Target landscape
Open Targets · retrieved 2026-09-30 · weekly12 genes recurrently implicated in breast 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: Breast cancer does have labelled therapy — 38 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 breast 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 |
|---|---|---|---|---|
| ESR1 across cancers → | 43 | 13 approvedBazedoxifene, Diethylstilbestrol, Diethylstilbestrol Diphosphate, Elacestrant, Estradiol, Estradiol Cypionate, Estrogens, Conjugated Synthetic A, Estrogens, Esterified, Estrone, Estropipate, Mestranol, Polyestradiol, QuinestrolApproved in breast cancer: Elacestrant, Estradiol.416 active of 1270 breast cancer trials | antibody, other clinical modality, protein degrader, small molecule | — |
| PGR across cancers → | 28 | 5 approvedDanazol, Ethynodiol Diacetate, Nomegestrol, Norgestrel, SegesteroneApproved in endometriosis, breast fibrocystic disease, Menorrhagia and 2 other indications. No breast cancer indication appears on these drugs’ labels.20 active of 179 breast cancer trials | antibody, protein degrader, small molecule | — |
| ERBB2 across cancers → | 43 | 10 approvedAfatinib, Dacomitinib, Lapatinib, Margetuximab, Masoprocol, Neratinib, Trastuzumab Duocarmazine, Tucatinib, Zanidatamab, ZenocutuzumabApproved in breast cancer: Lapatinib, Margetuximab, Neratinib, Tucatinib.456 active of 1148 breast cancer trials | antibody, other clinical modality, protein degrader, small molecule | 1 active of 1 trial |
| PIK3CA across cancers → | 31 | 2 approvedCopanlisib, InavolisibApproved in breast cancer: Inavolisib.55 active of 165 breast cancer trials | antibody, protein degrader, small molecule | — |
| AKT1 | 15 | 1 approvedCapivasertibApproved in breast cancer: Capivasertib.35 active of 76 breast cancer trials | antibody, protein degrader, small molecule | — |
| PTEN across cancers → | 0 | No drug— | antibody, protein degrader, small molecule | — |
| CDK4 across cancers → | 15 | 2 approvedRibociclib, TrilaciclibApproved in breast cancer: Ribociclib.275 active of 464 breast cancer trials | protein degrader, small molecule | — |
| CDK6 across cancers → | 10 | 2 approvedRibociclib, TrilaciclibApproved in breast cancer: Ribociclib.275 active of 464 breast cancer trials | protein degrader, small molecule | — |
| BRCA1 across cancers → | 0 | No drug— | antibody, protein degrader, small molecule | — |
| BRCA2 across cancers → | 0 | No drug— | protein degrader, small molecule | — |
| TP53 across cancers → | 8 | Phase 3Alrizomadlin, Cenersen, Contusugene Ladenovec, Eprenetapopt, Idasanutlin, Navtemadlin, Siremadlin, Teprasiran8 trials, none active | other clinical modality, protein degrader, small molecule | — |
| TACSTD2 across cancers → | 2 | 1 approvedDatopotamab DeruxtecanApproved in breast cancer: Datopotamab Deruxtecan.86 active of 102 breast cancer trials | antibody, other clinical modality, protein degrader | — |
Dataset evidence counts studies in the 3913-study ranked set whose title or abstract names the gene; the bar is scaled to CDK4. 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 · weekly38 drugs carry an FDA label naming breast cancer: Abemaciclib, Ado-Trastuzumab Emtansine, Alpelisib, Anastrozole, Camizestrant, Capivasertib, Datopotamab Deruxtecan, Elacestrant, Epirubicin, Eribulin, Estradiol, Estrogens, Conjugated, Everolimus, Exemestane, Fam-Trastuzumab Deruxtecan-Nxki, Fulvestrant, Goserelin, Imlunestrant, Inavolisib, Ixabepilone, Lapatinib, Letrozole, Margetuximab, Neratinib, Olaparib, Palbociclib, Pembrolizumab, Pertuzumab, Pertuzumab, Trastuzumab, Raloxifene, Ribociclib, Sacituzumab Govitecan, Talazoparib, Tamoxifen, Toremifene, Trastuzumab, Tucatinib, Vepdegestrant. Separately, 24 of the drugs returned for the genes in the table above are approved only for other diseases and reach breast cancer through trials, not through their labels.
