Target landscape
Open Targets · retrieved 2026-09-12 · weekly12 genes recurrently implicated in diffuse large b-cell lymphoma, 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: Diffuse large b-cell lymphoma does have labelled therapy — 11 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 diffuse large b-cell lymphoma 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 |
|---|---|---|---|---|
| MS4A1 | 18 | 11 approvedEpcoritamab, Glofitamab, Mosunetuzumab, Obinutuzumab, Ocrelizumab, Odronextamab, Ofatumumab, Rituximab, Tositumomab, Ublituximab, Yttrium Y 90 Ibritumomab TiuxetanApproved in diffuse large b-cell lymphoma: Epcoritamab, Glofitamab, Rituximab.138 active of 377 diffuse large b-cell lymphoma trials | antibody, other clinical modality, protein degrader, small molecule | 18 active of 32 trials |
| CD19 | 14 | 9 approvedAxicabtagene Ciloleucel, Blinatumomab, Brexucabtagene Autoleucel, Inebilizumab, Lisocabtagene Maraleucel, Loncastuximab Tesirine, Obecabtagene Autoleucel, Tafasitamab, TisagenlecleucelApproved in diffuse large b-cell lymphoma: Axicabtagene Ciloleucel, Lisocabtagene Maraleucel, Loncastuximab Tesirine, Tafasitamab, Tisagenlecleucel.44 active of 101 diffuse large b-cell lymphoma trials | antibody, other clinical modality, protein degrader | 57 active of 108 trials |
| CD79B | 1 | 1 approvedPolatuzumab VedotinApproved in diffuse large b-cell lymphoma: Polatuzumab Vedotin.46 active of 66 diffuse large b-cell lymphoma trials | antibody, other clinical modality, protein degrader, small molecule | 3 active of 3 trials |
| BCL2 across cancers → | 5 | 3 approvedNavitoclax, Oblimersen, VenetoclaxApproved in B-cell chronic lymphocytic leukemia. No diffuse large b-cell lymphoma indication appears on these drugs’ labels.12 active of 45 diffuse large b-cell lymphoma trials | antibody, other clinical modality, protein degrader, small molecule | — |
| BCL6 | 0 | No drug— | protein degrader, small molecule | — |
| MYC | 0 | No drug— | protein degrader, small molecule | — |
| EZH2 | 3 | 2 approvedTazemetostat, Tazemetostat HydrobromideApproved in follicular lymphoma, sarcoma. No diffuse large b-cell lymphoma indication appears on these drugs’ labels.4 active of 13 diffuse large b-cell lymphoma trials | protein degrader, small molecule | — |
| MYD88 | 0 | No drug— | antibody, protein degrader | — |
| CREBBP | 1 | Phase 2Pri-724No diffuse large b-cell lymphoma trial of any of these drugs | other clinical modality, protein degrader, small molecule | — |
| KMT2D | 0 | No drug— | antibody, protein degrader, small molecule | — |
| TP53 across cancers → | 8 | Phase 3Alrizomadlin, Cenersen, Contusugene Ladenovec, Eprenetapopt, Idasanutlin, Navtemadlin, Siremadlin, Teprasiran1 active of 4 diffuse large b-cell lymphoma trials | other clinical modality, protein degrader, small molecule | — |
| BTK | 20 | 8 approvedAcalabrutinib, Ibrutinib, Orelabrutinib, Pirtobrutinib, Rilzabrutinib, Ritlecitinib, Tirabrutinib, ZanubrutinibApproved in B-cell chronic lymphocytic leukemia, childhood leukemia, mantle cell lymphoma and 5 other indications. No diffuse large b-cell lymphoma indication appears on these drugs’ labels.79 active of 162 diffuse large b-cell lymphoma trials | antibody, protein degrader, small molecule | — |
Dataset evidence counts studies in the 362-study ranked set whose title or abstract names the gene; the bar is scaled to MYC. Sources: Open Targets Platform and NCBI GEO, retrieved 2026-09-12. 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 · weekly11 drugs carry an FDA label naming diffuse large b-cell lymphoma: Axicabtagene Ciloleucel, Brentuximab Vedotin, Epcoritamab, Glofitamab, Lisocabtagene Maraleucel, Loncastuximab Tesirine, Pembrolizumab, Polatuzumab Vedotin, Rituximab, Tafasitamab, Tisagenlecleucel. Separately, 25 of the drugs returned for the genes in the table above are approved only for other diseases and reach diffuse large b-cell lymphoma through trials, not through their labels.
