High-risk surgical stage 1 endometrial cancer: analysis of treatment outcome
© Viani et al; licensee BioMed Central Ltd. 2006
Received: 03 June 2006
Accepted: 03 August 2006
Published: 03 August 2006
To report the relapse and survival rates associated to treatment for patients with stage IC, grade 2 or grade 3 and IB grade 3 diseases considered high risk patients group for relapse.
Materials and methods
From January 1993 to December 2003, 106 patients with endometrial cancer stage I were managed surgically in our institution. Based on data from the medical records, 106 patients with epithelial endometrial cancer met the following inclusion criteria: stage IC grade 2 or 3 and IB grade 3 with or without lymphovascular invasion. Staging was defined according to the FIGO surgical staging system. Postoperative adjuvant radiotherapy consisted of external beam pelvic radiation, vaginal brachytherapy alone or both. The median age was 65 years (range, 32–83 years), lymph node dissection was performed in 45 patients (42.5%) and 14 patients (13.2%) received vaginal brachytherapy only, and 92 (86.8%) received combined vaginal brachytherapy and external beam radiotherapy. The median dose of external beam radiotherapy administered to the pelvis was 4500 cGy (range 4000 – 5040). The median dose to vaginal surface was 2400 cGy (range 2000 – 3000). Predominant pathological stage and histological grade were IC (73.6%) and grade 3 (51.9%). The lymphovascular invasion was present in 33 patients (31.1%) and pathological stage IC grade 2 was most common (48. 1%) combination of risk factors in this group.
With a follow up median of 58.3 months (range 12.8 – 154), five year overall survival and event free survival were 78.5% and 72.4%, respectively. Locoregional control in five year was 92.4%. Prognostic factors related with survival in univariate analyses were: lymphadenectomy (p = 0.045), lymphovascular invasion (p = 0.047) and initial failure site (p < 0.0001). In multivariate analyses the initial failure in distant sites (p < 0.0001) was the only factor associated with poor survival. Acute and chronic gastrointestinal and genitourinary toxicity grades 3 were not observed.
In conclusion, our results showed that the stage IC, grade 2, 3 and IB grade 3 endometrial cancer was associated with significantly increased risk of distant relapse and endometrial carcinoma-related death independently of salvage treatment modality.
Patients with stage I endometrial carcinoma, treated with total abdominal hysterectomy and bilateral salpingo-oophorectomy (TAH-BSO) and postoperative radiotherapy (RT) tailored to prognostic factors, have 5-year overall survival rates of 80% to 90%, 5-year cancer-specific survival of 90% to 95%, and locoregional recurrence rates of 4% to 8%. [1–8] However, the subgroup of patients with grade 3 tumors with deep (50% or more) myometrial invasion (stage IC, grade 3) has been reported to have a considerably higher risk of both locoregional and distant relapse. The Gynecological Oncology Group (GOG) staging study  showed the risk of microscopic pelvic node metastases for patients with clinical stage I endometrial carcinoma to be below 10%, except for those with outer 33% myometrial invasion, for whom the risk amounted to 18%. When designing the multicenter randomized Postoperative Radiation Therapy in Endometrial Carcinoma (PORTEC) trial for stage I endometrial carcinoma,  it was decided to exclude the subgroup of patients with grade 3 tumors with outer 50% myometrial invasion from random assignment in view of the reported higher relapse rates and because a survival benefit with pelvic RT had been suggested. In the Aalders et al.  study, a subgroup analysis in patients with deep myometrial invasion revealed that the rate of pelvic relapse was lower in the radiotherapy treated both grade 3 disease and deep invasion, a 10% decreased in the cancer death rate was seen with the addition of pelvic radiotherapy, and the pelvic relapse rate was lower, at 4.5% versus 20%. This series was done to report the relapse and survival rates for patients with stage IC, grade 2 or grade 3 and IB grade 3 disease with endometrial cancer considered high risk patients group for relapse. The secondary objective was to analyze the impact in survival of initial failure sites.
