Disease Briefing

Chronic lymphocytic leukemia: research and therapeutic landscape

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

Generated 2026-09-30Sources Open Targets · ClinicalTrials.gov · openFDA · GEO · PubMed · Europe PMC · iCite · RePORTERRanked 291 studies · 19,761 GEO samples
Page Reading as
Reorders emphasis only — nothing is hidden or loaded on demand.

Answer block

12 genes recurrently implicated in chronic lymphocytic leukemia — BTK, BCL2, PIK3CD, TP53, ATM, SF3B1, NOTCH1, MS4A1, CD19, ROR1, CD52, MYD88 — 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.

13
drugs carry an FDA label naming chronic lymphocytic leukemia: Acalabrutinib, Alemtuzumab, Bendamustine, Duvelisib, Ibrutinib, Idelalisib and 7 more. This counts labels, not treatment — the disease is also treated with agents approved under broader indications
4
of the 12 genes above carry a drug that is approved in chronic lymphocytic leukemia itself — BTK, CD19, MS4A1, PIK3CD. Across all of them 122 drug entries reach these genes, 111 distinct once salt forms are merged
50
registered CD19 cell-therapy trials in chronic lymphocytic leukemia, 23 active and 3 withdrawn. Counted from ClinicalTrials.gov across 4 synonyms, deduplicated by NCT id, interventional studies only — the query is published in the JSON beside this page so the number can be re-derived
4
targets carry an Open Targets tractability signal and no trial in chronic lymphocytic leukemia that the searches found (no trial naming a drug Open Targets lists for the gene, none naming it as a cell-therapy target): ATM, SF3B1, NOTCH1, MYD88. BTK, MS4A1, CD19, ROR1, CD52 all have cell-therapy trials, so they are undrugged rather than untouched
527
human GEO series match the disease; 291 survive on-topic filtering, and only 40 are patient cohorts of 100+ samples
64
Europe PMC full-text papers name GSE22762 — the highest accession-mention count in the set. A mention is not proof of reanalysis, so read it as reach rather than reuse
$25.9M
NIH obligations in FY2025, down 6% since 2013 — while distinct core projects went 45 to 34. Larger awards rather than more distinct core projects; core projects are not the same unit as laboratories

Target landscape

Open Targets · retrieved 2026-09-30 · weekly

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

Of 12 recurrently implicated genes, 9 carry any drug at all. That is a statement about these 12 gene targets, not about the disease: Chronic lymphocytic leukemia does have labelled therapy — 13 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 chronic lymphocytic leukemia 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
BTK across cancers → 20 5 approvedAcalabrutinib, Orelabrutinib, Rilzabrutinib, Ritlecitinib, TirabrutinibApproved in chronic lymphocytic leukemia: Acalabrutinib.168 active of 296 chronic lymphocytic leukemia trials antibody, protein degrader, small molecule 0 active of 2 trials
BCL2 across cancers → 5 2 approvedNavitoclax, Oblimersen79 active of 145 chronic lymphocytic leukemia trials antibody, other clinical modality, protein degrader, small molecule —
PIK3CD across cancers → 42 5 approvedCopanlisib, Duvelisib, Leniolisib, Parsaclisib, UmbralisibApproved in chronic lymphocytic leukemia: Duvelisib.10 active of 81 chronic lymphocytic leukemia trials antibody, protein degrader, small molecule —
TP53 across cancers → 8 Phase 3Alrizomadlin, Cenersen, Contusugene Ladenovec, Eprenetapopt, Idasanutlin, Navtemadlin, Siremadlin, Teprasiran1 active of 4 chronic lymphocytic leukemia trials other clinical modality, protein degrader, small molecule —
ATM across cancers → 0 No drug— protein degrader, small molecule —
SF3B1 across cancers → 0 No drug— protein degrader, small molecule —
NOTCH1 across cancers → 1 Phase 1BrontictuzumabNo chronic lymphocytic leukemia trial of any of these drugs antibody, protein degrader, small molecule —
MS4A1 across cancers → 18 5 approvedEpcoritamab, Mosunetuzumab, Obinutuzumab, Odronextamab, TositumomabApproved in chronic lymphocytic leukemia: Obinutuzumab.95 active of 365 chronic lymphocytic leukemia trials antibody, other clinical modality, protein degrader, small molecule 5 active of 11 trials
CD19 across cancers → 14 6 approvedBrexucabtagene Autoleucel, Lisocabtagene Maraleucel, Loncastuximab Tesirine, Obecabtagene Autoleucel, Tafasitamab, TisagenlecleucelApproved in chronic lymphocytic leukemia: Lisocabtagene Maraleucel.9 active of 22 chronic lymphocytic leukemia trials antibody, other clinical modality, protein degrader 23 active of 50 trials
ROR1 1 Phase 3Cirmtuzumab1 active of 4 chronic lymphocytic leukemia trials antibody, protein degrader, small molecule 0 active of 2 trials
CD52 2 WithdrawalAlemtuzumab, Alemtuzumab Beta2 active of 64 chronic lymphocytic leukemia trials antibody, small molecule 0 active of 1 trial
MYD88 across cancers → 0 No drug— antibody, protein degrader —