Every label that names breast cancer
| Drug | Role | What the label says |
|---|---|---|
| AbemaciclibVerzenio | Labelled here | Early Breast Cancer VERZENIO ® (abemaciclib) is indicated: in combination with endocrine therapy (tamoxifen or an aromatase inhibitor) for the adjuvant treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, node-positive, early breast cancer at high risk of recurrence. |
| Ado-Trastuzumab EmtansineKADCYLA | Labelled here | Early Breast Cancer (EBC) KADCYLA, as a single agent, is indicated for the adjuvant treatment of patients with HER2-positive early breast cancer who have residual invasive disease after neoadjuvant taxane and trastuzumab -based treatment. |
| AlpelisibPIQRAY | Labelled here | PIQRAY is a kinase inhibitor indicated in combination with fulvestrant for the treatment of adults with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, PIK3CA-mutated, advanced or metastatic breast cancer as detected by an FDA-approved test following progression on or after an endocrine-based regimen. |
| AnastrozoleANASTROZOLE, ARIMIDEX, Anastrozole | Labelled here | Treatment of advanced breast cancer in postmenopausal women with disease progression following tamoxifen therapy. |
| CamizestrantETCAMAH | Labelled here | ETCAMAH in combination with a CDK4/6 inhibitor (abemaciclib, palbociclib, or ribociclib) is indicated for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, locally advanced or metastatic breast cancer upon detection of ESR1 mutation during aromatase inhibitor and CDK4/6 inhibitor therapy, based on an FDA-authorized test . |
| CapivasertibTRUQAP | Labelled here | HR-positive, HER2-negative locally advanced or metastatic breast cancer TRUQAP, in combination with fulvestrant, is indicated for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, locally advanced or metastatic breast cancer with one or more PIK3CA/AKT1/PTEN -alteration as detected by an FDA-authorized test following p... |
| Datopotamab DeruxtecanDATROWAY | Labelled here | Unresectable or Metastatic Triple-Negative Breast Cancer (TNBC) DATROWAY is indicated for the treatment of adult patients with unresectable or metastatic triple-negative breast cancer (TNBC) who are not candidates for PD-1/PD-L1 inhibitor therapy. |
| ElacestrantORSERDU | Labelled here | ORSERDU is an estrogen receptor antagonist indicated for: treatment of postmenopausal women or adult men, with ER-positive, HER2-negative, ESR1 -mutated advanced or metastatic breast cancer, as detected by an FDA-authorized test, with disease progression following at least one line of endocrine therapy ( 1 ) |
| EpirubicinEllence | Labelled here | ELLENCE is indicated as a component of adjuvant therapy in patients with evidence of axillary node tumor involvement following resection of primary breast cancer . |
| EribulinERIBULIN MESYLATE, Eribulin Mesylate, Halaven | Labelled here | Me tastatic Breast Cancer HALAVEN is indicated for the treatment of patients with metastatic breast cancer who have previously received at least two chemotherapeutic regimens for the treatment of metastatic disease. |
| EstradiolESTRADIOL, Estradiol | Labelled here | Treatment of breast cancer (for palliation only) in appropriately selected women and men with metastatic disease. |
| Estrogens, ConjugatedConjugated Estrogens, PREMARIN, Premarin | Labelled here | Treatment of Breast Cancer (for Palliation Only) in Appropriately Selected Women and Men with Metastatic Disease |
| EverolimusAfinitor, Afinitor Disperz, EVEROLIMUS | Labelled here | Hormone Receptor-Positive, HER2-Negative Breast Cancer AFINITOR ® is indicated for the treatment of postmenopausal women with advanced hormone receptor-positive, HER2-negative breast cancer in combination with exemestane, after failure of treatment with letrozole or anastrozole. |
| ExemestaneAromasin, EXEMESTANE, Exemestane | Labelled here | Advanced Breast Cancer in Postmenopausal Women AROMASIN is indicated for the treatment of advanced breast cancer in postmenopausal women whose disease has progressed following tamoxifen therapy. |
| Fam-Trastuzumab Deruxtecan-NxkiEnhertu | Labelled here | HER2-Positive Early Breast Cancer ENHERTU followed by a taxane, trastuzumab, and pertuzumab (THP) is indicated for the neoadjuvant treatment of adult patients with HER2-positive (IHC 3+ or ISH+) Stage II or III breast cancer as determined by an FDA-authorized test. |
