A prospective population-based management program including primary surgery and postoperative risk assessment by means of DNA ploidy and histopathology. Adjuvant radiotherapy is not necessary for the majority of patients with FIGO stage I-II endometrial cancer

被引:25
作者
Hogberg, T [1 ]
Fredstorp-Lidebring, M
Alm, P
Baldetorp, B
Larsson, G
Ottosen, C
Svanberg, L
Lindahl, B
机构
[1] Univ Hosp, Dept Gynecol Oncol, SE-58185 Linkoping, Sweden
[2] Univ Hosp, Dept Gynecol Oncol, Lund, Sweden
[3] Univ Hosp, Dept Pathol, Lund, Sweden
[4] Univ Hosp, Oncol Lab, Dept Oncol, Lund, Sweden
[5] Karlskrona Hosp, Dept Obstet & Gynecol, Karlskrona, Sweden
[6] Helsingborg Hosp, Dept Obstet & Gynecol, Helsingborg, Sweden
[7] Univ Hosp, Dept Obstet & Gynecol, Malmo, Sweden
[8] Univ Hosp, Dept Obstet & Gynecol, Lund, Sweden
关键词
endometrial neoplasms/therapy; ploidies; prospective studies; risk factors;
D O I
10.1111/j.1048-891x.2004.014303.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A management program for FIGO stage I-II nonserous, nonclear-cell adenocarcinomas was evaluated. Histopathology and DNA ploidy were used to estimate postoperatively the risk of progression or death of disease and to tailor treatment. The patient material was a population-based consecutive cohort of all women with endometrial cancer in the Southern Swedish Health Care Region diagnosed between June 1993 and June 1996 (n = 553). Of these, 335 were eligible for the management program. Patients estimated to be at low risk were treated by surgery only, while high-risk patients also received vaginal brachytherapy. A large low-risk group consisting of 84% (n = 283) of the patients with an estimated disease-specific 5-year survival of 96% (95% CI = 93-98%) was identified. The high-risk group (n = 52, 16%) showed a worse outcome with an 80% 5-year disease-specific survival (95% CI = 65-89%). The difference in survival between the groups was highly significant (P < 0.0001). Half of the progressions were distant in the high-risk group. Although there is a clear indication for adjuvant therapy for this group, locoregional radiotherapy could be expected to fail in cases with distant progression. Thus, effective systemic treatments need to be developed. Low-risk patients, constituting the majority (84%) of the patients, can be safely treated by surgery only.
引用
收藏
页码:437 / 450
页数:14
相关论文
共 41 条
[1]  
AALDERS J, 1980, OBSTET GYNECOL, V56, P419
[2]   IDENTIFICATION OF SMALL AREAS OF SOLID GROWTH HAS A STRONG PROGNOSTIC IMPACT IN DIFFERENTIATED ENDOMETRIAL CARCINOMAS - A HISTOPATHOLOGIC AND MORPHOMETRIC STUDY [J].
ALM, P ;
GUDMUNDSSON, T ;
MARTENSSON, R ;
ANDERSON, H ;
HORVATH, G ;
HOGBERG, T .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 1995, 5 (02) :87-93
[3]   Cost-effectiveness of treatment of early stage endometrial cancer [J].
Ashih, H ;
Gustilo-Ashby, T ;
Myers, ER ;
Andrews, J ;
Clarke-Pearson, DL ;
Berry, D ;
Berchuck, A .
GYNECOLOGIC ONCOLOGY, 1999, 74 (02) :208-216
[4]   PROGNOSTIC SIGNIFICANCE OF PLOIDY LEVEL IN HUMAN TUMORS .1. CARCINOMA OF UTERUS [J].
ATKIN, NB .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1976, 56 (05) :909-910
[5]   STATISTICAL EVALUATION OF CELL KINETIC DATA FROM DNA FLOW-CYTOMETRY (FCM) BY THE EM ALGORITHM [J].
BALDETORP, B ;
DALBERG, M ;
HOLST, U ;
LINDGREN, G .
CYTOMETRY, 1989, 10 (06) :695-705
[6]   Do we know the best therapy for early endometrial cancer? [J].
Ball, HG .
GYNECOLOGIC ONCOLOGY, 1996, 60 (02) :173-175
[7]   A comparison of treatment strategies for endometrial adenocarcinoma: Analysis of financial impact [J].
Barnes, MN ;
Roland, PY ;
Straughn, M ;
Kilgore, LC ;
Alvarez, RD ;
Partridge, EE .
GYNECOLOGIC ONCOLOGY, 1999, 74 (03) :443-447
[8]  
BURKE TW, 1990, OBSTET GYNECOL, V75, P96
[9]  
CREASMAN WT, 1987, CANCER, V60, P2035, DOI 10.1002/1097-0142(19901015)60:8+<2035::AID-CNCR2820601515>3.0.CO
[10]  
2-8