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Propylthiouracil-induced chemical
hypothyroidism with high-dose tamoxifen prolongs survival in recurrent high
grade glioma: a phase I/II study
Hercbergs AA, Goyal LK, Suh JH, Lee S, Reddy CA, Cohen BH, Stevens GH, Reddy
SK, Peereboom DM, Elson PJ, Gupta MK, Barnett GH
Department of Radiation Oncology, Cleveland Clinic Foundation,
9500 Euclid Ave, S80, Cleveland, OH 44195, USA
Background. High-dose tamoxifen has had disappointing results as a
palliative therapy in recurrent glioma.
Insulin-like growth factor 1 (IGF-1) is a thyroid hormone modulated naturally
occurring antagonist of tamoxifen-induced cytotoxicity.
Thyroid function was suppressed to reduce IGF-1 levels in glioma patients and
high-dose tamoxifen administered.
Materials and Methods. Propylthiouracil was used to
induce chemical hypothyroidism in 22 patients with recurrent glioma.
Tamoxifen was started within one month and given in escalating doses from 40 mg
twice a day up to 80 mg 3 times a day.
No significant toxicity developed.
Results. Eleven out of 22 patients became
hypothyroid.
No patients experienced symptoms of clinical hypothyroidism.
Median survival was significantly longer in the hypothyroid group (10.1 months
versus 3.1 months); p = 0.03.
There was a significant decrease in blood levels of IGF-1 (p = 0.02). in
hypothyroid patients.
Conclusion. Patients treated for recurrent high-grade
gliomas with high-dose tamoxifen had significantly longer survival when chemical
hypothyroidism was induced with propylthiouracil.
PMID: 12680157 [PubMed - indexed for MEDLINE]
Source: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12680157&dopt=Abstract
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