| FulvestrantCLIGAVYX, FASLODEX, FULVESTRANT | Labelled here | (1) HR-positive advanced breast cancer in postmenopausal women with disease progression following endocrine therapy. |
| GoserelinZOLADEX | Labelled here | Advanced Breast Cancer ZOLADEX is indicated for use in the palliative treatment of advanced breast cancer in pre- and perimenopausal women. |
| ImlunestrantInluriyo | Labelled here | INLURIYO TM is an estrogen receptor antagonist indicated for: treatment of adults with ER-positive, HER2-negative, ESR1 -mutated advanced or metastatic breast cancer with disease progression following at least one line of endocrine therapy ( 1 ) |
| InavolisibItovebi | Labelled here | ITOVEBI is a kinase inhibitor indicated in combination with palbociclib and fulvestrant for the treatment of adults with endocrine-resistant, PIK3CA -mutated, hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, locally advanced or metastatic breast cancer, as detected by an FDA-approved test, following recurrence on or after completing adjuvant endocrine th... |
| IxabepiloneIXEMPRA | Labelled here | As a single agent for patients with metastatic or locally advanced breast cancer after failure of an anthracycline, a taxane, and capecitabine. |
| LapatinibLapatinib, TYKERB | Labelled here | Lapatinib tablets are indicated in combination with: capecitabine for the treatment of patients with advanced or metastatic breast cancer whose tumors overexpress human epidermal growth factor receptor 2 (HER2) and who have received prior therapy, including an anthracycline, a taxane, and trastuzumab.. . |
| LetrozoleFemara, LETROZOLE, Letrozole | Labelled here | Adjuvant Treatment of Early Breast Cancer Letrozole tablets are indicated for the adjuvant treatment of postmenopausal women with hormone receptor positive early breast cancer. |
| MargetuximabMARGENZA | Labelled here | MARGENZA is indicated, in combination with chemotherapy, for the treatment of adult patients with metastatic HER2-positive breast cancer who have received two or more prior anti-HER2 regimens, at least one of which was for metastatic disease. |
| NeratinibNerlynx | Labelled here | Advanced or Metastatic Breast Cancer NERLYNX in combination with capecitabine is indicated for the treatment of adult patients with advanced or metastatic HER2-positive breast cancer who have received two or more prior anti-HER2 based regimens in the metastatic setting . |
| OlaparibLynparza | Labelled here | ( 1.3 , 2.1 ) Breast cancer • for the adjuvant treatment of adult patients with deleterious or suspected deleterious g BRCA m human epidermal growth factor receptor 2 (HER2)-negative high risk early breast cancer who have been treated with neoadjuvant or adjuvant chemotherapy. |
| PalbociclibIbrance | Labelled here | HER2-Positive Metastatic Breast Cancer IBRANCE is indicated in combination with trastuzumab, with or without pertuzumab, and endocrine therapy for the maintenance treatment of adult patients with HR-positive, HER2-positive locally advanced or metastatic breast cancer following induction treatment. |
| PembrolizumabKEYTRUDA, KEYTRUDA QLEX | Labelled here | Triple-Negative Breast Cancer (TNBC) for the treatment of patients with high-risk early-stage TNBC in combination with chemotherapy as neoadjuvant treatment, and then continued as a single agent as adjuvant treatment after surgery. |
| PertuzumabPERJETA | Labelled here | Early Breast Cancer (EBC) PERJETA is indicated for use in combination with trastuzumab and chemotherapy for the neoadjuvant treatment of adults with HER2-positive, locally advanced, inflammatory, or early stage breast cancer (either greater than 2 cm in diameter or node positive) as part of a complete treatment regimen for early breast cancer . the adjuvant treatment of adults with HER2-positiv... |
| Pertuzumab, TrastuzumabPhesgo | Labelled here | Early Breast Cancer (EBC) PHESGO is indicated for use in combination with chemotherapy for the neoadjuvant treatment of adult patients with HER2-positive, locally advanced, inflammatory, or early stage breast cancer (either greater than 2 cm in diameter or node positive) as part of a complete treatment regimen for early breast cancer . the adjuvant treatment of adult patients with HER2-positive... |