Every label that names diffuse large b-cell lymphoma
| Drug | Role | What the label says |
|---|---|---|
| Axicabtagene CiloleucelYESCARTA | Labelled here | Large B-cell Lymphoma YESCARTA is indicated for the treatment of: Adult patients with large B-cell lymphoma that is refractory to first-line chemoimmunotherapy or that relapses within 12 months of first-line chemoimmunotherapy. |
| Brentuximab VedotinADCETRIS | Labelled here | Relapsed or Refractory Large B-Cell Lymphoma (LBCL) ADCETRIS in combination with lenalidomide and a rituximab product is indicated for the treatment of adult patients with relapsed or refractory LBCL, including diffuse large B-cell lymphoma (DLBCL) NOS, DLBCL arising from indolent lymphoma, or high-grade B-cell lymphoma (HGBL), after two or more lines of systemic therapy who are not eligible fo... |
| EpcoritamabEPKINLY | Labelled here | DLBCL and High-grade B-cell Lymphoma EPKINLY is indicated for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL), not otherwise specified, including DLBCL arising from indolent lymphoma, and high-grade B-cell lymphoma after two or more lines of systemic therapy. |
| GlofitamabColumvi | Labelled here | COLUMVI is indicated for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma, not otherwise specified (DLBCL, NOS) or large B-cell lymphoma (LBCL) arising from follicular lymphoma, after two or more lines of systemic therapy. |
| Lisocabtagene MaraleucelBREYANZI | Labelled here | Large B-cell Lymphoma (LBCL) BREYANZI is indicated for the treatment of adult patients with large B-cell lymphoma (LBCL), including diffuse large B-cell lymphoma (DLBCL) not otherwise specified (including DLBCL arising from indolent lymphoma), high-grade B-cell lymphoma, primary mediastinal large B-cell lymphoma, and follicular lymphoma grade 3B who have: • refractory disease to first-line chem... |
| Loncastuximab TesirineZYNLONTA | Labelled here | ZYNLONTA is indicated for the treatment of adult patients with relapsed or refractory large B-cell lymphoma after two or more lines of systemic therapy, including diffuse large B-cell lymphoma (DLBCL) not otherwise specified, DLBCL arising from low-grade lymphoma, and high-grade B-cell lymphoma. |
| PembrolizumabKEYTRUDA | Labelled here | Primary Mediastinal Large B-Cell Lymphoma (PMBCL) for the treatment of adult and pediatric patients with refractory PMBCL, or who have relapsed after 2 or more prior lines of therapy. |
| Polatuzumab VedotinPOLIVY | Labelled here | Previously Untreated DLBCL, NOS or HGBL POLIVY in combination with a rituximab product, cyclophosphamide, doxorubicin, and prednisone (R-CHP) is indicated for the treatment of adult patients who have previously untreated diffuse large B-cell lymphoma (DLBCL), not otherwise specified (NOS) or high-grade B-cell lymphoma (HGBL) and who have an International Prognostic Index score of 2 or greater. |
| RituximabRituxan, Rituxan Hycela | Labelled here | Previously untreated, advanced stage, CD20-positive, diffuse large B-cell lymphoma (DLBCL), Burkitt lymphoma (BL), Burkitt-like lymphoma (BLL) or mature B-cell acute leukemia (B-AL) in combination with chemotherapy. |
| TafasitamabMONJUVI | Labelled here | MONJUVI, in combination with lenalidomide, is indicated for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) not otherwise specified, including DLBCL arising from low grade lymphoma, and who are not eligible for autologous stem cell transplant (ASCT). |
| TisagenlecleucelKYMRIAH | Labelled here | Adult Relapsed or Refractory Diffuse Large B-cell Lymphoma KYMRIAH is indicated for treatment of adult patients with relapsed or refractory (r/r) large B-cell lymphoma after two or more lines of systemic therapy, including diffuse large B-cell lymphoma (DLBCL) not otherwise specified, high grade B-cell lymphoma and DLBCL arising from follicular lymphoma. |
14 labels match indications_and_usage:"diffuse large B-cell lymphoma" OR indications_and_usage:"large B-cell lymphoma"; they collapse to 11 distinct molecules once salt forms, biosimilars and co-formulated hyaluronidase are merged. Source: openFDA drug label API (api.fda.gov/drug/label.json), retrieved 2026-09-12. Labels change; this reflects the current label text, not the approval history. Not prescribing guidance.
