睾丸生殖细胞肿瘤:结果在西开普省三级医院,南非

Gérard Grobler, Petrus V. Spies, Henriette Burger, Heidi Van Deventer, André Van der Merwe
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引用次数: 0

摘要

背景:睾丸癌是一种罕见的恶性肿瘤,描述非洲临床特征和预后的数据有限。目的:我们总结了南非16年的数据,并将其与非洲的现有数据和国际数据进行了比较。背景:回顾性研究包括男性;2005年1月1日至2020年12月31日在泰格伯格医院诊断和治疗睾丸生殖细胞肿瘤12年。方法:自述种族包括白种人、混血儿、非洲人和亚洲人。患者从泌尿肿瘤学和病理记录中确定任何形式的睾丸癌。提取人口统计学、分期、治疗和结局数据。此外,作为内政部生活状况报告的一部分,患者被联系或跟踪,以确定生存结果的最后联系日期。结果:共纳入142例患者。最常见的危险因素是隐睾(14.1%),但大多数患者没有已知的危险因素(82.4%)。精原细胞瘤比非精原细胞生殖细胞瘤(nsgct)晚10年出现。没有危险因素似乎是保护性风险比(HR) 0.18, 40岁后被诊断出患有糖尿病的人死亡风险增加。组织病理学分类相当,精原细胞瘤70例,nsgct 72例。精原细胞瘤与nsgct的分期分布无统计学差异。精原细胞瘤的总体5年生存率为91%,nsgct为78%。在15年的时间范围内,精原细胞瘤组的患者预计存活时间延长16%(1.9年)。临床分期(CS) 3期患者的死亡风险高于CS1期和CS2期患者,而精原细胞瘤与nsgct之间无差异(HR = 12.6)。结论:本组患者的临床特征符合国际数据。有必要进行更好的健康教育,以确保患者及早就诊并获得适当的医疗护理。贡献:我们的数据代表了非洲单个中心最大的睾丸癌结果系列,目的是激励其他中心描述和分析他们的肿瘤结果,以确保我们在南非未来为所有患者提供最好的护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Testicular germ cell tumours: Outcomes at a tertiary hospital in the Western Cape, South Africa
Background: Testis cancer is a rare malignancy, and there are limited data describing Africa’s clinical characteristics and outcomes. Aim: We summarised 16 years of South African data, comparing it to available data for Africa and international data. Setting: The retrospective review included males > 12 years with testicular germ cell tumours diagnosed and treated at Tygerberg Hospital from 01 January 2005 to 31 December 2020. Methods: Self-declared racial status included Caucasian, mixed ethnicity, African and Asian. Patients were identified from uro-oncology and pathology records indicating any form of testicular cancer. Data were extracted for demographics, staging, treatment and outcomes. In addition, patients were contacted or tracked as part of a living status report by the Department of Home Affairs to determine the last contact date for survival outcomes. Results: There were 142 patients in the study. The most common risk factor was cryptorchidism (14.1%), but most patients reported no known risk factors (82.4%). Seminomas presented 10 years later than non-seminomatous germ cell tumours (NSGCTs). Having no risk factors seems to be protective hazard ratio (HR) 0.18 and being diagnosed after 40 years carries an increased risk of death. The histopathological classification was fairly equal, with 70 seminoma and 72 NSGCTs. There was no statistical difference in the stage distribution between seminoma and NSGCTs. The overall 5-year survival was 91% for seminoma compared with 78% in NSGCTs. With a time horizon of 15 years, a patient was expected to survive 16% (1.9 years) longer in the seminoma group. Clinical stage (CS) three patients had a higher risk of dying compared with CS1 and CS2, and there was no difference between seminoma and NSGCTs (HR = 12.6). Conclusion: The clinical characteristics of our patient population correspond to international data. There is a need for better health education to ensure patients present earlier and have access to appropriate medical care. Contribution: Our data represent the largest series of testis cancer outcomes at a single centre in Africa and the aim is to motivate other centres to describe and analyse their oncological outcomes to ensure we provide the best possible care to all our patients in South Africa’s future.
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