Metastatic Colorectal Cancer Clinical Trial
Official title:
FIRST-LINE FOLFOXIRI PLUS BEVACIZUMAB FOLLOWED BY REINTRODUCTION OF FOLFOXIRI PLUS BEVACIZUMAB AT PROGRESSION Versus FOLFOX PLUS BEVACIZUMAB FOLLOWED BY FOLFIRI PLUS BEVACIZUMAB AT PROGRESSION IN FIRST- AND SECOND-LINE TREATMENT OF UNRESECTABLE METASTATIC COLORECTAL CANCER.
Bev improves the efficacy of first-line chemotherapy in unresectable mCRC. In the phase III
TRIBE trial upfront FOLFOXIRI plus bev provided a significant advantage in terms of PFS and
RR compared to FOLFIRI plus bev. A trend toward better OS was also evidenced. The second-line
treatment was at investigator's choice. A manageable increase in diarrhea, mucositis and
neutropenia was reported, while no differences in febrile neutropenia, serious adverse events
and toxic deaths were evidenced.
A growing amount of data support the clinical relevance of achieving an early and deep tumor
shrinkage.
Phase III TML and BEBYP trials demonstrated that the continuation of bev beyond disease
progression combined with a switched chemotherapy regimen provided a significant advantage in
terms of OS and PFS.
Based on recent evidences, the partial interruption of the upfront "induction" chemotherapy
before disease progression and the prosecution of bev until disease progression as
maintenance treatment is a valid strategy in the treatment of mCRC.
On the basis of these considerations, a first-line doublet plus bev followed by a second-line
switched doublet (from oxaliplatin to irinotecan and viceversa) plus bev should be considered
a standard option for mCRC patients. Only retrospectively collected data are currently
available about the efficacy of first-line FOLFOXIRI plus bev followed by second-line
rechallenge with FOLFOXIRI plus bev. We therefore designed the present phase III randomized
trial of first-line FOLFOXIRI plus bev followed by reintroduction of FOLFOXIRI plus bev at
progression versus FOLFOX plus bev followed by FOLFIRI plus bev at progression in first- and
second-line treatment of unresectable mCRC patients.
n/a
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