Disease Briefing

Diffuse large B-cell lymphoma: research and therapeutic landscape

A live synthesis of what is being targeted, what is being trialled, which datasets exist, and where the actionable gaps sit — assembled from public APIs, with every figure traceable to its source.

Generated 2026-09-12Sources Open Targets · ClinicalTrials.gov · openFDA · GEO · PubMed · Europe PMC · iCite · RePORTERRanked 362 studies · 24,915 GEO samples
Reading as
Reorders emphasis only — nothing is hidden or loaded on demand.

Answer block

12 genes recurrently implicated in diffuse large b-cell lymphoma — MS4A1, CD19, CD79B, BCL2, BCL6, MYC, EZH2, MYD88, CREBBP, KMT2D, TP53, BTK — triaged for what can actually be aimed at them, alongside the trials, public datasets, literature and funding around the disease. Every figure below carries its source and retrieval date in the section it comes from.

11
drugs carry an FDA label naming diffuse large b-cell lymphoma: Axicabtagene Ciloleucel, Brentuximab Vedotin, Epcoritamab, Glofitamab, Lisocabtagene Maraleucel, Loncastuximab Tesirine and 5 more. This counts labels, not treatment — the disease is also treated with agents approved under broader indications
3
of the 12 genes above carry a drug that is approved in diffuse large b-cell lymphoma itself — CD19, CD79B, MS4A1. Across all of them 77 drug entries reach these genes, 70 distinct once salt forms are merged
108
registered CD19 cell-therapy trials in diffuse large b-cell lymphoma, 57 active and 2 withdrawn. Counted from ClinicalTrials.gov across 11 synonyms, deduplicated by NCT id, interventional studies only — the query is published in the JSON beside this page so the number can be re-derived
5
targets carry an Open Targets tractability signal and have no clinical programme of any kind: BCL6, MYC, MYD88, CREBBP, KMT2D. MS4A1, CD19, CD79B all have cell-therapy trials, so they are undrugged rather than untouched
858
human GEO series match the disease; 362 survive on-topic filtering, and only 22 are patient cohorts of 100+ samples
393
Europe PMC full-text papers name GSE10846 — the highest accession-mention count in the set. A mention is not proof of reanalysis, so read it as reach rather than reuse
$34.6M
NIH obligations in FY2025, up 428% since 2013 — while distinct core projects went 26 to 38. Larger awards rather than more distinct core projects; core projects are not the same unit as laboratories

Target landscape

Open Targets · retrieved 2026-09-12 · weekly

12 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.

GeneDrugsApproval, and whether it reached this diseaseOpen Targets tractabilitycomputed from protein features and literature — a signal that a modality is worth trying, not evidence that it worksCell therapy here
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 · weekly

11 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.

11Labelled for diffuse large b-cell lymphomaFDA INDICATIONS AND USAGE names the disease
25Approved, but for another diseasereturned for the genes in the table above
0Backbone agents listing itbroad cytotoxics whose labels name many tumours
57Active CD19 cell-therapy trialsof 108 registered

Every label that names diffuse large b-cell lymphoma

DrugRoleWhat the label says
Axicabtagene CiloleucelYESCARTALabelled hereLarge 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 VedotinADCETRISLabelled hereRelapsed 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...
EpcoritamabEPKINLYLabelled hereDLBCL 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.
GlofitamabColumviLabelled hereCOLUMVI 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 MaraleucelBREYANZILabelled hereLarge 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 TesirineZYNLONTALabelled hereZYNLONTA 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.
PembrolizumabKEYTRUDALabelled herePrimary 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 VedotinPOLIVYLabelled herePreviously 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 HycelaLabelled herePreviously 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.
TafasitamabMONJUVILabelled hereMONJUVI, 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).
TisagenlecleucelKYMRIAHLabelled hereAdult 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 · weekly

CD19 is the busiest cell-therapy antigen in diffuse large b-cell lymphoma: 108 registered trials, 57 still active, 2 withdrawn before enrolling anyone.

TrialPhaseStatusTitleLast update
NCT056596281RecruitingCD19 CAR-T Expressing IL-7 and CCL19 Combined With Anti-PD1 in RR-DLBCL2022-12-21
NCT060814782RecruitingCD19/CD22 Bispecific CAR-T Cell Therapy for Relapsed/Refractory B-cell Lymphoma or Acute Lymphoblastic Leukemia2023-10-13
NCT036765041/2RecruitingTreatment of Patients With Relapsed or Refractory CD19+ Lymphoid Disease With T Cells Expressing a Third-generation CAR2024-07-29
NCT056414282RecruitingComparison of Point-of-care Produced CAR T-cell with Commercial CAR T-cells in Patients with R/R LBCL2024-09-23
NCT062386482RecruitingEpcoritamab Compared to Observation for Treating B-cell Lymphoma Patients Not in Complete Remission After CD19-directed CAR-T Therapy2024-09-26
NCT052818092RecruitingLocal Manufacture of CAR T-Cell Products for the Treatment of B-Cell Lymphoma and B-Acute Lymphoblastic Leukemia2025-01-13
NCT064648611RecruitingSequential Treatment of CD19 CARNK and 7x19 CAR-T in R/R B Cell Lymphoma2025-02-07
NCT069189122RecruitingStudy 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 Failure2025-04-09
NCT053262431/2RecruitingPhase 1/2 Study of CD19 Chimeric Antigen Receptor T-cell (CD19 CAR-T; PL001) for Relapsed or Refractory B-cell Lymphoma2025-05-13
NCT062136361/2RecruitingFourth-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 · monthly

