Target landscape
Open Targets · retrieved 2026-09-30 · weekly14 genes recurrently implicated in lung cancer, triaged for whether anything can actually be aimed at them. The zeros are the informative rows.
Of 14 recurrently implicated genes, 13 carry any drug at all. That is a statement about these 14 gene targets, not about the disease: Lung cancer does have labelled therapy — 47 drugs, listed in the next section.
Two different questions
The table below asks what can be aimed at 14 recurrently implicated genes. That is narrower than what is approved for the disease, and narrower again than what lung 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 |
|---|---|---|---|---|
| EGFR across cancers → | 72 | 15 approvedAfatinib, Aumolertinib, Brigatinib, Cetuximab Sarotalocan, Dacomitinib, Erlotinib, Icotinib, Lapatinib, Lazertinib, Mobocertinib, Neratinib, Nimotuzumab, Olmutinib, Osimertinib, RociletinibApproved in lung cancer: Afatinib, Brigatinib, Dacomitinib, Erlotinib, Lazertinib, Osimertinib.283 active of 1170 lung cancer trials | antibody, other clinical modality, protein degrader, small molecule | — |
| ALK across cancers → | 11 | 3 approvedAlectinib, Brigatinib, EntrectinibApproved in lung cancer: Alectinib, Brigatinib, Entrectinib.101 active of 256 lung cancer trials | antibody, other clinical modality, protein degrader, small molecule | — |
| KRAS across cancers → | 3 | 2 approvedAdagrasib, SotorasibApproved in lung cancer: Adagrasib, Sotorasib.29 active of 57 lung cancer trials | antibody, protein degrader, small molecule | — |
| ROS1 | 4 | 2 approvedEntrectinib, RepotrectinibApproved in lung cancer: Entrectinib, Repotrectinib.33 active of 95 lung cancer trials | antibody, protein degrader, small molecule | — |
| BRAF across cancers → | 16 | 3 approvedDabrafenib, Sorafenib, TovorafenibApproved in lung cancer: Dabrafenib.14 active of 79 lung cancer trials | antibody, protein degrader, small molecule | — |
| MET across cancers → | 35 | 3 approvedCabozantinib, Capmatinib, TepotinibApproved in lung cancer: Capmatinib, Tepotinib.87 active of 235 lung cancer trials | antibody, other clinical modality, protein degrader, small molecule | — |
| RET across cancers → | 13 | 5 approvedAlectinib, Lestaurtinib, Quizartinib, Selpercatinib, SorafenibApproved in lung cancer: Alectinib, Selpercatinib.39 active of 177 lung cancer trials | antibody, other clinical modality, protein degrader, small molecule | — |
| ERBB2 across cancers → | 43 | 10 approvedAfatinib, Dacomitinib, Lapatinib, Margetuximab, Masoprocol, Neratinib, Trastuzumab Duocarmazine, Tucatinib, Zanidatamab, ZenocutuzumabApproved in lung cancer: Afatinib, Dacomitinib, Zenocutuzumab.82 active of 292 lung cancer trials | antibody, other clinical modality, protein degrader, small molecule | 2 active of 3 trials |
| NTRK1 across cancers → | 16 | 4 approvedEntrectinib, Larotrectinib, Lestaurtinib, RepotrectinibApproved in lung cancer: Entrectinib, Repotrectinib.18 active of 28 lung cancer trials | antibody, other clinical modality, protein degrader, small molecule | — |
| TP53 across cancers → | 8 | Phase 3Alrizomadlin, Cenersen, Contusugene Ladenovec, Eprenetapopt, Idasanutlin, Navtemadlin, Siremadlin, Teprasiran1 active of 10 lung cancer trials | other clinical modality, protein degrader, small molecule | — |
| STK11 | 0 | No drug— | protein degrader, small molecule | — |
| KEAP1 | 4 | 2 approvedDiroximel, MonomethylApproved in multiple sclerosis symptom measurement, relapsing-remitting multiple sclerosis, immune system disorder. No lung cancer indication appears on these drugs’ labels.1 active of 13 lung cancer trials | protein degrader, small molecule | — |
| CD274 across cancers → | 13 | 3 approvedAvelumab, Cosibelimab, SugemalimabApproved in Merkel cell skin cancer, urothelial carcinoma, neuroendocrine neoplasm and 2 other indications. No lung cancer indication appears on these drugs’ labels.211 active of 464 lung cancer trials | antibody, other clinical modality, protein degrader, small molecule | 0 active of 1 trial |
| DLL3 across cancers → | 2 | 1 approvedTarlatamabApproved in lung cancer: Tarlatamab.24 active of 36 lung cancer trials | antibody, other clinical modality, protein degrader | 5 active of 6 trials |
Dataset evidence counts studies in the 1986-study ranked set whose title or abstract names the gene; the bar is scaled to EGFR. 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 · weekly47 drugs carry an FDA label naming lung cancer: Adagrasib, Afatinib, Alectinib, Amivantamab, Atezolizumab, Bevacizumab, Binimetinib, Brigatinib, Capmatinib, Cemiplimab, Ceritinib, Crizotinib, Dabrafenib, Dacomitinib, Datopotamab Deruxtecan, Durvalumab, Encorafenib, Ensartinib, Entrectinib, Erlotinib, Fam-Trastuzumab Deruxtecan-Nxki, Gefitinib, Ipilimumab, Lazertinib, Lorlatinib, Lurbinectedin, Nivolumab, Osimertinib, Pembrolizumab, Pemetrexed, Porfimer, Pralsetinib, Ramucirumab, Repotrectinib, Selpercatinib, Sevabertinib, Sotorasib, Taletrectinib, Tarlatamab, Telisotuzumab Vedotin, Tepotinib, Trametinib, Tremelimumab, Vinorelbine, Zenocutuzumab, Zidesamtinib, Zongertinib. Separately, 25 of the drugs returned for the genes in the table above are approved only for other diseases and reach lung cancer through trials, not through their labels.
