Monoclonal antibodies in cancer therapy - New perspectives after the colorectal carcinoma trial

被引:7
作者
Holz, E
Gruber, R
Riethmuller, G
机构
[1] UNIV MUNICH, INST IMMUNOL, D-80336 MUNICH, GERMANY
[2] UNIV MUNICH, TUMORZENTRUM MUNCHEN, FAK MED, D-81377 MUNICH, GERMANY
[3] TECH UNIV MUNICH, W-8000 MUNICH, GERMANY
来源
CLINICAL IMMUNOTHERAPEUTICS | 1996年 / 5卷 / 03期
关键词
D O I
10.1007/BF03259084
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A new perspective for monoclonal antibodies (mAbs) is their use in patients presenting with minimal cancer burden or micrometastatic disease, i.e. in secondary prevention of metastatic cancer disease. The first proof of efficacy of a mAb in minimal residual disease has recently been published with mAb 17-1A in patients with colorectal cancer stage III after complete resection of the primary tumour. After a median follow-up of 5 years, antibody therapy reduced overall death rate by 30% and decreased the recurrence rate by 27%. This result is similar to the benefit obtained with (radio)chemotherapy trials, however, with notably less toxicity. Because the mechanisms of action of the different treatment modalities may be complementary in the control of tumour growth, more rationally designed clinical trials that combine conventional chemo-, hormonal or radiation therapy with immuno- or biotherapy need to be initiated. Also, with the more widespread use of prognostic parameters and increased abilities to characterise isolated tumour cells left behind in the patient, future therapy may eventually become more individualised and less consensus-oriented, thus leading to an improved risk: benefit ratio for the patient and reduced cost to society.
引用
收藏
页码:214 / 222
页数:9
相关论文
共 52 条
  • [1] Blottiere H M, 1991, Hum Antibodies Hybridomas, V2, P16
  • [2] BUCHLER M, 1991, CANCER-AM CANCER SOC, V68, P1507, DOI 10.1002/1097-0142(19911001)68:7<1507::AID-CNCR2820680707>3.0.CO
  • [3] 2-0
  • [4] CARRASQUILLO JA, 1988, J NUCL MED, V29, P1022
  • [5] CREEKMORE S, 1992, P ANN M AM SOC CLIN, V11, pA1186
  • [6] FAMILIAL DEFICIENCY OF DIHYDROPYRIMIDINE DEHYDROGENASE - BIOCHEMICAL BASIS FOR FAMILIAL PYRIMIDINEMIA AND SEVERE 5-FLUOROURACIL-INDUCED TOXICITY
    DIASIO, RB
    BEAVERS, TL
    CARPENTER, JT
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (01) : 47 - 51
  • [7] EASTON DF, 1993, AM J HUM GENET, V52, P678
  • [8] EASTON DF, IN PRESS AM J HUM GE
  • [9] Erlichman C., 1994, P AN M AM SOC CLIN, V13, P194
  • [10] FOGLER WE, 1988, CANCER RES, V48, P6303