Literature DB >> 9524096

High dose oral tamoxifen and subcutaneous interferon alpha-2a for recurrent glioma.

S M Chang1, F G Barker, S L Huhn, M K Nicholas, M Page, J Rabbitt, M D Prados.   

Abstract

Chemotherapeutic regimens in present use for recurrent glioma have substantial toxicity. Activity against recurrent gliomas has been reported for both tamoxifen and interferon alpha, agents that have more acceptable toxicity profiles and that can be administered in an outpatient setting. We tested the efficacy and toxicity of the combination of high-dose tamoxifen and interferon alpha in adults with recurrent glioma in a phase II trial. Eligible patients had radiographically measurable recurrent gliomas of any grade after initial radiation therapy. Interferon-alpha [6 x 10(6) U subcutaneously three times per week] and tamoxifen (240 mg/m2/day orally) were administered continuously. Treatment response was assessed at 6 week intervals using clinical and radiographic criteria. Eighteen patients (11 males and 7 females) were enrolled. Median age was 41 years (range 23-61 years). All patients had gliomas that progressed after radiation therapy and nitrosourea chemotherapy. The histologic diagnosis of the original tumor was glioblastoma multiforme in 8 patients, anaplastic astrocytoma in 5 patients, astrocytoma in 4 patients and mixed malignant glioma in 1 patient. Reversible moderate to severe neurological toxicity manifested by dizziness and unsteady gait was seen at tamoxifen doses of 240 mg/m2/day. Although the initial tamoxifen dose was reduced to 120 mg/m2/day, moderate neurotoxicity was noted at this dose as well and the trial was closed early. The combination of oral tamoxifen (120 to 240 mg/m2/day) and subcutaneous interferon-alpha [6 x 10(6) U three times per week] was associated with significant neurotoxicity in this group of recurrent glioma patients, resulting in early study closure. Of 16 evaluable patients, 12 had progressive disease after one cycle of treatment, 3 had stable disease, and there was one minor response. Gradual dose escalation may be required if similar patients are to be treated with high dose tamoxifen in conjunction with interferon.

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Year:  1998        PMID: 9524096     DOI: 10.1023/a:1005826323652

Source DB:  PubMed          Journal:  J Neurooncol        ISSN: 0167-594X            Impact factor:   4.130


  47 in total

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3.  A phase II study of high dose tamoxifen in progressive, metastatic renal cell carcinoma.

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4.  P-glycoprotein in the blood-brain barrier of mice influences the brain penetration and pharmacological activity of many drugs.

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6.  The efficacy of tamoxifen as an antiproliferative agent in vitro for benign and malignant pediatric glial tumors.

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7.  Clinical and radiographic response in a minority of patients with recurrent malignant gliomas treated with high-dose tamoxifen.

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Journal:  Neurosurgery       Date:  1993-03       Impact factor: 4.654

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Journal:  Cancer Chemother Pharmacol       Date:  1995       Impact factor: 3.333

9.  High-dose (480 mg/day) tamoxifen with etoposide: a study of a potential multi-drug resistance modulator.

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Review 10.  Decreased phenytoin levels in patients receiving chemotherapy.

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Journal:  Am J Med       Date:  1989-11       Impact factor: 4.965

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  11 in total

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Review 2.  Evidence and context of use for contrast enhancement as a surrogate of disease burden and treatment response in malignant glioma.

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Journal:  J Neurooncol       Date:  1999       Impact factor: 4.130

4.  Phase II study of concurrent continuous Temozolomide (TMZ) and Tamoxifen (TMX) for recurrent malignant astrocytic gliomas.

Authors:  Alexander M Spence; Richard A Peterson; Jeffrey D Scharnhorst; Daniel L Silbergeld; Robert C Rostomily
Journal:  J Neurooncol       Date:  2004-10       Impact factor: 4.130

5.  Phase 2 trial of radiation plus high-dose tamoxifen for glioblastoma multiforme: RTOG protocol BR-0021.

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Journal:  Neuro Oncol       Date:  2006-01       Impact factor: 12.300

Review 6.  Pharmacotherapy of malignant astrocytomas of children and adults: current strategies and future trends.

Authors:  M T Jennings; S Iyengar
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Authors:  William A Alaynick; James M Way; Stephanie A Wilson; William G Benson; Liming Pei; Michael Downes; Ruth Yu; Johan W Jonker; Jason A Holt; Deepak K Rajpal; Hao Li; Joan Stuart; Ruth McPherson; Katja S Remlinger; Ching-Yi Chang; Donald P McDonnell; Ronald M Evans; Andrew N Billin
Journal:  Mol Endocrinol       Date:  2009-12-04

8.  Targeted therapy in the treatment of malignant gliomas.

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Review 10.  The role of targeted therapies in the management of progressive glioblastoma : a systematic review and evidence-based clinical practice guideline.

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Journal:  J Neurooncol       Date:  2014-04-17       Impact factor: 4.130

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