Table 1. HRR gene alterations (deleterious somatic or germline) tested in major trials in mCRPC.
| Study | Genes tested | Prevalence |
|---|---|---|
| TOPARP-A [5] | BRCA1/2, ATM, FANCA, CHEK2, PALB2 | 33% |
| TOPARP-B [20] | BRCA1/2, ATM, CDK12,PALB2, CHEK1,CHEK2, ARID1A, ATRX,
FANCA, FANCF,FANCG, FANCI, FANCM, MSH2, NBN, RAD50, WRN |
15% (BRCA1/2), 6% (ATM), 28.3% (HRR) |
| PROFOUND [21] | Cohort A: BRCA1, BRCA2, and ATM
Cohort B: BRIP1, BARD1, CDK12, CHEK1, CHEK2, FANCL, PALB2, PPP2R2A, RAD51B, RAD51C, RAD51D, and RAD54L |
27.9% (HRR) |
| TRITON 2 [19] | BRCA1, BRCA2, ATM, BARD1, BRIP1, CDK12, CHEK2, FANCA, NBN, PALB2, RAD51, RAD51B, RAD51C, RAD51D, RAD54 | NA |
| TRITON 3 [22] | BRCA1, BRCA2, ATM | 25% (HRR) |
| GALAHAD [23] |
BRCA1, BRCA2, ATM, FANCA, PALB2, CHEK2, BRIP1,
or HDAC2 |
NA |
Abbreviations: ARID1A: AT-Rich Interaction Domain 1A; ATM: ataxia-telangiectasia mutated; BRCA: breast cancer gene; BRIP1: BRCA1 Interacting Protein C-terminal Helicase 1; CHEK2: Checkpoint kinase 2; CDK12: cyclin-dependent kinase 12; FANCA: Fanconi anemia complementation group A; FANCL: Fanconi anemia complementation group L; FANCF: Fanconi anemia complementation group F; FANCG: Fanconi anemia complementation group G; FANCI: Fanconi anemia complementation group I; FANCM: Fanconi anemia complementation group M; NA: not available; PALB2: partner and localizer of BRCA2; PPP2R2A: protein phosphatase 2 regulatory subunit B alpha.