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

被引:16
作者
Brook, Mark N. [1 ,4 ]
Ni Raghallaigh, Holly [1 ]
Govindasami, Koveela [1 ]
Dadaev, Tokhir [1 ]
Rageevakumar, Reshma [1 ]
Keating, Diana [1 ]
Hussain, Nafisa [1 ]
Osborne, Andrea [1 ]
Lophatananon, Artitaya [2 ]
Muir, Kenneth R. [2 ]
Kote-Jarai, Zsofia [1 ]
Eeles, Rosalind A. [1 ,3 ]
机构
[1] Inst Canc Res, London, England
[2] Univ Manchester, Hlth Serv Res & Primary Care, Div Populat Hlth, Manchester, England
[3] Royal Marsden NHS Fdn Trust, London, England
[4] Inst Canc Res, Div Genet & Epidemiol, Oncogenet Team, 15 Cotswold Rd, Sutton SM2 5NG, England
关键词
Prostate cancer; Family history; Survival; Screening; Awareness;
D O I
10.1016/j.eururo.2022.11.019
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: 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. Objective: To determine how the number, degree, and age of a PrCa patient's affected rel-atives are associated with OS and PCSS of those already diagnosed with PrCa. Design, setting, and participants: 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). Outcome measurements and statistical analysis: The primary outcome was all-cause mortality among PrCa patients. The risk of death with respect to FH was assessed by cal-culating hazard ratios from Cox proportional hazard regression models, adjusting for rel-evant factors. Results and limitations: 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. Conclusions: 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
引用
收藏
页码:257 / 266
页数:10
相关论文
共 13 条
  • [1] Alberti C, 2010, EUR REV MED PHARMACO, V14, P31
  • [2] [Anonymous], PROG GEN VERS 10
  • [3] Does family history of prostate cancer affect outcomes following radiotherapy?
    Bagshaw, Hilary
    Ruth, Karen
    Horwitz, Eric M.
    Chen, David Y. T.
    Buyyounouski, Mark K.
    [J]. RADIOTHERAPY AND ONCOLOGY, 2014, 110 (02) : 229 - 234
  • [4] Hereditary prostate cancer
    Bratt, O
    [J]. BJU INTERNATIONAL, 2000, 85 (05) : 588 - 598
  • [5] Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction
    Conti, David, V
    Darst, Burcu F.
    Moss, Lilit C.
    Saunders, Edward J.
    Sheng, Xin
    Chou, Alisha
    Schumacher, Fredrick R.
    Al Olama, Ali Amin
    Benlloch, Sara
    Dadaev, Tokhir
    Brook, Mark N.
    Sahimi, Ali
    Hoffmann, Thomas J.
    Takahashi, Atushi
    Matsuda, Koichi
    Momozawa, Yukihide
    Fujita, Masashi
    Muir, Kenneth
    Lophatananon, Artitaya
    Wan, Peggy
    Le Marchand, Loic
    Wilkens, Lynne R.
    Stevens, Victoria L.
    Gapstur, Susan M.
    Carter, Brian D.
    Schleutker, Johanna
    Tammela, Teuvo L. J.
    Sipeky, Csilla
    Auvinen, Anssi
    Giles, Graham G.
    Southey, Melissa C.
    MacInnis, Robert J.
    Cybulski, Cezary
    Wokolorczyk, Dominika
    Lubinski, Jan
    Neal, David E.
    Donovan, Jenny L.
    Hamdy, Freddie C.
    Martin, Richard M.
    Nordestgaard, Borge G.
    Nielsen, Sune F.
    Weischer, Maren
    Bojesen, Stig E.
    Roder, Martin Andreas
    Iversen, Peter
    Batra, Jyotsna
    Chambers, Suzanne
    Moya, Leire
    Horvath, Lisa
    Clements, Judith A.
    [J]. NATURE GENETICS, 2021, 53 (01) : 11 - 15
  • [6] The Heritability of Prostate Cancer in the Nordic Twin Study of Cancer
    Hjelmborg, Jacob B.
    Scheike, Thomas
    Holst, Klaus
    Skytthe, Axel
    Penney, Kathryn L.
    Graff, Rebecca E.
    Pukkala, Eero
    Christensen, Kaare
    Adami, Hans-Olov
    Holm, Niels V.
    Nuttall, Elizabeth
    Hansen, Steinbjorn
    Hartman, Mikael
    Czene, Kamila
    Harris, Jennifer R.
    Kaprio, Jaakko
    Mucci, Lorelei A.
    [J]. CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2014, 23 (11) : 2303 - 2310
  • [7] EVIDENCE OF AN X-LINKED OR RECESSIVE GENETIC COMPONENT TO PROSTATE-CANCER RISK
    MONROE, KR
    YU, MC
    KOLONEL, LN
    COETZEE, GA
    WILKENS, LR
    ROSS, RK
    HENDERSON, BE
    [J]. NATURE MEDICINE, 1995, 1 (08) : 827 - 829
  • [8] Clinical and histopathological characteristics of familial prostate cancer in Finland
    Pakkanen, Sanna
    Kujala, Paula M.
    Ha, Nati
    Matikainen, Mika P.
    Schleutker, Johanna
    Tammela, Teuvo L. J.
    [J]. BJU INTERNATIONAL, 2012, 109 (04) : 557 - 563
  • [9] StataCorp, 2021, STATA STAT SOFTWARE
  • [10] Men with family history of prostate cancer have a higher risk of disease recurrence after radical prostatectomy
    Thalgott, Mark
    Kron, Martina
    Brath, Johannes M.
    Ankerst, Donna P.
    Thompson, Ian M.
    Gschwend, Juergen E.
    Herkommer, Kathleen
    [J]. WORLD JOURNAL OF UROLOGY, 2018, 36 (02) : 177 - 185