Loehrer P J, Mandelbaum I, Hui S, Clark S, Einhorn L H, Williams S D, Donohue J P
J Thorac Cardiovasc Surg. 1986 Oct;92(4):676-83.
Fifty-one patients with primary testicular (N = 46) or mediastinal germ cell cancer (N = 5) were treated from April, 1975, through May, 1981, and had teratoma resected from residual disease after cisplatin-based combination chemotherapy. All patients had normal serum markers before resection of pulmonary (N = 12), mediastinal (N = 5), thoracoabdominal (N = 8), supraclavicular (N = 1) or abdominal disease (N = 25). Teratoma was classified as mature teratoma (N = 29), immature teratoma (N = 15), or immature teratoma with non-germ cell elements (N = 7). Thirty of 51 (60%) patients remain free of recurrent disease, whereas 20 patients have either recurrent carcinoma (N = 10) or teratoma (N = 10). One patient has a presumed second malignancy. After additional chemotherapy, four patients with recurrent carcinoma are alive and disease free and six have died. After an additional operation, eight of 10 patients with recurrent teratoma are long-term survivors. In four patients the initial relapse of carcinoma developed more than 2 years after therapy; in an additional patient carcinoma recurred after a 32 month disease-free survival period. Univariate factors predicting for relapse include tumor burden, immature teratoma with non-germ cell elements, and site (mediastinum), whereas only immature teratoma with non-germ cell elements and site predicted for survival. Immature teratoma and mature teratoma had similar relapse-free intervals and overall survival intervals. According to a multivariate analysis, primary tumor site at the mediastinum is the most significant adverse factor predictive for both relapse and survival (two of five patients survived). This study appears to support the various preclinical models that demonstrate multipotential capabilities of teratoma. Complete surgical excision of teratoma remains the most effective treatment with continued close follow-up recommended for high-risk patients (immature teratoma with non-germ cell elements, large tumor burden, or primary mediastinal tumors.
1975年4月至1981年5月期间,对51例原发性睾丸(n = 46)或纵隔生殖细胞癌(n = 5)患者进行了治疗,这些患者在基于顺铂的联合化疗后,从残留病灶中切除了畸胎瘤。所有患者在切除肺部(n = 12)、纵隔(n = 5)、胸腹(n = 8)、锁骨上(n = 1)或腹部疾病(n = 25)之前血清标志物均正常。畸胎瘤分为成熟畸胎瘤(n = 29)、未成熟畸胎瘤(n = 15)或伴有非生殖细胞成分的未成熟畸胎瘤(n = 7)。51例患者中有30例(60%)无疾病复发,而20例患者出现复发癌(n = 10)或畸胎瘤(n = 10)。1例患者疑似发生第二原发性恶性肿瘤。再次化疗后,4例复发癌患者存活且无疾病,6例死亡。再次手术后,10例复发畸胎瘤患者中有8例为长期幸存者。4例患者在治疗后2年多出现癌的初始复发;另有1例患者在无疾病生存期32个月后癌复发。预测复发的单因素包括肿瘤负荷、伴有非生殖细胞成分的未成熟畸胎瘤和部位(纵隔),而只有伴有非生殖细胞成分的未成熟畸胎瘤和部位可预测生存。未成熟畸胎瘤和成熟畸胎瘤的无复发生存期和总生存期相似。根据多因素分析,纵隔原发性肿瘤部位是预测复发和生存的最显著不利因素(5例患者中有2例存活)。本研究似乎支持各种临床前模型,这些模型证明了畸胎瘤的多潜能能力。畸胎瘤的完全手术切除仍然是最有效的治疗方法,建议对高危患者(伴有非生殖细胞成分的未成熟畸胎瘤、大肿瘤负荷或原发性纵隔肿瘤)进行持续密切随访。