, Masoprocol, Neratinib, Trastuzumab Duocarmazine, Tucatinib, Zanidatamab, ZenocutuzumabApproved in colorectal cancer: Tucatinib.66 active of 144 colorectal cancer trials antibody, other clinical modality, protein degrader, small molecule 0 active of 1 trial
PIK3CA across cancers → 31 2 approvedCopanlisib, InavolisibApproved in follicular lymphoma, non-Hodgkin lymphoma, neoplasm of mature B-cells and 1 other indications. No colorectal cancer indication appears on these drugs’ labels.5 active of 21 colorectal cancer trials antibody, protein degrader, small molecule —
MLH1 across cancers → 0 No drug— protein degrader, small molecule —
MSH2 across cancers → 0 No drug— protein degrader, small molecule —
NTRK1 across cancers → 16 4 approvedEntrectinib, Larotrectinib, Lestaurtinib, RepotrectinibApproved in non-small cell lung carcinoma, metastasis, acute myeloid leukemia by FAB classification. No colorectal cancer indication appears on these drugs’ labels.45 active of 149 colorectal cancer trials antibody, other clinical modality, protein degrader, small molecule —
CEACAM5 across cancers → 5 Phase 3Arcitumomab, Labetuzumab, Labetuzumab Govitecan, Medi-565, Tusamitamab Ravtansine9 trials, none active antibody, other clinical modality, small molecule 8 active of 18 trials

Dataset evidence counts studies in the 2072-study ranked set whose title or abstract names the gene; the bar is scaled to KRAS. Sources: Open Targets Platform and NCBI GEO, retrieved 2026-09-30. 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

15 drugs carry an FDA label naming colorectal cancer: Adagrasib, Bevacizumab, Cetuximab, Encorafenib, Fruquintinib, Ipilimumab, Nivolumab, Panitumumab, Pembrolizumab, Ramucirumab, Regorafenib, Sotorasib, Trifluridine And Tipiracil, Tucatinib, Ziv-Aflibercept. Separately, 29 of the drugs returned for the genes in the table above are approved only for other diseases and reach colorectal cancer through trials, not through their labels.

15Labelled for colorectal cancerFDA INDICATIONS AND USAGE names the disease
29Approved, but for another diseasereturned for the genes in the table above
4Backbone agents listing itbroad cytotoxics whose labels name many tumours
8Active cell-therapy trials naming CEAof 18 registered

