Canter Robert J
Division of Surgical Oncology, Department of Surgery, UC Davis Comprehensive Cancer Center, Davis School of Medicine, University of California, Suite 3010, 4501 X Street, Sacramento, CA 95817, USA.
Surg Oncol Clin N Am. 2016 Oct;25(4):861-72. doi: 10.1016/j.soc.2016.05.013. Epub 2016 Aug 5.
Since preoperative chemotherapy has been clearly shown to improve outcomes for patients with Ewing sarcoma, rhabdomyosarcoma, and osteosarcoma, practitioners have attempted to extend the use of adjuvant/neoadjuvant chemotherapy to other types of adult soft tissue sarcoma. Given the high risk of distant recurrence and disease-specific death for patients with soft tissue sarcoma tumors larger than 10 cm, these patients should be considered candidates for neoadjuvant chemotherapy as well as investigational therapies. Yet, potential toxicity from cytotoxic chemotherapy is substantial, and there remains little consensus and wide variation regarding the indications for use of chemotherapy in the adjuvant/neoadjuvant setting.
由于术前化疗已明确显示可改善尤因肉瘤、横纹肌肉瘤和骨肉瘤患者的预后,从业者已尝试将辅助/新辅助化疗的应用扩展到其他类型的成人软组织肉瘤。鉴于肿瘤大于10厘米的软组织肉瘤患者远处复发和疾病特异性死亡风险高,这些患者应被视为新辅助化疗以及研究性治疗的候选者。然而,细胞毒性化疗的潜在毒性很大,在辅助/新辅助治疗中使用化疗的指征方面,仍然几乎没有共识,差异很大。