Cell therapy against CD19
ClinicalTrials.gov · retrieved 2026-09-12 · weeklyCD19 is the busiest cell-therapy antigen in diffuse large b-cell lymphoma: 108 registered trials, 57 still active, 2 withdrawn before enrolling anyone.
| Trial | Phase | Status | Title | Last update |
|---|---|---|---|---|
| NCT05659628 | 1 | Recruiting | CD19 CAR-T Expressing IL-7 and CCL19 Combined With Anti-PD1 in RR-DLBCL | 2022-12-21 |
| NCT06081478 | 2 | Recruiting | CD19/CD22 Bispecific CAR-T Cell Therapy for Relapsed/Refractory B-cell Lymphoma or Acute Lymphoblastic Leukemia | 2023-10-13 |
| NCT03676504 | 1/2 | Recruiting | Treatment of Patients With Relapsed or Refractory CD19+ Lymphoid Disease With T Cells Expressing a Third-generation CAR | 2024-07-29 |
| NCT05641428 | 2 | Recruiting | Comparison of Point-of-care Produced CAR T-cell with Commercial CAR T-cells in Patients with R/R LBCL | 2024-09-23 |
| NCT06238648 | 2 | Recruiting | Epcoritamab Compared to Observation for Treating B-cell Lymphoma Patients Not in Complete Remission After CD19-directed CAR-T Therapy | 2024-09-26 |
| NCT05281809 | 2 | Recruiting | Local Manufacture of CAR T-Cell Products for the Treatment of B-Cell Lymphoma and B-Acute Lymphoblastic Leukemia | 2025-01-13 |
| NCT06464861 | 1 | Recruiting | Sequential Treatment of CD19 CARNK and 7x19 CAR-T in R/R B Cell Lymphoma | 2025-02-07 |
| NCT06918912 | 2 | Recruiting | Study of Loncastuximab Tesirine in Patients With Relapsed/Refractory Diffuse Large B-Cell Lymphoma (DLBCL) or High-Grade B-Cell Lymphoma (HGBCL) Following CAR-T Therapy Failure | 2025-04-09 |
| NCT05326243 | 1/2 | Recruiting | Phase 1/2 Study of CD19 Chimeric Antigen Receptor T-cell (CD19 CAR-T; PL001) for Relapsed or Refractory B-cell Lymphoma | 2025-05-13 |
| NCT06213636 | 1/2 | Recruiting | Fourth-gen CAR T Cells Targeting CD19/CD22 for Highly Resistant B-cell Lymphoma/Leukemia (PMBCL/CNS-BCL). | 2025-08-06 |
10 of 108 shown, most recently active first. Other antigens searched: CD20 (32), CD22 (7), CD79b (3), CD30 (3). Source: ClinicalTrials.gov API v2, retrieved 2026-09-12. Trials are matched on the antigen named in the title or intervention, so a trial stating only a product code is missed.
Research momentum
PubMed MeSH · monthlyEvery term below is a share of the diffuse large b-cell lymphoma literature, not a count, because the field itself grew: 2015–2018 (n=2,931) against 2021–2025 (n=5,059). A topic whose papers doubled while the field doubled has not risen.