Every label that names colorectal cancer

DrugRoleWhat the label says
AdagrasibKRAZATILabelled hereColorectal cancer (CRC)* • In combination with cetuximab, for the treatment of adult patients with KRAS G12C-mutated locally advanced or metastatic CRC, as determined by an FDA-approved test, who have received prior treatment with fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy.
BevacizumabALYMSYS, Avastin, JOBEVNELabelled hereMetastatic Colorectal Cancer MVASI, in combination with intravenous fluorouracil-based chemotherapy, is indicated for the first- or second-line treatment of patients with metastatic colorectal cancer (mCRC).
CetuximabERBITUXLabelled here( 1.1 , 14.1 ) Colorectal Cancer K-Ras wild-type, EGFR-expressing, metastatic colorectal cancer as determined by an FDA-approved test in combination with FOLFIRI for first-line treatment, in combination with irinotecan in patients who are refractory to irinotecan-based chemotherapy, as a single-agent in patients who have failed oxaliplatin- and irinotecan-based chemotherapy or who are intoleran...
EncorafenibBRAFTOVILabelled here( 1.1 , 2.1 ) Colorectal Cancer (CRC) • in combination with cetuximab and fluorouracil-based chemotherapy, for the treatment of adult patients with metastatic colorectal cancer (mCRC) with a BRAF V600E mutation, as detected by an FDA‑authorized test.
FruquintinibFruzaqlaLabelled hereFRUZAQLA is a kinase inhibitor indicated for the treatment of adult patients with metastatic colorectal cancer (mCRC) who have been previously treated with fluoropyrimidine‑, oxaliplatin‑, and irinotecan‑based chemotherapy, an anti‑VEGF therapy, and, if RAS wild‑type and medically appropriate, an anti-EGFR therapy.
IpilimumabYERVOYLabelled hereColorectal Cancer • Treatment of adults and pediatric patients 12 years and older with unresectable or metastatic microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) colorectal cancer (CRC) as determined by an FDA-authorized test in combination with nivolumab.
NivolumabOPDIVO, OPDIVO QVANTIGLabelled hereColorectal Cancer • adult and pediatric (12 years and older) patients with unresectable or metastatic microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) colorectal cancer (CRC) in combination with ipilimumab.
PanitumumabVectibixLabelled hereMetastatic Colorectal Cancer (mCRC) RAS Wild-Type mCRC Vectibix is indicated for the treatment of adult patients with wild-type RAS (defined as wild-type in both KRAS and NRAS as determined by an FDA-approved test) metastatic colorectal cancer (mCRC) [see Dosage and Administration
PembrolizumabKEYTRUDA, KEYTRUDA QLEXLabelled hereMicrosatellite Instability-High or Mismatch Repair Deficient Colorectal Cancer KEYTRUDA is indicated for the treatment of patients with unresectable or metastatic MSI-H or dMMR colorectal cancer (CRC) as determined by an FDA-authorized test [see Dosage and Administration
RamucirumabCYRAMZALabelled hereColorectal Cancer CYRAMZA, in combination with FOLFIRI (irinotecan, folinic acid, and fluorouracil), is indicated for the treatment of adults with metastatic colorectal cancer (mCRC) with disease progression on or after prior therapy with bevacizumab, oxaliplatin, and a fluoropyrimidine.
RegorafenibStivargaLabelled hereColorectal Cancer STIVARGA is indicated for the treatment of adult patients with metastatic colorectal cancer (CRC) who have been previously treated with fluoropyrimidine-, oxaliplatin- and irinotecan-based chemotherapy, an anti-VEGF therapy, and, if RAS wild-type, an anti-EGFR therapy.
SotorasibLUMAKRASLabelled hereKRAS G12C-mutated Metastatic Colorectal Cancer (mCRC) In combination with panitumumab, for the treatment of adult patients with KRAS G12C-mutated mCRC as determined by an FDA approved-test, who have received prior fluoropyrimidine-, oxaliplatin- and irinotecan-based chemotherapy.
Trifluridine And TipiracilLONSURFLabelled hereMetastatic Colorectal Cancer LONSURF, as a single agent or in combination with bevacizumab, is indicated for the treatment of adult patients with metastatic colorectal cancer previously treated with fluoropyrimidine-, oxaliplatin- and irinotecan-based chemotherapy, an anti-VEGF biological therapy, and if RAS wild-type, an anti-EGFR therapy.
TucatinibTUKYSALabelled hereUnresectable or Metastatic Colorectal Cancer TUKYSA is indicated in combination with trastuzumab for the treatment of adult patients with RAS wild-type, HER2-positive unresectable or metastatic colorectal cancer that has progressed following treatment with fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy.
Ziv-AfliberceptZALTRAPLabelled hereZALTRAP, in combination with fluorouracil, leucovorin, irinotecan-(FOLFIRI), is indicated for the treatment of patients with metastatic colorectal cancer (mCRC) that is resistant to or has progressed following an oxaliplatin-containing regimen.
CapecitabineCAPECITABINE, Capecitabine, Capecitabine 150mgBackboneColorectal Cancer XELODA is indicated as a single agent for adjuvant treatment in patients with Dukes' C colon cancer who have undergone complete resection of the primary tumor when treatment with fluoropyrimidine therapy alone is preferred.
IrinotecanCamptosar, IRINOTECAN HYDROCHLORIDE, Irinotecan HydrochlorideBackbone( 1 ) Patients with metastatic carcinoma of the colon or rectum whose disease has recurred or progressed following initial fluorouracil-based therapy.
Irinotecan HydrochloideIrinotecan hydrochloide, Irinotecan hydrochlorideBackbone( 1 ) Patients with metastatic carcinoma of the colon or rectum whose disease has recurred or progressed following initial fluorouracil-based therapy.
OxaliplatinOxaliplatin, USP, oxaliplatinBackbone(1) treatment of advanced colorectal cancer.
Leucovorin CalciumLEUCOVORIN CALCIUM, Leucovorin Calcium, Leucovorin calciumSupportiveTreatment of patients with metastatic colorectal cancer in combination with 5-fluorouracil.
LevoleucovorinKHAPZORY, LEVOLEUCOVORIN, LEVOLEUCOVORIN CALCIUMSupportive( 1 ) Treatment of adults with metastatic colorectal cancer in combination with fluorouracil.
Levoleucovorin CalciumLevoleucovorinSupportive( 1 ) Treatment of adults with metastatic colorectal cancer in combination with fluorouracil.

