Impact of Surgery Extent on Survival and Recurrence Rate of Stage ⅠEndometrial Adenocarcinoma

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Hou et al. / Cancer Cell Research 3 (2014) 65-69 Cancer Cell Research Available at http:// http://www.cancercellresearch.org/ ISSN 2161-2609 Impact of Surgery Extent on Survival and Recurrence Rate of Stage ⅠEndometrial Adenocarcinoma Wenping Hou, Zhumei Cui * Department of Gynecology, the Affiliated Hospital of Qingdao University, Qingdao, 266003, Shandong, China Article Information Abstract Article history: Received 18 March 2014 Revised 22 April 2014 Accepted 24 April 2014 Available online 25 April 2014 Keywords: Endometrial adenocarcinoma Surgery Survival rate Recurrence rate The total number of 349 patients of stage Ⅰ endometrial adenocarcinoma treated with surgery in Qingdao University Affiliated Hospital from January 2007 to December 2012 were analyzed retrospectively. They were divided into two groups: Group A (extrafascial hysterectomy plus bilateral salpingooophorectomy) and Group B (extrafascial hysterectomy or entensive hysterectomy, bilateral salpingo-oophorectomy, pelvic and para-aortic lymph node dissection), and then the survival and recurrence conditions were explored. The five-year survival rates of the two groups were 98.35% and 97.7% respectively (P>0.05). Among the 349 patients, there were 6 patients who recurred within 2 to 38months. The recurrence rates of Group A and Group B were 1.67% (3/178) and 1.75% (3/171) respectively (P>0.1). In this study, there were 129 stageⅠa moderately differentiated patients. None of the 17 patients who adopted adjuvant treatments relapsed; 4 of 112 patients without post-operative treatment recurred. There was no significant difference of recurrence rates (P>0.05). This study showed that to stage Ⅰendometrial adenocarcinoma patients, lymphadenectomy will not promote the survival rate and lower recurrence rate, however, to patients with risk factors it is still necessary to explore lymphadenectomy and adjuvant therapy. Perhaps adjuvant therapy can benefit the stage Ⅰ A moderately differentiated patients. 1. Introduction Endometrial carcinoma is one of the three major female genital tract malignant tumors, accounting for about 7% of female malignant tumors. Recently, with the rapid development of economy, the change of people's eating habits, 1 the occurrence of irregular hormone replacement Corresponding author:cuizhumei1966@126.com therapy and hormone abuse, the incidence of endometrial cancer tends to be higher and younger. Surgery is presently the main treatment for early stage endometrial cancer. Although 2011 national comprehensive cancer network (NCCN) guideline points out that comprehensive surgical staging is necessary, surgical scope draw our concern with the comprehensive cancer treatment and the continuous improvement of individual principle in clinical. In my study, clinical materials of 349 stage Ⅰ

Hou et al. / Cancer Cell Research 3 (2014) 65-69 66 endometrial adenocarcinoma patients were analyzed retrospectively. They were diagnosed with stage Ⅰin Qingdao University Affiliated Hospital according to the criterias made by Federation of International Gynecology and Obstetrics (FIGO) in 2009. Our study aims to provide some reference for the treatment of stage Ⅰendometrial adenocarcinoma. 2. Materials and Methods 2.1 Study Subjects 349 cases of stage Ⅰ endometrial adenocarcinoma who received operation in Qingdao University Affiliated Hospital between January 2007 and December 2012 were selected. All the 349 patients had complete clinical data and were pathologically diagnosed as stage Ⅰ by 2009 FIGO standards. Age ranged from 23 to 76 years old(mean age:54.2±7.9). A total of 236 cases, accounting for 67.6% of all the patients were with high-risk age (range from 45 to 63 years old). Telephone interviews were adopted to follow up patients and the follow-up time is 3-72 months. We had formal written consents of all the patients. 