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Gut 1999;44:767-769; doi:10.1136/gut.44.6.767
Copyright © 1999 BMJ Publishing Group Ltd & British Society of Gastroenterology.
Gut 1999;44:767-769 ( June )

Leading article

Towards immunotherapy of pancreatic cancer

The first 150 words of the full text of this article appear below.

    Article

A recent review of pancreatic carcinoma stated, "In spite of poor results, we must continue to search actively for more accurate methods of diagnosis and better methods of treatment"1; in light of this, further study of immunotherapy may be appropriate.

Gut readers will not be surprised to see this article as, every decade, immunotherapy becomes a "hot" topic and, as such, generates short lived enthusiasm. Thus, BCG, tumour lysates, and even interleukin (IL) 2 as a single agent, have recently been of interest to those involved in scientific research. Immunotherapy is currently at the fore as we can now, actively or passively, stimulate the immune system of patients with pancreatic cancer, creating an immunotherapeutic regimen which may be partially or completely effective in curing the disease. Why such optimism? Recently, developments in genetic engineering techniques have lead to breakthroughs identifying tumour antigens, the description of numerous cytokines (approximately 25, including IL . . . [Full text of this article]


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This article has been cited by other articles:

  • Brett, B. T., Smith, S. C., Bouvier, C. V., Michaeli, D., Hochhauser, D., Davidson, B. R., Kurzawinski, T. R., Watkinson, A. F., Van Someren, N., Pounder, R. E., Caplin, M. E. (2002). Phase II Study of Anti-Gastrin-17 Antibodies, Raised to G17DT, in Advanced Pancreatic Cancer. JCO 20: 4225-4231 [Abstract] [Full Text]  
  • Ito, M., Shichijo, S., Tsuda, N., Ochi, M., Harashima, N., Saito, N., Itoh, K. (2001). Molecular Basis of T Cell-mediated Recognition of Pancreatic Cancer Cells. Cancer Res. 61: 2038-2046 [Abstract] [Full Text]  

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