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Detection of a Circulating MicroRNA Custom Panel in Patients with Metastatic Colorectal Cancer
Published on: March 14, 2019
Clinical and molecular assessment of regorafenib monotherapy
Nao Kakizawa1, Koichi Suzuki1, Taro Fukui1
1Department of Surgery, Saitama Medical Center, Jichi Medical University, Omiya-ku, Saitama 330-8503, Japan.
Abstract:
Regorafenib has shown survival benefits in metastatic colorectal cancer patients who were exacerbated after all standard therapies. Some patients, however, exhibit severe adverse events (AEs) resulting in treatment discontinuation. Therefore, the selection of patients likely to benefit from regorafenib is crucial. Twenty patients were treated with regorafenib for metastatic colorectal cancer; 122 plasma samples were taken from 16 of these patients for monitoring of circulating tumor DNA (ctDNA) in the blood. The treatment response, AEs, overall survival (OS), progression-free survival (PFS) and tumor morphologic changes on CT images were evaluated. KRAS mutant ctDNA was determined using digital PCR. Median PFS and OS were 2.5 and 5.9 months, respectively. Treatment was discontinued because of disease progression (PD) in 10 patients, and AEs in another 10 patients. AEs included hyperbilirubinemia, severe fatigue and skin rash. Hyperbilirubinemia was seen in two patients with multiple bilateral liver metastases, and severe fatigue in another 2 patients with poor performance status (PS). These severe AEs resulted in treatment discontinuation. Ten patients had a median PFS of 2.1 months with AE related discontinuation; PD occurred at 3.5 months (p=0.00334). Four patients exhibited a morphologic response, achieving better PFS times of 3.5, 5.3, 5.6 and 14.2 months. Emergence of the KRAS mutation in ctDNA was observed during anti-EGFR antibody treatment in 3 patients among 11 with KRAS wild-type tumors; it was detectable in the blood prior to radiographic detection of PD. Moreover, the KRAS mutation declined in two patients during regorafenib monotherapy. These patients were re-challenged with anti-EGFR antibody. Patients with extensive multiple liver metastases or poor PS are unlikely to benefit from regorafenib. Patients with a morphologic response will probably benefit from regorafenib with adequate management of other AEs. KRAS monitoring in ctDNA could be useful regarding treatment response and in determining treatment strategy.
Insights
Regorafenib offers survival benefits for metastatic colorectal cancer patients but severe adverse events (AEs) can halt treatment. Patient selection is key, as those with extensive liver metastases or poor performance status may not benefit.
Area of Science:
- Oncology
- Medical Oncology
- Gastroenterology
Background:
- Regorafenib demonstrates survival benefits in refractory metastatic colorectal cancer (mCRC).
- Severe adverse events (AEs) frequently lead to treatment discontinuation.
- Identifying patients likely to benefit from regorafenib is critical for optimizing outcomes.
Purpose of the Study:
- To evaluate the efficacy and safety of regorafenib in mCRC patients.
- To identify predictors of response and treatment discontinuation.
- To assess the role of circulating tumor DNA (ctDNA) and KRAS mutations in treatment strategy.
Main Methods:
- Prospective study of 20 mCRC patients treated with regorafenib.
- Monitoring of circulating tumor DNA (ctDNA) using digital PCR in 122 plasma samples from 16 patients.
- Evaluation of treatment response, AEs, overall survival (OS), progression-free survival (PFS), and CT imaging.
Main Results:
- Median PFS was 2.5 months and median OS was 5.9 months.
- Treatment was discontinued due to disease progression (PD) in 10 patients and AEs in 10 patients.
- Severe AEs (hyperbilirubinemia, fatigue) were associated with liver metastases and poor performance status (PS).
- Morphologic response on CT scans correlated with improved PFS.
- KRAS mutations in ctDNA emerged during anti-EGFR therapy and declined with regorafenib, suggesting potential for treatment re-challenge.
Conclusions:
- Patients with extensive liver metastases or poor PS are unlikely to benefit from regorafenib.
- Morphologic response indicates potential benefit, necessitating AE management.
- Monitoring KRAS mutations in ctDNA can guide treatment response assessment and strategy adjustments.
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