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.

Oncology Reports
|March 6, 2017
PubMed

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.