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E-Poster Display

466P - FOLFOXIRI versus FOLFOX or FOLFIRI with targeted therapy in patients with mutant BRAF metastatic colorectal cancer: A systematic review and meta-analysis

Date

17 Sep 2020

Session

E-Poster Display

Topics

Tumour Site

Colon and Rectal Cancer

Presenters

Mikhail Fedyanin

Citation

Annals of Oncology (2020) 31 (suppl_4): S409-S461. 10.1016/annonc/annonc270

Authors

M. Fedyanin, E. Polyanskaya, H. Elsnukaeva, A. Tryakin, I. Pokataev, S. Tjulandin

Author affiliations

  • Clinical Pharmacology And Chemotherapy Dept, Federal State Budgetary Institution N.N. Blokhin National Medical Research Center of Oncology of the Ministry of Health of the Russian Federation (N.N. Blokhin NMRCO), 115478 - Moscow/RU

Resources

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Abstract 466P

Background

Based on the subgroup analysis of the TRIBE study FOLFOXIRI with bevacizumab is the recommended option for patients (pts) with mBRAF metastatic colorectal cancer (mCRC) in the 1st line. However, subgroup analysis of other studies showed conflicting results. Therefore, we performed systemic review and meta-analysis to compare efficacy FOLFOXIRI and doublets with targeted therapy in pts with mBRAF mCRC in terms of progression free survival (PFS), objective response rate (ORR) and overall survival (OS).

Methods

We performed a search of all prospective randomizes studies in PubMed, Embase, and Cochrane library for all years before May 2020, compared FOLFOXIRI plus bevacizumab or anti-EGFR antibodies and FOLFOX or FOLFIRI with targeted agents at the 1st line with information of the BRAF status. Primary outcome was hazard ratio (HR) for PFS and 95% confidence interval (CI); secondary – HR for OS and odds ratio (OD) for ORR. Fixed effects were used for analysis. Meta-analysis was conducted by «Review Manager» Ver. 5.3.

Results

We identified 6 trials (CHARTA, STEAM, TRIBE, TRIBE2, VISNU, VOLFI), which included 163 pts with mBRAF (FOLFOXIRI – 83 (51%) and doublets – 80 (49%). According to results of the meta-analysis there was a tendency for higher ORR in pts with FOLFOXIRI (OR 2.95, 95% CI 0.97-8.95; p = 0.06; I2 = 33%, p for heterogeneity 0.21; 4 trials). However we didn’t find any significant improvement in PFS (HR 0.91, 95% CI 0.66-1.24; p = 0.54; I2 = 0%, p for heterogeneity 0.74; 6 trials) or OS (HR 0.75, 95% CI 0.39-1.46; p = 0.4; I2 = 51%, p for heterogeneity 0.15; 2 trials) in the group of triplet.

Conclusions

FOLFOXIRI with targeted agents did not show statistical significant improvement in the PFS and OS in pts with mBRAF compared with FOLFOX or FOLFIRI with targeted antibodies. A prospective randomized trial is needed to determine the optimal chemotherapy regimen at the 1st line for pts with mBRAF mCRC.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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