Eilber F C, Rosen G, Eckardt J, Forscher C, Nelson S D, Selch M, Dorey F, Eilber F R
Division of Surgical Oncology, University of California Los Angeles Sarcoma Research Group, University of California Los Angeles, Los Angeles, CA, USA.
J Clin Oncol. 2001 Jul 1;19(13):3203-9. doi: 10.1200/JCO.2001.19.13.3203.
To determine whether treatment-induced pathologic necrosis correlates with local recurrence and overall survival in patients who receive neoadjuvant therapy for high-grade extremity soft tissue sarcomas.
Four hundred ninety-six patients with intermediate- to high-grade extremity soft tissue sarcomas received protocol neoadjuvant therapy. All patients underwent surgical resection after neoadjuvant therapy and had pathologic assessment of tumor necrosis in the resected specimens.
The 5- and 10-year local recurrence rates for patients with > or = 95% pathologic necrosis were significantly lower (6% and 11%, respectively) than the local recurrence rates for patients with less than 95% pathologic necrosis (17% and 23%, respectively). The 5- and 10-year survival rates for the patients with > or = 95% pathologic necrosis were significantly higher (80% and 71%, respectively) than the survival rates for the patients with less than 95% pathologic necrosis (62% and 55%, respectively). Patients with less than 95% pathologic necrosis were 2.51 times more likely to develop a local recurrence and 1.86 times more likely to die of their disease as compared with patients with > or = 95% pathologic necrosis. The percentage of patients who achieved > or /= 95% pathologic necrosis increased to 48% with the addition of ifosfamide as compared with 13% of the patients in all the other protocols combined.
Treatment-induced pathologic necrosis is an independent predictor of both local recurrence and overall survival in patients who receive neoadjuvant therapy for high-grade extremity soft tissue sarcomas. A complete pathologic response (> or = 95% pathologic necrosis) correlated with a significantly lower rate of local recurrence and improved overall survival.
确定接受新辅助治疗的高级别肢体软组织肉瘤患者中,治疗诱导的病理坏死与局部复发及总生存之间是否相关。
496例中高级别肢体软组织肉瘤患者接受了方案规定的新辅助治疗。所有患者在新辅助治疗后均接受了手术切除,并对切除标本进行了肿瘤坏死的病理评估。
病理坏死≥95%的患者5年和10年局部复发率显著低于病理坏死<95%的患者(分别为6%和11%与17%和23%)。病理坏死≥95%的患者5年和10年生存率显著高于病理坏死<95%的患者(分别为80%和71%与62%和55%)。与病理坏死≥95%的患者相比,病理坏死<95%的患者发生局部复发的可能性高2.51倍,死于疾病的可能性高1.86倍。与所有其他方案联合治疗的患者中13%相比,添加异环磷酰胺后病理坏死≥95%的患者比例增至48%。
治疗诱导的病理坏死是接受新辅助治疗的高级别肢体软组织肉瘤患者局部复发和总生存的独立预测因素。完全病理缓解(病理坏死≥95%)与显著更低的局部复发率及改善的总生存相关。