Retrospective study on thymidylate synthase as a predictor of outcome and sensitivity to adjuvant chemotherapy in patients with curatively resected colorectal cancer

被引:16
作者
Sugiyama, Y [1 ]
Kato, T [1 ]
Nakazato, H [1 ]
Ito, K [1 ]
Mizuno, I [1 ]
Kanemitsu, T [1 ]
Matsumoto, K [1 ]
Yamaguchi, A [1 ]
Nakai, K [1 ]
Inada, K [1 ]
Tatematsu, M [1 ]
机构
[1] TAC CR, Study Grp, Nagoya, Aichi, Japan
关键词
adjuvant chemotherapy and UFT; colorectal cancer; retrospective study; thymidylate synthase;
D O I
10.1097/00001813-200210000-00005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We carried out a retrospective evaluation of thymidylate synthase (TS) expression in tumor tissue, and its relation to outcome and response to treatment. The treatment consisted of chemotherapy with tegafur and uracil (UFT). The study group comprised 245 patients with curatively resected Dukes' stage B or C colorectal cancer who were postoperatively enrolled in a controlled study and assigned to receive UFT or no adjuvant chemotherapy. TS expression in tumor tissue was evaluated immunohistochemically with the use of recombinant humanTS-specific antibody. Results were as follows. There was no relation between TS expression and the rate of 5-year disease-free survival. Similar results were obtained in both colonic and rectal tumors. The rate of 5-year disease-free survival was significantly higher in the UFT group than in the group receiving no adjuvant chemotherapy (p=0.0055). The difference in survival became more marked among patients whose tumors had diffuse TS expression (p=0.0027). There was no difference in survival between the treatment groups among patients whose tumors had focal TS expression. We conclude that, although unrelated to outcome, TS activity may be useful in predicting the response to adjuvant chemotherapy with UFT in patients with curatively resected Dukes' stage B or C colorectal cancer. [(C) 2002 Lippincott Williams Wilkins.].
引用
收藏
页码:931 / 938
页数:8
相关论文
共 24 条
[1]  
Cascinu S, 1999, CLIN CANCER RES, V5, P1996
[2]  
CLARK JL, 1987, CANCER TREAT REP, V71, P261
[3]   STRUCTURES OF REVERSIBLE AND IRREVERSIBLE COMPLEXES OF THYMIDYLATE SYNTHETASE AND FLUORINATED PYRIMIDINE NUCLEOTIDES [J].
DANENBER.PV ;
LANGENBA.RJ ;
HEIDELBE.C .
BIOCHEMISTRY, 1974, 13 (05) :926-933
[4]   THYMIDYLATE SYNTHETASE - TARGET ENZYME IN CANCER CHEMOTHERAPY [J].
DANENBERG, PV .
BIOCHIMICA ET BIOPHYSICA ACTA, 1977, 473 (02) :73-92
[5]  
Diasio RB, 1999, ONCOLOGY-NY, V13, P17
[6]   Lack of correlation between thymidylate synthase levels in primary colorectal tumours and subsequent response to chemotherapy [J].
Findlay, MPN ;
Cunningham, D ;
Morgan, G ;
Clinton, S ;
Hardcastle, A ;
Aherne, GW .
BRITISH JOURNAL OF CANCER, 1997, 75 (06) :903-909
[7]  
Hoff PM, 1999, SEMIN ONCOL, V26, P52
[8]   THE ROLE OF THYMIDYLATE SYNTHASE EXPRESSION IN PROGNOSIS AND OUTCOME OF ADJUVANT CHEMOTHERAPY IN PATIENTS WITH RECTAL-CANCER [J].
JOHNSTON, PG ;
FISHER, ER ;
ROCKETTE, HE ;
FISHER, B ;
WOLMARK, N ;
DRAKE, JC ;
CHABNER, BA ;
ALLEGRA, CJ .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (12) :2640-2647
[9]   Thymidylate synthase expression and response to neoadjuvant chemotherapy in patients with advanced head and neck cancer [J].
Johnston, PG ;
Mick, R ;
Recant, W ;
Behan, KA ;
Dolan, ME ;
Ratain, MJ ;
Beckmann, E ;
Weichselbaum, RR ;
Allegra, CJ ;
Vokes, EE .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (04) :308-313
[10]  
JOHNSTON PG, 1992, CANCER RES, V52, P4306