Ben-Arush M, Kuten A, Perez-Nahum M, Cohen Y, Bialik V
Pediatric Oncology Unit, Northern Israel Oncology Center, Israel.
J Surg Oncol. 1991 Sep;48(1):51-5. doi: 10.1002/jso.2930480110.
A retrospective analysis was performed of 20 patients with Ewing's sarcoma treated by combined modality therapy, consisting of surgery, radiotherapy, and chemotherapy. Fourteen patients (70%) achieved complete remission and 5 patients (25%) were in partial remission at the end of treatment. One patient (5%) failed to respond to combined modality therapy. The overall 5 year actuarial survival was 64% and the disease free survival, 55%. Persistent or recurrent disease occurred in 8 patients (40%); one of them was salvaged by surgery and chemotherapy. Site and extent of primary lesion were prognosticators of patients' outcome. One patient developed radiation-related-sequelae. The efficacy of aggressive management consisting of wide surgery, radiotherapy and intermittent high dose chemotherapy is discussed.
对20例采用手术、放疗和化疗联合治疗的尤因肉瘤患者进行了回顾性分析。14例患者(70%)达到完全缓解,5例患者(25%)在治疗结束时部分缓解。1例患者(5%)对联合治疗无反应。5年总精算生存率为64%,无病生存率为55%。8例患者(40%)出现持续性或复发性疾病;其中1例通过手术和化疗挽救。原发病变的部位和范围是患者预后的预测因素。1例患者出现放疗相关后遗症。讨论了包括广泛手术、放疗和间歇性高剂量化疗在内的积极治疗方法的疗效。