Family History of Prostate Cancer and Survival Outcomes in the UK Genetic Prostate Cancer Study

医学 危险系数 前列腺癌 肿瘤科 内科学 比例危险模型 流行病学 家族史 人口 置信区间 相对存活率 前列腺 癌症 妇科 癌症登记处 环境卫生
作者
Mark N. Brook,Holly Ní Raghallaigh,Koveela Govindasami,Tokhir Dadaev,Reshma Rageevakumar,Diana Keating,Nafisa Hussain,Andrea Osborne,Artitaya Lophatananon,Kenneth Muir,Zsofia Kote‐Jarai,Rosalind Eeles
出处
期刊:European Urology [Elsevier BV]
卷期号:83 (3): 257-266 被引量:9
标识
DOI:10.1016/j.eururo.2022.11.019
摘要

A family history (FH) of prostate cancer (PrCa) is associated with an increased likelihood of PrCa diagnosis. Conflicting evidence exists regarding familial PrCa and clinical outcomes among PrCa patients, including all-cause mortality/overall survival (OS), PrCa-specific survival (PCSS), aggressive histology, and stage at diagnosis. To determine how the number, degree, and age of a PrCa patient’s affected relatives are associated with OS and PCSS of those already diagnosed with PrCa. The UK Genetic Prostate Cancer Study is a longitudinal, multi-institutional, observational study collecting baseline and follow-up clinical data since 1992. We examined OS and PCSS in 16 340 men by degree and number of relatives with prostate and genetically related cancers (breast, ovarian, and colorectal). The primary outcome was all-cause mortality among PrCa patients. The risk of death with respect to FH was assessed by calculating hazard ratios from Cox proportional hazard regression models, adjusting for relevant factors. A stronger FH was inversely associated with the risk of all-cause and PrCa-specific mortality. This association was greater in those with an increasing number (p-trend < 0.001) and increasing closeness (p-trend < 0.001) of the diagnosed relatives. Patients with at least one first-degree relative were at a lower risk of all-cause mortality than those with no FH (hazard ratio = 0.82 [95% confidence interval 0.75–0.89]). The population is largely of European ancestry, and this may cause an issue with representation and generalisation. Data are missing on epidemiological risk factors for death such as smoking and on comorbidities. Recall of family members' diagnoses may affect the classification of FH in unconfirmed cases. Based on the investigation of the type and timing of relatives’ cancers, it is likely that reductions in mortality are due almost completely to a greater awareness of the disease. This study provides information for clinicians guiding patients and their relatives based on their familial risk. It shows the importance of screening and awareness programmes, which are likely to improve survival among men with an FH. We were interested in how a family history of prostate cancer affects survival in prostate cancer patients. We studied 16 340 patients, categorised them according to the strength of their family history, and found that the stronger their family history, the better they did in terms of overall survival. We looked at the type and timing of patients’ diagnoses compared with those of their relatives and found that this effect is likely to be explained by awareness, which indicates the importance of screening and awareness programmes.
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