Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Clinical Trial
. 2019 Aug;24(8):e702-e708.
doi: 10.1634/theoncologist.2018-0839. Epub 2019 Mar 22.

Anlotinib Versus Sunitinib as First-Line Treatment for Metastatic Renal Cell Carcinoma: A Randomized Phase II Clinical Trial

Affiliations
Clinical Trial

Anlotinib Versus Sunitinib as First-Line Treatment for Metastatic Renal Cell Carcinoma: A Randomized Phase II Clinical Trial

Ai-Ping Zhou et al. Oncologist. 2019 Aug.

Abstract

Background: Anlotinib is a tyrosine kinase inhibitor inhibiting angiogenesis. This multicenter, randomized phase II trial aimed to investigate the efficacy and safety of anlotinib in comparison with sunitinib as first-line treatment for patients with metastatic renal cell carcinoma (mRCC).

Materials and methods: Patients with mRCC from 13 clinical centers were randomly assigned in a 2:1 ratio to receive anlotinib (n = 90) or sunitinib (n = 43). Anlotinib was given orally at a dose of 12 mg once daily (2 weeks on/1 week off), and sunitinib was given orally at 50 mg once daily (4 weeks on/2 weeks off). The primary endpoint was progression-free survival (PFS). Secondary endpoints included overall survival (OS), objective response rate (ORR), disease control rate (DCR), and safety.

Results: The median PFS was similar with anlotinib and sunitinib (17.5 vs. 16.6 months, p > .05). The median OS (30.9 vs. 30.5 months, p > .05), ORR (30.3% vs. 27.9%), and 6-week DCR (97.8% vs. 93.0%) were similar in the two groups. Adverse events (AEs) of grade 3 or 4 were significantly less frequent with anlotinib than with sunitinib (28.9% vs. 55.8%, p < .01), especially in terms of thrombocytopenia and neutropenia. AEs occurring at a lower frequency with anlotinib were hand-foot syndrome, eyelid edema, hair depigmentation, skin yellowing, neutropenia, thrombocytopenia, and anemia. The incidence of serious AEs was lower with anlotinib than with sunitinib.

Conclusion: The clinical efficacy of anlotinib was similar to that of sunitinib as the first-line treatment for mRCC, but with a more favorable safety profile.

Implications for practice: This study evaluated the efficacy and safety of anlotinib for the first-line treatment of metastatic renal cell carcinoma. Anlotinib, which was developed independently in China, is a new tyrosine kinase inhibitor inhibiting multiple kinases involved in angiogenesis and tumor proliferation. Results indicated that the efficacy of anlotinib is comparable to and the safety is better than that of sunitinib.

Keywords: Anlotinib; Metastatic renal cell cancer; Phase II clinical trial.

PubMed Disclaimer

Conflict of interest statement

Disclosures of potential conflicts of interest may be found at the end of this article.

Figures

Figure 1.
Figure 1.
Flowchart of patient disposition.
Figure 2.
Figure 2.
Kaplan‐Meier plot of progression free survival in the anlotinib group (black line) and the sunitinib group (red line). Abbreviations: CI, confidence interval; HR, hazard ratio.

References

    1. Chow WH, Dong LM, Devesa SS. Epidemiology and risk factors for kidney cancer. Nat Rev Urol 2010;7:245–257. - PMC - PubMed
    1. Hsieh JJ, Purdue MP, Signoretti S et al. Renal cell carcinoma. Nat Rev Dis Primers 2017;3:17009. - PMC - PubMed
    1. Motzer RJ. New perspectives on the treatment of metastatic renal cell carcinoma: An introduction and historical overview. The Oncologist 2011;16(suppl 2):1–3. - PMC - PubMed
    1. Hakimi AA, Reznik E, Lee CH et al. An integrated metabolic atlas of clear cell renal cell carcinoma. Cancer Cell 2016;29:104–116. - PMC - PubMed
    1. Rini BI. Vascular endothelial growth factor–targeted therapy in renal cell carcinoma: Current status and future directions. Clin Cancer Res 2007;13:1098–1106. - PubMed

Publication types

MeSH terms