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. 2019 Feb 1;10(10):1070-1084.
doi: 10.18632/oncotarget.26626.

Safety and effectiveness of FOLFOXIRI plus molecular target drug therapy for metastatic colorectal cancer: A multicenter retrospective study

Affiliations

Safety and effectiveness of FOLFOXIRI plus molecular target drug therapy for metastatic colorectal cancer: A multicenter retrospective study

Takatsugu Ogata et al. Oncotarget. .

Abstract

Introduction: FOLFOXIRI plus bevacizumab has a promising efficacy as first-line systemic chemotherapy for metastatic colorectal cancer (mCRC). This study aimed to evaluate the safety and effectiveness of FOLFOXIRI plus antibodies.

Results: Fifty-five patients were enrolled (median age: 60 years, males: 25, females: 30). Twenty-six subjects had RAS mutations and 29 had RAS wild-type. Anti-VEGF and anti-EGFR antibodies were administered to 38 and 17 patients, respectively. The most common severe adverse event was neutropenia (51%). The overall response rate (ORR) was 69% (55% with anti-VEGF antibodies and 100% with anti-EGFR antibodies; P = 0.190), and the disease control rate was 98% (stable disease: 16 patients). With a median follow-up period of 18.4 months, the median progression-free survival (mPFS) was 11.0 months and the median overall survival (mOS) was 41.9 months. The mPFS and mOS did not significantly differ between patients treated with anti-EGFR antibodies and those with anti-VEGF antibodies.

Methods: We retrospectively collected data from mCRC patients treated with FOLFOXIRI plus antibodies between March 2014 and December 2017.

Conclusions: FOLFOXIRI plus antibody therapy was effective in patients with mCRC. The response rate was higher in patients treated with anti-EGFR antibodies than in those treated with anti-VEGF antibodies.

Keywords: FOLFOXIRI therapy; anti-EGFR antibodies; anti-VEGF antibodies; metastatic colorectal cancer; triplet.

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Conflict of interest statement

CONFLICTS OF INTEREST The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1. Depth of response
Figure 2
Figure 2. Early tumor response
Figure 3
Figure 3. Progression-free survival (PFS) and overall survival (OS)
(A) PFS for all patients; (B) OS for all patients.
Figure 4
Figure 4. Progression-free survival by antibodies and tumor location
(A) Classified by antibodies; (B) Classified by sidedness; (C) Classified by antibodies and sidedness.
Figure 5
Figure 5. Overall survival by antibodies and tumor location
(A) Classified by antibodies; (B) Classified by sidedness; (C) Classified by antibodies and sidedness.
Figure 6
Figure 6. Overall survival in patients treated with conversion therapy
Figure 7
Figure 7. Changes in the neutrophil count during FOLFOXIRI plus molecular target drugs

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