THE POTENTIAL FOR ADJUVANT THERAPY IN EARLY-STAGE CERVICAL-CANCER

被引:6
作者
BUXTON, EJ
SAUNDERS, N
BLACKLEDGE, GRP
KELLY, K
REDMAN, CWE
MONAGHAN, J
PATERSON, MEL
LUESLEY, DM
机构
[1] West Midlands Cancer Research Campaign Clinical Trials Unit, Queen Elizabeth Hospital, Birmigham
关键词
D O I
10.1007/BF00685410
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Adjuvant therapy may potentially improve prognosis in women with early-stage cervical cancer who are at high risk of relapse after primary therapy. Patients with lymph node involvement at surgery are at high risk of recurrence and may benefit from adjuvant therapy, but many patients are treated with radical radiotherapy. At present there is no method of accurately identifying patients at high risk of recurrence in the latter group. A retrospective analysis of 141 surgically managed cases with state I/IIa cervical cancer is presented. The study aims were to characterize patients at high risk of relapse, identify independent prognostic variables predicting for relapse and, using these variables, develop a model, that would accurately predict high-risk patients. Univariate analysis identified depht of invasion, substage, lymph node involvement, lymphatic and blood vessel invasion and tumour differentiation as significant prognostic variables. After stratification for depth of invasion, which did not conform to the proportional hazards assumption implicit in the Cox model, Cox regression analysis showed substage, lymphatic and vascular invasion and histological tumour type to be independent prognostic variables. Using these variables, classification models were constructed that would be applicable to patients treated with either surgery or radiotherapy. Applying the models to 110 cases with >18 months follow-up, 11/18 (61%) and 11/19 cases (58%) predicted as being at high risk of relapse have developed recurrence. Highly active chemotherapy is now available for this disease. We have demonstrated that combined bleomycin, ifosfamide and cisplatin (BIP) is one of the most active regimens in this disease. BIP produces cytoreduction in around 70% of patients with recurrent and primary advanced disease. Responses are achieved rapidly and acute radiotherapy toxicity is not enhanced by giving chemotherapy prior to radical local radiotherapy. A multicentre, prospective randomized trial testing the role of BIP as adjuvant therapy in patients with positive nodes at radical hysterectomy is now in progress. A complementary study testing the role of adjuvant chemotherapy in high-risk patients treated with radical radiotherapy is in preparation. © 1990 Springer-Verlag.
引用
收藏
页码:S17 / S21
页数:5
相关论文
共 16 条
[1]  
BUXTON E, 1989, ACTA ONCOL, V27, P545
[2]   COMBINATION BLEOMYCIN, IFOSFAMIDE, AND CISPLATIN CHEMOTHERAPY IN CERVICAL-CANCER [J].
BUXTON, EJ ;
MEANWELL, CA ;
HILTON, C ;
MOULD, JJ ;
SPOONER, D ;
CHETIYAWARDANA, A ;
LATIEF, T ;
PATERSON, M ;
REDMAN, CW ;
LUESLEY, DM ;
BLACKLEDGE, GR .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1989, 81 (05) :359-361
[3]  
COX DR, 1972, J R STAT SOC B, V34, P187
[4]  
DISAIA PJ, 1975, GYNECOL ONCOL, P517
[5]  
DIXON WJ, 1985, BMDP STATISTICAL SOF
[6]   CERVICAL-CARCINOMA - A DRUG-RESPONSIVE TUMOR - EXPERIENCE WITH COMBINED CISPLATIN, VINBLASTINE, AND BLEOMYCIN THERAPY [J].
FRIEDLANDER, M ;
KAYE, SB ;
SULLIVAN, A ;
ATKINSON, K ;
ELLIOTT, P ;
COPPLESON, M ;
HOUGHTON, R ;
SOLOMON, J ;
GREEN, D ;
RUSSELL, P ;
HUDSON, CN ;
LANGLANDS, AO ;
TATTERSALL, MHN .
GYNECOLOGIC ONCOLOGY, 1983, 16 (02) :275-281
[7]  
HAKES T, 1984, KP AM SOC CLIN ONCOL, V3, P171
[8]   MUCIN PRODUCTION IN CERVICAL INTRAEPITHELIAL NEOPLASIA AND IN STAGE-1B CARCINOMA OF CERVIX WITH PELVIC LYMPH-NODE METASTASES [J].
IRELAND, D ;
COLE, S ;
KELLY, P ;
MONAGHAN, JM .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1987, 94 (05) :467-472
[9]  
KOTTMEIR M, 1976, FIGO16 REP
[10]   YOUNG AGE AS A PROGNOSTIC FACTOR IN CERVICAL-CANCER - ANALYSIS OF POPULATION BASED DATA FROM 10022 CASES [J].
MEANWELL, CA ;
KELLY, KA ;
WILSON, S ;
ROGINSKI, C ;
WOODMAN, C ;
GRIFFITHS, R ;
BLACKLEDGE, G .
BRITISH MEDICAL JOURNAL, 1988, 296 (6619) :386-391