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However, treatment with any of these agents in these trials

necessitated dose reduction and modification in some

patients; thus, the risk versus benefits of treatment must be

communicated clearly to patients

[8 10] .

Collectively, the efficacy of VEGF inhibitors in the

adjuvant RCC setting has been shown in principle, and

the current data strongly suggest that patient selection is

crucial: patients with high-risk clear cell tumours, who can

tolerate the full effective dose, are more likely to benefit.

Considering the increased risk of recurrence in these high-

risk patients, treatment that provides a meaningful

improvement in DFS is a clear clinical benefit and must

be discussed as an option for patients in this setting.

Conflicts of interest:

Bernard Escudier has received honorarium for

consultancy from P

fi

zer, Novartis, BMS, Ipsen, Roche, and Exilixis.

Michael Staehler has received consulting fees from P

fi

zer, GlaxoSmithK-

line, Novartis, Bayer, Roche, Aveo, EUSAPharm, Astellas, Ipsen, Exelixis,

Pelloton, and EISAI; honoraria from P

fi

zer, GlaxoSmithKline, AVEO,

Novartis, Bayer, EUSAPharm, Astellas, Ipsen, Exelixis, Pelloton, and EISAI;

and research funding from P

fi

zer, GlaxoSmithKline, AVEO, Novartis,

Bayer, Roche/Genentech, Immatics, Wilex, Ipsen, Exelixis, and EISAI.

Funding support:

This work was funded by P

fi

zer.

Acknowledgements:

Medical writing assistance was provided by Syner-

gy Medical Communications Ltd.

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Haas NB, Manola J, Uzzo RG, et al. Adjuvant sunitinib or sorafenib for high-risk, non-metastatic renal-cell carcinoma (ECOG-ACRIN E2805):a double-blind, placebo-controlled, randomised, phase 3 tri- al. Lancet 2016;387:2008 16

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