Adenosquamous histology predicts poor outcome in low-risk stage IB1 cervical adenocarcinoma

被引:53
作者
Lea, JS
Coleman, RL
Garner, EO
Duska, LR
Miller, DS
Schorge, JO
机构
[1] Univ Texas, SW Med Ctr, Div Gynecol Oncol, Dept Obstet & Gynecol, Dallas, TX 75390 USA
[2] Brigham & Womens Hosp, Boston, MA 02115 USA
[3] Massachusetts Gen Hosp, Boston, MA 02114 USA
关键词
D O I
10.1016/j.ygyno.2003.08.020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. The purpose of this study was to identify poor prognostic factors of low-risk stage 113 1 cervical adenocarcinoma. Methods. All women diagnosed with stage IB1 cervical adenocarcinoma between 1982 and 2002 were identified at our three institutions. Data were extracted from medical records. Patients were retrospectively assigned to a low- or intermediate/high-risk cohort based on the surgical-pathologic eligibility criteria of two randomized controlled trials of adjuvant therapy in early stage cervical cancer, Gynecologic Oncology Group protocols 92 and 109. Multivariate analysis was performed. Results. Two hundred thirty women diagnosed with stage 1131 cervical adenocarcinoma had an overall 5-year survival of 89%. Adenosquamous cell type (P < 0.01) was the only independent risk factor of disease recurrence in the low-risk group (n = 178). The 5-year disease-free survival for low-risk adenosquamous patients was 79%, compared to 96% for other histologic subtypes (P < 0.01). Low-risk case subjects developed fewer disease recurrences than those in the intermediate/high-risk (n = 52) category (7% vs 46%; P < 0.01). The 5-year disease-free survival for intermediate/high-risk patients was 51% and no additional risk factors were identified. Conclusion. Adenosquamous histology is predictive of disease recurrence and decreased survival in low-risk stage 1131 cervical adenocarcinoma. This risk factor should be considered in future clinical trials of adjuvant therapy. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:558 / 562
页数:5
相关论文
共 22 条
[1]  
Benedet JL, 2000, INT J GYNECOL OBSTET, V70, P209
[2]  
BEREK JS, 1985, OBSTET GYNECOL, V65, P46
[3]  
COX DR, 1972, J R STAT SOC B, V34, P187
[4]   COMPARISON OF THE PATTERN OF METASTATIC SPREAD OF SQUAMOUS-CELL CANCER AND ADENOCARCINOMA OF THE UTERINE CERVIX [J].
DRESCHER, CW ;
HOPKINS, MP ;
ROBERTS, JA .
GYNECOLOGIC ONCOLOGY, 1989, 33 (03) :340-343
[5]   ADENOCARCINOMA AS AN INDEPENDENT RISK FACTOR FOR DISEASE RECURRENCE IN PATIENTS WITH STAGE IB CERVICAL-CARCINOMA [J].
EIFEL, PJ ;
BURKE, TW ;
MORRIS, M ;
SMITH, TL .
GYNECOLOGIC ONCOLOGY, 1995, 59 (01) :38-44
[6]  
Grisaru D, 2001, CANCER, V92, P2999, DOI 10.1002/1097-0142(20011215)92:12<2999::AID-CNCR10145>3.0.CO
[7]  
2-1
[8]  
HOPKINS MP, 1991, OBSTET GYNECOL, V77, P912
[9]   NONPARAMETRIC-ESTIMATION FROM INCOMPLETE OBSERVATIONS [J].
KAPLAN, EL ;
MEIER, P .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1958, 53 (282) :457-481
[10]   Randomised study of radical surgery versus radiotherapy for stage Ib-IIa cervical cancer [J].
Landoni, F ;
Maneo, A ;
Colombo, A ;
Placa, F ;
Milani, R ;
Perego, P ;
Favini, G ;
Ferri, L ;
Mangioni, C .
LANCET, 1997, 350 (9077) :535-540