Adjuvant treatment for patients after resection of high-riskand regionally metastatic melanoma remains suboptimal. Despitethe Food and Drug Administration's approval of high-dose interferonalfa-2b, the substantial toxicity of the therapy and the factthat its benefit is limited to 20 to 30 percent of patientsat risk have hindered its general acceptance.
Attempts to identify patients who benefit from adjuvant treatmentwith interferon alfa-2b have been disappointing to date. Althoughanalyses of individual studies suggest that the benefit of high-doseinterferon alfa-2b might be restricted to certain subgroupsof patients, on the basis of the number of melanoma-involvedlymph . . . [Full Text of this Article]
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From Beth Israel Deaconess Medical Center, Boston.
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