Every label that names lung cancer
| Drug | Role | What the label says |
|---|---|---|
| AdagrasibKRAZATI | Labelled here | KRAS G12C-Mutated Locally Advanced or Metastatic Non-Small Cell Lung Cancer KRAZATI, as a single-agent, is indicated for the treatment of adult patients with KRAS G12C-mutated locally advanced or metastatic non-small cell lung cancer (NSCLC), as determined by an FDA-approved test [see Dosage and Administration |
| AfatinibAfatinib, Gilotrif | Labelled here | EGFR Mutation-Positive, Metastatic Non-Small Cell Lung Cancer GILOTRIF is indicated for the first-line treatment of patients with metastatic non-small cell lung cancer (NSCLC) whose tumors have non-resistant epidermal growth factor receptor (EGFR) mutations as detected by an FDA-approved test [see Dosage and Administration |
| AlectinibALECENSA | Labelled here | Adjuvant Treatment of Resected ALK-Positive Non-Small Cell Lung Cancer (NSCLC) ALECENSA is indicated as adjuvant treatment in adult patients following tumor resection of anaplastic lymphoma kinase (ALK)-positive non-small cell lung cancer (NSCLC) (tumors ≥ 4 cm or node positive), as detected by an FDA-approved test [see Dosage & Administration |
| AmivantamabRybrevant, Rybrevant Faspro | Labelled here | RYBREVANT is a bispecific EGF receptor-directed and MET receptor-directed antibody indicated: in combination with lazertinib for the first-line treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 L858R substitution mutations, as detected by an FDA-approved test. |
| AtezolizumabTECENTRIQ, Tecentriq Hybreza | Labelled here | Small Cell Lung Cancer (SCLC) in combination with carboplatin and etoposide, for the first-line treatment of adult patients with extensive-stage small cell lung cancer (ES-SCLC). |
| BevacizumabALYMSYS, Avastin, JOBEVNE | Labelled here | First-Line Non-Squamous Non-Small Cell Lung Cancer MVASI, in combination with carboplatin and paclitaxel, is indicated for the first-line treatment of patients with unresectable, locally advanced, recurrent or metastatic non-squamous non-small cell lung cancer (NSCLC). |
| BinimetinibMEKTOVI | Labelled here | BRAF V600E Mutation-Positive Metastatic Non-Small Cell Lung Cancer (NSCLC) MEKTOVI is indicated, in combination with encorafenib, for the treatment of adult patients with metastatic non-small cell lung cancer (NSCLC) with a BRAF V600E mutation, as detected by an FDA-approved test. [see Dosage and Administration |
| BrigatinibAlunbrig | Labelled here | ALUNBRIG is a kinase inhibitor indicated for the treatment of adult patients with anaplastic lymphoma kinase (ALK)-positive metastatic non-small cell lung cancer (NSCLC) as detected by an FDA-approved test. |
| CapmatinibTABRECTA | Labelled here | TABRECTA is a kinase inhibitor indicated for the treatment of adult patients with metastatic non-small cell lung cancer (NSCLC) whose tumors have a mutation that leads to mesenchymal-epithelial transition (MET) exon 14 skipping as detected by an FDA-approved test. |
| CemiplimabLIBTAYO | Labelled here | Non-Small Cell Lung Cancer (NSCLC) in combination with platinum‐based chemotherapy for the first‐line treatment of adult patients with non-small cell lung cancer (NSCLC) with no EGFR, ALK or ROS1 aberrations and is: locally advanced where patients are not candidates for surgical resection or definitive chemoradiation or metastatic. |
| CeritinibZYKADIA | Labelled here | ZYKADIA is a kinase inhibitor indicated for the treatment of adults with metastatic non-small cell lung cancer (NSCLC) whose tumors are anaplastic lymphoma kinase (ALK)-positive as detected by an FDA-approved test. |
| CrizotinibXalkori | Labelled here | ALK- or ROS1-Positive Metastatic Non-Small Cell Lung Cancer XALKORI is indicated for the treatment of adult patients with metastatic non-small cell lung cancer (NSCLC) whose tumors are anaplastic lymphoma kinase (ALK) or ROS1-positive as detected by an FDA-approved test [see Dosage and Administration |
| DabrafenibTafinlar | Labelled here | ( 1.3 , 2.1 ) the treatment of patients with metastatic non-small cell lung cancer (NSCLC) with BRAF V600E mutation as detected by an FDA-approved test. |