| RaloxifeneEVISTA, Evista, Raloxifene Hydrochloride | Labelled here | High risk of breast cancer is defined as at least one breast biopsy showing lobular carcinoma in situ (LCIS) or atypical hyperplasia, one or more first-degree relatives with breast cancer, or a 5-year predicted risk of breast cancer ≥1.66% (based on the modified Gail model). |
| RibociclibKISQALI | Labelled here | Early Breast Cancer KISQALI ® FEMARA ® CO-PACK is indicated for the adjuvant treatment of adults with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative stage II and III early breast cancer at high risk of recurrence. |
| Sacituzumab GovitecanTRODELVY | Labelled here | Locally Advanced or Metastatic Triple-Negative Breast Cancer First Line TRODELVY as a single agent is indicated for the first-line treatment of adult patients with unresectable locally advanced or metastatic triple negative breast cancer (TNBC) who are not candidates for PD-1 or PD-L1 inhibitor based therapy. |
| TalazoparibTalzenna | Labelled here | BRCA -mutated (g BRCA m) HER2-negative Locally Advanced or Metastatic Breast Cancer TALZENNA is indicated as a single agent for the treatment of adult patients with deleterious or suspected deleterious germline breast cancer susceptibility gene ( BRCA )-mutated (g BRCA m) human epidermal growth factor receptor 2 (HER2)-negative locally advanced or metastatic breast cancer. |
| TamoxifenSOLTAMOX, Tamoxifen Citrate | Labelled here | Metastatic Breast Cancer SOLTAMOX is indicated for the treatment of adult patients with estrogen receptor-positive metastatic breast cancer. |
| ToremifeneFARESTON, Fareston, toremifene citrate | Labelled here | FARESTON® is an estrogen agonist/antagonist indicated for the treatment of metastatic breast cancer in postmenopausal women with estrogen-receptor positive or unknown tumors. |
| TrastuzumabHERZUMA, Herceptin, Herceptin Hylecta | Labelled here | Adjuvant Breast Cancer Herceptin is indicated in adults for adjuvant treatment of HER2 overexpressing node positive or node negative (ER/PR negative or with one high risk feature ) breast cancer as part of a treatment regimen consisting of doxorubicin, cyclophosphamide, and either paclitaxel or docetaxel as part of a treatment regimen with docetaxel and carboplatin as a single agent following m... |
| TucatinibTUKYSA | Labelled here | Metastatic Breast Cancer TUKYSA is indicated in combination with trastuzumab and capecitabine for treatment of adult patients with advanced unresectable or metastatic HER2-positive breast cancer, including patients with brain metastases, who have received one or more prior anti-HER2-based regimens in the metastatic setting. |
| VepdegestrantVEPPANU | Labelled here | VEPPANU is indicated for the treatment of adults with estrogen receptor (ER)-positive, human epidermal growth factor receptor 2 (HER2)-negative, estrogen receptor-1 (ESR1) -mutated advanced or metastatic breast cancer, as detected by an FDA-authorized test, with disease progression following at least one line of endocrine therapy. |
| CapecitabineCAPECITABINE, Capecitabine, Capecitabine 150mg | Backbone | treatment of patients with advanced or metastatic breast cancer in combination with docetaxel after disease progression on prior anthracycline-containing chemotherapy. |
| DocetaxelBEIZRAY, DOCETAXEL, DOCIVYX | Backbone | Breast Cancer BEIZRAY is indicated for the treatment of patients with locally advanced or metastatic breast cancer after failure of prior chemotherapy. |
| DoxorubicinDOXOrubicin Hydrochloride, Doxorubicin Hydrochloride, Doxorubicin hydrochloride | Backbone | Doxorubicin is also indicated for use as a component of adjuvant therapy in women with evidence of axillary lymph node involvement following resection of primary breast cancer. |
| GemcitabineAVGEMSI, GEMCITABINE, Gemcitabine | Backbone | — |
| MethotrexateMETHOTREXATE, Methotrexate | Backbone | Breast Cancer Methotrexate Injection is indicated for the treatment of adults with breast cancer as part of a combination chemotherapy regimen. |
| PaclitaxelABRAXANE, PACLITAXEL, PACLITAXEL PACLITAXEL | Backbone | TAXOL is indicated for the adjuvant treatment of node-positive breast cancer administered sequentially to standard doxorubicin-containing combination chemotherapy. |