Rising, with a real baseline
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Receptors, Chimeric Antigen | 0.34% | 9.27% | 27.16× | 469 papers |
| Immunotherapy, Adoptive | 0.99% | 12.85% | 12.98× | 650 papers |
| Antigens, CD19 | 1.09% | 7.16% | 6.55× | 362 papers |
| Immunoconjugates | 0.44% | 2.47% | 5.57× | 125 papers |
| Circulating Tumor DNA | 0.24% | 1.13% | 4.72× | 57 papers |
| Central Nervous System | 0.38% | 1.72% | 4.58× | 87 papers |
| Receptors, Antigen, T-Cell | 0.68% | 2.98% | 4.37× | 151 papers |
| Lymphoma, Non-Hodgkin | 1.74% | 5.99% | 3.44× | 303 papers |
| Progression-Free Survival | 0.82% | 2.71% | 3.31× | 137 papers |
| Antibodies, Monoclonal | 0.72% | 2.31% | 3.23× | 117 papers |
Cooling
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Multivariate Analysis | 2.32% | 0.28% | 0.12× | 14 papers |
| Gene Expression | 1.81% | 0.24% | 0.13× | 12 papers |
| Antibodies, Monoclonal, Murine-Derived | 12.73% | 1.8% | 0.14× | 91 papers |
| Disease-Free Survival | 11.63% | 1.74% | 0.15× | 88 papers |
| Neoplasm Staging | 9.01% | 1.44% | 0.16× | 73 papers |
| Time Factors | 3.28% | 0.53% | 0.16× | 27 papers |
Biggest topics now
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Antineoplastic Combined Chemotherapy Protocols | 33.57% | 25.38% | 0.76× | 1284 papers |
| Prognosis | 24.7% | 23.72% | 0.96× | 1200 papers |
| Rituximab | 22.79% | 17.75% | 0.78× | 898 papers |
| Cyclophosphamide | 19.17% | 13.16% | 0.69× | 666 papers |
| Doxorubicin | 19.0% | 12.93% | 0.68× | 654 papers |
| Immunotherapy, Adoptive | 0.99% | 12.85% | 12.98× | 650 papers |
| Vincristine | 18.97% | 12.41% | 0.65× | 628 papers |
| Prednisone | 17.5% | 11.15% | 0.64× | 564 papers |
| Treatment Outcome | 18.9% | 10.69% | 0.57× | 541 papers |
| Neoplasm Recurrence, Local | 4.57% | 10.2% | 2.23× | 516 papers |
Publication mix
| Type | 2015–18 | 2021–25 |
|---|---|---|
| Clinical Trial | 0.0% | 0.1% |
| Randomized Controlled Trial | 1.9% | 1.1% |
| Review | 9.8% | 8.7% |
| Meta-Analysis | 1.1% | 1.0% |
| Case Reports | 0.0% | 4.9% |
Query: Lymphoma, Large B-Cell, Diffuse[MeSH Major Topic] NOT ("Hodgkin Disease"[MeSH] OR "Lymphoma, Mantle-Cell"[MeSH] OR "Burkitt Lymphoma"[MeSH] OR "Leukemia, Lymphocytic, Chronic, B-Cell"[MeSH] OR "Multiple Myeloma"[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. 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.
| Measure | Value | Match | What it counts |
|---|---|---|---|
| New cases each year | 79,320 cases/year | proxy | counts non-hodgkin lymphoma, which is broader than this disease; 2026 SEER Cancer Stat Facts, Non-Hodgkin Lymphoma, retrieved 2026-09-12 |
| Deaths each year | 19,970 deaths/year | proxy | counts non-hodgkin lymphoma, which is broader than this disease; 2026 SEER Cancer Stat Facts, Non-Hodgkin Lymphoma, retrieved 2026-09-12 |
| Incidence rate | 18.7 cases per 100,000 per year | proxy | counts non-hodgkin lymphoma, which is broader than this disease; 2019-2023 SEER Cancer Stat Facts, Non-Hodgkin Lymphoma, retrieved 2026-09-12 |
| Death rate | 4.8 deaths per 100,000 per year | proxy | counts non-hodgkin lymphoma, which is broader than this disease; 2020-2024 SEER Cancer Stat Facts, Non-Hodgkin Lymphoma, retrieved 2026-09-12 |
| People living with it | 872,940 people living with the disease | proxy | counts non-hodgkin lymphoma, which is broader than this disease; 2023 SEER Cancer Stat Facts, Non-Hodgkin Lymphoma, retrieved 2026-09-12 |
| Median age at diagnosis | 68.0 years | proxy | counts non-hodgkin lymphoma, which is broader than this disease; 2019-2023 SEER Cancer Stat Facts, Non-Hodgkin Lymphoma, retrieved 2026-09-12 |
| median age at death | 76 years | proxy | counts non-hodgkin lymphoma, which is broader than this disease; 2020-2024 SEER Cancer Stat Facts, Non-Hodgkin Lymphoma, retrieved 2026-09-12 |
| Five-year relative survival | 74.3% | proxy | counts non-hodgkin lymphoma, which is broader than this disease; 2016-2022 SEER Cancer Stat Facts, Non-Hodgkin Lymphoma, retrieved 2026-09-12 |
| New cases each year, estimated | 26,176 cases/year | derived proxy | 79,320 x 0.33, from non-hodgkin lymphoma; 2026 SEER Cancer Stat Facts, Non-Hodgkin Lymphoma, retrieved 2026-09-12 |
Years of life lost
2.7 years per case, 69,963 a year, from survival and age at diagnosis rather than from a death count. derived proxy What this costs to fund is in Funding.
