Adjuvant brachytherapy removes survival disadvantage of local disease extension in stage IIIC endometrial cancer: A SEER registry analysis

被引:31
作者
Rossi, Peter J. [1 ]
Jani, Ashesh B. [1 ]
Horowitz, Ira R. [2 ]
Johnstone, Peter A. S. [1 ]
机构
[1] Emory Univ, Sch Med, Dept Radiat Oncol, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Dept Obstet & Gynecol, Atlanta, GA 30322 USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2008年 / 70卷 / 01期
关键词
endometrial neoplasms; radiotherapy; brachytherapy; SEER;
D O I
10.1016/j.ijrobp.2007.05.048
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To assess the role of radiotherapy (RT) in women with Stage IIIC endometrial cancer. Methods and Materials: The 17-registry Survival, Epidemiology, and End Results (SEER) database was searched for patients with lymph node-positive non-Stage IV epithelial endometrial cancer diagnosed and treated between 1988 and 1998. Two subgroups were identified: those with organ-confined Stage IIIC endometrial cancer and those with Stage IIIC endometrial cancer with direct extension of the primary tumor. RT was coded as external beam RT (EBRT) or brachytherapy (BT). Observed survival (OS) was reported with a minimum of 5 years of follow-up; the survival curves were compared using the log-rank test. Results: The therapy data revealed 611 women with Stage IIIC endometrial cancer during this period. Of these women, 51% were treated with adjuvant EBRT, 21% with EBRT and BT, and 28% with no additional RT (NAT). Of the 611 patients, 293 had organ-confined Stage IIIC endometrial cancer and 318 patients had Stage IIIC endometrial cancer with direct extension of the primary tumor. The 5-year OS rate for all patients was 40% with NAT, 56% after EBRT, and 64% after EBRT/BT. Adjuvant RT improved survival compared with NAT (p < 0.001). In patients with organ-confined Stage IIIC endometrial cancer, the 5-year OS rate was 50% for NAT, 64% for EBRT, and 67% for EBRT/BT. Again, adjuvant RT contributed to improved survival compared with NAT (p = 0.02). In patients with Stage IIIC endometrial cancer and direct tumor extension, the 5-year OS rate was 34% for NAT, 47% for EBRT, and 63% for EBRT/BT. RT improved OS compared with NAT (p < 0.001). Also, in this high-risk subgroup, adding BT to EBRT was superior to EBRT alone (P = 0.002). Conclusion: Women with Stage IIIC endometrial cancer receiving adjuvant EBRT and EBRT/BT had improved OS compared with patients receiving NAT. When direct extension of the primary tumor was present, the addition of BT to EBRT was even more beneficial. (c) 2008 Elsevier Inc.
引用
收藏
页码:134 / 138
页数:5
相关论文
共 16 条
[1]  
AALDERS J, 1980, OBSTET GYNECOL, V56, P419
[2]   ENDOMETRIAL CANCER WITH PARAAORTIC ADENOPATHY - PATTERNS OF FAILURE AND OPPORTUNITIES FOR CURE [J].
CORN, BW ;
LANCIANO, RM ;
GREVEN, KM ;
SCHULTZ, DJ ;
REISINGER, SA ;
STAFFORD, PM ;
HANKS, GE .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1992, 24 (02) :223-227
[3]   Surgery and postoperative radiotherapy versus surgery alone for patients with stage-1 endometrial carcinoma:: multicentre randomised trial [J].
Creutzberg, CL ;
van Putten, WLJ ;
Koper, PCM ;
Lybeert, MLM ;
Jobsen, JJ ;
Wárlám-Rodenhuis, CC ;
De Winter, KAJ ;
Lutgens, LCHW ;
van den Bergh, ACM ;
van de Steen-Banasik, E ;
Beerman, H ;
van Lent, M .
LANCET, 2000, 355 (9213) :1404-1411
[4]   A pilot trial of TAC (paclitaxel, doxorubicin, and carboplatin) chemotherapy with filgastrim (r-metHuG-CSF) support followed by radiotherapy in patients with "high-risk" endometrial cancer [J].
Duska, LR ;
Berkowitz, R ;
Matulonis, U ;
Muto, M ;
Goodman, A ;
Mcintyre, JF ;
Klein, A ;
Atkinson, T ;
Seiden, MV ;
Campos, S .
GYNECOLOGIC ONCOLOGY, 2005, 96 (01) :198-203
[5]   Final analysis of RTOG 9708: Adjuvant postoperative irradiation combined with cisplatin/paclitaxel chemotherapy following surgery for patients with high-risk endometrial cancer [J].
Greven, Kathryn ;
Winter, Kathryn ;
Underhill, Kelly ;
Fontenesci, Jim ;
Cooper, Jay ;
Burke, Tom .
GYNECOLOGIC ONCOLOGY, 2006, 103 (01) :155-159
[6]   MEDICALLY INOPERABLE STAGE-I ADENOCARCINOMA OF THE ENDOMETRIUM TREATED WITH RADIOTHERAPY ALONE [J].
GRIGSBY, PW ;
KUSKE, RR ;
PEREZ, CA ;
WALZ, BJ ;
CAMEL, MH ;
KAO, MS ;
GALAKATOS, A .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1987, 13 (04) :483-488
[7]   SURVIVAL IN PATIENTS WITH PARAAORTIC LYMPH-NODE METASTASES FROM ENDOMETRIAL ADENOCARCINOMA CLINICALLY LIMITED TO THE UTERUS [J].
HICKS, ML ;
PIVER, MS ;
PURETZ, JL ;
HEMPLING, RE ;
BAKER, TR ;
MCAULEY, M ;
WALSH, DL .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1993, 26 (04) :607-611
[8]   A phase III trial of surgery with or without adjunctive external pelvic radiation therapy in intermediate risk endometrial adenocarcinoma: a Gynecologic Oncology Group study [J].
Keys, HM ;
Roberts, JA ;
Brunetto, VL ;
Zaino, RJ ;
Spirtos, NM ;
Bloss, JD ;
Pearlman, A ;
Maiman, MA ;
Bell, JG .
GYNECOLOGIC ONCOLOGY, 2004, 92 (03) :744-751
[9]   Surgery and postoperative radiation therapy in FIGO Stage IIIC endometrial carcinoma [J].
Mundt, AJ ;
Murphy, KT ;
Rotmensch, J ;
Waggoner, SE ;
Yamada, SD ;
Connell, PP .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2001, 50 (05) :1154-1160
[10]   FIGO stage IIIC endometrial carcinoma with metastases confined to pelvic lymph nodes: Analysis of treatment outcomes, prognostic variables, and failure patterns following adjuvant radiation therapy [J].
Nelson, G ;
Randall, M ;
Sutton, G ;
Moore, D ;
Hurteau, J ;
Look, K .
GYNECOLOGIC ONCOLOGY, 1999, 75 (02) :211-214