Colorectal Cancer
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Mar 15, 2003; 9(3): 495-498
Published online Mar 15, 2003. doi: 10.3748/wjg.v9.i3.495
Application of autologous tumor cell vaccine and NDV vaccine in treatment of tumors of digestive traet
Wei Liang, Hui Wang, Tie-Mie Sun, Wen-Qing Yao, Li-Li Chen, Yu Jin, Chun-Ling Li, Fan-Juan Meng
Wei Liang, Tie-Mie Sun, Wen-Qing Yao, Li-Li Chen, Yu Jin, Chun-Ling Li, Fan-Juan Meng, Liaoning Provincal Tumor Research Institute, Shenyang 110042, Liaoning Province, China
Hui Wang, Department of Coloproctology Surgery of Liaoning Tumor Hospital, Shenyang 110042, Liaoning Province, China
Author contributions: All authors contributed equally to the work.
Supported by Scientific Foundation of Liaoning Province, No. 895215
Correspondence to: Wen-Qing Yao, Liaoning Provincal Tumor Research Institute, 44 xiaoheYan Road, Dadong District, Shenyang 110042, Liaoning Province, China. yaowenq@mail.sy.ln.cn Telephone: +86-24-24324202
Received: August 3, 2002
Revised: August 23, 2002
Accepted: September 12, 2002
Published online: March 15, 2003
Abstract

AIM: To treat patients with stage I-IV malignant tumors of digestive tract using autologous tumor cell vaccine and NDV (Newcastle disease virus) vaccine, and observe the survival period and curative effect.

METHODS: 335 patients with malignant tumors of digestive tract were treated with autologous tumor cell vaccine and NDV vaccine. The autologous tumor cell vaccine received were assigned for long-term survival observation. While these failed to obtain the autologous tumor tissue were given with NDV vaccine for a received short-term observation on curative effect.

RESULTS: The colorectal cancer patients treated with autologous tumor cell vaccine were divided into two groups: the controlled group (subjected to resection alone) (n = 257), the vaccine group (subjected to both resection and immunotherapy) (n = 310). 25 patients treated with NDV immunotherapy were all at stage IV without having resection. In postoperation adjuvant therapy patients, the 5, 6 and 7-year survival rates were 66.51%, 60.52%, 56.50% respectively; whereas in patients with resection alone, only 45.57%, 44.76% and 43.42% respectively. The average survival period was 5.13 years (resection alone group 4.15 years), the median survival period was over 7 years (resection alone group 4.46 years). There were significant differences between the two groups. The patients treated with resection plus vaccine were measured delayed-type hypersensitivity (DTH) reactions after vaccination, (indurative scope > 5 mm). The magnitude of DTH was related to the prognosis. The 5-year survival rate was 80% for those with indurations greater than 5 mm, compared with 30% for those with indurations less than 5 mm. The 1-year survival rate was 96% for 25 patients treated with NDV immunotherapy. The total effective rate (CR+PR) was 24.00% in NDV immunotherapy; complete remission (CR) in 1 case (4.00%), partial remission (PR) in 5 cases (20.00%), stabilizedin in 16 cases (64.00%), progression (PD) in 1 case (4.00%). After NDV vaccine immunotherapy, the number of NK cell increased and immune function imporved obviously.

CONCLUSION: The autologous tumor cell vaccine and NDV vaccine can prolong the patients’ life. NDV vaccine is notably effective for short-term with promotion of quality of life and can be used whenever necessary with good prospects.

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