2.2 Methods and data collections Surgery extent depended on preoperative curettage, intraoperative frozen pathologic findings or intraoperative cross-sectional condition of uterine. Poorly differentiated, type Ⅱ endometrial cancer, more than 1/2 of muscular invasion or over 50% of the uterine cavity were high risk factors for cancer tissues. Therefore, patients with high risk factors were necessary to obtain extrafascial hysterectomy, salpingo- oophorectomy, pelvic and para-aortic lymphadenectomy. In this study, the 349 patients were divided into two groups: Group A extrafascial hysterectomy and bilateral salpingo-oophorectomy(a total of 178 cases), and Group B-extrafascial hysterectomy, bilateral salpingo-oophorectomy, pelvic and para-aortic lymphadenectomy (a total of 171 cases). After operation, patients with high risk factors accepted adjuvant therapy, including pelvic external radiation therapy for one course (22cases, about 6.30% of the whole patients), chemotherapy for one to six courses(30cases, taking up 8.60%) and hormone therapy (14 cases, accounting for 4.01%). Among these patients, the number of those who accepted two kinds of adjuvant therapy is 6, accounting for 10%. 2.3 Statistical methods Qualitative variable was analyzed using chi-square test and Fisher exact test and survival data was analyzed through Kaplan-Meier method. All analyses were conducted using SPSS17.0 software packet. 3. Results Basic information of 349 cases of patient was shown in table 1 below. Table 1 The comparison of basic information in both Group A and Group B Total Group Group P cases A B value Total cases 349 178 171 age 53.75 54.31 >0.05 Hypertension 160 123 37 >0.05 Diabetes 155 53 102 >0.05 Well differentiated 34 2 32 <0.05 moderately differentiated 299 162 137 Poorly differentiated 50 16 34 myometrial invasion depth <1/2 128 54 74 <0.05 myometrial invasion depth 1/2 50 27 23 3.1 Influence of operation scope on survival rate Survival data of patients with stageⅠ endometrial adenocarcinoma who were diagnosed through surgical pathology staging was analyzed using Kaplan-Meier method, and five-year survival rate of Group A and Group B was 98.3% and 97.7% respectively. There was no statistical significance between the two groups (P>0.05). Survival curves were shown in Fig1. 3.2 Impact of operation scope on recurrence rate Among the 349 patients, 6 cases relapsed, and 3 cases relapsed in both Group A and Group B,with the recurrence rate of 1.67% and 1.75%

Hou et al. / Cancer Cell Research 3 (2014) 65-69 67 respectively. There was no statistical significance (P>0.1).There was three pelvic metastasis out of six, two cases in Group A and one case in Group B. The other three cases had distant metastasis, including one case in Group A and two cases in Group B. Local recurrence rate was 66.67% and 33.33% respectively, and distant metastasis rate was 33.33% and 66.67% respectively. Fig1. Survival curves of Group A and Group B were shown. Note: Group A stands for extrafascial hysterectomy and bilateral salpingo-oophorectomy, Group B stands for extrafascial hysterectomy, bilateral salpingo-oophorectomy, pelvic and para-aortic lymphadenectomy. 3.3 Choose adjuvant therapy or not for stage Ⅰ A moderately differentiated endometrial adenocarcinoma? 129 cases diagnosed with stage ⅠA moderately differentiated endometrial adenocarcinoma, no one relapsed among the 17 cases who accepted adjuvant therapy and four cases recurred among 112 patients without adjuvant therapy. The recurrence rate was no statistical significance (P>0.05). 3.4 The choice of surgery procedure and adjuvant therapy for those with high risk factors The number of patients with high risk factors was 84 out of 349 patients. Most cases underwent extrafascial hysterectomy plus bilateral salpingo-oophorectomy and pelvic and para-aortic lymphadenectomy (66/84), there were 38 patients who adopted adjuvant therapy after operation. The survival rate is 98.81% (83/84). 