Hoekstra H J, Schraffordt Koops H, Molenaar W M, Oldhoff J
Division of Surgical Oncology, Groningen University Hospital, The Netherlands.
Cancer. 1987 Oct 15;60(8):1703-7. doi: 10.1002/1097-0142(19871015)60:8<1703::aid-cncr2820600802>3.0.co;2-j.
High-grade soft tissue sarcomas of the extremities continue to pose problems of local disease control and deaths from distant metastases. Between 1969 and 1976, eight patients with primary and six with recurrent high-grade soft tissue sarcomas of the extremities were treated by isolated regional perfusion with cytostatics and local excision. None received systemic adjuvant chemotherapy or external-beam radiotherapy. During the follow-up (median, 13 years) five patients (36%) developed distant metastases. One was cured after resection of a pulmonary metastasis. In one other patient (7%) recurrent local disease was diagnosed after 48 months; he was cured after resection of the local lesion followed by postoperative external beam radiotherapy. The actuarial 5-year and 10-year survival was 69%. Treatment caused no cardiovascular complications and there was no postoperative mortality.
肢体高级别软组织肉瘤在局部疾病控制以及远处转移导致的死亡方面仍然存在问题。1969年至1976年间,对8例原发性和6例复发性肢体高级别软组织肉瘤患者采用细胞抑制剂进行孤立区域灌注并联合局部切除治疗。无一例接受全身辅助化疗或外照射放疗。在随访期间(中位随访时间为13年),5例患者(36%)出现远处转移。1例患者在切除肺部转移灶后治愈。另有1例患者(7%)在48个月后被诊断为局部疾病复发;在切除局部病灶并术后进行外照射放疗后治愈。5年和10年精算生存率为69%。治疗未引起心血管并发症,也无术后死亡病例。