Dataset evidence counts studies in the 291-study ranked set whose title or abstract names the gene; the bar is scaled to CD19. Sources: Open Targets Platform and NCBI GEO, retrieved 2026-09-30. Clinical stage is the highest reached for any indication — see the per-drug indications noted in each row. Target-prioritisation reference only; not clinical or prescribing guidance.

What is actually approved here

openFDA drug labels · weekly

13 drugs carry an FDA label naming chronic lymphocytic leukemia: Acalabrutinib, Alemtuzumab, Bendamustine, Duvelisib, Ibrutinib, Idelalisib, Lisocabtagene Maraleucel, Obinutuzumab, Ofatumumab, Pirtobrutinib, Rituximab, Venetoclax, Zanubrutinib. Separately, 19 of the drugs returned for the genes in the table above are approved only for other diseases and reach chronic lymphocytic leukemia through trials, not through their labels.

13Labelled for chronic lymphocytic leukemiaFDA INDICATIONS AND USAGE names the disease
19Approved, but for another diseasereturned for the genes in the table above
2Backbone agents listing itbroad cytotoxics whose labels name many tumours
23Active cell-therapy trials naming CD19of 50 registered

Every label that names chronic lymphocytic leukemia

DrugRoleWhat the label says
AcalabrutinibCALQUENCELabelled hereChronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma CALQUENCE is indicated for the treatment of adult patients with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL).
AlemtuzumabCampathLabelled hereCAMPATH is indicated as a single agent for the treatment of B-cell chronic lymphocytic leukemia (B-CLL).
BendamustineBELRAPZO, BENDAMUSTINE HYDROCHLORIDE, BendamustineLabelled hereChronic Lymphocytic Leukemia (CLL) BELRAPZO is indicated for the treatment of patients with chronic lymphocytic leukemia.
DuvelisibCOPIKTRALabelled hereChronic Lymphocytic Leukemia (CLL)/Small Lymphocytic Lymphoma (SLL) COPIKTRA is indicated for the treatment of adult patients with relapsed or refractory CLL or SLL after at least two prior therapies.
IbrutinibImbruvicaLabelled hereChronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma IMBRUVICA is indicated for the treatment of adult patients with chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL). 1. 2 Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma with 17p deletion IMBRUVICA is indicated for the treatment of adult patients with chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SL...
IdelalisibZydeligLabelled hereZydelig is a kinase inhibitor indicated for the treatment of patients with: Relapsed chronic lymphocytic leukemia (CLL), in combination with rituximab, in patients for whom rituximab alone would be considered appropriate therapy due to other co-morbidities.
Lisocabtagene MaraleucelBREYANZILabelled hereChronic Lymphocytic Leukemia (CLL) or Small Lymphocytic Lymphoma (SLL) BREYANZI is indicated for the treatment of adult patients with relapsed or refractory chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) who have received at least 2 prior lines of therapy including, a Bruton tyrosine kinase (BTK) inhibitor and a B-cell lymphoma 2 (BCL-2) inhibitor.
ObinutuzumabGazyvaLabelled hereChronic Lymphocytic Leukemia (CLL) GAZYVA, in combination with chlorambucil, is indicated for the treatment of patients with previously untreated chronic lymphocytic leukemia.
OfatumumabARZERRALabelled hereARZERRA ® (ofatumumab) is indicated for the treatment of patients with chronic lymphocytic leukemia (CLL) refractory to fludarabine and alemtuzumab.
PirtobrutinibJAYPIRCALabelled hereChronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma JAYPIRCA is indicated for the treatment of adult patients with relapsed or refractory chronic lymphocytic leukemia or small lymphocytic lymphoma (CLL/SLL) who have previously been treated with a covalent BTK inhibitor.
RituximabRiabni, Rituxan, Rituxan HycelaLabelled hereChronic Lymphocytic Leukemia (CLL)
VenetoclaxVenclextaLabelled hereChronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma VENCLEXTA is indicated for the treatment of adult patients with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL).
ZanubrutinibBRUKINSALabelled hereChronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL).
CyclophosphamideCYCLOPHOSPHAMIDE, Cyclophosphamide, FrindovyxBackboneMalignant Diseases Cyclophosphamide for injection is indicated for the treatment of adult and pediatric patients with: malignant lymphomas (Stages III and IV of the Ann Arbor staging system), Hodgkin's disease, lymphocytic lymphoma (nodular or diffuse), mixed-cell type lymphoma, histiocytic lymphoma, Burkitt's lymphoma multiple myeloma leukemias: chronic lymphocytic leukemia, chronic granulocyt...
FludarabineFludarabine, Fludarabine Phosphate, Fludarabine phosphateBackboneFludarabine Phosphate Injection, USP is indicated for the treatment of patients with B-cell chronic lymphocytic leukemia (CLL) who have not responded to or whose disease has progressed during treatment with at least one standard alkylating-agent containing regimen.

