Jayram Gautam, Szmulewitz Russell Z, Eggener Scott E
Section of Urology, Department of Surgery, University of Chicago Medical Center, USA.
Indian J Urol. 2010 Jan-Mar;26(1):92-7. doi: 10.4103/0970-1591.60449.
INTRODUCTION/METHODS: Approximately 30% of nonseminomatous germ-cell tumors (NSGCT) of the testis present with metastatic disease. In 1997, the International Germ Cell Cancer Collaborative Group (IGCCCG) stratified all patients with metastatic NSGCT into various risk groups based on serum tumor markers and presence of visceral disease. We review the literature and present optimal stage-dependent management strategies in patients with favorable-risk metastatic NSGCT.
Primary chemotherapy (3 cycles BEP or 4 cycles EP) has been shown to be the preferred modality in patients with Clinical Stage IS (cIS) and in patients with bulky metastatic disease (>/=CS IIb) due to their high risk of systemic disease and recurrence. Primary retroperitoneal lymph node dissection appears to be the most efficient primary therapy for retroperitoneal disease <2 cm (CS IIa), with adjuvant chemotherapy reserved for patients who are pathologically advanced (>5 nodes involved, single node > 2 cm) and for those who are non-compliant with surveillance regimens. Following primary chemotherapy, STM and radiographic evaluation are used to assess treatment response. For patients with normalization of STM and retroperitoneal masses < 1 cm, retroperitoneal lymph node dissection or observation with treatment at disease progression are considered options. Due to risk of teratoma or chemoresistant GCT, masses >1 cm and extra-retroperitoneal masses should be treated with surgical resection, which should be performed with nerve-sparing, if possible.
In patients with favorable disease based on IGCCCG criteria, clinical stage, STM, and radiographic evaluation are used to guide appropriate therapy to provide excellent long-term cure rates (>92%) in patients with metastatic NSGCT.
引言/方法:约30%的睾丸非精原细胞瘤(NSGCT)患者初诊时即有转移性疾病。1997年,国际生殖细胞癌协作组(IGCCCG)根据血清肿瘤标志物和内脏疾病情况,将所有转移性NSGCT患者分为不同风险组。我们回顾文献,介绍低危转移性NSGCT患者基于分期的最佳治疗策略。
对于临床分期IS(cIS)患者以及有大块转移性疾病(≥临床分期IIb)的患者,由于其发生全身疾病和复发的风险高,原发性化疗(3周期BEP或4周期EP)已被证明是首选治疗方式。对于直径<2 cm的腹膜后疾病(临床分期IIa),原发性腹膜后淋巴结清扫术似乎是最有效的初始治疗方法,辅助化疗适用于病理分期较晚(受累淋巴结>5个,单个淋巴结>2 cm)以及不遵守监测方案的患者。原发性化疗后,采用血清肿瘤标志物(STM)和影像学评估来评估治疗反应。对于STM恢复正常且腹膜后肿块<1 cm的患者,可考虑腹膜后淋巴结清扫术或在疾病进展时进行观察并给予治疗。由于存在畸胎瘤或化疗耐药性生殖细胞肿瘤的风险,对于直径>1 cm的肿块和腹膜后以外的肿块,应进行手术切除,如有可能应行保留神经的手术。
对于基于IGCCCG标准属于低危疾病的患者,根据临床分期、STM和影像学评估来指导恰当的治疗,可使转移性NSGCT患者获得优异的长期治愈率(>92%)。