Second-line angiogenesis inhibition in metastatic colorectal cancer patients: Straightforward or overcrowded?

Riccardo Giampieri, Marta Caporale, Filippo Pietrantonio, Francesca V. Negri, Filippo De Braud, Francesco Giuliani, Valeria Pusceddu, Laura Demurtas, Angelo Restivo, Caterina Fontanella, Giuseppe Aprile, Stefano Cascinu, Mario Scartozzi

Research output: Contribution to journalArticle

Abstract

Although the number of therapeutic options targeting tumour angiogenesis is becoming increasingly relevant, the question of the optimal choice for second-line anti-angiogenic inhibition in combination with chemotherapy for metastatic colorectal cancer patients remains largely unanswered.In fact the lack of head to head comparison between consolidated options such as bevacizumab and new treatment alternatives such as aflibercept and ramucirumab makes the selection in the clinical practice challenging, particularly when the patient has already received an anti-angiogenic-based combination up-front.In the following pages we described the biological scenario validating second-line angiogenesis inhibition in colorectal cancer along with potential mechanism of resistance. We also critically described the available evidence recommending the use of the bevacizumab, aflibercept and ramucirumab in this setting with the final aim to guide the choice in the clinical practice.

Original languageEnglish
Pages (from-to)99-106
Number of pages8
JournalCritical Reviews in Oncology/Hematology
Volume100
DOIs
Publication statusPublished - Apr 1 2016

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Keywords

  • Aflibercept
  • Angiogenesis
  • Bevacizumab
  • Colorectal cancer
  • Ramucirumab
  • Second line

ASJC Scopus subject areas

  • Oncology
  • Hematology
  • Geriatrics and Gerontology

Cite this

Giampieri, R., Caporale, M., Pietrantonio, F., Negri, F. V., De Braud, F., Giuliani, F., Pusceddu, V., Demurtas, L., Restivo, A., Fontanella, C., Aprile, G., Cascinu, S., & Scartozzi, M. (2016). Second-line angiogenesis inhibition in metastatic colorectal cancer patients: Straightforward or overcrowded? Critical Reviews in Oncology/Hematology, 100, 99-106. https://doi.org/10.1016/j.critrevonc.2016.02.005