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Management of regorafenib-related toxicities: a review
Saravanan K Krishnamoorthy1, Valerie Relias2, Sunit Sebastian3
1Columbia University Medical Center, New York, New York, USA.
Abstract:
Regorafenib (Stivarga, BAY 73-4506; Bayer Pharma AG, Berlin, Germany) is an oral multikinase inhibitor that targets the angiogenic tumor microenvironment and oncogenic kinases including vascular endothelial growth factor receptor 2 (VEGFR2), VEGFR1, VEGFR3, fibroblast growth factor receptor 1 (FGFR1), RAF, KIT, RET and BRAF. Its antiangiogenic effect is greater than that of its related drug, sorafenib. Regorafenib has been approved by the US Food and Drug Administration (FDA) for the treatment of metastatic colorectal cancer (mCRC) in patients who have failed treatment with fluoropyrimidine, oxaliplatin and irinotecan based chemotherapy, an anti-VEGF therapy and, if KRAS wild type, an anti-EGFR therapy. The FDA based this approval on data from the CORRECT trial, which showed the efficacy of regorafenib compared with placebo. The most common grade 3-4 adverse reactions with the drug are hand foot skin reactions (HFSR), diarrhea, hypertension and fatigue. This review discusses the efficacy data, and the incidence and management of regorafenib's toxicities.
Insights
Regorafenib is an effective treatment for metastatic colorectal cancer (mCRC) after other therapies fail. This review details its efficacy and management of common side effects like hand foot skin reactions and fatigue.
Area of Science:
- Oncology
- Pharmacology
Background:
- Regorafenib is an oral multikinase inhibitor targeting tumor microenvironment and oncogenic kinases.
- It exhibits a greater antiangiogenic effect compared to sorafenib.
Purpose of the Study:
- To review the efficacy of regorafenib in metastatic colorectal cancer (mCRC).
- To discuss the incidence and management of regorafenib's toxicities.
Main Methods:
- Review of data from the CORRECT trial comparing regorafenib to placebo.
- Analysis of adverse reactions associated with regorafenib treatment.
Main Results:
- Regorafenib demonstrated efficacy in patients with mCRC who failed prior treatments.
- Common severe adverse reactions include hand foot skin reactions, diarrhea, hypertension, and fatigue.
Conclusions:
- Regorafenib is an FDA-approved treatment option for refractory mCRC.
- Understanding and managing toxicities is crucial for patient care.
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