113 labels carry a positive indication naming the disease under indications_and_usage:"colorectal cancer" OR indications_and_usage:"colon cancer" OR indications_and_usage:"rectal cancer" OR indications_and_usage:"carcinoma of the colon or rectum" OR indications_and_usage:"colorectal carcinoma"; they collapse to 22 distinct molecules once salt forms, biosimilars and co-formulated hyaluronidase are merged. Supportive agents (Leucovorin Calcium, Levoleucovorin, Levoleucovorin Calcium) are given in the disease but do not act on it. 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.

Labels that name colorectal cancer without indicating for it

A label can name a disease under Limitations of Use, in a contraindication or as a risk. These were read and are not counted above.

DrugWhy notWhat the label says
DabrafenibTafinlarExcluded by labelLimitations of Use : TAFINLAR is not indicated for treatment of patients with colorectal cancer because of known intrinsic resistance to BRAF inhibition.
TrametinibMekinistExcluded by labelLimitations of Use : MEKINIST is not indicated for treatment of patients with colorectal cancer because of known intrinsic resistance to BRAF inhibition.

Cell therapy against CEA

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

CEA is the busiest cell-therapy target among those this briefing searched in colorectal cancer: 18 registered trials naming it, 8 still active, 2 withdrawn before enrolling anyone. It has no gene entry of its own and is reached through CEACAM5: the surface glycoprotein CEACAM5 encodes, the CEA of the blood test.

TrialPhaseStatusTitleLast update
NCT052409501RecruitingAnti-CEA CAR-T Cells to Treat Colorectal Liver Metastases2022-03-11
NCT060434661RecruitingA Clinical Trial Targeting CEA Chimeric Antigen Receptor T (CAR-T) for CEA Positive Advanced Malignant Solid Tumors2023-09-21
NCT060108621RecruitingClinical Study of CEA-targeted CAR-T Therapy for CEA-positive Advanced/Metastatic Malignant Solid Tumors2023-11-08
NCT061264061RecruitingClinical Study of CEA Targeting Chimeric Antigen Receptor T Lymphocytes(CAR-T) for CEA Positive Advanced Malignant Solid Tumors2023-11-13
NCT071796921RecruitingCEA-Targeted CAR-T Therapy in CEA-Positive Advanced Solid Tumors2025-10-02
NCT072473961RecruitingCEA CAR-T Therapy After Cytoreduction in Colorectal Cancer Patients With Peritoneal Metastases2025-11-25
NCT068210481RecruitingStudy of CEA Targeting CAR-T (PTC13) in the Treatment of CEA-Positive Advanced Malignant Solid Tumors2026-01-23
NCT057367311/2ActiveA Study to Evaluate the Safety and Efficacy of A2B530, a Logic-gated CAR T, in Participants With Solid Tumors That Express CEA and Have Lost HLA-A*02 Expression2025-04-25
NCT017233062SuspendedPhase II/Pilot Study of 2nd Generation Anti-CEA Designer T Cells in Adenocarcinomas2016-06-14
NCT023497241UnknownA Clinical Research of CAR T Cells Targeting CEA Positive Cancer2017-04-25

10 of 18 shown, most recently active first. Other targets searched: NKG2D (7), PD-1 (6), EGFR (3), MUC1 (3), GUCY2C (1), HER2 (1), TROP2 (1), LGR5 (1). Source: ClinicalTrials.gov API v2, retrieved 2026-09-18. A trial counts here when its registered conditions name colorectal 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 colorectal 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 32,289 and 48,775 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
Deep Learning0.08%1.67%20.0×100 papers
Artificial Intelligence0.08%1.42%17.0×85 papers
Machine Learning0.22%2.33%10.77×140 papers
Drugs, Chinese Herbal0.12%0.92%7.86×55 papers
Molecular Docking Simulation0.23%1.63%7.0×98 papers
Tumor Microenvironment1.35%8.4%6.22×504 papers
Probiotics0.13%0.82%6.12×49 papers
Lipid Metabolism0.1%0.53%5.33×32 papers
Diagnosis, Computer-Assisted0.12%0.6%5.14×36 papers
Glycolysis0.2%0.9%4.5×54 papers

