4.7 Article

Phase 2 study evaluating the combination of sorafenib and temsirolimus in the treatment of radioactive iodine-refractory thyroid cancer

Journal

CANCER
Volume 123, Issue 21, Pages 4114-4121

Publisher

WILEY
DOI: 10.1002/cncr.30861

Keywords

anaplastic thyroid cancer; v-Raf murine sarcoma viral oncogene homolog B (BRAF) mutation; mammalian target of rapamycin (mTOR) inhibition; sorafenib; thyroid cancer

Categories

Funding

  1. National Comprehensive Cancer Network from Pfizer
  2. National Institutes of Health by the Memorial Sloan Kettering Cancer Center Support Grant/Core Grant [P30 CA008748]
  3. Specialized Programs of Research Excellence [P50 CA172012-01A1]

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BACKGROUNDPatients with recurrent and/or metastatic, radioactive iodine-refractory thyroid carcinoma have limited treatment options. Sorafenib, an oral kinase inhibitor, is approved by the US Food and Drug Administration for the treatment of radioactive iodine-refractory thyroid carcinoma, although it demonstrated low response rates (12.2%) as a single agent in the first-line setting. The objective of the current study was to determine whether adding the mammalian target of rapamycin inhibitor temsirolimus to sorafenib could improve on these results. METHODSIn this single-institution, phase 2 study, 36 patients with metastatic, radioactive iodine-refractory thyroid carcinoma of follicular origin received treatment with the combination of oral sorafenib (200 mg twice daily) and intravenous temsirolimus (25 mg weekly). The receipt of prior systemic treatment with cytotoxic chemotherapy and targeted therapy, including sorafenib, was permitted. The primary endpoint was the radiographic response rate. RESULTSThe best response was a partial response in 8 patients (22%), stable disease in 21 (58%), and progressive disease in 1 (3%). Six patients were not evaluable for a response. Patients who had received any prior systemic treatment had a response rate of 10% compared with 38% of those who had not received prior systemic treatment. One of 2 patients with anaplastic thyroid cancer had an objective response. The progression-free survival rate at 1 year was 30.5%. The most common grade 3 and 4 toxicities associated with sorafenib and temsirolimus included hyperglycemia, fatigue, anemia, and oral mucositis. CONCLUSIONSSorafenib and temsirolimus appear to be an active combination in patients with radioactive iodine-refractory thyroid carcinoma, especially in patients who received no prior treatment compared with historic data from single-agent sorafenib. Activity is also observed in patients who previously received sorafenib. This regimen warrants further investigation. Cancer 2017;123:4114-4121. (c) 2017 American Cancer Society. Sorafenib and temsirolimus appear to be an active combination in patients with radioactive-iodine refractory thyroid cancer, even in those who previously received sorafenib. This regimen also may have activity in anaplastic thyroid cancer.

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