Liver Metastasis Colon Cancer Clinical Trial
Official title:
Observational Study on Transarterial Chemoembolization With Irinotecan-loaded Embolics Associated With Systemic Bevacizumab for the Treatment of Refractory Liver Metastases From Colorectal Cancer
Transarterial chemoembolization (TACE) is an effective, minimally invasive therapy that is
widely used for unresectable colorectal cancer liver metastases (CRC-LM) treatment.
Chemoembolization, however, induces a hypoxic micro-environment, which increases
neo-angiogenesis, and may promote early progression. For this reason, efficacy may be
improved by associating TACE with an angiogenesis inhibitor, such as bevacizumab.
The use of FOLFIRI associate to Bevacizumab is part of clinical practice and is commonly used
for the therapy of patients with CRC-LM both wild type and mutant.
This case-control observational study aim to compare patients treated with TACE using
Irinotecan-loaded embolics followed by systemic Bevacizumab versus patients treated with
FILFIRI+ Bevacizumab
TACE is indicated for the treatment of unresectable CRC_LM, patients who are refractory to
systemic chemotherapy, elderly, or have a poor performance status, and is usually performed
using irinotecan (IRI) covalently loaded onto embolics.
Although chemoembolization with irinotecan-loaded embolics results in an objective response,
this method creates a hypoxic micro-environment. Hypoxia induces and activates the HIF-1 and
HIF 2 hypoxia-inducible transcription factors, which promote high-level VEGF expression and
subsequent neo-angiogenesis.
This may provide a mechanism for early relapse and progression following TACE and strongly
support a rational for following TACE therapy with a therapeutic inhibitor of angiogenesis,
such as bevacizumab.
The use of FOLFIRI associate to Bevacizumab is part of clinical practice and is commonly used
for the therapy of patients with CRC-LM both wild type and mutant.
This case-control observational study aim to compare patients treated with TACE using
Irinotecan-loaded embolics followed by systemic Bevacizumab versus patients treated with
FILFIRI+ Bevacizumab
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