| DacomitinibVizimpro | Labelled here | VIZIMPRO is a kinase inhibitor indicated for the first-line treatment of patients with metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 19 deletion or exon 21 L858R substitution mutations as detected by an FDA-approved test. |
| Datopotamab DeruxtecanDATROWAY | Labelled here | Locally Advanced or Metastatic EGFR-Mutated Non-Small Cell Lung Cancer (NSCLC) DATROWAY is indicated for the treatment of adult patients with locally advanced or metastatic epidermal growth factor receptor (EGFR)-mutated non-small cell lung cancer (NSCLC) who have received prior EGFR-directed therapy and platinum-based chemotherapy. |
| DurvalumabIMFINZI | Labelled here | Small Cell Lung Cancer • IMFINZI, as a single agent, is indicated for the treatment of adult patients with limited-stage small cell lung cancer (LS-SCLC) whose disease has not progressed following concurrent platinum-based chemotherapy and radiation therapy (cCRT). • IMFINZI, in combination with etoposide and either carboplatin or cisplatin, is indicated for the first-line treatment of adult pa... |
| EncorafenibBRAFTOVI | Labelled here | ( 1.2 , 2.1 ) Non-Small Cell Lung Cancer (NSCLC) • in combination with binimetinib, for the treatment of adult patients with metastatic non–small cell lung cancer (NSCLC) with a BRAF V600E mutation, as detected by an FDA-authorized test. |
| EnsartinibENSACOVE | Labelled here | ENSACOVE is a kinase inhibitor indicated for the treatment of adult patients with anaplastic lymphoma kinase (ALK)-positive locally advanced or metastatic non-small cell lung cancer (NSCLC) as detected by an FDA-approved test who have not previously received an ALK-inhibitor. |
| EntrectinibRozlytrek | Labelled here | ROS1 -Positive Non-Small Cell Lung Cancer ROZLYTREK is indicated for the treatment of adult patients with ROS1- positive metastatic non-small cell lung cancer (NSCLC), as detected by an FDA-approved test. |
| ErlotinibERLOTINIB, ERLOTINIB HYDROCHLORIDE, Erlotinib | Labelled here | Non-Small Cell Lung Cancer (NSCLC) TARCEVA monotherapy is indicated for the treatment of patients with locally advanced or metastatic non-small cell lung cancer after failure of at least one prior chemotherapy regimen [see Clinical Studies |
| Fam-Trastuzumab Deruxtecan-NxkiEnhertu | Labelled here | HER2-Mutant Unresectable or Metastatic Non-Small Cell Lung Cancer as monotherapy for the treatment of adult patients with unresectable or metastatic non-small cell lung cancer (NSCLC) whose tumors have activating HER2 (ERBB2) mutations, as detected by an FDA-authorized test, and who have received a prior systemic therapy* |
| GefitinibGefitinib, IRESSA | Labelled here | IRESSA is indicated for the first-line treatment of patients with metastatic non-small cell lung cancer (NSCLC) whose tumors have epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 (L858R) substitution mutations as detected by an FDA-approved test .. . |
| IpilimumabYERVOY | Labelled here | Non-Small Cell Lung Cancer (NSCLC) • Treatment of adult patients with metastatic non-small cell lung cancer expressing PD-L1 (≥1%) as determined by an FDA-authorized test, with no EGFR or ALK genomic tumor aberrations, as first-line treatment in combination with nivolumab. |
| LazertinibLAZCLUZE | Labelled here | LAZCLUZE is a kinase inhibitor indicated in combination with amivantamab for the first-line treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 L858R substitution mutations, as detected by an FDA-approved test. |
| LorlatinibLorbrena | Labelled here | LORBRENA is a kinase inhibitor indicated for the treatment of adult patients with metastatic non-small cell lung cancer (NSCLC) whose tumors are anaplastic lymphoma kinase (ALK)-positive as detected by an FDA-approved test. |
| LurbinectedinZEPZELCA | Labelled here | Metastatic Small Cell Lung Cancer ZEPZELCA is indicated for the treatment of adult patients with metastatic small cell lung cancer (SCLC) with disease progression on or after platinum-based chemotherapy. |
