Adjuvant Radiotherapy Approach in Stage I High Risk and High-intermediate Risk Endometrioid-type Uterine Cancers TROD 04-005 Gynecological Tumors Subgroup Survey Study

Introduction

Methods

Study Variables
The independent variables of the study are questions containing socio-demographic data, and the dependent variables are the scenarios provided according to the risk classification.

Data Collection Method and Tools
In the study, the participants were asked 19 questions, six of which were about socio-demographic data. Apart from the socio-demographic data questions, the first two questions were about the guidelines/protocols used in making treatment decisions. The second one was about the prognostic factors that determine the adjuvant therapy decision in endometrial cancer in the literature. Questions 9-19 asked which adjuvant therapy option(s) would be preferred by the participants in scenarios with HIRG and HRG patients created according to the risk groups defined in the ESMO-ESGO-ESTRO 2016 guidelines. For each scenario example, the following choices were presented: (a) Observation, (b) vaginal brachytherapy (VB), (c) external radiotherapy (ERT), (d) ERT+VB, and (e) Other. Again, for each scenario, the participants were asked whether they would recommend staging surgery (SS) before an adjuvant therapy decision if SS had not been performed. Table 1 presents the survey questions. In addition, we also asked about participant preferences according to whether SS was performed or not when making a treatment decision.

Table 1: Survey questions

Statistical Analysis
Statistical analyzes were performed using SPSS version 17.0 software. The compliance of the variables to normal distribution was examined using analytical methods (Kolmogorov-Smirnov/Shapiro-Wilk tests). Descriptive analyzes were presented using mean ± standard deviation for normally distributed variables. Descriptive statistics were made by giving frequency and percentage values in categorical data. In continuous data, a t-test was used in independent groups in normal distribution to compare two groups. One-Way ANOVA analysis was used to compare more than two groups. Bonferroni analysis was used for post hoc analysis. Pearson"s Chisquare or Fisher"s Exact Chi-square test was used in the analysis of categorical data. Cases where the P-value was below 0.05 were considered statistically significant.

Results

Table 2: Socio-demographic data

101 (84%) of the participants were using NCCN, 33 (27.5%) ASTRO, 23 (19%) ESGO guidelines, and 30 (25%) their own clinical protocols for ATP. In this question, participants were allowed to select more than one choice.

Myometrial invasion was chosen by 112 (93%) and grade by 109 (91%) people as the most frequently evaluated prognostic factors when making treatment decisions. Among the given options, tumor size was chosen as the least evaluated prognostic factor by 36 (30%) participants. In this question, participants were allowed to select more than one choice. In Table 3, the evaluation percentage of prognostic markers given in the survey while performing ATP is given.

Table 3: The ratio of prognostic markers to be evaluated in ATP

In (LVI) (+) (HIRG) patients with Stage 1A-B, Grade 1-2, LVI who had undergone SS, the ATP percentage was 68% for VB, 11% for ERT, 9% for ERT+VB, and 7.5% for observation (p<0.0001 in favor of VB). If SS had not been performed on the same group, 72 (60%) of the participants recommended SS. In 48 (40%) participants who did not recommend SS to this group, the recommendations were ERT+VB in 33%, VB in 26%, ERT in 24%, and observation in 4.5% (p=0.001 in favor of ERT+VB).

In Stage 1A, Grade 3, LVI (?) patients (HIRG) who had undergone SS, the ATP was 63% for VB, 22.5% for ERT+VB, 9% for ERT, and 5% for observation (p<0.0001 in favor of VB). For LVI (+) patients in the same group, the ATP was 43% for ERT+VB, 41% for VB, 14% for ERT, and 1% for observation (p<0.0001 in favor of ERT+VB). 81 (67.5%) participants recommended SS for Stage 1A, Grade 3 patients who had not undergone SS. In 39 (32.5%) participants who did not recommend SS for this group, the recommendations were ERT+VB in 43%, ERT in 24.5%, VB in 20%, and observation in 1.5% (p<0.0001 in favor of ERT+VB).

In Stage 1B, Grade 3, LVI (?) patients (HRG) who had undergone SS, ATP was 45% for ERT+VB, 35% for VB, 19% for ERT, and observation was not recommended (p<0.0001 in favor of ERT+VB). For the LVI (+) patients in the same group, the ATP was 71% for ERT+VB, 14% for ERT, 13% for VB, and 1% for observation (p<0.0001 in favor of ERT+VB). 89 (74%) participants recommended SS to Stage 1B, Grade 3 patients who had not undergone SS. In 31 (26%) participants who did not recommend SS, the recommendations were ERT+VB in 55%, ERT in 20%, and VB in 11% (p<0.0001 in favor of ERT+VB).

