The role of omental biopsy in endometrial cancer staging
© Springer-Verlag 2009
Received: 31 January 2009
Accepted: 27 February 2009
Published: 19 March 2009
Omental biopsy is not part of FIGO staging for endometrial cancer. The few studies that have looked into this matter have had conflicting results. This is the largest study in terms of the number of cases studying the incidence of omental involvement in endometrioid and non-endometrioid endometrial cancer. A retrospective study assessing 248 cases of endometrial cancer with omental biopsy at the time of primary surgical treatment for endometrial cancer at the Gynaecological Oncology Centre, Norfolk and Norwich University Hospital between January 2004 and May 2008. Demographic, clinico-pathologic and surveillance data were collected from hospital records, operative notes and histopathology results. The histology included tumour type, stage, grade and omental biopsy. All histological types were included in the study. Two hundred and forty eight patients had an omental biopsy at the time of primary surgical treatment for endometrial cancer during the study period. Of them, 187 cases were stage I, 27 stage II, 27 stage III and seven stage IV. According to histological type, 202 (81.4%) had endometrioid, 20 (8.0%) serous papillary, 20 (8.0%) malignant mixed Mullerian tumour (MMMT), three (1.2%) clear cell and three (1.2%) sarcoma. Overall, six cases (2.4%) had omental involvement, 4/202 (1.98%) with endometrioid type, 1/20 (5.0%) with serous papillary type and 1/20 (5.0%) MMMT. Eighty four percent of omental metastases (five cases) were macroscopic and noted at operation .The overall risk of omental metastases is 2.4% and in the absence of gross lesions the risk is around 0.4%. Most omental metastases can be diagnosed by careful inspection and palpation of the omentum. The possibility of missing microscopic disease is low. Based on these figures and possible increase in morbidity and operative time, omental biopsy cannot be justified as a standard procedure in endometrial cancer staging.
Uterine cancer is the second most common gynaecological malignancy and the fifth most common cancer in women in the UK with around 6,400 cases diagnosed each year . Seventy five percent of patients survive for 5 years, the majority is diagnosed in an early stage and most present with postmenopausal bleeding. Worldwide, the number of deaths from endometrial cancer has increased significantly since 1987 . Endometrial cancer metastasizes by direct spread into the myometrium, extending to the cervix , haematogenous dissemination, lymphatic embolisation and peritoneal seeding . Endometrial cancer can metastasize to the omentum through peritoneal seeding by-passing the myometrium and regional lymphatics.
FIGO adopted surgico-pathologic staging for endometrial cancer in 1988. The standard staging involves total abdominal hysterectomy and bilateral salpingo-oophorectomy, evaluation of pelvic and para-aortic lymph nodes, peritoneal washings, palpation and inspection of the abdominal organs in attempt to identify extrauterine spread . Omental biopsy is not part of FIGO staging for endometrial cancer.
In the UK, lymphadenectomy is not done in all cases of endometrial cancer and the role of lymphadenectomy remains debatable. We thought omental biopsy may improve staging; detection of occult omental metastases will upstage the cancer to stage IVb.
Previous studies including by one of the current authors had suggested that the omentum might be involved in up to 10% of the cases [6–10]. Gehrig et al.  suggested that most omental metastases can be diagnosed by gross visualisation of the omentum. The sensitivity of a visually negative omentum is 0.89. It remains uncertain whether omental biopsy should be part of routine staging of endometrial cancer. So far, few studies have looked into this and have had conflicting results. Up to date, this is the largest study in terms of the number of cases studying the incidence of omental involvement in endometrioid and non-endometrioid endometrial cancer.
Materials and methods
A retrospective study assessing 248 cases of endometrial cancer having omental biopsy at the time of primary surgical treatment for endometrial cancer at the Gynaecological Oncology Centre, Norfolk and Norwich University Hospital between January 2004 and May 2008 was conducted. Demographic, clinico-pathologic and surveillance data were collected from hospital records, operative notes and histopathology results. The histology included tumour type, stage, grade and omental biopsy. All histological types were included in the study.
The omentum was inspected and infracolic omentectomy was performed in the presence of gross lesions. Otherwise, a representative sample of the omentum was obtained. The relationship between grade, depth of myometrial invasion, histological type, peritoneal cytology and omental metastases was assessed.
Patients who had an omental biopsy at the time of surgical staging for endometrial cancer
Moreover, 202 (81.4%) had endometrioid, 20 (8.1%) serous papillary, 20 (8.1%) MMMT, three (1.2%) clear cell and three (1.2%) sarcoma.
Clinical features of six patients with omental involvement
Follow-up (month) to June 08
A discrepancy between clinical and surgical staging has been reported earlier . Recent data suggested adding omentectomy as part of surgical staging. In some cases, appendicectomy has also been suggested . However, the role of omental biopsy in surgical staging for endometrial cancer is unclear; although the procedure is simple and associated with minimal morbidity, it has an effect on the cost and overall length of the operation.
Recent studies looking at omental biopsy in endometrial cancer
Chen SS  found that, in the absence of gross omental lesions, microscopic omental metastases were found in 1.5% of cases. In our study, microscopic omental metastases were (1/248) 0.4%.
The overall risk of omental metastasis is low (2.4%). However, metastatic omental lesions will upstage endometrial cancer to stage IVb; post-operative radiotherapy is not indicated as the disease already spread outside the pelvis. Randomised controlled trials are needed to decide on the best management for these patients, prognosis being poor. Peritoneal washings as expected were found to be positive in most cases with omental metastases.
In half of the patients with omental disease, the adnexa were free of disease and this seems to be associated with a better prognosis.
Most omental metastases can be diagnosed by careful inspection and palpation of the omentum and the possibility of missing microscopic disease is around 0.4%. Based on these figures and possible increased in morbidity and operative time, omental biopsy cannot be justified as a standard procedure in endometrial cancer staging. However, the importance of careful inspection and biopsy of suspicious lesions cannot be overemphasised.
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