Lieberman P H, Brennan M F, Kimmel M, Erlandson R A, Garin-Chesa P, Flehinger B Y
Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York.
Cancer. 1989 Jan 1;63(1):1-13. doi: 10.1002/1097-0142(19890101)63:1<1::aid-cncr2820630102>3.0.co;2-e.
In the period from 1923 to 1986 our pathologists examined pathologic material from 102 patients with alveolar soft-part sarcoma (ASPS). Followup clinical data is available for 91. Median followup is 7 years (range 1 month to 27 years). Local recurrence was only found if residual disease was left at the time of the original excision. Survival in those patients who presented without metastases was 77% at 2 years, 60% at 5 years, 38% at 10 years and 15% at 20 years (median 6 years). No survival advantage could be demonstrated for patients who received chemo and/or radiotherapy, although numbers are small and staging not uniform. An evaluation by electron microscopy and immunohistochemistry cannot confirm recent claims that ASPS is a muscle tumor. ASPS is an unusual neoplasm; the primary therapeutic option is aggressive surgical excision. Survival even with the development of metastases can be long.
在1923年至1986年期间,我们的病理学家检查了102例肺泡软组织肉瘤(ASPS)患者的病理材料。91例患者有随访临床数据。中位随访时间为7年(范围1个月至27年)。仅在初次切除时残留疾病的情况下才发现局部复发。无转移患者的2年生存率为77%,5年生存率为60%,10年生存率为38%,20年生存率为15%(中位生存时间6年)。尽管病例数少且分期不统一,但接受化疗和/或放疗的患者未显示出生存优势。通过电子显微镜和免疫组织化学评估无法证实最近关于ASPS是一种肌肉肿瘤的说法。ASPS是一种不常见的肿瘤;主要的治疗选择是积极的手术切除。即使发生转移,生存期也可能很长。