Bevacizumab in combination with cetuximab and irinotecan after failure of cetuximab and irinotecan in patients with metastatic colorectal cancer

Authors

  • Finn Ole Larsen Department of Oncology, Herlev Hospital, University of Copenhagen, Denmark
  • Per Pfeiffer Department of Oncology, Odense University Hospital, Odense, Denmark
  • Dorte Nielsen Department of Oncology, Herlev Hospital, University of Copenhagen, Denmark
  • Kristin Skougaard Department of Oncology, Herlev Hospital, University of Copenhagen, Denmark
  • Camilla Qvortrup Department of Oncology, Odense University Hospital, Odense, Denmark
  • Kirsten Vistisen Department of Oncology, Herlev Hospital, University of Copenhagen, Denmark
  • Anne-Lene Fromm Department of Oncology, Herlev Hospital, University of Copenhagen, Denmark
  • Trine L. Jørgensen Department of Oncology, Odense University Hospital, Odense, Denmark
  • Jon K. Bjerregaard Department of Oncology, Odense University Hospital, Odense, Denmark
  • Estrid Hoegdall Department of Pathology, Herlev Hospital, University of Copenhagen, Denmark
  • Benny V. Jensen Department of Oncology, Herlev Hospital, University of Copenhagen, Denmark

DOI:

https://doi.org/10.3109/0284186X.2010.546369

Abstract

Background. The efficacy and safety of concurrent administration of irinotecan with the two monoclonal antibodies cetuximab and bevacizumab as fourth line therapy in heavily pretreated patients with metastatic colorectal cancer were evaluated. Patients and methods. Patients with metastatic colorectal cancer who had progressed on therapy with 5-FU, oxaliplatin and irinotecan in the first and second line setting and on the combination of irinotecan and cetuximab in third line setting independent of their KRAS mutation status, were treated with irinotecan and cetuximab combined with bevacizumab in a dosage of 5 mg/kg. All drugs were administered every second week. Results. From January 2007 to November 2008 27 patients were treated with cetuximab, irinotecan and bevacizumab. The triple-combination was well tolerated. Progression free survival (PFS) was 8.3 months and median overall survival (mOS) was 12.0 months. Two patients without KRAS mutation (7%) obtained a partial response and 17 (63%) had stable disease for at least two months. A retrospective KRAS mutation analysis revealed that there was a trend toward longer PFS and mOS in patients without KRAS mutations compared to patients with KRAS mutations with a PFS of 8.9 vs. 5.1 months and a mOS of 12.7 vs. 9.0 months. Conclusion. Bevacizumab is safe to add to irinotecan and cetuximab with a toxicity profile that seems to be similar to what would be expected from the agents alone. The results indicate that adding bevacizumab to irinotecan and cetuximab in a fourth line setting may induce a high rate of disease control in heavily pretreated patients with metastatic colorectal cancer.

Downloads

Download data is not yet available.

Downloads

Published

2011-05-01

How to Cite

Ole Larsen, F., Pfeiffer, P., Nielsen, D., Skougaard, K., Qvortrup, C., Vistisen, K., … Jensen, B. V. (2011). Bevacizumab in combination with cetuximab and irinotecan after failure of cetuximab and irinotecan in patients with metastatic colorectal cancer. Acta Oncologica, 50(4), 574–577. https://doi.org/10.3109/0284186X.2010.546369