QUANTITATION OF INTRATUMORAL THYMIDYLATE SYNTHASE EXPRESSION PREDICTS FOR RESISTANCE TO PROTRACTED INFUSION OF 5-FLUOROURACIL AND WEEKLY LEUCOVORIN IN DISSEMINATED COLORECTAL CANCERS - PRELIMINARY-REPORT FROM AN ONGOING TRIAL

被引:110
作者
LEICHMAN, L
LENZ, HJ
LEICHMAN, CG
GROSHEN, S
DANENBERG, K
BARANDA, J
SPEARS, CP
BOSWELL, W
SILBERMAN, H
ORTEGA, A
STAIN, S
BEART, R
DANENBERG, P
机构
[1] UNIV SO CALIF, DEPT MED, DIV MED ONCOL, LOS ANGELES, CA 90089 USA
[2] UNIV SO CALIF, DEPT MED, DEPT BIOCHEM, LOS ANGELES, CA 90089 USA
[3] UNIV SO CALIF, DEPT MED, DEPT PREVENT MED, LOS ANGELES, CA 90089 USA
[4] UNIV SO CALIF, DEPT MED, DEPT RADIOL, LOS ANGELES, CA 90089 USA
[5] UNIV SO CALIF, DEPT MED, DEPT SURG, LOS ANGELES, CA 90089 USA
关键词
D O I
10.1016/0959-8049(95)00326-E
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A clinical trial for patients with measurable, disseminated colorectal cancer is being conducted to determine: (1) if intratumoral expression of thymidylate synthase (TS) affects response to protracted-infusion 5-fluorouracil (5FU); and (2) whether intratumoral expression of TS increases when clinical resistance is found after response to 5-FU. Polymerase chain reaction technology is employed to determine TS expression. Using p-actin as an internal standard, TS expressions for 26 patients range from 0.5 x 10(-3) to 22.6 x 10(-3). Currently, 22 patients are evaluable for response and TS quantitation of their measurable tumour. 8 patients (36%) have had partial responses; 3 responding patients had been previously treated with 5-FU. A strong statistical association between TS expression and resistance to therapy has been found (P = 0.004). No patient with TS expression of 4.0 x 10(-3) or greater has responded. On average, patients previously treated with 5-FU have slightly higher levels of TS expression in their measurable tumours (P = 0.4). Whether responding patients will develop increased expressions of TS upon clinical progression of their cancer remains to be determined. Confirmation of these results in a larger cohort could lead to a scientific rationale for deciding upon specific therapy for patients with disseminated colorectal cancers.
引用
收藏
页码:1306 / 1310
页数:5
相关论文
共 28 条
  • [1] [Anonymous], 1985, NEW ENGL J MED, V312, P1465
  • [2] A RANDOMIZED PHASE-I AND PHASE-II STUDY OF SHORT-TERM INFUSION OF HIGH-DOSE FLUOROURACIL WITH OR WITHOUT N-(PHOSPHONACETYL)-L-ASPARTIC ACID IN PATIENTS WITH ADVANCED PANCREATIC AND COLORECTAL CANCERS
    ARDALAN, B
    SINGH, G
    SILBERMAN, H
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (06) : 1053 - 1058
  • [3] BERGER SH, 1985, MOL PHARMACOL, V28, P461
  • [4] BERGER SH, 1984, MOL PHARMACOL, V25, P303
  • [5] SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION
    CHOMCZYNSKI, P
    SACCHI, N
    [J]. ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) : 156 - 159
  • [6] CHU E, 1991, MOL PHARMACOL, V39, P136
  • [7] UNSTABLE METHOTREXATE RESISTANCE IN HUMAN SMALL-CELL CARCINOMA ASSOCIATED WITH DOUBLE MINUTE CHROMOSOMES
    CURT, GA
    CARNEY, DN
    COWAN, KH
    JOLIVET, J
    BAILEY, BD
    DRAKE, JC
    KAOSHAN, CS
    MINNA, JD
    CHABNER, BA
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1983, 308 (04) : 199 - 202
  • [8] EISENSTEIN BI, 1990, NEW ENGL J MED, V322, P178
  • [9] EVANS RM, 1981, CANCER RES, V41, P3288
  • [10] MAXIMALLY SELECTED CHI-SQUARE STATISTICS FOR SMALL SAMPLES
    HALPERN, J
    [J]. BIOMETRICS, 1982, 38 (04) : 1017 - 1023