71 labels carry a positive indication naming the disease under indications_and_usage:"chronic lymphocytic leukemia" OR indications_and_usage:"small lymphocytic lymphoma"; they collapse to 15 distinct molecules once salt forms, biosimilars and co-formulated hyaluronidase are merged. Source: openFDA drug label API (api.fda.gov/drug/label.json), retrieved 2026-09-18. Labels change; this reflects the current label text, not the approval history. Not prescribing guidance.

Labels that name chronic lymphocytic leukemia without indicating for it

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

DrugWhy notWhat the label says
LenalidomideLenalidomideExcluded by labelLimitations of Use: Lenalidomide capsules are not indicated and are not recommended for the treatment of patients with chronic lymphocytic leukemia (CLL) outside of controlled clinical trials
PemivibartpemgardaExcluded by labelMedical conditions or treatments that may result in moderate to severe immune compromise and an inadequate immune response to COVID-19 vaccination include: Active treatment for solid tumor and hematologic malignancies Hematologic malignancies associated with poor responses to COVID-19 vaccines regar
ThioguanineTABLOIDExcluded by labelReliance upon thioguanine alone is seldom justified for initial remission induction of acute nonlymphocytic leukemias because combination chemotherapy including thioguanine results in more frequent remission induction and longer duration of remission than thioguanine alone. b) Other Neoplasms TABLOI

Cell therapy against CD19

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

CD19 is the busiest cell-therapy target among those this briefing searched in chronic lymphocytic leukemia: 50 registered trials naming it, 23 still active, 3 withdrawn before enrolling anyone.

TrialPhaseStatusTitleLast update
NCT036765041/2RecruitingTreatment of Patients With Relapsed or Refractory CD19+ Lymphoid Disease With T Cells Expressing a Third-generation CAR2024-07-29
NCT057055701RecruitingClinical Trial Using CAR- T Cells for Treatment of Patients With Refractory or Relapsed CD19-positive B Lymphoid Malignancies2025-09-25
NCT018536311RecruitingActivated T-Cells Expressing 2nd or 3rd Generation CD19-Specific CAR, Advanced B-Cell NHL, ALL, and CLL (SAGAN)2026-01-05
NCT057028531/2RecruitingMetabolically Fit CD19 CAR T-cell Therapy With CD34 Selection in Patients With CD19+ Relapsed/Refractory NHL, CLL/SLL2026-03-27
NCT054180881RecruitingGenetically Engineered Cells (Anti-CD19/CD20/CD22 CAR T-cells) for the Treatment of Relapsed or Refractory Lymphoid Malignancies2026-05-29
NCT048922771RecruitingCD19-Directed CAR-T Cell Therapy for the Treatment of Relapsed/Refractory B Cell Malignancies2026-06-09
NCT059632171RecruitingStudy of TBI-2001(Autologous CD19 Specific Chimeric Antigen Receptor (CAR) Gene-transduced T Lymphocytes) for Relapsed or Refractory CD19+ B-cell Lymphoma, CLL/SLL2026-06-09
NCT045457621RecruitingAnti-CD19 Chimeric Antigen Receptor T Cells for Treatment of Relapsed or Refractory Non-Hodgkin Lymphoma2026-06-22
NCT063644231/2RecruitingAnti-CD19 Chimeric Antigen Receptor T-Cell Immunotherapy for Leukemias2026-07-16
NCT067624311/2RecruitingPhase I/II Open-label Study Evaluating The Safety And Efficacy of Concomitant Administration of Anti-CD19 CAR T-cell Therapy and Lenalidomide in Refractory/Relapsed Chronic Lymphocytic Leukemia Patients.2026-08-13

