Aldinger K A, Samaan N A, Ibanez M, Hill C S
Cancer. 1978 Jun;41(6):2267-75. doi: 10.1002/1097-0142(197806)41:6<2267::aid-cncr2820410627>3.0.co;2-7.
Eighty-four cases of spindle and giant cell carcinoma of the thyroid were reviewed. This is a swiftly growing, and rapidly fatal neoplasm that generally develops in the elderly. Treatment of this disease was generally unsuccessful with a 7.1% five-year survival rate and a mean survival period of 6.2 months from the time of tissue diagnosis. In the majority of cases, areas of well-differentiated thyroid carcinoma could be identified, supporting the concept that spindle and giant cell carcinoma results from the transformation of preexisting well-differentiated thyroid carcinoma. Because of the aggressive biologic activity of this neoplasm, we treat all cases as disseminated disease at the time of presentation. Our best therapeutic results have been obtained with a combination of surgery, irradiation, and chemotherapy; however, these results still leave much to be desired. Patients with only small foci of spindle and giant cell carcinoma, at the time of diagnosis, may have a better chance of prolonged survival.
对84例甲状腺梭形细胞癌和巨细胞癌进行了回顾性研究。这是一种生长迅速、预后凶险的肿瘤,多见于老年人。该疾病的治疗通常效果不佳,五年生存率为7.1%,自组织诊断起平均生存期为6.2个月。在大多数病例中,可以识别出高分化甲状腺癌区域,这支持了梭形细胞癌和巨细胞癌由先前存在的高分化甲状腺癌转变而来的观点。由于这种肿瘤具有侵袭性生物学活性,我们在就诊时将所有病例视为播散性疾病。我们通过手术、放疗和化疗联合治疗取得了最佳治疗效果;然而,这些结果仍不尽人意。诊断时仅有小灶性梭形细胞癌和巨细胞癌的患者可能有更好的延长生存期的机会。