Treatment of metastatic refractory colorectal cancer following regorafenib failure

Nobumichi Takeuchi1, Kumiko Koike1, Sonomi Yoshida1

  • 1Department of Medical Oncology, Ina Central Hospital, Ina, Nagano 396-8555, Japan.

Insights

Regorafenib (RGR) shows promise as a salvage therapy for metastatic colorectal cancer. Many patients remain fit for further treatment after RGR failure, leading to longer survival without compromising supportive care.

Area of Science:

  • Oncology
  • Gastroenterology

Background:

  • Standard treatment strategies for metastatic colorectal cancer (mCRC) after initial therapy failure are limited, with regorafenib (RGR) and TAS-102 being primary options.
  • RGR is recognized for its potential to resensitize tumors resistant to prior anticancer drugs, positioning it as a key salvage therapy for mCRC.

Purpose of the Study:

  • To evaluate the efficacy and patient fitness for subsequent treatments after regorafenib (RGR) failure in metastatic colorectal cancer (mCRC).
  • To determine if RGR salvage therapy impacts the duration of best supportive care and overall survival in mCRC patients.

Main Methods:

  • Retrospective study involving 17 patients with metastatic colorectal cancer (mCRC).
  • Patients received regorafenib (RGR) treatment after failure of standard therapies.
  • Analysis of patient fitness for further anticancer treatment and survival outcomes post-RGR failure.

Main Results:

  • 71% of patients were fit for further anticancer treatment after regorafenib (RGR) failure.
  • Patients who received subsequent anticancer treatment after RGR failure exhibited longer survival periods.
  • Regorafenib (RGR) treatment did not shorten the duration of best supportive care.

Conclusions:

  • Regorafenib (RGR) is a viable salvage option for metastatic colorectal cancer (mCRC) patients, enabling subsequent treatments and prolonging survival.
  • Further research should investigate the optimal timing for transitioning from RGR to other anticancer therapies to maximize patient benefit.