This study from the Gynecology Oncology Group investigated the use of postoperative whole abdominal radiation therapy in women with stage III and IV endometrial cancer. In the period between December 1986 and February 1994, 180 patients who met study criteria were enrolled in the study. Seventy-seven patients (mean age 63 years) had typical endometrial carcinoma (adenocarcinoma, endometrioid, glassy cell, mixed epithelial, adenosquamous, villoglandular, or undifferentiated) and 103 had papillary serous (median age 68.5 years) or clear cell carcinoma (median age 71 years) (P < .001 for age difference between typical and higher-risk tumors). Papillary serous tumors were more common in black women (78%) than in white women (53%), and grade 3 disease was more common in women with papillary serous/clear cell tumors (66%) than in those with typical endometrial cancer (44%). All patients underwent total abdominal hysterectomy, bilateral salpingo-oophorectomy, pelvic washings, and selective paraaortic and pelvic lymph node sampling. Radiation therapy was begun within 8 weeks of surgery and consisted of daily doses of 150 cGy to the whole abdomen for 20 days (total 3000 cGy) followed by 180 cGy per day to the pelvis for 11 treatments (total 1980 cGy). Women with positive paraaortic lymph nodes received a paraaortic boost totaling 1500 cGy. The frequency of gross disease and the extent and pattern of spread were similar in both groups except that metastases to the diaphragm were seen more frequently in women with papillary serous/clear cell disease (7.8%) than in those with typical disease (1.3%) (P = .05). Pelvic nodes and paraaortic nodes were positive in 45% and 39%, respectively, of patients with typical endometrial cancer and 51% and 31%, respectively, of patients with high-risk tumors. In this study, 22 patients (21%) had grade 3 or 4 hematologic toxicity associated with treatment. Nearly half of the participants (n = 78, 45%) had at least grade 2, and 11% (n = 20) had grade 3 gastrointestinal toxicity. Seven women developed severe gastrointestinal toxicity (grade 4), including 3 patients with no evidence of disease who died from complications of bowel obstruction. Two patients died from severe hemorrhages, one with a gastrointestinal bleeding 5 months after radiation and one who hemorrhaged after anticoagulation for deep venous thrombosis 60 days after surgery. Grade 3 or 4 hepatic toxicity was seen in 4 women (3%). Twelve patients (7%) experienced serious (grade 3 or 4) cardiovascular complications, including 4 pulmonary emboli and 2 instances of congestive heart failure. Sixty-five percent of patients with typical endometrial cancer and 67% of those with papillary serous/clear cell cancer had a recurrence of disease. Women with typical disease had recurrent disease diagnosed at various locations, but pelvis, abdomen, and lung were the most common (n = 7, 9, and 9, respectively). In the high-risk group, 21 of 69 recurrences were in the abdomen and 15 were in the lung. Among the 77 women with typical endometrial cancers, 58 had stage III disease and 19 had stage IV disease. Three-year survival rates for these patients were 34.5% and 21.1%, respectively. Seventy-five of the 103 participants with papillary serous/clear cell tumors were stage III and 28 were stage IV. Their 3-year survival rates were 48.1% and 10.7%, respectively. Overall survival rates were 31% for patients with typical endometrial cancers and 35% for patients with high-risk tumors. At 3 years, the disease-free survival rates for these groups were 29% and 27%, respectively.
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