4. Discussion Endometrial carcinoma is a common gynecological tumor. Women have probability to suffer from it from reproductive age to postmenopausal age. Besides, women from 50 to 69 have a high incidence [1-3]. In this study, the age of patients with stageⅠ endometrial adenocarcinoma was from 45 to 63 years old, younger than those reported in papers. This may be due to endometrial adenocarcinoma belonging to type Ⅰ endometrial cancer, which occurs in relatively young age; or perhaps the age of endometrial carcinoma is indeed younger than that in the past. For these patients, it is very important to receive a proper surgery procedure and adjuvant therapy. 70% to 90% endometrial carcinoma patients are diagnosed in early stage for irregular vaginal bleeding and increased vaginal drainage, only a few of patients in advanced stage [4]. Early stage endometrial cancer is still given priority to surgery, but as the improvement of comprehensive treatment and individualized principle, operation scope has become a growing focus point. It is reported that incidence of lymph node metastasis in clinical stage Ⅰ is 5%-16% [5-8]. Although the complications of lymph node dissection are rare, it can t be neglected [8-10]. Lin et al. [11] explored the recurrence conditions of stage Ⅰ endometrial carcinoma patients who underwent hysterectomy and bilateral oophorectomy only, and followed up for two years,then they found that nobody relapsed for those stage Ⅰa and Ⅰb (that is stage ⅠA according to FIGO 2009 staging system), and recurrence rate was up to 33% for stage Ⅰc patients (that is stage ⅠB according to FIGO 2009 staging system) who had bulky lump or deep myometrial invasion or was in poorly differentiated condition, for which they believed stage Ⅰ c patients with risk factors should accept expanded surgery procedure and adjuvant therapy. However, Gao Jinsong et al. [12] believed that there was no increased survival rate

Hou et al. / Cancer Cell Research 3 (2014) 65-69 68 after expanding surgery scope or undergoing lymph node dissection for patients surgical staging diagnosed with stage Ⅰ endometrial carcinoma. For those with risk factors, lymph node dissection or lymph node biopsy can help clarify staging and prognosis, besides, in the presence of risk factors, adjuvant therapy is helpful. At present, special type of endometrial cancer is an essential element to expand operation scope or undergo lymphadenectomy or accept adjuvant therapy [13], but there is still some controversy to choose surgery extents for early stage endometrioid adenocarcinoma patients. In this study 349 cases diagnosed by surgical pathology staging with stage Ⅰ endometrial adenocarcinoma were retrospectively analyzed. There was no significant difference between the five-year survival rate of the two groups, with the survival rates of 98.3% and 97.7% respectively. It is reported that five-year survival rate of stage Ⅰ A/ⅠB well/moderately differentiated endometrial adenocarcinoma was 95%[14], which is consistent with survival rate in this study. The recurrence rate of the two groups is not statistically significant. So we can conclude that expanded surgery extent can not improve survival rate and reduce recurrence rate for stage Ⅰ endometrial adenocarcinoma. As reported, early stage endometrial cancer patients with distant metastasis accounted for more than 50% of those who relapsed, and most relapsed in 3 years [15]. In this study, there were six cases who relapsed ranging from postoperative 2 to 38 months, of which three cases metastasized to the distant, this is consistent with reported papers. For those with risk factors, most cases tend to undergo extrafascial hysterectomy or entensive hysterectomy plus bilateral salpingo-oophorectomy and pelvic and para-aortic lymphadenectomy, and only a few choose extrafascial hysterectomy plus bilateral salpingo-oophorectomy because of their old age, complex complications. According to treatment guideline, for patients with stage ⅠA moderately differentiated endometrial adenocarcinoma, extrafascial hysterectomy plus bilateral salpingo-oophorectomy can be used as standard surgery procedure. In this study, there are 129 patients with stage ⅠA moderately differentiated endometrial adenocarcinoma. Among 112 cases without adjuvant therapy four cases relapsed, and none recurred of 17patients with adjuvant therapy. Although there is no significant difference, however, the relapsed patients are few and the sample is limited, the meaning of adjuvant therapy for stage ⅠA moderately differentiated endometrial adenocarcinoma need further study. 