10 of 50 shown, most recently active first. Other targets searched: CD20 (11), ROR1 (2), BTK (2), CD52 (1). Source: ClinicalTrials.gov API v2, retrieved 2026-09-18. A trial counts here when its registered conditions name chronic lymphocytic leukemia or a tumour-agnostic basket, its title names an administered cell product, and the title names this target: a HER2 CAR-T trial that adds a PD-1 antibody is a HER2 trial. A trial stating only a product code is missed.

Research momentum

PubMed MeSH · monthly

Every term below is a share of the chronic lymphocytic leukemia literature, not a count, because the field itself grew: 2015–2018 (n=2,666) against 2021–2025 (n=2,902). A topic whose papers doubled while the field doubled has not risen.

Rising, with a real baseline

MeSH term2015–182021–25ChangeShare now
Vaccination0.23%1.62%7.2×47 papers
Benzamides0.64%4.14%6.48×120 papers
Lymphoma, B-Cell, Marginal Zone0.23%1.34%5.97×39 papers
Pyrazines0.71%4.14%5.8×120 papers
Hematologic Neoplasms0.34%1.72%5.1×50 papers
Receptors, Chimeric Antigen0.34%1.65%4.9×48 papers
Progression-Free Survival0.49%2.31%4.73×67 papers
Leukemia0.19%0.72%3.86×21 papers
Hypertension0.19%0.62%3.31×18 papers
Receptors, Immunologic0.19%0.59%3.12×17 papers

Cooling

MeSH term2015–182021–25ChangeShare now
Disease-Free Survival6.15%0.76%0.12×22 papers
Protein-Tyrosine Kinases3.49%0.45%0.13×13 papers
Kaplan-Meier Estimate3.79%0.48%0.13×14 papers
Neoplasm Staging5.36%0.83%0.15×24 papers
Survival Analysis4.76%0.86%0.18×25 papers
Time Factors2.74%0.52%0.19×15 papers

Biggest topics now

MeSH term2015–182021–25ChangeShare now
Piperidines12.68%16.26%1.28×472 papers
Adenine12.49%15.13%1.21×439 papers
Antineoplastic Combined Chemotherapy Protocols16.02%13.4%0.84×389 papers
Protein Kinase Inhibitors7.5%12.54%1.67×364 papers
Prognosis17.44%12.47%0.72×362 papers
Antineoplastic Agents17.25%10.79%0.63×313 papers
Bridged Bicyclo Compounds, Heterocyclic4.05%9.41%2.32×273 papers
Sulfonamides4.5%9.3%2.07×270 papers
Mutation11.1%9.3%0.84×270 papers
Agammaglobulinaemia Tyrosine Kinase3.45%8.06%2.34×234 papers

Publication mix

Type2015–182021–25
Clinical Trial0.0%0.0%
Randomized Controlled Trial2.6%2.2%
Review16.0%13.7%
Meta-Analysis0.8%1.1%
Case Reports0.0%1.7%

Query: Leukemia, Lymphocytic, Chronic, B-Cell[MeSH Major Topic] NOT ("Lymphoma, Mantle-Cell"[MeSH] OR "Precursor Cell Lymphoblastic Leukemia-Lymphoma"[MeSH] OR "Leukemia, Myeloid"[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 year22,760 cases/yeardirect2026
Deaths each year4,350 deaths/yeardirect2026
Incidence rate4.8 cases per 100,000 people per yeardirect2019-2023
Death rate1 deaths per 100,000 people per yeardirect2020-2024
People living with it235,781 people living with the diseasedirect2023
Median age at diagnosis71.0 yearsdirect2019-2023
median age at death82 yearsdirect2020-2024
Five-year relative survival90.2%direct2016-2022

Years of life lost (proxy)

0.7 years per case, 16,506 a year, from survival and age at diagnosis rather than from a death count. derived proxy Not the WHO/GBD measure, which uses age at death and a life table; comparable across these briefings, not with published YLL figures. What this costs to fund is in Funding.