| DenosumabBILDYOS, BOSAYA, Boncresa | Supportive | Treatment of Bone Loss in Women Receiving Adjuvant Aromatase Inhibitor Therapy for Breast Cancer Enoby is indicated as a treatment to increase bone mass in women at high risk for fracture receiving adjuvant aromatase inhibitor therapy for breast cancer . |
| DexrazoxaneDEXRAZOXANE, Dexrazoxane, Totect | Supportive | ( 1 ) Reducing the incidence and severity of cardiomyopathy associated with doxorubicin administration in women with metastatic breast cancer who have received a cumulative doxorubicin dose of 300 mg/m 2 and who will continue to receive doxorubicin therapy to maintain tumor control. |
| PamidronatePamidronate Disodium | Supportive | Osteolytic Bone Metastases of Breast Cancer and Osteolytic Lesions of Multiple Myeloma Pamidronate disodium is indicated, in conjunction with standard antineoplastic therapy, for the treatment of osteolytic bone metastases of breast cancer and osteolytic lesions of multiple myeloma. |
| Fluoroestradiol F 18CERIANNA | Not a therapy | CERIANNA is indicated for use with positron emission tomography (PET) imaging for the detection of estrogen receptor (ER)-positive lesions as an adjunct to biopsy in patients with recurrent or metastatic breast cancer. |
| PegulicianineLUMISIGHT | Not a therapy | LUMISIGHT is indicated for fluorescence imaging in adults with breast cancer as an adjunct for the intraoperative detection of cancerous tissue within the resection cavity following removal of the primary specimen during lumpectomy surgery. |
| Technetium Tc 99M Sulfur ColloidKit for the Prepartion of Technetium Tc99m Sulfur Colloid | Not a therapy | Technetium Tc 99m Sulfur Colloid Injection is indicated: In adults, to assist in the: localization of lymph nodes draining a primary tumor in patients with breast cancer or malignant melanoma when used with a hand-held gamma counter. evaluation of peritoneo-venous (LeVeen) shunt patency. |
| Technetium Tc 99M Sulfur Colloid KitKit for the Preparation of Technetium Tc 99m Sulfur Colloid | Not a therapy | Technetium Tc 99m Sulfur Colloid Injection is indicated: In adults, to assist in the: Localization of lymph nodes draining a primary tumor in patients with breast cancer or malignant melanoma when used with a hand-held gamma counter. |
| TilmanoceptKit for the preparation of Lymphoseek (technetium Tc 99m tilmanocept) | Not a therapy | ( 1 ) • Guiding sentinel lymph node biopsy using a handheld gamma counter in patients with clinically node negative squamous cell carcinoma of the oral cavity, breast cancer or melanoma. |
436 labels carry a positive indication naming the disease under indications_and_usage:"breast cancer"; they collapse to 52 distinct molecules once salt forms, biosimilars and co-formulated hyaluronidase are merged. Supportive agents (Denosumab, Dexrazoxane, Pamidronate) are given in the disease but do not act on it. Diagnostic and contrast agents (Fluoroestradiol F 18, Pegulicianine, Technetium Tc 99M Sulfur Colloid, Technetium Tc 99M Sulfur Colloid Kit, Tilmanocept) are listed but are not treatments. Source: openFDA drug label API (api.fda.gov/drug/label.json), retrieved 2026-09-19. Labels change; this reflects the current label text, not the approval history. Not prescribing guidance.
Labels that name breast 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.
| Drug | Why not | What the label says |
|---|---|---|
| Kit For The Preparation Of Technetium Tc99M SestamibiKit for the Preparation of Technetium Tc99m Sestamibi | Excluded by label | Technetium Tc 99m Sestamibi is not indicated for breast cancer screening, to confirm the presence or absence of malignancy, and it is not an alternative to biopsy. |
| Technetium Tc 99M SestamibiTECHNETIUM TC 99M SESTAMIBI | Excluded by label | Kit for the preparation of Technetium Tc 99m Sestamibi Injection is not indicated for breast cancer screening, to confirm the presence or absence of malignancy, and it is not an alternative to biopsy. |
| Tetrakis(2-Methoxyisobutylisocyanide)Copper(I) TetrafluoroborateCardiolite | Excluded by label | MIRALUMA ® is not indicated for breast cancer screening, to confirm the presence or absence of malignancy, and it is not an alternative to biopsy. |
Cell therapy against MUC1
ClinicalTrials.gov · retrieved 2026-09-18 · weeklyMUC1 is the busiest cell-therapy target among those this briefing searched in breast cancer: 5 registered trials naming it, 2 still active.