5. Conclusion In conclusion, it is useful of lymph node dissection for determining staging and getting prognosis known, however, lymphadenectomy can not improve survival rate and reduce recurrence rate. Besides, lymphadenectomy can increase incidence of complications and reduce life quality. For stage Ⅰpatients without risk factors, it is a good choice to undergo extrafascial hysterectomy plus bilateral salpingo oophorectomy. Further studies are needed to decide whether adjuvant therapy is necessary for patients with stage ⅠA moderately differentiated endometrial adenocarcinoma due to the limited sample and follow-up time and the few of recurrence. References [1] Liu X, Zhang WY, Dai YX: Advances in risk factors related to endometrial cancer. Chinese General Practice,12: 2009 1128-1131. [2] Jia ZW: Clinical analysis of 59 cases on endometrial cancer. Chinese Primary Medicine and Pharmacy, 16: 2009 1425-1426. [3] Chen JG, Wen M, Zhang B: Clinical analysis of 10 cases of young women with early endometrial cancer by conservative treatment. Practical Journal of Medicine, 23: 2007 2891-2893. [4] DiSaia PJ,Creasman WT,Lang Jinghe: Clinical Gynecologic Oncology (Edition 6). In Beijing: People's Health Publishing Hous, 2003. [5] Creasman, W. T., Morrow, C. P., Bundy, B. N., Homesley, H. D., Graham, J. E., & Heller, P. B. Surgical pathologic spread patterns of endometrial cancer: a Gynecologic Oncology Group study. Cancer, 60: 1987

2035-2041. [6] Chuang, Linus, et al. "Staging laparotomy for endometrial carcinoma: assessment of retroperitoneal lymph nodes." Gynecologic oncology 58.2 (1995): 189-193. [7] Lo, K. W. K., Cheung, T. H., Yu, M. Y., Yim, S. F., Chung, T. K. H. The value of pelvic and para-aortic lymphadenectomy in endometrial cancer to avoid unnecessary radiotherapy. International Journal of Gynecological Cancer, 13: 2003 863-869. [8] Orr Jr, James W., James L. Holimon, and Pamela F. Orr. Stage Ⅰ corpus cancer: is teletherapy necessary? American journal of obstetrics and gynecology, 176: 1997 777-789. [9] Cragun, J. M., Havrilesky, L. J., Calingaert, B., Synan, I., Secord, A. A. Berchuck, A. Retrospective analysis of selective lymphadenectomy in apparent early-stage endometrial cancer. Journal of Clinical Oncology, 23: 2005 3668-3675. [10] Homesley HD, Kadar N, Barrett RJ, Lentz SS: Selective pelvic and periaortic lymphadenectomy does not increase morbidity in surgical staging of endometrial carcinoma. Am J Obstet Gynecol, 167: 1992 1225-1230. [11] Lin, H. H., Chen, C. D., Chen, C. K., Chen, C. L., Chow, S. N., & Huang, S. C. Is total abdominal hysterectomy with bilateral salpingo oophorectomy adequate for new FIGO Stage I endometrial carcinoma?bjog: An International Journal of Obstetrics & Gynaecology, 102: 1995 148-152. [12] Gao JS, Shen K, Influence of different surgery procedure on survival and recurrence rate of stage I endometrial cancer. Chinese Journal of Obstetrics and Gynecology, 37: 2002 90-93. [13] Hamilton, Chad A., Daniel S. Kapp, and John K. Chan. Clinical aspects of uterine papillary serous carcinoma. Current Opinion in Obstetrics and Gynecology, 20: 2008 26-33. [14] Gotlieb, W. H., Beiner, M. E., Shalmon, B., Korach, Y., Segal, Y., Zmira, N., Ben-Baruch, G. Outcome of fertility-sparing treatment with progestins in young patients with endometrial cancer. Obstetrics & Gynecology, 102: 2003 718-725. [15] Ayhan, A., Tuncer, Z. S., Tuncer, R., Yüce, K., Küçükali, T. Risk factors for recurrence in clinically early endometrial carcinoma: an analysis of 183 consecutive cases. European Journal of Obstetrics & Gynecology and Reproductive Biology, 57: 1994 167-170. Hou et al. / Cancer Cell Research 3 (2014) 65-69 69