Avastin controls tumour growth
The Avastin MoA has multiple clinical implications
- Angiogenesis is one of the key acquired characteristics or ‘hallmarks’ essential for the growth and development of all tumour types1
- the anti-angiogenic agent Avastin has demonstrated clinical efficacy in a range of different tumour types, regardless of tumour or patient characteristics2–5
- clinical trials have reported that Avastin can be combined safely and effectively with both chemotherapy and immunotherapy.2–5
Efficacy of Avastin
- The continuous expression of VEGF throughout the tumour life cycle validates the use of Avastin up to tumour progression
- this is supported by data from Avastin clinical trials.6–9
Optimal duration of Avastin therapy
- Precise VEGF inhibition by Avastin limits the development of additional toxicity such as the AEs produced by ‘off-target’ effects of multitargeted TKIs.10–11
Precise VEGF inhibition limits toxicity
References
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- Sandler A, Gray R, Perry MC, et al. N Engl J Med 2006;355:2542–50.
- Gray R, Bhattacharya S, Bowden C, Miller K, Comis RL. J Clin Oncol 2009;27:4966–72.
- Escudier B, Pluzanska A, Koralewski P, et al. Lancet 2007;370:2103–11.
- Saltz L, Clarke S, Díaz-Rubio E, et al. J Clin Oncol 2008;26:2013–9.
- Saltz L, Clarke S, Díaz-Rubio E, et al. J Clin Oncol 2007;25(June 20 Suppl.):170s (Abstract 4028 and associated poster and oral presentations).
- Grothey A, Sugrue MM, Purdie DM, et al. J Clin Oncol 2008;26:5326–34.
- Grothey A, Sugrue M, Hedrick E, et al. J Clin Oncol 2007;25(June 20 suppl):172s (Abstract 4036 and associated poster presentation).
- Kamba T, McDonald DM. Br J Cancer 2007;96:1788–95.
- Verheul HMW, Pinedo HM. Nat Rev Cancer 2007;7:475–85.