Purpose: Soft tissue sarcoma (STS) encompasses a group of neoplasms that ar
e anatomically and biologically diverse. Retroperitoneal/visceral (RP/V) tu
mors have a poorer prognosis than extremity/trunk (E/T) lesions, and this h
as been attributed to frequent presentation with tumors Of large size and m
ultiorgan involvement that precludes complete resection. The worse prognosi
s that is associated with RP/V tumors has also been thought to be histopath
ologically dependent and not necessarily related to anatomic site. The aim
of this study was to determine the role of anatomic site and biologic featu
res in prognosis and outcome in patients after complete resection by examin
ing a large cohort of STS patients with a single histopathology, ie, liposa
rcoma.
Methods: All patients who were treated for liposarcoma from July 1, 1982, t
hrough July 1, 1998, were included, Univariate analyses were performed usin
g log-rank test and Kaplan-Meier estimates, and multivariate analyses were
performed using Cox regression. The three end points examined were local re
currence (LR), distant recurrence, and disease-specific survival [DSS].
Results: Seven hundred twenty patients with liposarcoma were evaluated, and
of these, 460 had completely resected primary or completely resected local
ly recurrent disease. Breakdown of anatomic site was 65% E/T (n = 301)and 3
5% RP/V (n = 159). The median follow-up period for patients who underwent c
omplete resection was 42 months (range, 1 to 194 months). We found that RP/
V site is a poor prognosticator that is independent of patient sex and age;
tumor size, grade, and margin; and recurrent presentation. Sixty-nine perc
ent of patients with RP/V tumors who died had local disease only and no dis
tant metastasis at the time of death.
Conclusion: In liposarcoma, tumor location exerts as strong an influence on
prognosis as biology. In contrast to extremity liposarcoma, LR without dis
tant metastasis often results in death for patients with RP/V tumors. For t
hese patients, local control accomplished by complete surgical resection +/
- adjuvant radiation therapy should impact strongly on DSS.
J Clin Oncol 18:1637-1643. (C) 2000 by American Society of Clinical Oncolog
y.