Abstract | PURPOSE: EXPERIMENTAL DESIGN:
Carcinoma tissue samples were obtained from client-owned dogs presented for medical care. The tissues were assessed for Le(y) antigen expression using immunohistochemical methods. Dogs with tumors expressing Le(y) antigen were offered enrollment in a clinical trial to receive twice-weekly infusions of 4 to 12 mg/m(2) BR96 sFv-PE40. Clinical toxicity and response data were assessed at each treatment. RESULTS: Twenty-two of 61 carcinomas evaluated were positive for Le(y) expression, including mammary, prostate, lung, and rectal carcinomas, and 12 dogs were enrolled in the clinical trial. The primary side effect was transient emesis. Partial responses or disease stabilization were noted in dogs with inflammatory mammary, bronchogenic, rectal, and tonsillar carcinoma. At least nine of the dogs developed antibodies to the immunotoxin after two to five infusions. CONCLUSIONS: Although development of anti-BR96 sFv-PE40 antibodies limited the long-term effectiveness of this immunotoxin in dogs, rapid clinical responses in several aggressive canine carcinomas suggest the immunotoxin has utility for treatment of certain naturally occurring tumors and that its clinical evaluation for treatment of similar human carcinomas is warranted.
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Authors | Carolyn J Henry, Michael S Buss, Ingegerd Hellström, Karl Erik Hellström, William G Brewer, Jeffrey N Bryan, Clay B Siegall |
Journal | Clinical cancer research : an official journal of the American Association for Cancer Research
(Clin Cancer Res)
Vol. 11
Issue 2 Pt 1
Pg. 751-5
(Jan 15 2005)
ISSN: 1078-0432 [Print] United States |
PMID | 15701865
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antibodies, Monoclonal
- BR96 sFv-PE40
- Immunotoxins
- Lewis Blood Group Antigens
- Lewis Y antigen
- Recombinant Fusion Proteins
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Topics |
- Animals
- Antibodies, Monoclonal
- Dogs
- Female
- Immunotherapy
- Immunotoxins
(therapeutic use)
- Lewis Blood Group Antigens
(immunology, metabolism)
- Lung Neoplasms
(immunology, metabolism, therapy)
- Male
- Mammary Neoplasms, Experimental
(immunology, metabolism, therapy)
- Mice
- Neoplasm Invasiveness
(immunology, pathology, prevention & control)
- Prostatic Neoplasms
(immunology, metabolism, therapy)
- Recombinant Fusion Proteins
(therapeutic use)
- Rectal Neoplasms
(immunology, metabolism, therapy)
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