Wolfson A H, Sightler S E, Markoe A M, Schwade J G, Averette H E, Ganjei P, Hilsenbeck S G
Department of Radiation Oncology, University of Miami School of Medicine, Florida 33101.
Gynecol Oncol. 1992 May;45(2):142-6. doi: 10.1016/0090-8258(92)90276-o.
This study is based on a retrospective review of 156 patients with endometrial carcinoma from 1978 through 1984 who underwent primary surgical evaluation. All cases were retrospectively restaged using the newly adopted FIGO surgical staging. The preoperative FIGO clinical stage distribution for this study was as follows: 121 (77.6%) Stage I, 22 (14.1%) Stage II, 5 (3.2%) Stage III, 2 (1.3%) Stage IV, and 6 (3.8%) unstaged patients. Most patients had TAH-BSO with a collection of peritoneal washings and retroperitoneal lymph node sampling. Surgical staging revealed 122 (78.2%) Stage I, 9 (5.8%) Stage II, 12 (7.7%) Stage III, and 13 (8.3%) Stage IV patients. Surgery upstaged 12.4% of clinical Stage I. In clinical stage II, 59.0% were downstaged while 27.3% were upstaged. For clinical Stage III, 60.6% were upstaged, but no downstaging occurred. No change in stage occurred for clinical Stage IV patients. Ninety-seven surgically staged patients received no adjuvant therapy. The remaining 59 patients had adjunctive treatment which consisted of radiotherapy (59.3%), hormonal therapy (25.4%), chemotherapy (5.1%), or combined modality treatment (10.2%). All patients were followed until death or a minimum of 5 years (60-139 months; median, 82 months) with the exception of 13 patients who were lost to follow-up (2-58 months; median, 34 months). Five-year survival by clinical staging was as follows: 86.2% for Stage I, 85.9% for Stage II, and 0% for Stage III and IV. Five-year survival by surgical staging was 90.6% for Stage I, 85.7% for Stage II, 58.3% for Stage III, and 0% for Stage IV. The 13 patients who were lost to follow-up were censored in all survival analyses at the time of last contact. Stepwise regression analysis using a parametric proportional hazards model identified surgical stage as the most significant prognostic factor (P = 0.02). Univariate analysis showed that patients with surgical Stage IC had significantly worse prognosis (75.0%, 5 years) than those in surgical Stage IA (93.8% 5 YS) or IB (95.4% 5 years). In summary, this study demonstrates that surgical staging as recommended by FIGO is indicated to accurately determine the initial extent of disease in endometrial carcinoma. In addition, surgical staging is the strongest predictor of survival. Deep myometrial invasion appears to be a significant independent prognostic factor within surgical Stage I. The role of adjunctive radiotherapy in Stage I disease awaits the results from an ongoing multi-institutional, prospectively randomized trial.
本研究基于对1978年至1984年间接受初次手术评估的156例子宫内膜癌患者的回顾性分析。所有病例均采用新采用的国际妇产科联盟(FIGO)手术分期系统进行回顾性重新分期。本研究术前FIGO临床分期分布如下:I期121例(77.6%),II期22例(14.1%),III期5例(3.2%),IV期2例(1.3%),未分期患者6例(3.8%)。大多数患者接受了全子宫双附件切除术,并收集了腹腔冲洗液和进行了腹膜后淋巴结取样。手术分期显示I期患者122例(78.2%),II期9例(5.8%),III期12例(7.7%),IV期13例(8.3%)。手术使12.4%的临床I期患者分期上升。在临床II期,59.0%的患者分期下降,而27.3%的患者分期上升。对于临床III期,60.6%的患者分期上升,但没有患者分期下降。临床IV期患者分期无变化。97例经手术分期的患者未接受辅助治疗。其余59例患者接受了辅助治疗,包括放疗(59.3%)、激素治疗(25.4%)、化疗(5.1%)或综合治疗(10.2%)。除13例失访患者(随访时间2 - 58个月;中位数34个月)外,所有患者均随访至死亡或至少5年(60 - 139个月;中位数82个月)。按临床分期的5年生存率如下:I期为86.2%,II期为85.