| Trial | Phase | Status | Title | Last update |
|---|---|---|---|---|
| NCT04020575 | 1 | Recruiting | Autologous huMNC2-CAR44 or huMNC2-CAR22 T Cells for Breast Cancer Targeting Cleaved Form of MUC1 (MUC1*) | 2023-06-18 |
| NCT05239143 | 1 | Active | P-MUC1C-ALLO1 Allogeneic CAR-T Cells in the Treatment of Subjects With Advanced or Metastatic Solid Tumors | 2026-02-09 |
| NCT02587689 | 1/2 | Unknown | Phase I/II Study of Anti-Mucin1 (MUC1) CAR T Cells for Patients With MUC1+ Advanced Refractory Solid Tumor | 2016-12-05 |
| NCT02839954 | 1/2 | Unknown | CAR-pNK Cell Immunotherapy in MUC1 Positive Relapsed or Refractory Solid Tumor | 2016-12-06 |
| NCT05812326 | 1/2 | Completed | PD-1 Knockout Anti-MUC1 CAR-T Cells in the Treatment of Advanced Breast Cancer | 2023-04-13 |
5 of 5 shown, most recently active first. Other targets searched: mesothelin (3), HER2 (1), PD-L1 (1), ROR1 (1), Nectin-4 (1). Source: ClinicalTrials.gov API v2, retrieved 2026-09-18. A trial counts here when its registered conditions name breast 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 · monthlyEvery term below is a share of the breast 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 46,801 and 68,867 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 |
|---|---|---|---|---|
| Artificial Intelligence | 0.1% | 1.8% | 18.0× | 108 papers |
| Camptothecin | 0.1% | 1.0% | 10.0× | 60 papers |
| Deep Learning | 0.27% | 2.42% | 9.06× | 145 papers |
| Molecular Dynamics Simulation | 0.12% | 0.92% | 7.86× | 55 papers |
| Immunoconjugates | 0.22% | 1.42% | 6.54× | 85 papers |
| Molecular Docking Simulation | 0.42% | 2.55% | 6.12× | 153 papers |
| Copper | 0.1% | 0.5% | 5.0× | 30 papers |
| Extracellular Vesicles | 0.12% | 0.58% | 5.0× | 35 papers |
| Machine Learning | 0.52% | 2.47% | 4.77× | 148 papers |
| Ubiquitination | 0.1% | 0.47% | 4.67× | 28 papers |
Cooling
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Tumor Cells, Cultured | 2.47% | 0.27% | 0.11× | 16 papers |
| Survival Analysis | 2.83% | 0.43% | 0.15× | 26 papers |
| Biomarkers | 1.5% | 0.25% | 0.17× | 15 papers |
| Biopsy | 2.12% | 0.4% | 0.19× | 24 papers |
| Odds Ratio | 1.03% | 0.2% | 0.19× | 12 papers |
| Up-Regulation | 1.75% | 0.35% | 0.2× | 21 papers |
Biggest topics now
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Triple Negative Breast Neoplasms | 7.6% | 13.88% | 1.83× | 833 papers |
| Prognosis | 13.35% | 12.85% | 0.96× | 771 papers |
| Biomarkers, Tumor | 10.63% | 12.0% | 1.13× | 720 papers |
| Gene Expression Regulation, Neoplastic | 11.62% | 11.65% | 1.0× | 699 papers |
| Antineoplastic Agents | 8.17% | 11.08% | 1.36× | 665 papers |
| Cell Proliferation | 10.58% | 10.9% | 1.03× | 654 papers |
| Erb-b2 Receptor Tyrosine Kinases | 8.17% | 9.02% | 1.1× | 541 papers |
| Apoptosis | 6.37% | 7.0% | 1.1× | 420 papers |
| Tumor Microenvironment | 1.93% | 6.9% | 3.57× | 414 papers |
| Treatment Outcome | 8.23% | 6.32% | 0.77× | 379 papers |
Publication mix
| Type | 2015–18 | 2021–25 |
|---|---|---|
| Clinical Trial | 0.0% | 0.1% |
| Randomized Controlled Trial | 3.2% | 3.9% |
| Review | 8.4% | 9.3% |
| Meta-Analysis | 2.0% | 2.4% |
| Case Reports | 0.0% | 2.2% |
Query: Breast Neoplasms[MeSH Major Topic] NOT ("Phyllodes Tumor"[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. The same figures for every disease on the site are on one table.
