Skip to main content

Advertisement

Advertisement

Advertisement

Advertisement

ADVERTISEMENT

Poster P-415

The importance of RAS and BRAF in metastatic colorectal cancer – real-world evidence from North-East Romania

Afrasanie V. 1 Stratulat T. Alexa 1 Froicu E. 2 Gafton B. 2 Regional Institute of Oncology Iasi, Iasi, Romania Grigore T. Popa University of Medicine and Pharmacy, Iasi, Romania
Background

RAS genes are prognostic and predictive genetic biomarkers for the anti-EGFR treatment in metastatic colorectal cancer (mCRC), having an important impact on treatment management. BRAF mutation is associated with poor prognosis and resistance to anti-EGFR treatment.

Methods

We performed a retrospective analysis of patients data diagnosed with mCRC who were tested for RAS and BRAF mutations and treated in RIO Iași from April 2012 to April 2017.

Results

We identified 212 patients in which mutational status of RAS and BRAF was determined. The patients received palliative chemotherapy in association with biological therapies. 24.3% of tumors were located in the right colon, 71% in the left colon and in 4.7% of patients, the primary tumor location couldn’t be evaluated. Most of the tumors were located in the rectum: 32.7%. 47.8% of tumors had KRAS mutation, 23.3% had NRAS mutation, 14.9% had BRAF mutation and only 14% were wild type tumors. Patients with RAS and BRAF wild type tumors had a PFS of 14.2 months, those with RAS mutations a PFS of 12.6 months and those with BRAF mutations a PFS of 10.2 months.

Conclusions

Comparing the results in our study group with literature data, RAS mutations were more frequent in our population and BRAF mutations had a similar prevalence. PFS of first-line treatment was different depending on the mutational status of the tumor. The results were comparable with other studies in literature.

Legal entity responsible for the study

The authors.

Funding

This work/ paper/ article was co-funded from the European Social Fund - the Human Capital Operational Programme, Project/ Grant No: POCU/993/6/13/154722.

Disclosure

All authors have declared no conflicts of interest.

Publisher
Elsevier Ltd
Source Journal
Annals of Oncology
E ISSN 1569-8041 ISSN 0923-7534

Advertisement

Advertisement

Advertisement

Advertisement