| NivolumabOPDIVO, OPDIVO QVANTIG | Labelled here | Non-Small Cell Lung Cancer (NSCLC) • adult patients with resectable (tumors ≥4 cm or node positive) NSCLC in the neoadjuvant setting, in combination with platinum-doublet chemotherapy. |
| OsimertinibTAGRISSO | Labelled here | Adjuvant Treatment of EGFR Mutation-Positive Non-Small Cell Lung Cancer (NSCLC) TAGRISSO is indicated as adjuvant therapy after tumor resection in adult patients with non-small cell lung cancer (NSCLC) whose tumors have epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 L858R mutations, as detected by an FDA-approved test [see Dosage and Administration |
| PembrolizumabKEYTRUDA, KEYTRUDA QLEX | Labelled here | Non-Small Cell Lung Cancer (NSCLC) in combination with pemetrexed and platinum chemotherapy, as first-line treatment of patients with metastatic nonsquamous NSCLC, with no EGFR or ALK genomic tumor aberrations. |
| PemetrexedAXTLE, Alimta, PEMETREXED | Labelled here | Non-Squamous Non-Small Cell Lung Cancer (NSCLC) PEMRYDI RTU ® is indicated: in combination with pembrolizumab and platinum chemotherapy, for the initial treatment of patients with metastatic non-squamous non-small cell lung cancer (NSCLC), with no EGFR or ALK genomic tumor aberrations. in combination with cisplatin for the initial treatment of patients with locally advanced or metastatic, non-s... |
| PorfimerPhotofrin | Labelled here | — |
| PralsetinibGavreto | Labelled here | Metastatic RET Fusion-Positive Non-Small Cell Lung Cancer GAVRETO is indicated for the treatment of adult patients with metastatic RET fusion-positive non-small cell lung cancer (NSCLC) as detected by an FDA approved test. |
| RamucirumabCYRAMZA | Labelled here | Non-Small Cell Lung Cancer CYRAMZA, in combination with erlotinib, is indicated for the first-line treatment of adults with metastatic non-small cell lung cancer (NSCLC) whose tumors have epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 (L858R) substitution mutations. |
| RepotrectinibAugtyro | Labelled here | ROS1 -Positive Non-Small Cell Lung Cancer AUGTYRO is indicated for the treatment of adult patients with locally advanced or metastatic ROS1 -positive non-small cell lung cancer (NSCLC) [see Dosage and Administration |
| Selpercatinib{, ', M | Labelled here | RET Fusion-Positive Non-Small Cell Lung Cancer RETEVMO ® is indicated for the treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) with a rearranged during transfection (RET) gene fusion, as detected by an FDA-approved test. |
| SevabertinibHYRNUO | Labelled here | HYRNUO is a kinase inhibitor indicated for the treatment of adult patients with locally advanced or metastatic non-squamous non-small cell lung cancer (NSCLC) whose tumors have HER2 ( ERBB2 ) tyrosine kinase domain (TKD) activating mutations, as detected by an FDA-approved test, and who have received a prior systemic therapy. |
| SotorasibLUMAKRAS | Labelled here | KRAS G12C-mutated Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC) LUMAKRAS as a single agent is indicated for the treatment of adult patients with KRAS G12C -mutated locally advanced or metastatic non-small cell lung cancer (NSCLC), as determined by an FDA-approved test [see Dosage and Administration |
| TaletrectinibIBTROZI | Labelled here | IBTROZI is a kinase inhibitor indicated for the treatment of adult patients with locally advanced or metastatic ROS1 -positive non-small cell lung cancer (NSCLC). |
| TarlatamabIMDELLTRA (AMG757) | Labelled here | IMDELLTRA is indicated for the treatment of adult patients with extensive stage small cell lung cancer (ES-SCLC) with disease progression on or after platinum-based chemotherapy. |
| Telisotuzumab VedotinEMRELIS | Labelled here | EMRELIS is indicated for the treatment of adult patients with locally advanced or metastatic, non-squamous non-small cell lung cancer (NSCLC) with high c-Met protein overexpression [≥50% of tumor cells with strong (3+) staining], as determined by an FDA-approved test [see Dosage and Administration |