Patients and methods
From January 1993 to December 2003, 250 patients with endometrial cancer stage I were managed surgically at Hospital do cancer (Sao Paulo, Brazil). Based on data from the medical records, 106 patients with epithelial endometrial cancer met the following inclusion criteria: (1) total hysterectomy and removal of existing adnexal structures with or without additional surgical staging procedures for endometrial cancer, (2) stage IC grade 2 or 3 and IB grade 3 with or without lymphovascular invasion and (3) no other malignancy diagnosed within 5 years before or after the diagnosis of endometrial cancer (except for carcinoma in situ or skin cancer other than melanoma). Staging was defined according to the International Federation of Gynecology and Obstetrics (FIGO-1992) surgical staging system. Postoperative adjuvant radiotherapy consisted of external beam pelvic radiation or vaginal brachytherapy or both. The interval time between surgery and radiotherapy treatment did not exceeded 4 weeks. The decision to deliver adjuvant radiotherapy depended predominantly on the assessment by gynecologic oncologists and radiation oncologists of the risks of local or regional both recurrence after pathologic evaluation of the surgical specimen. This decision usually was dictated by presence of grade 3 differentiation, nonendometrioid histological subtype, or deep myometrial invasion, or a combination of these pathologic features. The most part of patients were treated with pelvic "box technique" for a dose of 45 Gy in 5 weeks, with daily fractions of 1.8 Gy. Radiation was initiated no later than 8 weeks after surgery via cobalt60 teletherapy or linear accelerator with energy of 4 MeV or greater. Pelvic radiotherapy fields were standard with an upper border of L5-S1, while the inferior border was at the mid-portion of the obturator foramen. The lateral borders were set at 1 cm beyond the lateral margins of the bony pelvic wall at the widest plane of the pelvis. Lateral field borders were the posterior border of the S3 vertebral body and the anterior border of the symphysis pubis. Beam arrangement was 4-field. During irradiation patients were checked weekly with X-ray portal of control. Following pelvic radiation, the hypofractionated high dose rate vaginal vault brachytherapy was delivered postoperatively. All the patients completed the treatment in 8 weeks after the initial date of pelvic radiation. Under sterile conditions, a Foley catheter was placed. The simulation treatment planning process initially included placement of an auto-suture radio-opaque clip at the vaginal apex. The largest possible diameter of the vaginal cylinder was selected for treatment to decrease the vaginal mucosa dose and improve depth dose. Dummy sources were placed in the vaginal applicator during simulation and subsequently prior to each treatment for appropriate placement under fluoroscopic guidance. The position of the vaginal applicator was documented on ventrodorsal and lateral X-ray prior to every treatment. The intracavitary treatment radiation was delivered in four high dose rate applications with a median dose of 24 Gy (range 20–30 Gy). The point of prescription dose used in the vaginal brachytherapy was the vaginal surface or to 5 mm of the surface of applicator when vaginal brachytherapy was used alone. During irradiation patients were checked weekly for adverse treatment-related effects and post treatment during follow up time. Patients who experience acute gastrointestinal (frequency, diarrhea), genitourinary (frequency, dysuria), and chronic gastrointestinal (rectite, obstruction), genitourinary (hematuria, disury) classified according to RTOG criteria were registered.
After treatment, patients were followed every 4 months for 2 years and then every 6 months for 1 year and then yearly. Pap smear and chest radiographs were performed yearly. History and physical examination, Karnofsky performance status (KPS), and documentation of major symptoms or adverse effects were performed at every visit. Blood work with count blood cells (CBC), platelets, liver enzyme tests, and creatinine as well as pap smears and chest X-rays were assessed when necessary. If sufficient follow-up information about survival and recurrence was not available in the clinical records, death certificates were obtained and letters were sent or telephone calls were made to patients and family physicians to obtain the information.
The primary purpose of study was report the locoregional failure, distant failure, event free survival, overall survival rates associated with treatment. Local failure was defined as recurrence with the area of the pelvis and vaginal cuff encompassed by the pelvic radiation field. Distance failure refers to recurrence in distance sites outside the treated area. The patients were followed after relapses and probability of death was calculated of according with primary relapse site and salvage treatment modality.
Patterns of recurrence were primary endpoints in this study, pelvic failure, locoregional failure, and distant metastases failure rates were estimated using the cumulative incidence method. Absolute survival and disease-free survival rates were estimated using the Kaplan-Meier method. The covariates examined in all cases for survival were: age, lymphovascular invasion, lymphadenectomy, initial site of relapse, pathological stage, histological grade, combination of pathological and histological grade, pelvic radiotherapy and salvage treatment. The time point for survival analyses was from the end date of the radiotherapy treatment. The log rank test was applied using the intent-to-treat analysis of all eligible patients to evaluate differences between regimens with respect to event free survival (EFS), Local control (LC) and overall Survival (OS). All factors with a P-value ≤ 0.05 at univariate analysis were entered into a multivariate analysis using the proportional hazards model (Cox Regression) with confidential interval of 99%. The hazard function survival (Kaplan Meier method) was used to estimate the probability to death of according with initial failure site in the period of follow up. The Fisher test was used to identify an association between endometrial cancer mortality and relapse, differences were considered statistically significant at P < 0.05.
