A Phase 1 Study of Everolimus and Sorafenib for Metastatic Clear Cell Renal Cell Carcinoma

被引:52
作者
Harzstark, Andrea L. [1 ]
Small, Eric J. [1 ]
Weinberg, Vivian K.
Sun, Janine [1 ]
Ryan, Charles J. [1 ]
Lin, Amy M. [1 ]
Fong, Lawrence [1 ]
Brocks, Dion R. [2 ]
Rosenberg, Jonathan E. [3 ]
机构
[1] Univ Calif San Francisco, Dept Med, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94143 USA
[2] Univ Alberta, Edmonton, AB, Canada
[3] Dana Farber Canc Inst, Dept Med, Lank Ctr Genitourinary Oncol, Boston, MA 02115 USA
关键词
renal cell carcinoma; clear cell; everolimus; sorafenib; mammalian target of rapamycin (mTOR) inhibitor; tyrosine kinase inhibitor; combination therapy; INTERFERON-ALPHA; RAPAMYCIN; EFFICACY;
D O I
10.1002/cncr.25931
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: The current study was conducted to assess the maximum tolerated dose (MTD), safety, pharmacokinetics, and preliminary antitumor effect of everolimus, a mammalian target of rapamycin inhibitor, in combination with sorafenib, a tyrosine kinase inhibitor, in patients with metastatic clear cell renal cell carcinoma. METHODS: Sequential cohorts of patients received escalating doses of everolimus and sorafenib in 28-day cycles in the absence of a dose-limiting toxicity (DLT) or disease progression were examined. RESULTS: Twenty patients with a median age of 65 years received therapy in 3 cohorts. Dose level 1 was comprised of everolimus at a dose of 2.5 mg daily and sorafenib at a dose of 400 mg twice daily (6 patients), dose level 2 was comprised of everolimus at a dose of 5 mg daily and sorafenib at a dose of 400 mg twice daily (8 patients), and dose level 3 was comprised of everolimus at a dose of 10 mg daily and sorafenib at a dose of 200 mg twice daily (6 patients). DLTs included grade 4 (according to National Cancer Institute Common Terminology Criteria for Adverse Events [version 3.0]) hyperuricemia with grade 2 gout and grade 3 lipase associated with grade 2 pancreatitis at dose level 2, and grade 3 rash in 2 patients at dose level 3. Dose level 2 (everolimus at a dose of 5 mg daily and sorafenib at a dose of 400 mg twice daily) was established as the maximum tolerated dose. Treatment-related adverse events occurring in >20% of patients included diarrhea, hand-foot syndrome, hypertension, hypophosphatemia, hypothyroidism, and rash. Five of 20 patients achieved Response Evaluation Criteria In Solid Tumors (RECIST)-defined partial responses, all of which occurred in patients without a history of prior systemic therapy. Seven of 8 patients treated at dose level 2 experienced a partial response or stable disease. Pharmacokinetic analysis revealed no interaction between everolimus and sorafenib. CONCLUSIONS: The combination of everolimus and sorafenib was associated with acceptable toxicity and evidence of antitumor activity in previously untreated patients with metastatic renal cell carcinoma. Cancer 2011;117:4194-200. (C) 2011 American Cancer Society.
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页码:4194 / 4200
页数:7
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