Every 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 term2015–182021–25ChangeShare now
Receptors, Chimeric Antigen0.34%9.27%27.16×469 papers
Immunotherapy, Adoptive0.99%12.85%12.98×650 papers
Antigens, CD191.09%7.16%6.55×362 papers
Immunoconjugates0.44%2.47%5.57×125 papers
Circulating Tumor DNA0.24%1.13%4.72×57 papers
Central Nervous System0.38%1.72%4.58×87 papers
Receptors, Antigen, T-Cell0.68%2.98%4.37×151 papers
Lymphoma, Non-Hodgkin1.74%5.99%3.44×303 papers
Progression-Free Survival0.82%2.71%3.31×137 papers
Antibodies, Monoclonal0.72%2.31%3.23×117 papers

Cooling

MeSH term2015–182021–25ChangeShare now
Multivariate Analysis2.32%0.28%0.12×14 papers
Gene Expression1.81%0.24%0.13×12 papers
Antibodies, Monoclonal, Murine-Derived12.73%1.8%0.14×91 papers
Disease-Free Survival11.63%1.74%0.15×88 papers
Neoplasm Staging9.01%1.44%0.16×73 papers
Time Factors3.28%0.53%0.16×27 papers

Biggest topics now

MeSH term2015–182021–25ChangeShare now
Antineoplastic Combined Chemotherapy Protocols33.57%25.38%0.76×1284 papers
Prognosis24.7%23.72%0.96×1200 papers
Rituximab22.79%17.75%0.78×898 papers
Cyclophosphamide19.17%13.16%0.69×666 papers
Doxorubicin19.0%12.93%0.68×654 papers
Immunotherapy, Adoptive0.99%12.85%12.98×650 papers
Vincristine18.97%12.41%0.65×628 papers
Prednisone17.5%11.15%0.64×564 papers
Treatment Outcome18.9%10.69%0.57×541 papers
Neoplasm Recurrence, Local4.57%10.2%2.23×516 papers

Publication mix

Type2015–182021–25
Clinical Trial0.0%0.1%
Randomized Controlled Trial1.9%1.1%
Review9.8%8.7%
Meta-Analysis1.1%1.0%
Case Reports0.0%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.

MeasureValueMatchWhat it counts
New cases each year79,320 cases/yearproxycounts non-hodgkin lymphoma, which is broader than this disease; 2026
Deaths each year19,970 deaths/yearproxycounts non-hodgkin lymphoma, which is broader than this disease; 2026
Incidence rate18.7 cases per 100,000 per yearproxycounts non-hodgkin lymphoma, which is broader than this disease; 2019-2023
Death rate4.8 deaths per 100,000 per yearproxycounts non-hodgkin lymphoma, which is broader than this disease; 2020-2024
People living with it872,940 people living with the diseaseproxycounts non-hodgkin lymphoma, which is broader than this disease; 2023
Median age at diagnosis68.0 yearsproxycounts non-hodgkin lymphoma, which is broader than this disease; 2019-2023
median age at death76 yearsproxycounts non-hodgkin lymphoma, which is broader than this disease; 2020-2024
Five-year relative survival74.3%proxycounts non-hodgkin lymphoma, which is broader than this disease; 2016-2022
New cases each year, estimated26,176 cases/yearderived proxy79,320 x 0.33, from non-hodgkin lymphoma; 2026

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 · quarterly

NIH 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.

$34.6MNIH obligations, FY2025from $6.6M in FY2013 · +428%
38distinct projects funded26 in FY2013
$34.6Mpeak year was FY2025obligations, all institutes
89%of FY2025 awards from NCI40 of 45

NIH obligations by fiscal year

$9M$17M$26M$35M13151719212325
YearObligationsAwardsDistinct projectsDropped as off-topic
FY2013$6.6M262670
FY2014$7.1M262568
FY2015$7.7M222277
FY2016$13.8M332782
FY2017$20.1M393473
FY2018$18.9M403495
FY2019$18.6M4335100
FY2020$18.8M4640104
FY2021$18.7M4141105
FY2022$18.9M3938120
FY2023$26.2M4443112
FY2024$29.3M4944115
FY2025$34.6M4538113

Where FY2025 money went

InstitutionObligationsAwards
Division Of Basic Sciences - Nci$9.1M6
Weill Medical Coll Of Cornell Univ$5.2M9
University Of Tx Md Anderson Can Ctr$3.6M4
University Of Miami School Of Medicine$2.6M1
National Institute Of Arthritis And Musculoskeletal And Skin Diseases$2.0M0
Feinstein Institute For Medical Research$1.2M2
Columbia University Health Sciences$1.1M2
Avm Biotechnology, Llc$1.0M0
Beth Israel Deaconess Medical Center$0.8M0
New York Genome Center$0.8M0

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

NCI40 · 89%
NIGMS3 · 7%
VA1 · 2%
NIAMS1 · 2%

Projects by administering institute. The rows above are the top 4 and account for 45 of 45.