Table 4 summarizes data considered statistically significant after evaluating the correlation between questions nine through 19 in which demographic questions, selected guides, and possible scenarios are given. Each of the demographic data and question choices was compared separately, and data with p<0.05 were shared in the table. There was no significant value in statistics regarding years of experience and age. Gender was not taken into consideration. In terms of guidelines, only data of those who preferred NCCN were considered significant in six questions.

Table 4: Relationship between demographic data, selected guidelines, and scenarios

Discussion

In early-stage endometrial cancer, the location of SS, that is, of lymph node dissection, is controversial.[] Although the therapeutic effect of lymph node dissection is unclear, it is complementary to the surgical procedure. The surgery performed allows for the final surgical staging of the patients and makes it easier to decide on adjuvant therapy. However, is lymph node dissection really necessary in early-stage endometrial cancer? Especially in the presence of grade 1-2, <50% myometrial invasion, the possibility of these patients to benefit from lymph node dissection is very low, since the possibility of pathological lymph node will be very low.[] In a randomized controlled study by Panici et al.[] 514 patients diagnosed with early-stage endometrial cancer, there was no difference in overall survival and diseasefree survival between the two groups with and without lymph node dissection. Similarly, in the ASTEC study, 1.408 Stage I endometrial cancer patients were randomized. No difference was found in the group in which lymph node dissection was performed compared to the group with no lymph node dissection.[] In the ASTEC study, the small number of lymph nodes removed and the lack of para-aortic dissection were criticized.

There are groups that recommend dissection according to the grade of the tumor, apart from the stage. In the study by Trimble et al.,[] lymph node dissection was recommended for high-grade tumors. The analysis of Kim et al.,[] in which 16,995 patients were evaluated in nine studies, showed that ten or more lymph nodes removed were of limited benefit in low-risk endometrial cancer but had an overall survival benefit in intermediate- and high-risk endometrial cancer.

The guidelines state that lymph node dissection does not provide a survival advantage in HIRG patients, but it can be performed for surgical staging, and recommend lymph node dissection for HRG patients.[]

In the SEPAL study, unlike other studies, lymph node dissection was also recommended for HIRG patients, and in the study that included 671 patients, the survival of 407 HIRG and HRG patients who underwent pelvic and para-aortic lymph node dissection was found to be higher (p=0.0009).[]

In our study, in the scenarios where HIRG and HRG were given, the answer to the question "Would you recommend SS if SS had not been performed" (questions 10, 14, and 18), was "I would recommend SS" with 71% for question 10, 67% for question 14, and 89% for question 18, respectively. All the participants who did not recommend SS when responding to these questions selected the ERT+VB choice in a statistically significant manner. The fact that most of the participants recommend SS indicates that staging by dissection is still preferred by physicians or that lymph node dissection is thought to have therapeutic effect. Those who did not recommend SS preferred ERT+VB to dissection. The preference of combined therapy shows that physicians believe that dual-modality will be more successful in this group of patients.

Age, myometrial invasion, stage, grade, and LVI are among the most important prognostic factors in endometrial cancer.[] Prognostic factors used in risk classification in ESMO-ESGO-ESTRO guidelines are LVI, stage, and grade.[] The GOG-99, ASTEC/ EN5, and PORTEC-1 studies determined the risk groups of the study using similar prognostic factors. [-] In our study, the participants chose the prognostic markers evaluated during ATP as myometrial invasion with 93%, grade with 90.83%, and LVI with 79.16%, respectively. Although there are studies considering tumor size above 2 cm as a risk factor,[] tumor size is not among the risk factors in the decision of adjuvant therapy in current guidelines.[,] In our study, tumor size was the least evaluated prognostic factor with 30%.

As a result of three extensive, randomized studies comparing ERT and observation in early-stage endometrial cancer, a statistically significant decrease in locoregional recurrence rates was observed in the arm receiving ERT, without observing the overall survival difference.[-]

In the PORTEC study, 714 Stage 1B, Grade 2-3, and Stage 1C, Grade 1-2 patients (HIRG) were evaluated according to FIGO 1988. The 10-year locoregional recurrence rate without any difference in survival was found to be 5% and 14% in the RT group and the observation group, respectively (p<0.0001). In the subgroup analysis, the 5-year local recurrence rate in the low-risk group with superficial invasion was the same as the observation group (5%). It was determined that Grade 3 patients in the HRG who had deep invasion were the group that benefited from ERT.[]

In the GOG-99 study, 392 Stage IB-C and IIA patients were evaluated, and in this study in which LVI was included in the risk classification, the 2-year local recurrence rate in the observation group against RT in HIRG was found to be 6% and 27%, respectively, while a 58% reduction was observed in 2-year vaginal and pelvic recurrence.[]

