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. 2022 Jul 26;14(15):3623. doi: 10.3390/cancers14153623

Table 2.

Clinical characteristics for ATM, CHEK2, and HOXB13 germline mutations.

ATM Mutation Carriers
Age at Diagnosis PSA 1 Grade Group Stage Architecture 2 D’Amico Primary Treatment Age at Death Cause of Death Age at Diagnosis of Other Primary Malignancy
78 13.6 - - - Int Radiation 87 PCa -
90 210 5 T1c No High Non-curative 93 PCa -
57 160 - - - High Radiation 75 MDS 3 70, MDS
65 20 5 T1c Cribriform High Radiation - - 66, Renal
75 5 3 T3aN1 Cribriform High Prostatectomy - -
68 12 5 T3b IDCP High Prostatectomy - - -
49 2.6 3 T2a IDCP, Cribriform Int Prostatectomy - - -
42 6.9 1 - Low Prostatectomy - - -
61 12 2 T2c - High Prostatectomy - - 83, Lung, Melanoma
CHEK2 Mutation Carriers
80 - 5 T4 - High Prostatectomy 81 Cardiac 78, Bladder, Colon
56 8.8 2 T2c - High Prostatectomy - - 47, Breast
HOXB13G84E Mutation Carriers
68 6.7 1 T1c Low Radiation 92 - 80, Breast
69 5.3 2 T2N0 Int Prostatectomy - - -
47 3.8 2 T3a High Prostatectomy - - -
64 - 2 T2a Int - 89 PCa -

1 PSA immediately prior to undergoing diagnostic biopsy; 2 High-risk pathology features identified within prostatic adenocarcinoma; Abbreviations: Myelodysplastic syndrome (MDS), D’Amico Intermediate-risk (Int), intraductal carcinoma of the prostate (IDCP).