Phase 3 Trial of Cabozantinib to Treat Advanced Neuroendocrine Tumors
Jennifer A Chan1, Susan Geyer2, Tyler Zemla2
1Dana-Farber Cancer Institute, Boston.
Background:
Treatment options for patients with advanced neuroendocrine tumors are limited. The efficacy of cabozantinib in the treatment of previously treated, progressive extrapancreatic or pancreatic neuroendocrine tumors is unclear.
Methods:
We enrolled two independent cohorts of patients - those with extrapancreatic neuroendocrine tumors and those with pancreatic neuroendocrine tumors - who had received peptide receptor radionuclide therapy or targeted therapy or both. Patients were randomly assigned in a 2:1 ratio to receive cabozantinib at a dose of 60 mg daily or placebo. The primary end point was progression-free survival as assessed by blinded independent central review. Key secondary end points included objective response, overall survival, and safety.
Results:
In the cohort of 203 patients with extrapancreatic neuroendocrine tumors, the median progression-free survival with cabozantinib was 8.4 months, as compared with 3.9 months with placebo (stratified hazard ratio for progression or death, 0.38; 95% confidence interval [CI], 0.25 to 0.59; P<0.001). In the cohort of 95 patients with pancreatic neuroendocrine tumors, the median progression-free survival with cabozantinib was 13.8 months, as compared with 4.4 months with placebo (stratified hazard ratio, 0.23; 95% CI, 0.12 to 0.42; P<0.001). The incidence of confirmed objective response with cabozantinib was 5% and 19% among patients with extrapancreatic and pancreatic neuroendocrine tumors, respectively, as compared with 0% with placebo. Grade 3 or higher adverse events were noted in 62 to 65% of the patients treated with cabozantinib, as compared with 23 to 27% of the patients who received placebo. Common treatment-related adverse events of grade 3 or higher included hypertension, fatigue, diarrhea, and thromboembolic events.
Conclusions:
Cabozantinib, as compared with placebo, significantly improved progression-free survival in patients with previously treated, progressive advanced extrapancreatic or pancreatic neuroendocrine tumors. Adverse events were consistent with the known safety profile of cabozantinib. (Funded by the National Cancer Institute and others; CABINET ClinicalTrials.gov number, NCT03375320.).
Insights
Cabozantinib significantly improved progression-free survival in advanced neuroendocrine tumors. This study found cabozantinib effective for patients with previously treated, progressive extrapancreatic or pancreatic neuroendocrine tumors.
Area of Science:
- Oncology
- Medical Science
Background:
- Limited treatment options exist for advanced neuroendocrine tumors.
- The efficacy of cabozantinib in progressive neuroendocrine tumors remains unclear.
Purpose of the Study:
- To evaluate the efficacy and safety of cabozantinib in patients with advanced neuroendocrine tumors.
- To compare progression-free survival in patients treated with cabozantinib versus placebo.
Main Methods:
- Two independent cohorts (extrapancreatic and pancreatic neuroendocrine tumors) were enrolled.
- Patients received prior peptide receptor radionuclide therapy or targeted therapy.
- Randomized controlled trial comparing cabozantinib (60 mg daily) to placebo in a 2:1 ratio.
Main Results:
- Median progression-free survival was significantly longer with cabozantinib (8.4 months extrapancreatic, 13.8 months pancreatic) compared to placebo (3.9 months extrapancreatic, 4.4 months pancreatic).
- Objective response rates were 5% (extrapancreatic) and 19% (pancreatic) with cabozantinib, versus 0% with placebo.
- Grade 3 or higher adverse events occurred in 62-65% of cabozantinib patients versus 23-27% of placebo patients, including hypertension, fatigue, diarrhea, and thromboembolic events.
Conclusions:
- Cabozantinib demonstrated significant improvement in progression-free survival for advanced neuroendocrine tumors.
- Adverse events were consistent with the known safety profile of cabozantinib.
- Cabozantinib is an effective treatment option for previously treated, progressive neuroendocrine tumors.
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