Cheriyan Salim K, Nicholson Marilin, Aydin Ahmet M, Azizi Mounsif, Peyton Charles C, Sexton Wade J, Gilbert Scott M
Department of Genitourinary Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Department of Health Outcomes and Behavior, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Transl Androl Urol. 2020 Jan;9(Suppl 1):S45-S55. doi: 10.21037/tau.2019.05.14.
Early stage nonseminomatous germ cell tumor (NSGCT) remains a treatable disease, with stage I cancer specific survival exceeding 95%. Using a risk-adapted approach; active surveillance (AS), adjuvant chemotherapy, and retroperitoneal lymph node dissection (RPLND) all options for treatment; with surveillance being increasingly used. With persistently elevated markers (stage IS), chemotherapy remains the hallmark of treatment. Management of stage II NSGCT varies based on status of tumor markers. With negative markers, both induction chemotherapy and upfront RPLND remain options. Management of a residual mass <1 cm after chemotherapy remains controversial, with AS and nerve-sparing RPLND considered options. The development of miR-371a-3p microRNA shows promise a novel biomarker for testicular cancer (GCT). Despite controversies in management, cures for NSGCT are achievable in 95-99% of patients.
早期非精原细胞瘤性生殖细胞肿瘤(NSGCT)仍然是一种可治疗的疾病,I期癌症特异性生存率超过95%。采用风险适应性方法;主动监测(AS)、辅助化疗和腹膜后淋巴结清扫术(RPLND)都是治疗选择;监测的使用越来越多。对于肿瘤标志物持续升高的情况(IS期),化疗仍然是治疗的关键。II期NSGCT的管理因肿瘤标志物状态而异。肿瘤标志物为阴性时,诱导化疗和 upfront RPLND仍然都是选择。化疗后残留肿块<1 cm的处理仍存在争议,AS和保留神经的RPLND被认为是选择。miR-371a-3p微小RNA的出现有望成为睾丸癌(GCT)的一种新型生物标志物。尽管在管理方面存在争议,但95-99%的NSGCT患者可以实现治愈。