Characteristics of patients
Characteristic of patients and treatment
Stage – IB
Stage – IC
Grade and Pathological stage
RT + VB
Radiotherapy dose Gy
40 – 50.4
20 – 30
Overall survival, event free survival and local control in five and ten year
Univariate analysis to prognostic factors associates with OS in 5 years
Five years OS
55 – 51.8
12 – 80.4
51 – 48.2
14 – 76.8
Stage – IB
28 – 26.4
5 – 82
Stage – IC
78 – 73.6
25 – 7 7
51 – 48.1
12 – 84
55 – 51.9
14 – 73.7
Grade and Pathological stage
28 – 26.4
5 – 82.3
51 – 48.1
12 – 83.9
27 – 25.5
9 – 64.7
First failure site
76 – 71.6
6 – 94.5
8 – 4.7
3 – 75.5
22 – 20.7
17 – 39
Radiotherapy or surgery
13 – 12.2
5 – 77.4
17 – 16.6
15 – 26.1
61 – 37.5
6 – 88.7
45 – 42.5
20 – 71,6
73 – 68.9
13 – 71.2
33 – 31.1
13 – 82.2
Outcome by initial failure site and cause of death for patients with or without relapse.
Initial failure site
Multivariate analyses of significant factors for survival (Cox Regression)
99% confidential interval
No or Local distance
All of the prospective studies made attempts to identify subgroups of patients at higher risk for recurrence. In the GOG study , a "high intermediate" group was defined by a combination of risk factors that included advanced age, lymphovascular invasion, outer-third invasion, and moderate to high tumor grade. As the first site of failure, the control arm of the low intermediate risk group (which comprised approximately two thirds of the patients) had an observed failure rate of 5%, while the higher risk group had a 13% risk for local-regional failure. The high intermediate risk patients were also at risk for failing distantly, with a 48-month observed distant failure rate of 19% in the control arm. The PORTEC trial  identified high-risk patients included patients older than 60, patients with stage IC, grade 1 or 2 tumors, and patients with stage IB, grade 3 tumors. This group of patients had a 5-year local-regional relapse rate of 19%, with the majority of relapses occurring in the vagina.
This analysis was done to investigate whether stage IC, grade 2 or grade 3 and IB grade 3 endometrial carcinoma should be considered a separate entity from the other prognostic subgroups of stage I endometrial carcinoma. The others objectives this study was report the relapses rate post radiotherapy and evaluate the impact of the initial failure site in patients survival. In the GOG 99 trial , patients with stage I to II endometrial cancer were randomly assigned after TAH-BSO with lymphadenectomy to receive pelvic RT or no further treatment. Interestingly, the results are strikingly similar to those obtained in the PORTEC study : 88% 2-year relapse-free survival in the control group (17 locoregional recurrences in 200 patients) and 96% 2-year relapse-free survival in the RT group (three recurrences in 190 patients), with mainly vaginal recurrences in the control group.
There are limited data regarding outcome of surgically staged stage IC patients treated with observation alone for survival. Straughn et al.  reported the largest series (121 patients) treated with full surgical staging and no adjuvant radiotherapy; there was a 12% overall failure rate with 6% of patients failing locally; again, the vast majority of these local-regional failures were in the vagina and any benefit to survival was not showed.
Pelvic RT is generally recommended for grade 3 tumors with deep myometrial invasion. [13–16] In their review of radiation therapy for endometrial cancer, Koh et al strongly recommend pelvic RT for surgically staged IC, grade 3 cancer, and suggest that RT be considered for grade 2 with outer 33% myometrial invasion. In a survey performed after the first results of GOG 99 had been reported, it was found that most GOG members (79%) would still recommended pelvic RT for stage IC, grade 3 disease.
In our data pelvic lymphadenectomy was associated with better survival (p = 0.04) and was not related with any benefit to EFS and LC. This fact, in our study may be associated with reduced number of patients in the sample, compared to other studies, and the majority of patients was not submitted for pelvic lymphadenectomy (57. 5%).
The original GOG surgical-pathologic study found that lymphovascular invasion placed patients at high risk for lymph node metastases. Other investigators have confirmed this , and the risk for lymph node disease with lymphavascular invasion ranges from 20%–50% . In our data, lymphavascular invasion was associated with poor overall survival rate in five year (81.1% vs. 52.8%, p = 0.043). Due to this, our data suggest that patients managed surgically without lymphadenectomy should be treated with pelvic radiotherapy in the presence of lymphovascular invasion, regardless of other risk factors.
Acute and chronic toxicities according to RTOG.
Radiotherapy treatment (%)
Genitourinary ( disury , frequency )
Gastrointestinal ( diarrheia , nausea )
Radiotherapy treatment (%)
Genitourinary ( disury , hematuria )
Gastrointestinal ( obstruction , rectite )
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