Award mechanisms

R0116 · 36%
ZIA6 · 13%
P016 · 13%
U543 · 7%
R352 · 4%
R002 · 4%

R01 is an investigator-initiated grant; ZIA is NIH intramural, meaning the work happens inside NIH rather than being funded outside it. The rows above are the top 15 and account for 45 of 45.

Where it lands

Division Of Basic Sciences - Nci$9.1M · 26.4%
Weill Medical Coll Of Cornell Univ$5.2M · 14.9%
University Of Tx Md Anderson Can Ctr$3.6M · 10.3%
University Of Miami School Of Medicine$2.6M · 7.6%
National Institute Of Arthritis And Musc$2.0M · 5.9%
Feinstein Institute For Medical Research$1.2M · 3.4%

Share of $34.6M in FY2025. The top three hold 52%.

Public datasets, ranked

NCBI GEO + Europe PMC + iCite · weekly

858 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

unspecified 121cell line 96patient 94mixed 47xenograft 4
121 unspecified96 cell line94 patient47 mixed4 xenograft205 carry clinical annotation127 carry survival22 patient cohorts ≥100 GEO samples24,915 GEO samples totalin 11 single-cell series a GEO sample is one cell, not one patient

Established

high reuse, older
AccessionStudySamplesMentionsEurope PMCRCREvidence
GSE10846Prediction of survival in diffuse large B cell lymphoma treated with chemotherapy plus Rituximab2008 · array42039328.8
patient cohortAPT 0.95survivalmolecularRITUXIMAB1,470 cites
GSE117556Molecular definition of high grade B cell lymphoma: a centroblast-like group with potential for more effective therapy2019 · array928718.3
patient cohortAPT 0.95survivalstagemolecularBCL2BCL6MYC247 cites
GSE181063Whole genome expression profiling based on paraffin embedded tissue of a large DLBCL cohort2021 · array1,3107717.6
patient cohortAPT 0.95427 cites
GSE31312Development 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 · array4981707.3
APT 0.95molecularRITUXIMAB295 cites
GSE56315Diffuse Large B-Cell Lymphoma Classification System That Associates Normal B-Cell Subset Phenotypes With Prognosis2015 · array881063.1
patient cohortAPT 0.75survivalmolecularRITUXIMABTP53111 cites
GSE98588Genetically-defined Diffuse Large B-cell Lymphoma Subsets Arise by Distinct Pathogenetic Mechanisms and Predicts Outcome2018 · array1374053.8
APT 0.95survival1,629 cites
GSE60Diffuse large B-cell lymphoma2002 · array13310130.7
mixedAPT 0.95survival6,794 cites
GSE11318Molecular subtypes of DLBCL have distinct chromosomal aberrations2008 · array4068715.1
APT 0.95791 cites

Recent

2022 onward, by score
AccessionStudySamplesMentionsEurope PMCRCREvidence
GSE248835Impact of Tumor Microenvironment on Efficacy of CD19 CAR T-Cell Therapy or Chemotherapy and Transplant in Large B-Cell Lymphoma2024 · array256512.4
APT 0.95survivalmolecularAXI-CELAXICABTAGENECD19111 cites
GSE223655Characteristics of premanufacture CD8+T cells determine CAR-T efficacy in patients with diffuse large B-cell lymphoma2023 · sequencing6565.5
patient cohortAPT 0.75molecularCD19CD2074 cites
GSE207192Two-Stage CAR T-Cell Differentiation in Patients with Large B-Cell Lymphoma2025 · single-cell6023.5
patient cohortAPT 0.75stagemolecularAXICABTAGENE16 cites
GSE182214H3K27Ac mapping in DLBCL cell lines2022 · chromatin8427.0
mixedAPT 0.75molecularBCL2BCL6128 cites
GSE232853Spatially-resolved transcriptomics reveal macrophage heterogeneity and prognostic significance in diffuse large B-cell lymphoma2024 · spatial59225.4
APT 0.75survival47 cites
GSE255548EZH2 INHIBITION ENHANCES T CELL IMMUNOTHERAPIES BY INDUCING LYMPHOMA IMMUNOGENICITY AND IMPROVING T CELL FUNCTION (RNA-Seq)2025 · sequencing35016.2
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 refresh

Each card below is a disagreement between two of the tables on this page — a drug that exists but was never tried here, a target that looks tested and was not, a gene with no drug whose product has a busy clinical programme. They are computed from the same facts as the tables, so they cannot contradict them.

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

Static

This page is written to be quoted correctly by a model as much as read by a person. The same facts are available as JSON at the sibling URL below, which is what to cite.

Fully server-rendered

Every figure is in the HTML at first byte. No JavaScript runs, no figure is fetched after load, and nothing on this page requires a renderer to see.

Every number carries a source

Each section names the API it came from and the date it was retrieved: Open Targets (2026-09-12), 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."
}