Cooling

MeSH term2015–182021–25ChangeShare now
Survival Analysis4.17%0.32%0.08×19 papers
Multivariate Analysis1.88%0.25%0.13×15 papers
Cell Cycle1.28%0.23%0.18×14 papers
Biopsy1.27%0.25%0.2×15 papers
Tumor Burden2.05%0.45%0.22×27 papers
Down-Regulation2.47%0.53%0.22×32 papers

Biggest topics now

MeSH term2015–182021–25ChangeShare now
Prognosis15.18%15.27%1.01×916 papers
Gene Expression Regulation, Neoplastic12.02%14.43%1.2×866 papers
Rectal Neoplasms15.33%13.98%0.91×839 papers
Colonic Neoplasms21.22%13.42%0.63×805 papers
Biomarkers, Tumor10.68%12.42%1.16×745 papers
Cell Proliferation11.02%11.27%1.02×676 papers
Treatment Outcome12.97%9.55%0.74×573 papers
Tumor Microenvironment1.35%8.4%6.22×504 papers
Early Detection of Cancer7.3%7.87%1.08×472 papers
Risk Factors7.83%7.68%0.98×461 papers

Publication mix

Type2015–182021–25
Clinical Trial0.0%0.1%
Randomized Controlled Trial3.1%3.4%
Review7.4%8.5%
Meta-Analysis2.6%3.1%
Case Reports0.0%3.5%

Query: Colorectal Neoplasms[MeSH Major Topic] NOT ("Anus Neoplasms"[MeSH] OR "Neuroendocrine Tumors"[MeSH] OR "Appendiceal 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 year158,850 cases/yeardirect2026
Deaths each year55,230 deaths/yeardirect2026
Incidence rate37.6 cases per 100,000 per yeardirect2019-2023
Death rate12.7 deaths per 100,000 per yeardirect2020-2024
People living with it1,478,528 people living with the diseasedirect2023
Median age at diagnosis66.0 yearsdirect2019-2023
median age at death72 yearsdirect2020-2024
Five-year relative survival65.4%direct2016-2022

Years of life lost (proxy)

4.3 years per case, 681,530 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 colorectal cancer, after removing the 9,685 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.

$211.7MNIH obligations, FY2025from $150.7M in FY2013 · +40%
370distinct projects funded326 in FY2013
$211.7Mpeak year was FY2025obligations, all institutes
94%of FY2025 awards from NCI391 of 415

NIH obligations by fiscal year

$53M$106M$159M$212M13151719212325
YearObligationsAwardsDistinct projectsDropped as off-topic
FY2013$150.7M387326609
FY2014$129.1M348299624
FY2015$134.2M375313652
FY2016$139.0M340311650
FY2017$147.5M343314636
FY2018$198.2M413367852
FY2019$161.4M416367756
FY2020$176.0M423373805
FY2021$189.1M457404833
FY2022$200.6M468417853
FY2023$198.0M447388845
FY2024$190.9M446386833
FY2025$211.7M417370737

Where FY2025 money went

InstitutionObligationsAwards
Fred Hutchinson Cancer Center$14.1M25
Vanderbilt University Medical Center$10.3M14
University Of Tx Md Anderson Can Ctr$8.3M12
University Of Michigan At Ann Arbor$8.2M11
Weill Medical Coll Of Cornell Univ$6.5M12
University Of Southern California$6.0M0
Division Of Basic Sciences - Nci$5.4M0
Massachusetts General Hospital$5.3M11
Utah State Higher Education System--University Of Utah$4.9M11
Washington University$4.5M10

Text search colorectal 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 681,530 years of life lost a year, FY2025 obligations are $311 per life-year — $1,333 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

NCI391 · 94%
NIMHD8 · 2%
NIGMS5 · 1%
NIA3 · 1%
NIBIB2 · 0%
NIEHS2 · 0%

Projects by administering institute. The rows above are the top 10 and account for 415 of 417.

Award mechanisms

R01198 · 47%
R3724 · 6%
U0122 · 5%
U5421 · 5%
P5014 · 3%
R2113 · 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 364 of 417.

Where it lands

Fred Hutchinson Cancer Center$14.1M · 6.7%
Vanderbilt University Medical Center$10.3M · 4.9%
University Of Tx Md Anderson Can Ctr$8.3M · 3.9%
University Of Michigan At Ann Arbor$8.2M · 3.9%
Weill Medical Coll Of Cornell Univ$6.5M · 3.1%
University Of Southern California$6.0M · 2.8%

Share of $211.7M in FY2025. The top three hold 15%.