| Measure | Value | Match | What it counts |
|---|---|---|---|
| New cases each year | 321,910 cases/year | direct | 2026 SEER Cancer Stat Facts, Female Breast Cancer, retrieved 2026-09-11 |
| Deaths each year | 42,140 deaths/year | direct | 2026 SEER Cancer Stat Facts, Female Breast Cancer, retrieved 2026-09-11 |
| Incidence rate | 132.5 cases per 100,000 women per year | direct | 2019-2023 SEER Cancer Stat Facts, Female Breast Cancer, retrieved 2026-09-11 |
| Death rate | 18.9 deaths per 100,000 women per year | direct | 2020-2024 SEER Cancer Stat Facts, Female Breast Cancer, retrieved 2026-09-11 |
| People living with it | 4,238,585 women living with the disease | direct | 2023 SEER Cancer Stat Facts, Female Breast Cancer, retrieved 2026-09-11 |
| Median age at diagnosis | 64.0 years | direct | 2019-2023 SEER Cancer Stat Facts, Female Breast Cancer, retrieved 2026-09-11 |
| median age at death | 71 years | direct | 2020-2024 SEER Cancer Stat Facts, Female Breast Cancer, retrieved 2026-09-11 |
| Five-year relative survival | 91.9% | direct | 2016-2022 SEER Cancer Stat Facts, Female Breast Cancer, retrieved 2026-09-11 |
Years of life lost (proxy)
1.2 years per case, 375,476 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 · quarterlyNIH obligations naming breast cancer, after removing the 31,741 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 | $421.3M | 1,050 | 896 | 2,478 |
| FY2014 | $424.8M | 1,098 | 926 | 2,453 |
| FY2015 | $398.5M | 1,139 | 950 | 2,391 |
| FY2016 | $384.0M | 1,032 | 912 | 2,348 |
| FY2017 | $412.8M | 1,040 | 927 | 2,305 |
| FY2018 | $453.9M | 1,133 | 948 | 2,902 |
| FY2019 | $433.0M | 1,141 | 994 | 2,554 |
| FY2020 | $485.3M | 1,135 | 990 | 2,491 |
| FY2021 | $462.2M | 1,115 | 992 | 2,412 |
| FY2022 | $481.6M | 1,163 | 1,008 | 2,406 |
| FY2023 | $504.3M | 1,188 | 1,030 | 2,445 |
| FY2024 | $472.7M | 1,144 | 996 | 2,409 |
| FY2025 | $509.2M | 993 | 883 | 2,147 |
Where FY2025 money went
| Institution | Obligations | Awards |
|---|---|---|
| Division Of Basic Sciences - Nci | $34.9M | 27 |
| University Of California, San Francisco | $24.4M | 29 |
| Univ Of North Carolina Chapel Hill | $11.9M | 29 |
| Sloan-Kettering Inst Can Research | $10.4M | 15 |
| Division Of Cancer Epidemiology And Genetics | $10.3M | 0 |
| Washington University | $9.7M | 19 |
| Mayo Clinic Rochester | $8.9M | 17 |
| Dana-Farber Cancer Inst | $8.8M | 19 |
| University Of California At Davis | $8.4M | 23 |
| University Of Wisconsin-Madison | $8.0M | 0 |
Text search breast 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 375,476 years of life lost a year, FY2025 obligations are $1,356 per life-year — $1,582 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 980 of 993.
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 878 of 993.
Where it lands
Share of $509.2M in FY2025. The top three hold 14%.
