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Thyrotoxicosis with pegylated interferon alfa-2b.

AbstractBACKGROUND:
Despite adequate surgery, a diagnosis of stage III melanoma carries a high risk of relapse, and hence mortality. Interferon alfa is the only treatment that has currently been shown to alter the natural history of the disease, delaying relapse-free survival, particularly in patients with micrometastatic disease. There is also recent evidence of a prognostic advantage conferred by the development of autoimmune conditions in patients receiving adjuvant interferon therapy.
OBSERVATIONS:
We present the case of a 27-year-old woman with stage IIIa melanoma who was entered into the European Organisation for the Research and Treatment of Cancer 18991 trial of 5-year adjuvant treatment with pegylated interferon (peginterferon) alfa-2b. The patient developed thyrotoxicosis 3 months after commencing treatment, which required treatment with propylthiouracil. The degree of thyrotoxicosis corresponded closely to the dose of peginterferon alfa-2b given. However, in this patient, the hyperthyroidism resolved spontaneously after 4 years when peginterferon treatment was still ongoing. Seven years following the initial diagnosis, the patient has not had disease relapse.
CONCLUSION:
Hyperthyroidism is less common than hypothyroidism as a consequence of interferon therapy, and this case is atypical in that it resolved spontaneously during interferon therapy but is in accordance with the recent evidence of a positive association between interferon-associated autoimmunity and prognosis.
AuthorsSarah A Lowndes, Ruth Asher, Mark R Middleton
JournalArchives of dermatology (Arch Dermatol) Vol. 146 Issue 11 Pg. 1273-5 (Nov 2010) ISSN: 1538-3652 [Electronic] United States
PMID21079065 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Interferon alpha-2
  • Interferon-alpha
  • Recombinant Proteins
  • Polyethylene Glycols
  • peginterferon alfa-2b
Topics
  • Adult
  • Female
  • Humans
  • Interferon alpha-2
  • Interferon-alpha (adverse effects)
  • Melanoma (drug therapy, pathology)
  • Polyethylene Glycols (adverse effects)
  • Recombinant Proteins
  • Skin Neoplasms (drug therapy, pathology)
  • Thyrotoxicosis (chemically induced, drug therapy)

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