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ANTIBODY-TARGETED IMMUNOTHERAPY FOR TREATMENT OF MALIGNANCY
Despite testing since the mid-1900s, only in the past three years have some monoclonal antibodies provided sufficient efficacy and safety data to support regulatory approval as cancer therapy. Adjuvant-edrecolomab monoclonal antibody was approved in Germany after demonstration of a statistically sig...
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Published in: | Annual review of medicine 2001-01, Vol.52 (1), p.125-145 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Despite testing since the mid-1900s, only in the past three years have some
monoclonal antibodies provided sufficient efficacy and safety data to support
regulatory approval as cancer therapy. Adjuvant-edrecolomab monoclonal antibody
was approved in Germany after demonstration of a statistically significant
32% improvement over observation alone in the seven-year mortality rate
for patients with colorectal cancer. Similarly, trastuzumab monoclonal antibody
combined with chemotherapy prolonged the median time to the progression of
breast cancer compared to chemotherapy alone. Unconjugated monoclonal
antibodies investigated for the treatment of hematologic malignancies include
anti-idiotype, CAMPATH-1, and rituximab. Rituximab was the first such therapy
approved in the United States for relapsed or refractory low-grade or
follicular B-cell non-Hodgkin's lymphoma after demonstration of an overall
response rate of 48% and a duration of response of 11.7 months. The
radioisotope-conjugated monoclonal antibodies tested as therapy include
anti-B1, LYM-1, LL2, anti-CD33, and ibritumomab tiuxetan. Clearly, the full
potential of immunotherapy still lies ahead. |
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ISSN: | 0066-4219 1545-326X |
DOI: | 10.1146/annurev.med.52.1.125 |