Public datasets, ranked
NCBI GEO + Europe PMC + iCite · weekly8,692 human GEO series match breast cancer. Keyword relevance cannot tell a 4,113-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 3912-study ranked set
Established
high reuse, older| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE81540 | Clinical Value of RNA Sequencing–Based Classifiers for Prediction of the Five Conventional Breast Cancer Biomarkers: A Report From the Population-Based Multicenter Sweden Cancerome Analysis Network—Breast Initiative [superseries]2018 · sequencing | 3,814 | 325 | 5.4 | patient cohortAPT 0.75survivalstagemolecularHER2PGR170 cites |
| GSE176078 | A single-cell and spatially resolved atlas of human breast cancers2021 · single-cell | 26 | 527 | 68.8 | patient cohortAPT 0.75survivalmolecularPD-L11,347 cites |
| GSE2034 | Breast cancer relapse free survival2005 · array | 286 | 727 | 39.6 | patient cohortAPT 0.95survival2,020 cites |
| GSE3494 | An expression signature for p53 in breast cancer predicts mutation status, transcriptional effects, and patient survival2005 · array | 502 | 538 | 17.6 | patient cohortAPT 0.95survivalstage948 cites |
| GSE6532 | Definition of clinically distinct molecular subtypes in estrogen receptor positive breast carcinomas using genomic grade2007 · array | 741 | 484 | 12.2 | APT 0.95survivalstagemolecularERBB2617 cites |
| GSE2990 | Gene Expression Profiling in Breast Cancer: Understanding the Molecular Basis of Histologic Grade To Improve Prognosis2006 · array | 189 | 277 | 30.1 | patient cohortAPT 0.95survivalstage1,530 cites |
| GSE4922 | Genetic Reclassification of Histologic Grade Delineates New Clinical Subtypes of Breast Cancer2006 · array | 578 | 335 | 10.5 | patient cohortAPT 0.95survivalstage537 cites |
| GSE7390 | Strong Time Dependence of the 76-Gene Prognostic Signature2007 · array | 198 | 618 | 14.5 | patient cohortAPT 0.95survival731 cites |
Recent
2022 onward, by score| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE196096 | I-SPY2-990 mRNA/RPPA Data Resource2022 · array | 1,724 | 109 | 17.0 | patient cohortAPT 0.95stagemolecularHER2290 cites |
| GSE202203 | Clinical associations of ESR2 (estrogen receptor beta; ERβ) expression across thousands of primary breast tumors2022 · sequencing | 3,207 | 44 | 4.7 | patient cohortAPT 0.75survivalstagemolecularESR159 cites |
| GSE47994 | Tumor-infiltrating lymphocytes, prognosis and trastuzumab benefit in early-stage breast cancer patients from the FinHER trial2022 · array | 337 | 8 | 28.2 | patient cohortAPT 0.95survivalstagemolecularHER2TRASTUZUMAB1,039 cites |
| GSE266919 | Distinct Cellular Mechanisms Underlie Chemotherapies and Their Combinations with PD-L1 Checkpoint Inhibitor in Triple-Negative Breast Cancer [TNBC]2025 · single-cell | 117 | 10 | 27.3 | patient cohortAPT 0.75molecularATEZOLIZUMABPD-L1115 cites |
| GSE246613 | Single-cell and spatial profiling identify three response trajectories to pembrolizumab and radiation therapy in triple negative breast cancer2024 · single-cell | 266 | 26 | 15.2 | patient cohortAPT 0.75150 cites |
| GSE233242 | Tumor circadian clock strength influences metastatic potential and predicts patient prognosis in Luminal A breast cancer2024 · sequencing | 86 | 17 | 6.3 | patient cohortAPT 0.75survivalmolecularHER244 cites |
Sources: NCBI GEO + Europe PMC + iCite, retrieved 2026-09-19. SubSeries are collapsed to one row per study by linked PMID. Of 7,202 series retrieved, 31 were dropped by the profile’s exclusion rules and 2,051 named the disease only in passing. 1 further series named in the profile as contamination are excluded here. 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.
PTEN
Open Targets lists no drug against it and no trial in breast cancer names it. A bounded negative: the sources and search terms are in the JSON beside this page.
BRCA1
Open Targets lists no drug against it and no trial in breast cancer names it. A bounded negative: the sources and search terms are in the JSON beside this page.
BRCA2
Open Targets lists no drug against it and no trial in breast cancer names it. A bounded negative: the sources and search terms are in the JSON beside this page.
TP53
8 registered trials, 1 withdrawn before enrolling anyone and none active. This target reads as tried; it was not.
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. 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 (2026-09-19), NCBI GEO (2026-09-19), PubMed (2026-09-11), NIH RePORTER (2026-09-19).
Negatives stated explicitly
Where the searches find nothing for breast 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 MCF-7, MDA-MB-231, 4T1 and MCF-10A is used as a model system in endocrine-disruptor screening (MCF-7), natural-product cytotoxicity (MCF-7, MDA-MB-231), syngeneic tumour immunology and drug delivery (4T1, E0771), mammary epithelial biology (MCF-10A). What was removed and why is stated in each section rather than silently applied.
{
"disease": "Breast cancer",
"mesh": "Breast Neoplasms",
"facts": "https://usebiotransfer.org/disease/breast-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."
}