Halperin E C, Friedman H S, Schold S C, Fuchs H E, Oakes W J, Hockenberger B, Burger P C
Department of Radiation Oncology, Duke University Medical Center, Durham, North Carolina 27710.
Surg Neurol. 1993 Oct;40(4):278-83. doi: 10.1016/0090-3019(93)90138-q.
Supratentorial embryonal neuroepithelial tumors are undifferentiated neoplasms. We have used this term in preference to the controversial classification primitive neuroectodermal tumors (PNET). These lesions in children are malignant neoplasms which are usually fatal within 2 years of diagnosis in spite of therapy with surgery, radiotherapy, and chemotherapy. We have adopted an aggressive approach to the treatment of these tumors with surgical resection, hyperfractionated craniospinal irradiation of 30.6-43.9 Gy followed by a tumor boost to a total dose of 50-63.7 Gy, and adjuvant chemotherapy with cyclophosphamide, vincristine, and cis-platinum. We have treated five children, aged 4-18 years, with this approach. In contrast to the results reported in the literature, four children are alive without evidence of tumor from 4.3 to 8.0 years following diagnosis. One has suffered a tumor relapse at 2.3 years following diagnosis but remains alive. The basis of our therapeutic strategy for childhood supratentorial embryonal neuroepithelial tumors and the implications of our clinical results are discussed.
幕上胚胎性神经上皮肿瘤是未分化肿瘤。我们更倾向于使用这个术语,而非存在争议的原始神经外胚层肿瘤(PNET)分类。儿童中的这些病变是恶性肿瘤,尽管接受了手术、放疗和化疗,通常在诊断后2年内致命。我们采用了积极的方法来治疗这些肿瘤,包括手术切除、30.6 - 43.9 Gy的超分割全脑全脊髓照射,随后对肿瘤进行加量照射,总剂量达50 - 63.7 Gy,以及使用环磷酰胺、长春新碱和顺铂进行辅助化疗。我们用这种方法治疗了5名年龄在4至18岁的儿童。与文献报道的结果不同,4名儿童在诊断后4.3至8.0年存活且无肿瘤迹象。1名儿童在诊断后2.3年肿瘤复发,但仍存活。本文讨论了我们针对儿童幕上胚胎性神经上皮肿瘤的治疗策略依据及临床结果的意义。