Target, across the briefings

BCL2 across 9 cancers

BCL2 is on the target list of 9 of the briefings. No drug aimed at it carries an FDA label naming any of them; a drug against it is approved somewhere in 9. In the reference cohorts of the 7 with a mutation landscape it is altered in at least 5% of patients in 2 and in under 2% in 5 (Mantle cell lymphoma, Acute myeloid leukemia, Chronic lymphocytic leukemia, Myelodysplastic syndromes, Small cell lung cancer) — 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
Mantle cell lymphomaapproved elsewhereapproved51 via BCL-20.0% mut n=29
Acute myeloid leukemiaapproved elsewhereapproved5—0.0% mut n=200
Chronic lymphocytic leukemiaapproved elsewhereapproved50 via BCL-20.47% mut n=1074
Chronic myeloid leukemiaapproved elsewhereapproved50 via BCL-2no landscape
Diffuse large B-cell lymphomaapproved elsewhereapproved50 via BCL-29.69% mut n=1001
Follicular lymphomaapproved elsewhereapproved50 via BCL-234.72% mut · 0.52% amp n=193
Myelodysplastic syndromesapproved elsewhereapproved50 via BCL-20.06% mut n=3323
Small cell lung cancerapproved elsewhereapproved5—0.83% mut n=120
Waldenström macroglobulinaemiaapproved elsewhereapproved50 via BCL-2no landscape

"Approved here" means a drug Open Targets records as aimed at BCL2 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.