| TepotinibTEPMETKO | Labelled here | TEPMETKO is a kinase inhibitor indicated for the treatment of adult patients with metastatic non-small cell lung cancer (NSCLC) harboring mesenchymal-epithelial transition ( MET ) exon 14 skipping alterations. |
| TrametinibMekinist | Labelled here | ( 1.2 , 2.1 ) the treatment of patients with metastatic non-small cell lung cancer (NSCLC) with BRAF V600E mutation as detected by an FDA-approved test. |
| TremelimumabIMJUDO | Labelled here | Non-Small Cell Lung Cancer (NSCLC) IMJUDO, in combination with durvalumab and platinum-based chemotherapy, is indicated for the treatment of adult patients with metastatic NSCLC with no sensitizing epidermal growth factor receptor (EGFR) mutations or anaplastic lymphoma kinase (ALK) genomic tumor aberrations. |
| VinorelbineNAVELBINE, TARTRATE, Vinorelbine | Labelled here | VINORELBINE is indicated as a single agent or in combination with cisplatin for the first-line treatment of ambulatory patients with unresectable, advanced non-small cell lung cancer (NSCLC). |
| ZenocutuzumabBIZENGRI | Labelled here | Advanced Unresectable or Metastatic NRG1 Fusion-Positive Non-Small Cell Lung Cancer BIZENGRI is indicated for the treatment of adults with advanced unresectable or metastatic non-small cell lung cancer (NSCLC) harboring a neuregulin 1 ( NRG1 ) gene fusion with disease progression on or after prior systemic therapy. |
| ZidesamtinibJIDEYTRO | Labelled here | JIDEYTRO is a kinase inhibitor indicated for the treatment of adult patients with locally advanced or metastatic ROS1 -positive non-small cell lung cancer (NSCLC) who received a prior ROS1 kinase inhibitor.( 1 ) |
| ZongertinibHERNEXEOS | Labelled here | HERNEXEOS is a kinase inhibitor indicated for the treatment of adult patients with unresectable or metastatic non-squamous non-small cell lung cancer (NSCLC) whose tumors have HER2 (ERBB2) tyrosine kinase domain activating mutations, as detected by an FDA-authorized test. |
| DocetaxelBEIZRAY, DOCETAXEL, DOCIVYX | Backbone | Non-small Cell Lung Cancer (NSCLC): single agent for locally advanced or metastatic NSCLC after platinum therapy failure; and with cisplatin for unresectable, locally advanced or metastatic untreated NSCLC |
| EtoposideAvopef, ETOPOPHOS, ETOPOSIDE | Backbone | Small cell lung cancer |
| GemcitabineAVGEMSI, GEMCITABINE, Gemcitabine | Backbone | Non-Small Cell Lung Cancer AVGEMSI in combination with cisplatin is indicated for the first-line treatment of patients with inoperable, locally advanced (Stage IIIA or IIIB) or metastatic (Stage IV) non-small cell lung cancer (NSCLC). |
| MethotrexateMethotrexate | Backbone | Methotrexate is used alone or in combination with other anticancer agents in the treatment of breast cancer, epidermoid cancers of the head and neck, advanced mycosis fungoides (cutaneous T cell lymphoma), and lung cancer, particularly squamous cell and small cell types. |
| PaclitaxelABRAXANE, PACLITAXEL, PACLITAXEL PROTEIN BOUND PARTICLES ALBUMIN BOUND | Backbone | TAXOL, in combination with cisplatin, is indicated for the first-line treatment of non-small cell lung cancer in patients who are not candidates for potentially curative surgery and/or radiation therapy. |
| TopotecanHYCAMTIN, Topotecan, Topotecan Hydrochloride | Backbone | Topotecan is a topoisomerase inhibitor indicated for: small cell lung cancer sensitive disease after failure of first-line chemotherapy. |
| TrilaciclibCOSELA | Supportive | COSELA is a kinase inhibitor indicated to decrease the incidence of chemotherapy-induced myelosuppression in adult patients when administered prior to a platinum/etoposide-containing regimen or topotecan-containing regimen for extensive-stage small cell lung cancer. |
208 labels carry a positive indication naming the disease under indications_and_usage:"lung cancer" OR indications_and_usage:"non-small cell lung cancer" OR indications_and_usage:"small cell lung cancer" OR indications_and_usage:"non-small cell lung carcinoma"; they collapse to 54 distinct molecules once salt forms, biosimilars and co-formulated hyaluronidase are merged. Supportive agents (Trilaciclib) 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.
