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. Author manuscript; available in PMC: 2020 Jan 28.
Published in final edited form as: Semin Oncol. 2016 Aug 18;43(5):560–565. doi: 10.1053/j.seminoncol.2016.08.001

Table 1.

Risk estimates for prostate cancer (PCA) by genes associated with hereditary cancer syndromes.

Gene Risk for PCA* Risk for aggressive PCA features*, *+Risk for early-onset PCA (age at diagnosis < 65)*,§ PCA-specific outcomes
BRCA1 1.07–3.81 [26,53,8992] -- 1.82 [90] 5.16 [56]
BRCA2 3.18–8.6 [26,56,57,89,9395] 3.18–4.38 [30,55,96] 7.33 [89] HR for death 2.4–5.48 [56,9698], decreased survival [31]
Mismatch repair genes 1.99–3.67 [38,99] -- 2.48 [38] --
HOXB13 2.8–8.47 [41,44,47,50] -- 2.7–10.11 [41,44,47,50,100] --
*

Risks are a combination of odds ratios, relative risks, hazard ratios, or standardized incidence ratios depending on the study. Risks vary based on strength of family history reported.

Outcomes are a combination of survival estimates or mortality depending on the study.

Definition of aggressive prostate cancer features include Gleason score ≥ 7, depending on the study. Additional studies have described an association of BRCA1 and BRCA2 in particular to features of aggressiveness. The table highlights those studies with reported risk estimates.

§

While definitions for early-onset prostate cancer can vary, risks are reported for age at diagnosis < 65 years to encompass the majority of studies with an age-related focus.