Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/9178
Title: Monoclonal antibody-directed cytotoxic therapy: potential in malignant diseases of aging.
Austin Authors: Panousis, C;Pietersz, Geoffrey A
Affiliation: The Austin Research Institute, Austin Hospital, Melbourne, Victoria, Australia
Issue Date: 1-Jul-1999
Publication information: Drugs & Aging; 15(1): 1-13
Abstract: The advent of monoclonal antibodies has allowed the development of tumour directed therapies utilising antibody-dependent effector mechanisms and immunoconjugates (e.g. drug, isotope and toxin coupled antibodies) against human malignancies. Preclinical studies in mouse tumour models have been most impressive and have led to numerous clinical trials. Whereas the majority of these phase I/II trials have been less impressive, a few trials have shown efficacy in highly pre-treated refractory patients and have led to phase III trials. The therapeutic monoclonal antibodies examined in these trials will become clinically available in the near future. In this review, various methods of utilising antibody-directed anticancer strategies are presented, with emphasis on recent advances in the field. The advantages and disadvantages of these methods together with the role of antibody-directed therapeutics in cancer management are discussed.
Gov't Doc #: 10459728
URI: https://ahro.austin.org.au/austinjspui/handle/1/9178
Journal: Drugs & aging
URL: https://pubmed.ncbi.nlm.nih.gov/10459728
Type: Journal Article
Subjects: Aging.immunology
Animals
Antibiotics, Antineoplastic.administration & dosage.therapeutic use
Antibodies, Monoclonal.administration & dosage.therapeutic use
Humans
Immunoconjugates.administration & dosage
Mice
Neoplasms.etiology.immunology.therapy
Neoplasms, Experimental.therapy
Appears in Collections:Journal articles

Show full item record

Page view(s)

20
checked on Feb 22, 2025

Google ScholarTM

Check


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.