Cell therapy against CEACAM5
ClinicalTrials.gov · retrieved 2026-09-18 · weeklyCEACAM5 is the busiest cell-therapy target among those this briefing searched in lung cancer: 14 registered trials naming it, 10 still active, 1 withdrawn before enrolling anyone.
| Trial | Phase | Status | Title | Last update |
|---|---|---|---|---|
| NCT06043466 | 1 | Recruiting | A Clinical Trial Targeting CEA Chimeric Antigen Receptor T (CAR-T) for CEA Positive Advanced Malignant Solid Tumors | 2023-09-21 |
| NCT06010862 | 1 | Recruiting | Clinical Study of CEA-targeted CAR-T Therapy for CEA-positive Advanced/Metastatic Malignant Solid Tumors | 2023-11-08 |
| NCT06126406 | 1 | Recruiting | Clinical Study of CEA Targeting Chimeric Antigen Receptor T Lymphocytes(CAR-T) for CEA Positive Advanced Malignant Solid Tumors | 2023-11-13 |
| NCT06768151 | 1 | Recruiting | A Clinical Trial of CEA Targeting CAR-T for CEA Positive Advanced Lung Cancer | 2025-01-10 |
| NCT06903117 | 1 | Recruiting | Anti-CEA CAR-T for Advanced CEA-Positive Lung Carcinoma | 2025-04-03 |
| NCT06992583 | 1 | Recruiting | Targeted Anti-CEA CAR-T Immunotherapy for Advanced Lung Cancer | 2025-05-28 |
| NCT06945523 | 1 | Recruiting | Clinical Study on Chimeric Antigen Receptor T Lymphocyte (CAR-T) Targeting CEA for the Treatment of CEA - Positive Advanced Lung Cancer | 2025-06-04 |
| NCT07179692 | 1 | Recruiting | CEA-Targeted CAR-T Therapy in CEA-Positive Advanced Solid Tumors | 2025-10-02 |
| NCT07250386 | 1 | Recruiting | A Study of CEA-Targeted CAR-T Therapy in Patients With CEA-Positive Advanced Solid Tumors | 2025-11-26 |
| NCT05736731 | 1/2 | Active | A 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 Expression | 2025-04-25 |
10 of 14 shown, most recently active first. Other targets searched: mesothelin (10), NY-ESO-1 (7), DLL3 (6), MUC1 (5), HER2 (3), B7-H3 (3), PD-L1 (1). Source: ClinicalTrials.gov API v2, retrieved 2026-09-18. A trial counts here when its registered conditions name lung 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 lung 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 34,781 and 56,231 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 |
|---|---|---|---|---|
| Deep Learning | 0.1% | 2.18% | 21.83× | 131 papers |
| Machine Learning | 0.5% | 2.93% | 5.87× | 176 papers |
| Nomograms | 0.28% | 1.53% | 5.41× | 92 papers |
| DNA Helicases | 0.08% | 0.43% | 5.2× | 26 papers |
| Molecular Docking Simulation | 0.35% | 1.77% | 5.05× | 106 papers |
| Quinolines | 0.18% | 0.88% | 4.82× | 53 papers |
| Ubiquitination | 0.13% | 0.63% | 4.75× | 38 papers |
| Tumor Escape | 0.1% | 0.47% | 4.67× | 28 papers |
| CRISPR-Cas Systems | 0.08% | 0.37% | 4.4× | 22 papers |
| Tumor Microenvironment | 1.78% | 7.78% | 4.36× | 467 papers |
Cooling
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Survival Analysis | 6.62% | 0.38% | 0.06× | 23 papers |
| Disease-Free Survival | 4.37% | 0.68% | 0.16× | 41 papers |
| Crizotinib | 1.35% | 0.23% | 0.17× | 14 papers |
| DNA Mutational Analysis | 1.23% | 0.22% | 0.18× | 13 papers |
| Down-Regulation | 2.2% | 0.45% | 0.2× | 27 papers |
| RNA, Small Interfering | 1.62% | 0.33% | 0.21× | 20 papers |
Biggest topics now
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Carcinoma, Non-Small-Cell Lung | 42.17% | 39.87% | 0.95× | 2392 papers |
| Prognosis | 15.18% | 16.52% | 1.09× | 991 papers |
| Adenocarcinoma of Lung | 9.93% | 12.98% | 1.31× | 779 papers |
| Gene Expression Regulation, Neoplastic | 11.1% | 12.97% | 1.17× | 778 papers |