3 assumptions behind this estimate
  • Five-year relative survival stands in for cure; a death after five years is not counted.
  • The median age at diagnosis stands in for the whole age distribution.
  • Life expectancy at birth (78.4 years) is the reference, rather than remaining expectancy at the age of death from a life table.
  • Each assumption moves the result by more than the difference between the two diseases currently on this site, so this figure separates a disease from one ten times its size, not from a close neighbour.

Funding

NIH RePORTER · quarterly

NIH obligations naming chronic lymphocytic leukemia, after removing the 3,029 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.

$25.9MNIH obligations, FY2025from $27.6M in FY2013 · -6%
34distinct projects funded45 in FY2013
$56.6Mpeak year was FY2014obligations, all institutes
90%of FY2025 awards from NCI37 of 41

NIH obligations by fiscal year

$14M$28M$42M$57M13151719212325
YearObligationsAwardsDistinct projectsDropped as off-topic
FY2013$27.6M5645276
FY2014$56.6M5545271
FY2015$30.2M6251290
FY2016$28.9M6551271
FY2017$23.7M4642281
FY2018$22.4M3734226
FY2019$20.0M3832195
FY2020$18.0M3431194
FY2021$26.5M4438187
FY2022$23.9M4135186
FY2023$26.0M4436232
FY2024$27.8M4639215
FY2025$25.9M4134205

Where FY2025 money went

InstitutionObligationsAwards
Division Of Cancer Epidemiology And Genetics$5.3M2
Dana-Farber Cancer Inst$5.0M11
National Heart, Lung, And Blood Institute$3.4M0
Mayo Clinic Rochester$3.3M5
Ut Southwestern Medical Center$1.2M2
Ohio State University$1.2M2
Utah State Higher Education System--University Of Utah$0.9M0
Methodist Hospital Research Institute$0.9M2
Beckman Research Institute/City Of Hope$0.9M2
H. Lee Moffitt Cancer Ctr & Res Inst$0.7M0

Text search chronic lymphocytic leukemia 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 16,506 years of life lost a year, FY2025 obligations are $1,572 per life-year — $1,140 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

NCI37 · 90%
NHLBI2 · 5%
NIA1 · 2%
NIAID1 · 2%

Projects by administering institute. The rows above are the top 4 and account for 41 of 41.

Award mechanisms

R0118 · 44%
P017 · 17%
R503 · 7%
K083 · 7%
ZIA3 · 7%
R212 · 5%

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 11 and account for 41 of 41.

Where it lands

Division Of Cancer Epidemiology And Gene$5.3M · 20.3%
Dana-Farber Cancer Inst$5.0M · 19.3%
National Heart, Lung, And Blood Institut$3.4M · 13.1%
Mayo Clinic Rochester$3.3M · 12.7%
Ut Southwestern Medical Center$1.2M · 4.4%
Ohio State University$1.2M · 4.4%

Share of $25.9M in FY2025. The top three hold 53%.

Public datasets, ranked

NCBI GEO + Europe PMC + iCite · weekly

527 human GEO series match chronic lymphocytic leukemia. Keyword relevance cannot tell a 843-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 291-study ranked set

patient 146unspecified 80mixed 38cell line 27
146 patient80 unspecified38 mixed27 cell line178 carry clinical annotation102 carry survival40 patient cohorts ≥100 GEO samples19,761 GEO samples totalin 12 single-cell series the GEO sample count is the submitter’s unit (cells, libraries or pools), not patients