3 assumptions behind this estimate
- Five-year relative survival stands in for cure; a death after five years is not counted.
- The median age at diagnosis stands in for the whole age distribution.
- Life expectancy at birth (78.4 years) is the reference, rather than remaining expectancy at the age of death from a life table.
- Each assumption moves the result by more than the difference between the two diseases currently on this site, so this figure separates a disease from one ten times its size, not from a close neighbour.
Funding
NIH RePORTER · quarterlyNIH obligations naming diffuse large b-cell lymphoma, after removing the 1,234 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 | $6.6M | 26 | 26 | 70 |
| FY2014 | $7.1M | 26 | 25 | 68 |
| FY2015 | $7.7M | 22 | 22 | 77 |
| FY2016 | $13.8M | 33 | 27 | 82 |
| FY2017 | $20.1M | 39 | 34 | 73 |
| FY2018 | $18.9M | 40 | 34 | 95 |
| FY2019 | $18.6M | 43 | 35 | 100 |
| FY2020 | $18.8M | 46 | 40 | 104 |
| FY2021 | $18.7M | 41 | 41 | 105 |
| FY2022 | $18.9M | 39 | 38 | 120 |
| FY2023 | $26.2M | 44 | 43 | 112 |
| FY2024 | $29.3M | 49 | 44 | 115 |
| FY2025 | $34.6M | 45 | 38 | 113 |
Where FY2025 money went
| Institution | Obligations | Awards |
|---|---|---|
| Division Of Basic Sciences - Nci | $9.1M | 6 |
| Weill Medical Coll Of Cornell Univ | $5.2M | 9 |
| University Of Tx Md Anderson Can Ctr | $3.6M | 4 |
| University Of Miami School Of Medicine | $2.6M | 1 |
| National Institute Of Arthritis And Musculoskeletal And Skin Diseases | $2.0M | 0 |
| Feinstein Institute For Medical Research | $1.2M | 2 |
| Columbia University Health Sciences | $1.1M | 2 |
| Avm Biotechnology, Llc | $1.0M | 0 |
| Beth Israel Deaconess Medical Center | $0.8M | 0 |
| New York Genome Center | $0.8M | 0 |
Text search diffuse large B-cell lymphoma 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 2026-09-12.
What that buys
Against 69,963 years of life lost a year, FY2025 obligations are $495 per life-year — $1,322 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 4 and account for 45 of 45.
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 45 of 45.
Where it lands
Share of $34.6M in FY2025. The top three hold 52%.
Public datasets, ranked
NCBI GEO + Europe PMC + iCite · weekly858 human GEO series match diffuse large b-cell lymphoma. Keyword relevance cannot tell a 2,511-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 362-study ranked set
Established
high reuse, older| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE10846 | Prediction of survival in diffuse large B cell lymphoma treated with chemotherapy plus Rituximab2008 · array | 420 | 393 | 28.8 | patient cohortAPT 0.95survivalmolecularRITUXIMAB1,470 cites |
| GSE117556 | Molecular definition of high grade B cell lymphoma: a centroblast-like group with potential for more effective therapy2019 · array | 928 | 71 | 8.3 | patient cohortAPT 0.95survivalstagemolecularBCL2BCL6MYC247 cites |
| GSE181063 | Whole genome expression profiling based on paraffin embedded tissue of a large DLBCL cohort2021 · array | 1,310 | 77 | 17.6 | patient cohortAPT 0.95427 cites |
| GSE31312 | Development and application of a new immunophenotypic algorithm for molecular subtype classification of Diffuse Large B-Cell Lymphoma (DLBCL): Report from an International DLBCL Rituximab-CHOP Consortium Program Study2012 · array | 498 | 170 | 7.3 | APT 0.95molecularRITUXIMAB295 cites |
| GSE56315 | Diffuse Large B-Cell Lymphoma Classification System That Associates Normal B-Cell Subset Phenotypes With Prognosis2015 · array | 88 | 106 | 3.1 | patient cohortAPT 0.75survivalmolecularRITUXIMABTP53111 cites |
| GSE98588 | Genetically-defined Diffuse Large B-cell Lymphoma Subsets Arise by Distinct Pathogenetic Mechanisms and Predicts Outcome2018 · array | 137 | 40 | 53.8 | APT 0.95survival1,629 cites |
| GSE60 | Diffuse large B-cell lymphoma2002 · array | 133 | 10 | 130.7 | mixedAPT 0.95survival6,794 cites |
| GSE11318 | Molecular subtypes of DLBCL have distinct chromosomal aberrations2008 · array | 406 | 87 | 15.1 | APT 0.95791 cites |
