A phase 1b clinical trial of the multi-targeted tyrosine kinase inhibitor lenvatinib (E7080) in combination with everolimus for treatment of metastatic renal cell carcinoma (RCC) Journal Article
| Authors: | Molina, A. M.; Hutson, T. E.; Larkin, J.; Gold, A. M.; Wood, K.; Carter, D.; Motzer, R.; Michaelson, M. D. |
| Article Title: | A phase 1b clinical trial of the multi-targeted tyrosine kinase inhibitor lenvatinib (E7080) in combination with everolimus for treatment of metastatic renal cell carcinoma (RCC) |
| Abstract: | Purpose: Lenvatinib is an oral multi-targeted tyrosine kinase inhibitor of VEGFR1-3, FGFR1-4, PDGFRβ, RET, and KIT. Everolimus is an oral mammalian target of rapamycin inhibitor approved for advanced renal cell carcinoma (RCC). This phase 1b study assessed safety, maximum tolerated dose (MTD), and preliminary antitumor activity of lenvatinib plus everolimus in metastatic RCC (mRCC) patients. Methods: Patients with advanced unresectable or mRCC and Eastern Cooperative Oncology Group performance status 0-1 were eligible (number of prior treatments not restricted). Starting dose was lenvatinib 12 mg once daily with everolimus 5 mg once daily administered continuously in 28-day cycles using a conventional 3 + 3 dose-escalation design. At the MTD, additional patients were enrolled in an expansion cohort. Results: Twenty patients (mean 58.4 years) received lenvatinib [12 mg (n = 7); 18 mg (n = 11); 24 mg (n = 2)] plus everolimus 5 mg. MTD was established as once daily lenvatinib 18 mg plus everolimus 5 mg. The most common treatment-related treatment-emergent adverse events (all dosing cohorts) were fatigue 60 % (Grade ≥3: 10 %), mucosal inflammation 50 %, proteinuria (Grade ≥3: 15 %), diarrhea (Grade ≥3: 10 %), vomiting (Grade ≥3: 5 %), hypertension, and nausea, each 40 %. In MTD and lowest-dose cohorts (n = 18), best responses of partial response and stable disease were achieved in 6 (33 %) and 9 (50 %) patients, respectively. Conclusions: Lenvatinib 18 mg combined with everolimus 5 mg was associated with manageable toxicity consistent with individual agents and no new safety signals. Observed activity warrants further evaluation of the combination in advanced RCC patients. © 2013 The Author(s). |
| Keywords: | everolimus; mtor; vegf; metastatic renal cell carcinoma; antitumor; lenvatinib |
| Journal Title: | Cancer Chemotherapy and Pharmacology |
| Volume: | 73 |
| Issue: | 1 |
| ISSN: | 0344-5704 |
| Publisher: | Springer |
| Date Published: | 2014-01-01 |
| Start Page: | 181 |
| End Page: | 189 |
| Language: | English |
| DOI: | 10.1007/s00280-013-2339-y |
| PROVIDER: | scopus |
| PMCID: | PMC3889692 |
| PUBMED: | 24190702 |
| DOI/URL: | |
| Notes: | Export Date: 3 March 2014 -- CODEN: CCPHD -- Source: Scopus |
Altmetric
Citation Impact
BMJ Impact Analytics
Related MSK Work