Phase III trial of 5-fluorouracil and leucovorin plus either 3H1 anti-idiotype monoclonal antibody or placebo in patients with advanced colorectal cancer

被引:26
作者
Chong, G
Bhatnagar, A
Cunningham, D
Cosgriff, TM
Harper, PG
Steward, W
Bridgewater, J
Moore, M
Cassidy, J
Coleman, R
Coxon, F
Redfern, CH
Jones, JJ
Hawkins, R
Northfelt, D
Sreedharan, S
Valone, F
Carmichael, J
机构
[1] Royal Marsden Hosp, Dept Med, Sutton SM2 5PT, Surrey, England
[2] Titan Pharmaceut, San Francisco, CA USA
[3] Hematol Serv, New Orleans, LA USA
[4] Oncol Serv, New Orleans, LA USA
[5] Guys Hosp, London SE1 9RT, England
[6] Leicester Royal Infirm, Leicester, Leics, England
[7] N Middlesex Hosp, Edmonton, England
[8] Georgia Canc Res Ctr, Decatur, GA USA
[9] Univ Aberdeen, Aberdeen, Scotland
[10] Weston Pk Hosp NHS Trust, Sheffield, S Yorkshire, England
[11] Newcastle Gen Hosp, Newcastle Upon Tyne NE4 6BE, Tyne & Wear, England
[12] Sharp Hlth Care, San Diego, CA USA
[13] Columbus CCOP, Columbus, OH USA
[14] Christie Hosp, Withington, England
[15] Univ Calif San Diego, San Diego, CA 92103 USA
[16] City Hosp, Nottingham NG5 1PB, England
关键词
anti-idiotype; antibody; carcinoembryonic antigen; response; colorectal;
D O I
10.1093/annonc/mdj090
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The monoclonal antibody 3H1 mimics the external structure of the carcinoembryonic antigen (CEA). It therefore has the potential, via the anti-idiotypic network, to stimulate immune responses to CEA that may benefit colorectal cancer patients. Patients and methods: A total of 630 patients with previously untreated metastatic colorectal cancer were randomised in a 2:1 fashion to receive bolus 5-fluorouracil (5-FU) and leucovorin (LV) plus either 3H1 (n = 422) or placebo (n = 208). Results: The addition of 3H1 to 5-FU and LV did not result in increased toxicity. Survival for the full intent-to-treat population was 14.7 months for the 3H1 arm and 15.2 months for the placebo arm (P = 0.80). Anti-CEA antibody responses were observed in 70% of patients treated with 3H1. Patients with a negative CEA response had a median survival of 8.3 months (95% CI 7.5-11.0) compared with patients with a strong response: median survival not reached (P < 0.001). Conclusion: 3H1 is safe and effectively induces immune responses to CEA. Addition of 3H1 to 5-FU and LV was not shown to improve overall patient outcomes. However, improved survival in patients developing anti-CEA responses to 3H1 are provocative and should be studied in further clinical trials.
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页码:437 / 442
页数:6
相关论文
共 18 条
[1]  
BHATTACHARYACHATTERJEE M, 1990, J IMMUNOL, V145, P2758
[2]   Immune responses in breast cancer patients immunized with an anti-idiotype antibody mimicking NeuGc-containing gangliosides [J].
Díaz, A ;
Alfonso, M ;
Alonso, R ;
Saurez, G ;
Troche, M ;
Catalá, M ;
Díaz, RM ;
Pérez, R ;
Vázquez, AM .
CLINICAL IMMUNOLOGY, 2003, 107 (02) :80-89
[3]  
Durrant LG, 2000, CLIN CANCER RES, V6, P422
[4]   Clinical and immune responses in advanced melanoma patients immunized with an anti-idiotype antibody mimicking disialoganglioside GD2 [J].
Foon, KA ;
Lutzky, J ;
Baral, RN ;
Yannelli, JR ;
Hutchins, L ;
Teitelbaum, A ;
Kashala, OL ;
Das, R ;
Garrison, J ;
Reisfeld, RA ;
Bhattacharya-Chatterjee, M .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (02) :376-384
[5]   Clinical and immune responses in resected colon cancer patients treated with anti-idiotype monoclonal antibody vaccine that mimics the carcinoembryonic antigen [J].
Foon, KA ;
John, WJ ;
Chakraborty, M ;
Das, R ;
Teitelbaum, A ;
Garrison, J ;
Kashala, O ;
Chatterjee, SK ;
Bhattacharya-Chatterjee, M .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (09) :2889-2895
[6]  
Foon KA, 2001, CLIN CANCER RES, V7, P1112
[7]   DEMONSTRATION OF TUMOR-SPECIFIC ANTIGENS IN HUMAN COLONIC CARCINOMATA BY IMMUNOLOGICAL TOLERANCE AND ABSORPTION TECHNIQUES [J].
GOLD, P ;
FREEDMAN, SO .
JOURNAL OF EXPERIMENTAL MEDICINE, 1965, 121 (03) :439-+
[8]  
JERNE NK, 1974, ANN INST PASTEUR IMM, VC125, P373
[9]   ANTITUMOR-ACTIVITY AND IMMUNE-RESPONSES INDUCED BY A RECOMBINANT CARCINOEMBRYONIC ANTIGEN-VACCINIA VIRUS-VACCINE [J].
KANTOR, J ;
IRVINE, K ;
ABRAMS, S ;
KAUFMAN, H ;
DIPIETRO, J ;
SCHLOM, J .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1992, 84 (14) :1084-1091
[10]  
LINDENMANN J, 1973, ANN INST PASTEUR IMM, VC124, P171