Abstract | BACKGROUND: METHODS: The application of radiolabelled Mabs for the treatment of solid cancers is discussed, and clinical trials investigating RIT for colorectal cancer listed in the Medline and Embase databases are reviewed. RESULTS: Uptake of radiolabelled Mabs in tumour and, consequently, the therapeutic efficacy of RIT is inversely correlated with tumour size. The bone marrow is the most important dose-limiting organ. Twenty-three phase I/II studies were found that investigated the feasibility and efficacy of RIT using five radionuclides and 15 Mabs against carcinoembryonic antigen, tumour-associated glycoprotein 72, epithelial cellular adhesion molecule, A33 or colon-specific antigen p, mainly in patients with advanced colorectal cancer. A few responses were recorded but no particular antibody construct seemed superior. CONCLUSION:
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Authors | M J Koppe, R P Bleichrodt, W J G Oyen, O C Boerman |
Journal | The British journal of surgery
(Br J Surg)
Vol. 92
Issue 3
Pg. 264-76
(Mar 2005)
ISSN: 0007-1323 [Print] England |
PMID | 15739250
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
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Copyright | Copyright (c) 2005 British Journal of Surgery Society Ltd. |
Chemical References |
- Antibodies, Monoclonal
- Antigens, Neoplasm
- Carcinoembryonic Antigen
- Cell Adhesion Molecules
- GPA33 protein, human
- Glycoproteins
- Membrane Glycoproteins
- Radioisotopes
- tumor-associated antigen 72
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Topics |
- Antibodies, Monoclonal
(therapeutic use)
- Antigens, Neoplasm
(metabolism)
- Carcinoembryonic Antigen
(metabolism)
- Cell Adhesion Molecules
(metabolism)
- Clinical Trials, Phase I as Topic
- Clinical Trials, Phase II as Topic
- Colorectal Neoplasms
(metabolism, radiotherapy)
- Dose-Response Relationship, Radiation
- Glycoproteins
(metabolism)
- Humans
- Membrane Glycoproteins
(metabolism)
- Radioimmunotherapy
(methods)
- Radioisotopes
(adverse effects, therapeutic use)
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