Taveira-Barbosa José, Morais Samantha, Garcia Teresa, Bento Maria José, Lunet Nuno
Departamento de Ciências da Saúde Pública e Forenses e Educação Médica, Faculdade de Medicina, Universidade do Porto, Al. Prof. Hernâni Monteiro, 4200-319, Porto, Portugal.
Serviço de Epidemiologia, Instituto Português de Oncologia do Porto FG, EPE, Porto, Portugal.
Clin Exp Med. 2025 Apr 21;25(1):122. doi: 10.1007/s10238-025-01654-7.
Increased survival and life expectancy among patients with prostate cancer results in an increased risk of developing a second primary cancer (SPC). We aimed to describe the occurrence of SPCs in a population-based cohort with a prostate first primary cancer (FPC), in Northern Portugal. A cohort of 13,222 patients with a prostate FPC from the North Region Cancer Registry of Portugal, diagnosed between 2000 and 2009, was followed until 31 December 2021, for synchronous (within six months of FPC diagnosis) and metachronous SPCs (all others). We describe absolute and relative frequencies of SPCs, incidence rates and standardized incidence ratios of SPCs (compared to the male general population), and cumulative incidence of metachronous SPCs. A total of 1953 (14.8%) patients with a prostate FPC developed an SPC, mostly of the colon, lung and bladder; synchronous SPCs occurred mainly in the bladder. Compared to the general male population, patients with a prostate FPC had a globally lower incidence of all cancers, and lung and oesophagus cancers, but a higher incidence of bladder and pancreas cancers. Overall, the incidence of synchronous SPCs was also significantly higher, likely reflecting the incidental diagnosis of SPCs. The 20-year cumulative incidence of metachronous SPCs was 15.4%. Patients with a prostate FPC had a lower overall incidence of SPCs than the general male population, despite a higher incidence in the first six-months after the SPC diagnosis. After that period, one out of seven may be expected to develop an SPC within two decades. Continued cancer surveillance among survivors is needed.
前列腺癌患者生存率和预期寿命的提高导致患第二原发性癌症(SPC)的风险增加。我们旨在描述葡萄牙北部以前列腺癌作为首发原发性癌症(FPC)的人群队列中SPC的发生情况。对葡萄牙北部地区癌症登记处13222例2000年至2009年间诊断为前列腺FPC的患者进行队列研究,随访至2021年12月31日,观察同步性(FPC诊断后6个月内)和异时性SPC(其他所有情况)。我们描述了SPC的绝对和相对频率、SPC的发病率和标准化发病率(与男性普通人群相比)以及异时性SPC的累积发病率。共有1953例(14.8%)前列腺FPC患者发生了SPC,主要为结肠癌、肺癌和膀胱癌;同步性SPC主要发生在膀胱。与普通男性人群相比,前列腺FPC患者所有癌症、肺癌和食管癌的总体发病率较低,但膀胱癌和胰腺癌的发病率较高。总体而言,同步性SPC的发病率也显著更高,这可能反映了SPC的偶然诊断。异时性SPC的20年累积发病率为15.4%。前列腺FPC患者SPC的总体发病率低于普通男性人群,尽管在SPC诊断后的前六个月发病率较高。在那段时间之后,预计七分之一的患者在二十年内可能会发生SPC。需要对幸存者继续进行癌症监测。