| Biomarkers, Tumor | 10.83% | 12.82% | 1.18× | 769 papers |
| Cell Proliferation | 10.92% | 10.97% | 1.0× | 658 papers |
| Mutation | 10.9% | 10.27% | 0.94× | 616 papers |
| Neoplasm Staging | 13.32% | 9.87% | 0.74× | 592 papers |
| Treatment Outcome | 10.95% | 9.85% | 0.9× | 591 papers |
| Tomography, X-Ray Computed | 9.43% | 9.7% | 1.03× | 582 papers |
Publication mix
| Type | 2015–18 | 2021–25 |
|---|---|---|
| Clinical Trial | 0.0% | 0.1% |
| Randomized Controlled Trial | 2.2% | 2.5% |
| Review | 8.2% | 10.7% |
| Meta-Analysis | 1.8% | 2.2% |
| Case Reports | 0.0% | 5.3% |
Query: Lung Neoplasms[MeSH Major Topic] NOT ("Mesothelioma"[MeSH] OR "Mesothelioma, Malignant"[MeSH] OR "Pleural Neoplasms"[MeSH] OR "Thymus Neoplasms"[MeSH] OR "Thymoma"[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 | 229,410 cases/year | direct | 2026 SEER Cancer Stat Facts, Lung and Bronchus Cancer, retrieved 2026-09-11 |
| Deaths each year | 124,990 deaths/year | direct | 2026 SEER Cancer Stat Facts, Lung and Bronchus Cancer, retrieved 2026-09-11 |
| Incidence rate | 47.2 cases per 100,000 per year | direct | 2019-2023 SEER Cancer Stat Facts, Lung and Bronchus Cancer, retrieved 2026-09-11 |
| Death rate | 30.2 deaths per 100,000 per year | direct | 2020-2024 SEER Cancer Stat Facts, Lung and Bronchus Cancer, retrieved 2026-09-11 |
| People living with it | 661,853 people living with the disease | direct | 2023 SEER Cancer Stat Facts, Lung and Bronchus Cancer, retrieved 2026-09-11 |
| Median age at diagnosis | 71.0 years | direct | 2019-2023 SEER Cancer Stat Facts, Lung and Bronchus Cancer, retrieved 2026-09-11 |
| median age at death | 73 years | direct | 2020-2024 SEER Cancer Stat Facts, Lung and Bronchus Cancer, retrieved 2026-09-11 |
| Five-year relative survival | 29.5% | direct | 2016-2022 SEER Cancer Stat Facts, Lung and Bronchus Cancer, retrieved 2026-09-11 |
Years of life lost (proxy)
5.2 years per case, 1,196,832 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 lung cancer, after removing the 30,409 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 | $157.1M | 401 | 326 | 2,070 |
| FY2014 | $144.2M | 382 | 320 | 2,133 |
| FY2015 | $154.1M | 398 | 339 | 2,101 |
| FY2016 | $171.9M | 424 | 369 | 2,184 |
| FY2017 | $194.8M | 466 | 393 | 2,205 |
| FY2018 | $218.1M | 495 | 408 | 2,608 |
| FY2019 | $229.0M | 536 | 456 | 2,378 |
| FY2020 | $241.6M | 554 | 471 | 2,480 |
| FY2021 | $269.9M | 634 | 528 | 2,449 |
| FY2022 | $303.6M | 663 | 541 | 2,477 |
| FY2023 | $303.0M | 679 | 553 | 2,518 |
| FY2024 | $308.0M | 684 | 562 | 2,512 |
| FY2025 | $311.2M | 614 | 547 | 2,294 |
Where FY2025 money went
| Institution | Obligations | Awards |
|---|---|---|
| University Of Tx Md Anderson Can Ctr | $19.8M | 39 |
| Division Of Basic Sciences - Nci | $18.2M | 20 |
| H. Lee Moffitt Cancer Ctr & Res Inst | $13.9M | 21 |
| New York University School Of Medicine | $12.7M | 24 |
| Sloan-Kettering Inst Can Research | $12.6M | 24 |
| Yale University | $10.2M | 19 |
| Dana-Farber Cancer Inst | $9.8M | 16 |
| Fred Hutchinson Cancer Center | $9.5M | 16 |
| Stanford University | $8.3M | 15 |
| Ohio State University | $7.8M | 16 |
Text search lung 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 1,196,832 years of life lost a year, FY2025 obligations are $260 per life-year — $1,356 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 614 of 614.
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 536 of 614.
Where it lands
Share of $311.2M in FY2025. The top three hold 17%.
