Department of Growth and Reproduction, Copenhagen University Hospital, Rigshospitalet, Copenhagen.
Department of Biostatistics, University of Copenhagen, Copenhagen, Denmark.
BJU Int. 2022 Nov;130(5):646-654. doi: 10.1111/bju.15774. Epub 2022 Jun 13.
To evaluate whether optimized and standardized diagnostic procedures would improve detection of germ cell neoplasia in situ (GCNIS) in the contralateral testis of patients with testicular germ cell tumour (TGCT) and decrease the rate of metachronous tumours, which in a nationwide Danish study was estimated to be 1.9%.
This was a retrospective analysis of outcomes in 655 patients with TGCT who underwent contralateral biopsies (1996-2007) compared with those in 459 non-biopsied TGCT controls (1984-1988). The biopsies were performed using a standardized procedure with immunohistochemical GCNIS markers and assessed by experienced evaluators. Initial histopathology reports were reviewed, and pathology and survival data were retrieved from national Danish registers. In 604/608 patients diagnosed as GCNIS-negative (four were lost to follow-up), the cumulative incidence of metachronous TGCT was estimated in a competing risk setting using the Grey method. All cases of metachronous TGCT were re-examined using immunohistochemistry.
Germ cell neoplasia in situ was found in 47/655 biopsied patients (7.2%, 95% confidence interval [CI] 5.4-9.5%). During the follow-up period (median 17.3 years) five of the 604 GCNIS-negative patients developed a TGCT. In 1/5 false-negative biopsies, GCNIS was found on histological revision using immunohistochemistry and 2/5 biopsies were inadequate because of too small size. The estimated cumulative incidence rate of second tumour after 20 years of follow-up was 0.95% (95% CI 0.10%-1.8%) compared with 2.9% (95% CI 1.3%-4.4%) among the non-biopsied TGCT patients (P = 0.012). The estimates should be viewed with caution due to the small number of patients with metachronous TGCT.
Optimized diagnostic procedures improved the detection rate of GCNIS in patients with TGCT and minimized their risk of developing metachronous bilateral cancer. Urologists should be aware of the importance of careful tissue excision (to avoid mechanical compression) and the need of adequate biopsy size. Performing contralateral biopsies is beneficial for patients' care and should be offered as a part of their management.
评估优化和标准化的诊断程序是否会提高对睾丸生殖细胞肿瘤(TGCT)患者对侧睾丸生殖细胞原位肿瘤(GCNIS)的检出率,并降低其同时性肿瘤的发生率。在一项全国性丹麦研究中,该发生率估计为 1.9%。
这是一项回顾性分析,纳入了 655 例接受对侧活检的 TGCT 患者(1996-2007 年)和 459 例未接受活检的 TGCT 对照组患者(1984-1988 年)的结局。活检采用标准化程序进行,使用免疫组织化学 GCNIS 标志物,并由经验丰富的评估者进行评估。对初始组织病理学报告进行了回顾,并从丹麦国家登记处检索了病理学和生存数据。在 604/608 例诊断为 GCNIS 阴性的患者(4 例失访)中,使用 Grey 法在竞争风险环境中估计了同时性 TGCT 的累积发生率。所有同时性 TGCT 病例均使用免疫组织化学重新检查。
在 655 例接受活检的患者中,47 例(7.2%,95%置信区间[CI]为 5.4-9.5%)发现 GCNIS。在中位随访时间为 17.3 年期间,604 例 GCNIS 阴性患者中有 5 例发生 TGCT。在 1 例假阴性活检中,使用免疫组织化学对组织学复查发现 GCNIS,2 例活检因体积过小而不充分。20 年随访后,第二肿瘤累积发生率在接受活检的 TGCT 患者中为 0.95%(95%CI为 0.10%-1.8%),而非接受活检的 TGCT 患者中为 2.9%(95%CI 为 1.3%-4.4%)(P=0.012)。由于同时性 TGCT 患者数量较少,因此应谨慎解读这些估计值。
优化的诊断程序提高了 TGCT 患者 GCNIS 的检出率,并降低了他们发生双侧同时性癌症的风险。泌尿科医生应注意组织切除(避免机械性压迫)的重要性和足够活检体积的必要性。进行对侧活检有助于患者的治疗,应作为其治疗的一部分提供。