Public datasets, ranked

NCBI GEO + Europe PMC + iCite · weekly

5,232 human GEO series match colorectal cancer. Keyword relevance cannot tell a 2,503-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 2072-study ranked set

unspecified 631patient 630cell line 576mixed 206xenograft 29
631 unspecified630 patient576 cell line206 mixed29 xenograft779 carry clinical annotation503 carry survival141 patient cohorts ≥100 GEO samples91,851 GEO samples totalin 78 single-cell series the GEO sample count is the submitter’s unit (cells, libraries or pools), not patients

Established

high reuse, older
AccessionStudySamplesMentionsEurope PMCRCREvidence
GSE14333Expression data from 290 primary colorectal cancers2010 · array2906116.9
patient cohortAPT 0.75survivalstage363 cites
GSE81861Reference component analysis of single-cell transcriptomes elucidates cellular heterogeneity in human colorectal tumors2017 · single-cell1,22011323.8
patient cohortAPT 0.75survival841 cites
GSE17538Experimentally Derived Metastasis Gene Expression Profile Predicts Recurrence and Death in Colon Cancer Patients2009 · array24498412.7
patient cohortAPT 0.75survival615 cites
GSE178341A Single Cell Atlas of MMRd and MMRp Colorectal Cancer2021 · spatial18118732.7
patient cohortAPT 0.75710 cites
GSE132465Single cell 3' RNA sequencing of 23 Korean colorectal cancer patients2020 · single-cell3336423.8
patient cohortAPT 0.75668 cites
GSE41258Expression data from colorectal cancer patients2012 · array3904786.2
patient cohortAPT 0.75324 cites
GSE146771Single-Cell Analyses Inform Mechanisms of Myeloid-Targeted therapies in colon cancer2020 · single-cell2021348.0
patient cohortAPT 0.751,275 cites
GSE40967Gene expression Classification of Colon Cancer defines six molecular subtypes with distinct clinical, molecular and survival characteristics2013 · array1,0481,73830.4
APT 0.95survival1,169 cites

Recent

2022 onward, by score
AccessionStudySamplesMentionsEurope PMCRCREvidence
GSE205506Remodeling of the Immune and Stromal Cell Compartment by PD-1 Blockade in Mismatch Repair-Deficient Colorectal Cancer2023 · single-cell407623.3
patient cohortAPT 0.75molecularPD-1318 cites
GSE236581Spatiotemporal single-cell analysis decodes cellular dynamics underlying different responses to immunotherapy in Colorectal Cancer2024 · single-cell1695015.3
patient cohortAPT 0.75molecularPD-1168 cites
GSE225857Single-cell and spatial transcriptome analysis reveals the cellular heterogeneity of liver metastatic colorectal cancer2023 · single-cell87516.8
patient cohortAPT 0.75survival218 cites
GSE200997Refining Colorectal Cancer Classification and Clinical Stratification Through a Single-Cell Atlas2022 · single-cell239812.1
patient cohortAPT 0.75194 cites
GSE164522Single-cell analyses reveal phenotypic linkage between colorectal cancer and liver metastasis2022 · single-cell173322.2
patient cohortAPT 0.75372 cites
GSE245552Th17 cells secrete TWEAK to trigger epithelial-mesenchymal transition and promote colorectal cancer liver metastasis (scRNA-seq)2024 · single-cell39208.2
patient cohortAPT 0.75survival70 cites

Sources: NCBI GEO + Europe PMC + iCite, retrieved 2026-09-19. SubSeries are collapsed to one row per study by linked PMID. Of 5,101 series retrieved, 96 were dropped by the profile’s exclusion rules and 2,473 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.

APC

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

SMAD4

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

MLH1

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

MSH2

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

CEACAM5

18 cell-therapy trials against CEA, 8 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. 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 colorectal 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

4 exclusion patterns are applied to free text before anything is ranked, because HCT116, HT-29 and Caco-2, with MC38 and CT26 is used as a model system in DNA-damage and cell-cycle biology (HCT116), intestinal barrier and drug absorption (Caco-2), syngeneic tumour immunology (MC38, CT26). What was removed and why is stated in each section rather than silently applied.

{
  "disease": "Colorectal cancer",
  "mesh": "Colorectal Neoplasms",
  "facts": "https://usebiotransfer.org/disease/colorectal-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."
}