Target, across the briefings

CD19 across 7 cancers

CD19 is on the target list of 7 of the briefings. A drug aimed at it carries an FDA label naming the disease in 5, and is approved for some indication in 7. In the reference cohorts of the 5 with a mutation landscape it is altered in at least 5% of patients in 0 and in under 2% in 5 (Diffuse large B-cell lymphoma, Acute lymphoblastic leukemia, Follicular lymphoma, Mantle cell lymphoma, Chronic lymphocytic leukemia) — a target there by expression, dependency or drug label, not by mutation.

DiseaseLabel statusFurthest stage (Open Targets)Distinct drugsCell-therapy trialsAltered in the reference cohort
Diffuse large B-cell lymphomaapproved here Lisocabtagene Maraleucel, Loncastuximab Tesirine, Tafasitamab, Tisagenlecleucelapproved1450 via CD190.0% mut n=1001
Acute lymphoblastic leukemiaapproved here Brexucabtagene Autoleucel, Obecabtagene Autoleucel, Tisagenlecleucelapproved1497 via CD190.0% mut · 0.15% amp · 0.15% del n=137
Follicular lymphomaapproved here Lisocabtagene Maraleucel, Tafasitamab, Tisagenlecleucelapproved1427 via CD19 n=193
Mantle cell lymphomaapproved here Brexucabtagene Autoleucel, Lisocabtagene Maraleucelapproved1425 via CD190.0% mut n=29
Chronic lymphocytic leukemiaapproved here Lisocabtagene Maraleucelapproved1450 via CD190.19% mut n=1074
Burkitt lymphomaapproved elsewhereapproved145 via CD19no landscape
Waldenström macroglobulinaemiaapproved elsewhereapproved142 via CD19no landscape

"Approved here" means a drug Open Targets records as aimed at CD19 carries an FDA label that names that disease, per the briefing's openFDA stage. "Approved elsewhere" means the drug is approved for some other indication. Stage is the furthest Open Targets clinical stage among drugs aimed at the gene, in any indication; the database is reported as it is, and it lags some approvals. Cell-therapy trials are counted on the antigen the briefing maps the gene to, from ClinicalTrials.gov. The last column is the disease's mutation landscape: non-silent mutation, high-level amplification and deep deletion as percentages of the reference cohort's patients, each over its own denominator; "not on panel" means the reference cohort could not have called the gene.