Fazal Faizan, Ur Rehman Mohammad Ebad, Khokhar Arham A, Tahir Saad, Tanveer Usama, Ijaz Ali A, Maqbool Shahzaib, Abid Areesha, Raja Hafsa Arshad Azam, Malik Bilal Haider
Medicine, Holy Family Hospital, Rawalpindi, PAK.
Surgery, Oxford University Hospitals NHS Foundation Trust, Oxford, GBR.
Cureus. 2025 Aug 13;17(8):e90017. doi: 10.7759/cureus.90017. eCollection 2025 Aug.
This study aimed to identify the sites and risks of developing second primary malignancies (SPMs) after urogenital cancers, as well as their associations with race, gender, and age.
This was a retrospective cohort study involving 140,620 subjects with primary urogenital cancer. The data were extracted from the Surveillance, Epidemiology, and End Results (SEER) database, covering the duration from January 1975 to April 2025. This study included only those patients who were diagnosed with primary urogenital cancer. Descriptive statistics, absolute excess risk (AER), and observed-to-expected ratios (O/E) were calculated.
Out of the 140,620 patients observed, 106,377 (75.64%) were male. Among the patients diagnosed with urogenital cancer, 33,680 (23.9%) developed an SPM. The mean age for the development of an SPM was 75.12 years. The risk of developing an SPM in patients with urogenital cancer was significantly higher compared to the general population (O/E = 1.31, confidence interval (CI) = 1.30-1.33, AER = 67.83). Male genital system cancers (O/E = 1.27, CI = 1.24-1.30, AER = 13.41), respiratory system cancers (O/E = 1.75, CI = 1.71-1.80, AER = 26.02), and urinary system cancers (O/E = 2.28, CI = 2.22-2.33, AER = 29.16) were among the most commonly identified SPMs. A total of 17,869 (53%) patients with an SPM belonged to the >75 years age group.
Compared to the general population, patients with urogenital cancer had a considerably higher risk of developing an SPM. Most SPM cases were observed in individuals aged 50-74 years and those over 75. A latency period of 12-59 months was commonly noted before the development of an SPM. The most frequently reported SPMs involved the male genital, respiratory, and urinary systems.
本研究旨在确定泌尿生殖系统癌症后发生第二原发性恶性肿瘤(SPM)的部位和风险,以及它们与种族、性别和年龄的关联。
这是一项回顾性队列研究,涉及140,620例原发性泌尿生殖系统癌症患者。数据从监测、流行病学和最终结果(SEER)数据库中提取,涵盖1975年1月至2025年4月的时间段。本研究仅纳入那些被诊断为原发性泌尿生殖系统癌症的患者。计算了描述性统计数据、绝对超额风险(AER)和观察到的与预期的比率(O/E)。
在观察的140,620例患者中,106,377例(75.64%)为男性。在被诊断为泌尿生殖系统癌症的患者中,33,680例(23.9%)发生了SPM。发生SPM的平均年龄为75.12岁。与一般人群相比,泌尿生殖系统癌症患者发生SPM的风险显著更高(O/E = 1.31,置信区间(CI)= 1.30 - 1.33,AER = 67.83)。男性生殖系统癌症(O/E = 1.27,CI = 1.24 - 1.30,AER = 13.41)、呼吸系统癌症(O/E = 1.75,CI = 1.71 - 1.80,AER = 26.02)和泌尿系统癌症(O/E = 2.28,CI = 2.22 - 2.33,AER = 29.16)是最常被确定的SPM。共有17,869例(53%)发生SPM的患者属于75岁以上年龄组。
与一般人群相比,泌尿生殖系统癌症患者发生SPM的风险要高得多。大多数SPM病例出现在50 - 74岁以及75岁以上的个体中。在发生SPM之前,通常会有12 - 59个月的潜伏期。最常报告的SPM涉及男性生殖、呼吸和泌尿系统。