Metastatic colorectal cancer first-line treatment with bevacizumab: the impact of K-ras mutation
Received 9 February 2013
Accepted for publication 8 April 2013
Published 29 November 2013 Volume 2013:6 Pages 1761—1769
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 3
Luigi Rossi,1,2 Enzo Veltri,3 Angelo Zullo,4 Federica Zoratto,1 Maria Colonna,5 Flavia Longo,6 Marcella Mottolese,7 Diana Giannarelli,8 Luigi Ruco,9 Paolo Marchetti,10 Adriana Romiti,10 Viola Barucca,10 Giuseppe Giannini,11 Loredana Bianchi,1 Silverio Tomao1
1Department of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Rome, Italy; 2Oncology Unit, ICOT Hospital, Latina, Italy; 3Oncology Unit, SM Goretti Hospital, Latina, Italy; 4Gastroenterology and Digestive Endoscopy Unit, Nuovo Regina Margherita Hospital, Rome, Italy; 5Oncology Unit, Don Luigi di Liegro Hospital, Gaeta, Italy; 6Oncology Unit, Umberto I Policlinico di Roma Hospital, Sapienza University of Rome, Rome, Italy; 7Department of Pathology, 8Biostatistics and Scientific Direction, Regina Elena National Cancer Institute, Rome, Italy; 9Department of Pathology, 10Oncology Unit, Sant'Andrea Hospital, 11Department of Pathology, Umberto I Policlinico di Roma Hospital, Sapienza University of Rome, Rome, Italy
Background: Bevacizumab plus chemotherapy prolongs progression-free survival (PFS) and overall survival (OS) in metastatic colorectal cancer (mCRC). Although there is strong evidence to suggest that the mutational status of the K-ras oncogene has a role as a predictive factor for activity in patients treated with cetuximab and panitumumab, few data have been obtained in patients treated with bevacizumab. We conducted an additional retrospective analysis to investigate the prognostic value of K-ras mutation relative to mCRC first-line treatment with bevacizumab.
Materials and methods: A total of 108 patients were retrospectively reviewed. K-ras status was assessed in the overall population by sequencing. Statistical association for PFS and OS was analyzed using the Kaplan–Meier method, and the prognostic role of K-ras was determined using the logrank test.
Results: Median PFS was 10 months both for patients with wild-type (WT) K-ras and mutated (MT) K-ras (hazard ratio [HR] 0.94, P=0.75); neither difference in median OS was significant (27 months WT K-ras versus 26 months MT K-ras, HR 0.92; P=0.70). A further analysis was carried out in the two groups according to metastatic sites. No statistically significant difference in terms of PFS and OS was demonstrated between WT K-ras and MT K-ras with liver metastases only and in those with extrahepatic disease.
Conclusion: Although further study is required, our results seem to confirm that K-ras mutation does not have a prognostic role in mCRC patients receiving first-line treatment with bevacizumab.
Keywords: K-ras, bevacizumab, prognostic factor, metastatic colorectal cancer, liver metastases, extrahepatic disease
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