In the ASTEC/EN5 study, 905 early-stage patients were evaluated. However, in this study, nonendometrioid- type patients were also included in the group, and RT and VB were applied to both groups (53%). The 5-year cumulative recurrence was 6.1% in the observation group and 3.2% in the RT group, and it was emphasized that the low recurrence in the observation group was caused by VB given to 53% of the patients in this group.[]

Considering the success of VB in local control, the PORTEC-2 study was designed, and 427 patients with HIR factors of FIGO 1988 Stage IB, Grade 3; Stage IC, Grade 1, 2; and Stage IIA, Grade 1, 2 (all Stage I patients according to FIGO 2009 staging) were randomized to ERT and VB arms. There was no statistically significant difference in overall survival and local control, but VB was superior in side effects and function evaluation. In the 10-year analysis, pelvic recurrence was slightly higher in the VB arm, though not statistically significant, with 2.5% versus 0.5%, but most of these recurrences were associated with distant metastasis. It was reported that ERT provided better pelvic control in patients with LVI compared to VB.[]

In Sorbe's et al.[] study, VB and ERT+VB groups were compared in HIRG. It was emphasized that combined therapy should be used in the HRG.BRT is considered the international standard treatment in HIRG, taking into account the side effects and quality of life data.[]

In guidelines, the first choice of NCCN in HIRG is VB, and it is recommended to consider it for ERT, especially in the presence of LVI, by looking at other risk factors.[] The ESGO guidelines determine whether SS is performed in the presence of Stage IA-B, Grade 1-2, LVI, and recommend BRT if SS is performed, and ERT if it is not. In Stage IA, Grade 3, VB is recommended regardless of LVI. In HRG, on the other hand, ERT appears as the first option.[]

In our study, in accordance with the literature, the recommendation for patients who had undergone SS in questions 9-12, which asked about adjuvant treatment preference in HIRG, was 68% and 63% VB, respectively. In question 13, in the presence of two important prognostic factors of Grade 3 and LVI, combined treatment (ERT+BRT) was preferred at 43%, similar to the Norwegian study.[]

In our study, in HRG which had undergone SS, the response to questions 16 and 17 was ERT+VB at 45% and 71%, respectively. Participants preferred combined therapy in the presence of two main risk factors, as in HIRG, although ERT was recommended in the guidelines. In patients without SS, combined ERT+VB was the most preferred option regardless of LVI. As 16% of the participants who answered no in this question preferred the "Other" option, we understand that they considered a treatment option combined with possible chemotherapy.

Factors such as the guidelines chosen in treatment decisions, the experience of the physician, whether he/ she works as academic staff, and the technical facilities of the institution he/she works for gain importance. In our study, when we compared these data and treatment preferences, no significant correlation was found between physician age and duration of experience and treatment preferences (p>0.05). However, in the case that non-academic staff members did not recommend SS in any scenario, their treatment preference was ERT+VB in a statistically significant manner (for questions 11, 15 and 19, p=0.023, p=0.007, and p=0.004, respectively). Combined therapies were considered as a safer and preferable option, especially by non-academic physicians. Similarly, it was observed that those who used the NCCN guidelines recommended SS in a statistically significant manner in questions 10 and 14 (p=0.037 and 0.019 for questions 10 and 14, respectively).

The inadequacies of the study were the lack of elaboration about systemic therapy due to questioning the choice of adjuvant RT, and failure to discuss genetic markers as they had not yet been put into daily practice.

Although the preferences of Turkish Radiation Oncology physicians in the choice of adjuvant therapy in early-stage endometrial cancer were different from each other, they were compatible with current guidelines. However, the preference of ERT+VB was observed to increase with the increase in risk factors, unlike the guidelines. Especially in Grade 3 disease without SS, the preference of ERT+VB was observed to be prominent among physicians not working in university and training hospitals. The fact that these choices are not dependent on demographics is proof that the treatments in our discipline are planned in the light of evidence-based data. The evaluation of our results in line with our treatment decisions in a national database, and the creation of our own data and treatment algorithm, should be among our most important goals.

Peer-review: Externally peer-reviewed.

Conflict of Interest: All authors declared no conflict of interest.

Ethics Committee Approval: The study was approved by the University of Health Sciences, Tepecik Training and Research Hospital Clinical Research Ethics Committee (No: 2020/14-32, Date: 23/12/2020).

Financial Support: None declared.

Authorship contributions: Concept - Z.G., F.E., Z.Ö.; Design - Z.G., F.E., Z.Ö.; Supervision - Z.G., F.E., Z.Ö.; Funding - Z.G., F.E., Z.Ö.; Materials - Z.G., F.E.; Data collection and/ or processing - Z.G., F.E.; Data analysis and/or interpretation - Z.G., F.E., Z.Ö.; Literature search - Z.G., F.E., Z.Ö.; Writing - Z.G., F.E., Z.Ö.; Critical review - Z.Ö., Z.G.

References