Recent
2022 onward, by score| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE248835 | Impact of Tumor Microenvironment on Efficacy of CD19 CAR T-Cell Therapy or Chemotherapy and Transplant in Large B-Cell Lymphoma2024 · array | 256 | 5 | 12.4 | APT 0.95survivalmolecularAXI-CELAXICABTAGENECD19111 cites |
| GSE223655 | Characteristics of premanufacture CD8+T cells determine CAR-T efficacy in patients with diffuse large B-cell lymphoma2023 · sequencing | 65 | 6 | 5.5 | patient cohortAPT 0.75molecularCD19CD2074 cites |
| GSE207192 | Two-Stage CAR T-Cell Differentiation in Patients with Large B-Cell Lymphoma2025 · single-cell | 60 | 2 | 3.5 | patient cohortAPT 0.75stagemolecularAXICABTAGENE16 cites |
| GSE182214 | H3K27Ac mapping in DLBCL cell lines2022 · chromatin | 84 | 2 | 7.0 | mixedAPT 0.75molecularBCL2BCL6128 cites |
| GSE232853 | Spatially-resolved transcriptomics reveal macrophage heterogeneity and prognostic significance in diffuse large B-cell lymphoma2024 · spatial | 592 | 2 | 5.4 | APT 0.75survival47 cites |
| GSE255548 | EZH2 INHIBITION ENHANCES T CELL IMMUNOTHERAPIES BY INDUCING LYMPHOMA IMMUNOGENICITY AND IMPROVING T CELL FUNCTION (RNA-Seq)2025 · sequencing | 35 | 0 | 16.2 | patient cohortAPT 0.75survivalmolecularEZH271 cites |
Sources: NCBI GEO + Europe PMC + iCite, retrieved 2026-09-12. SubSeries are collapsed to one row per study by linked PMID. Of 858 series retrieved, 121 were dropped by the profile’s exclusion rules and 273 named the disease only in passing. The ranked set is a relevance-ranked sample, not a census, so the composition figures describe the sample only.
Where the gaps are
Derived from the sections above · recomputed on every refreshEach card below is a disagreement between two of the tables on this page — a drug that exists but was never tried here, a target that looks tested and was not, a gene with no drug whose product has a busy clinical programme. They are computed from the same facts as the tables, so they cannot contradict them.
BCL6
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
MYC
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
MYD88
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
KMT2D
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
How a machine reads this page
StaticThis page is written to be quoted correctly by a model as much as read by a person. The same facts are available as JSON at the sibling URL below, which is what to cite.
Fully server-rendered
Every figure is in the HTML at first byte. No JavaScript runs, no figure is fetched after load, and nothing on this page requires a renderer to see.
Every number carries a source
Each section names the API it came from and the date it was retrieved: Open Targets (2026-09-12), ClinicalTrials.gov (2026-09-12), openFDA (2026-09-12), NCBI GEO (2026-09-12), PubMed (2026-09-12), NIH RePORTER (2026-09-12).
Negatives stated explicitly
Where nothing exists for diffuse large b-cell lymphoma — no drug, no trial, no approval — the page says so in those words rather than omitting the row. An absent row is unquotable; a stated negative is the finding.
Denominators, not just percentages
Every share is printed with the count and the total it came from, so a figure can be checked rather than taken.
The filters are published
3 exclusion patterns are applied to free text before anything is ranked, because none of consequence; Raji and Daudi as CD20-positive targets is used as a model system in antibody and CAR-T functional assays that use a Burkitt line as the CD19/CD20 target. What was removed and why is stated in each section rather than silently applied.
{
"disease": "Diffuse large B-cell lymphoma",
"mesh": "Lymphoma, Large B-Cell, Diffuse",
"facts": "https://usebiotransfer.org/disease/diffuse-large-b-cell-lymphoma.json",
"methods": "https://usebiotransfer.org/methods/",
"note": "Every figure on the page is in that JSON with its source and retrieval date. Quote from it rather than from the HTML."
}