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Evolving role of regorafenib for the treatment of advanced cancers
Axel Grothey1, Jean-Yves Blay2, Nick Pavlakis3
1West Cancer Center, Germantown, TN, USA.
Abstract:
Regorafenib is an oral tyrosine kinase inhibitor (TKI) approved for the treatment of refractory metastatic colorectal cancer (mCRC), advanced gastrointestinal stromal tumors (GIST) previously treated with imatinib and sunitinib, and unresectable hepatocellular carcinoma (HCC) following progression on sorafenib. Regorafenib was initially approved for mCRC based on improved overall survival (OS) in the randomized, placebo-controlled, phase 3 CORRECT trial, which was confirmed in an expanded population of Asian patients in the randomized, placebo-controlled phase 3 CONCUR trial. Approvals in GIST, and more recently in HCC, were based on the results from the randomized, placebo-controlled, phase 3 GRID and RESORCE trials, respectively. In this review, we provide a comprehensive summary of the clinical evidence for approval of regorafenib in mCRC, GIST, and HCC, present emerging evidence of regorafenib activity in other tumor types (namely, gastroesophageal cancer, sarcomas, biliary tract cancer, and glioblastoma), and discuss trials in progress within the context of regorafenib's mechanism of action. We describe recent advances and key lessons learned with regorafenib, including the importance of managing common drug-related toxicities using dose-optimization strategies, the search for biomarkers to predict response to treatment, and highlight some of the unaddressed questions and future directions for regorafenib across tumors.
Insights
Regorafenib is an effective treatment for metastatic colorectal cancer, advanced gastrointestinal stromal tumors, and liver cancer. Ongoing research explores its potential in other cancers and optimizing patient outcomes.
Area of Science:
- Oncology
- Pharmacology
Background:
- Regorafenib is an oral tyrosine kinase inhibitor (TKI).
- It is approved for metastatic colorectal cancer (mCRC), advanced gastrointestinal stromal tumors (GIST), and unresectable hepatocellular carcinoma (HCC).
Purpose of the Study:
- To comprehensively review clinical evidence for regorafenib's approval in mCRC, GIST, and HCC.
- To present emerging evidence of regorafenib activity in other cancer types.
- To discuss ongoing trials and future directions for regorafenib.
Main Methods:
- Review of pivotal phase 3 trials (CORRECT, CONCUR, GRID, RESORCE).
- Summary of clinical evidence supporting regorafenib's efficacy.
- Exploration of emerging data in other tumor types.
Main Results:
- Regorafenib demonstrated improved overall survival in mCRC, GIST, and HCC.
- Emerging evidence suggests activity in gastroesophageal cancer, sarcomas, biliary tract cancer, and glioblastoma.
- Management of toxicities and biomarker identification are crucial for optimal use.
Conclusions:
- Regorafenib is an established therapy for refractory mCRC, GIST, and HCC.
- Further research is warranted to expand its application and optimize treatment strategies.
- Understanding its mechanism of action and managing toxicities are key for future directions.
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