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Department of Oncology, Montefiore Medical Center and the Albert Einstein Cancer Center, Bronx, New York, USA
Correspondence: Scott Wadler, M.D., Department of Oncology, Hofheimer One, Montefiore Medical Center, 111 East 210th Street, Bronx, New York 10467, USA. Telephone: 718-920-4830; Fax: 718-798-7474.
Substantial increases in both the understanding of the cellular mechanisms of actions of interferon (IFN) and in its clinical use in cancer have occurred in recent years. The efficacy of interferon for the treatment of select malignancies has been established, and IFN-
and IFN-ß have been approved by the Food and Drug Administration for multiple clinical indications. IFN-
increased median survival and relapse-free survival in patients with locally advanced melanoma when used as adjuvant therapy and had modest activity against advanced disease. In other tumors where studies indicated that IFN lacked direct therapeutic activity, clinical trials suggested that it increased the antitumor activity of cytotoxic chemotherapeutic agents when used in combination therapy. IFN has substantial activity in chronic myelogenous leukemia, increasing survival in patients in early chronic phase when compared with conventional chemotherapy, and has some activity in non-Hodgkins lymphoma in combination with cytotoxic agents. Recent molecular and pharmacologic studies defining cellular receptor activation, signal transduction pathways, and biochemical modulating activities of interferon have yet to be fully incorporated into clinical development. Further preclinical advances along with the expanding identification of potentially clinically sensitive tumors make it likely that the use of IFN in cancer chemotherapy will continue to grow.
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