Public datasets, ranked
NCBI GEO + Europe PMC + iCite · weekly4,354 human GEO series match lung cancer. Keyword relevance cannot tell a 3,924-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 1984-study ranked set
Established
high reuse, older| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE31210 | Gene expression data for pathological stage I-II lung adenocarcinomas2011 · array | 246 | 1,849 | 18.7 | patient cohortAPT 0.95survivalstagemolecularALKEGFRKRAS764 cites |
| GSE68465 | caArray_jacob-00182: Gene expression-based survival prediction in lung adenocarcinoma: a multi-site, blinded validation study2015 · array | 462 | 667 | 18.1 | patient cohortAPT 0.95survivalstagemolecular921 cites |
| GSE72094 | KRAS mutation-associated gene expression, p53 and STK11 mutations, proliferation and immune surveillance in lung adenocarcinoma2015 · array | 442 | 721 | 9.1 | patient cohortAPT 0.75survivalmolecularEGFRKRASSTK11326 cites |
| GSE30219 | "Off-context" gene expression in lung cancer identifies a group of metastatic-prone tumors2013 · array | 307 | 1,153 | 11.8 | patient cohortAPT 0.95survivalmolecular480 cites |
| GSE16716 | MicroArray Quality Control Phase II (MAQC-II) Project2010 · array | 1,343 | 228 | 14.6 | patient cohortAPT 0.95survivalstagemolecular630 cites |
| GSE50081 | Validation of a histology-independent prognostic gene signature for early stage, non-small cell lung cancer including stage IA patients2013 · array | 181 | 835 | 7.0 | patient cohortAPT 0.75survivalstagemolecular283 cites |
| GSE19188 | Expression data for early stage NSCLC2010 · array | 156 | 644 | 14.4 | patient cohortAPT 0.95survivalstage629 cites |
| GSE131907 | Single cell RNA sequencing of lung adenocarcinoma2020 · single-cell | 58 | 590 | 40.5 | patient cohortAPT 0.75molecular1,064 cites |
Recent
2022 onward, by score| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE207422 | Tumor microenvironment remodeling after neoadjuvant immunotherapy in non-small cell lung cancer revealed by single-cell RNA sequencing2023 · single-cell | 39 | 111 | 23.1 | patient cohortAPT 0.75307 cites |
| GSE243013 | A single-cell atlas of immune heterogeneity in anti-PD1-treated non-small cell lung cancer2025 · single-cell | 243 | 10 | 25.5 | patient cohortAPT 0.75survival120 cites |
| GSE241934 | Neoadjuvant sintilimab plus chemotherapy in early-stage EGFR-mutant NSCLC: phase 2 trial interim results (NEOTIDE/CTONG2104)2024 · single-cell | 88 | 8 | 4.1 | patient cohortAPT 0.95survivalstagemolecularEGFRMET47 cites |
| GSE119911 | Comprehensive transcriptomic profiles of non-small cell lung cancer by single-cell RNA-seq2022 · single-cell | 106 | 10 | 4.1 | patient cohortAPT 0.75survivalstagemolecular66 cites |
| GSE200563 | Spatial gene expression-based, non-small cell lung carcinoma patients with paired brain metastases2022 · spatial | 120 | 14 | 10.7 | patient cohortAPT 0.75molecular178 cites |
| GSE162520 | Immunologically active phenotype is associated with response to PD-1/PD-L1 inhibitors in patients with advanced non-small cell lung cancer2022 · sequencing | 92 | 18 | 3.1 | patient cohortAPT 0.5survivalstagemolecularPD-L148 cites |
Sources: NCBI GEO + Europe PMC + iCite, retrieved 2026-09-19. SubSeries are collapsed to one row per study by linked PMID. Of 4,311 series retrieved, 148 were dropped by the profile’s exclusion rules and 1,709 named the disease only in passing. 2 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.
STK11
Open Targets lists no drug against it and no trial in lung cancer names it. A bounded negative: the sources and search terms are in the JSON beside this page.
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 (2026-09-18), NCBI GEO (2026-09-19), PubMed (2026-09-11), NIH RePORTER (2026-09-19).
Negatives stated explicitly
Where the searches find nothing for lung 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
5 exclusion patterns are applied to free text before anything is ranked, because A549, with Calu-3 and Lewis lung carcinoma is used as a model system in toxicology and particle exposure, respiratory virology, airway epithelial barrier and drug permeability (A549, Calu-3); syngeneic tumour immunology (Lewis lung). What was removed and why is stated in each section rather than silently applied.
{
"disease": "Lung cancer",
"mesh": "Lung Neoplasms",
"facts": "https://usebiotransfer.org/disease/lung-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."
}