Established

high reuse, older
AccessionStudySamplesMentionsEurope PMCRCREvidence
GSE136634Clinical and biological implications of target occupancy in chronic lymphocytic leukemia treated with acalabrutinib2020 · sequencing12463.6
patient cohortAPT 0.95survivalstagemolecularACALABRUTINIBBTK89 cites
GSE22762An eight-gene expression signature for the prediction of survival and time to treatment in chronic lymphocytic leukemia2011 · array195641.3
patient cohortAPT 0.5survivalmolecular59 cites
GSE39671Expression data from untreated CLL patients2012 · array130311.6
patient cohortAPT 0.5survivalmolecular63 cites
GSE143673Reduced representation bisulfite sequencing (RRBS) of chronic lymphocytic leukemia (CLL) samples2021 · methylation45142.7
patient cohortAPT 0.5survivalmolecularIBRUTINIBTP5364 cites
GSE111015Chromatin mapping and single-cell immune profiling defines the temporal dynamics of ibrutinib drug response in chronic lymphocytic leukemia2019 · chromatin18892.5
patient cohortAPT 0.5molecularBTKIBRUTINIB74 cites
GSE109085Epigenetic evolution and lineage histories of chronic lymphocytic leukemia2019 · methylation84361.7
patient cohortAPT 0.5molecularIBRUTINIB64 cites
GSE50252Genomic profiling of Richter-syndrome Chronic Lymphocytic Leukemia2013 · array14634.9
patient cohortAPT 0.95survivalmolecularTP53206 cites
GSE21029The lymph node microenvironment promotes B-cell receptor signaling, NF-κB activation, and tumor proliferation in chronic lymphocytic leukemia (CLL)2010 · array621715.5
APT 0.95709 cites

Recent

2022 onward, by score
AccessionStudySamplesMentionsEurope PMCRCREvidence
GSE161711Interdependencies of Intratumoral Genetic Heterogeneity and the Immune Microenvironment in Chronic Lymphocytic Leukemia (Bulk RNA)2022 · single-cell9643.5
patient cohortAPT 0.75molecular43 cites
GSE254718Multi-omics exploration of microenvironmental changes during BTK covalent inhibition in chronic lymphocytic leukemia2024 · sequencing4521.3
patient cohortAPT 0.75survivalmolecularBTKIBRUTINIB5 cites
GSE178208HIGH-RISK SUBTYPES OF CHRONIC LYMPHOCYTIC LEUKEMIA ARE DETECTABLE AS EARLY AS 16 YEARS BEFORE DIAGNOSIS2022 · other27712.4
patient cohortAPT 0.75survivalstage36 cites
GSE249956Trascriptional profiling of proliferating and resting fracntions in ibrutinib-treated CLL2024 · sequencing4031.3
patient cohortAPT 0.5survivalmolecularBTKIBRUTINIB11 cites
GSE192685High Expression Level of ROR1 and ROR1-signaling Associates With Venetoclax Resistance In Chronic Lymphocytic Leukemia2022 · sequencing1632.0
patient cohortAPT 0.5molecularROR1VENETOCLAX30 cites
GSE214763miRNA profile at diagnosis predicts treatment outcome in patients with B-chronic lymphocytic leukemia: A filo study.2022 · sequencing7910.7
patient cohortAPT 0.5survivalmolecularRITUXIMAB8 cites

Sources: NCBI GEO + Europe PMC + iCite, retrieved 2026-09-19. SubSeries are collapsed to one row per study by linked PMID. Of 527 series retrieved, 29 were dropped by the profile’s exclusion rules and 137 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.

ATM

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

SF3B1

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

ROR1

2 cell-therapy trials against ROR1, 0 active, and no approved product. The clinical activity is real and none of it has reached a label.

CD52

1 cell-therapy trials against CD52, 0 active, and no approved product. The clinical activity is real and none of it has reached a label.

MYD88

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

How a machine reads this page

Static

This page is written to be quoted correctly by a model as much as read by a person. The same facts are available as JSON at the sibling URL below, which is what to cite. The cross-disease layer — burden, genes, drugs and antigens across every briefing — is described at /disease/api.json.

Fully server-rendered

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

Every number carries a source

Each section names the API it came from and the date it was retrieved: Open Targets (2026-09-30), ClinicalTrials.gov (2026-09-18), openFDA (2026-09-18), NCBI GEO (2026-09-19), PubMed (2026-09-12), NIH RePORTER (2026-09-19).

Negatives stated explicitly

Where the searches find nothing for chronic lymphocytic leukemia — 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

2 exclusion patterns are applied to free text before anything is ranked, because none is used as a model system in none: the disease has no widely used cell line, which is itself a fact about it. What was removed and why is stated in each section rather than silently applied.

{
  "disease": "Chronic lymphocytic leukemia",
  "mesh": "Leukemia, Lymphocytic, Chronic, B-Cell",
  "facts": "https://usebiotransfer.org/disease/chronic-lymphocytic-leukemia.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."
}