Department of Urology, Albertinen-Krankenhaus, Hamburg, Germany.
Ann Oncol. 2013 May;24(5):1332-7. doi: 10.1093/annonc/mds628. Epub 2013 Jan 4.
The treatment of testicular intraepithelial neoplasia (TIN), the progenitor of testicular germ cell tumours (GCTs), is based on little data.
Two hundred and twenty-eight GCT patients with contralateral TIN were retrospectively enrolled. Ten had surveillance, 122 radiotherapy to testis with 18-20 Gy, 30 cisplatin-based chemotherapy (two cycles), 51 chemotherapy (three cycles), and 15 carboplatin. The study end point was a malignant event (ME), defined as detection of TIN upon control biopsy or occurrence of a second GCT. The Secondary end point was hypogonadism during follow-up.
Numbers, proportions of ME, and median event-free survival (EFS) times were: radiotherapy N = 3, 2.5%, 11.08 years; chemotherapy (two cycles) N = 15, 50%, 3.0 years; chemotherapy (three cycles) N = 12, 23.5%, 9.83 years; carboplatin N = 10, 66%, 0.9 years; surveillance N = 5, 50%, 7.08 years. EFS is significantly different among the groups. Hypogonadism rates were in radiotherapy patients 30.8%, chemotherapy (two cycles) 13%, chemotherapy (three cycles) 17.8%, carboplatin 40%, surveillance 40%.
Local radiotherapy is highly efficacious in curing TIN. Chemotherapy is significantly less effective and the cure rates are dose-dependent. Though hypogonadism occurs in one-third of patients, radiotherapy with 20 Gy remains the standard management of TIN.
睾丸上皮内肿瘤(TIN)是睾丸生殖细胞肿瘤(GCT)的前体,其治疗主要基于有限的数据。
回顾性纳入 228 例伴有对侧 TIN 的 GCT 患者。其中 10 例接受监测,122 例接受 18-20 Gy 睾丸放疗,30 例接受顺铂为基础的化疗(两周期),51 例接受化疗(三周期),15 例接受卡铂治疗。研究终点为恶性事件(ME),定义为在控制活检时检测到 TIN 或发生第二例 GCT。次要终点为随访期间发生性腺功能减退症。
ME 的数量、比例和中位无事件生存(EFS)时间分别为:放疗 N = 3,2.5%,11.08 年;化疗(两周期)N = 15,50%,3.0 年;化疗(三周期)N = 12,23.5%,9.83 年;卡铂 N = 10,66%,0.9 年;监测 N = 5,50%,7.08 年。各组之间 EFS 有显著差异。放疗患者的性腺功能减退症发生率为 30.8%,化疗(两周期)为 13%,化疗(三周期)为 17.8%,卡铂为 40%,监测为 40%。
局部放疗对 TIN 有很高的疗效。化疗的效果明显较低,且治愈率与剂量相关。尽管三分之一的患者会发生性腺功能减退症,但 20 Gy 的放疗仍然是 TIN 的标准治疗方法。