Preliminary study on BRICS sequential therapeutic regimen as salvage treatment for refractory advanced colorectal

Yonghai Peng1, Jian Wang2, Junhui Wang3

  • 1Department of Oncology, Cangshan Hospital Area, 900 Hospital of the Joint Logistics Support Force, Fujian, Fuzhou, China.

Frontiers in Immunology
|October 6, 2025
PubMed
Abstract

Insights

The novel BRICS regimen shows promise for refractory mismatch repair-proficient/microsatellite stable metastatic colorectal cancer, improving outcomes with an 88.9% disease control rate and 12.3-month median overall survival. This approach offers a new treatment option for patients resistant to standard therapies.

Area of Science:

  • Oncology
  • Immunotherapy
  • Gastroenterology

Background:

  • Metastatic colorectal cancer (CRC) that is mismatch repair-proficient/microsatellite stable (pMMR/MSS) is resistant to current treatments.
  • Patients with refractory pMMR/MSS CRC have a poor prognosis, with median overall survival (OS) under 10 months.

Purpose of the Study:

  • To evaluate the efficacy and safety of the novel BRICS sequential regimen in patients with refractory pMMR/MSS metastatic CRC.
  • To assess objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), and OS.

Main Methods:

  • A retrospective analysis of 27 patients with refractory pMMR/MSS metastatic CRC treated with the BRICS regimen.
  • BRICS includes Stereotactic body radiotherapy, high-dose probiotics, low-dose chemotherapy, and PD-1 inhibitor therapy.

Main Results:

  • The BRICS regimen achieved an ORR of 33.3% and a DCR of 88.9%.
  • Median PFS was 7.20 months and median OS was 12.30 months.
  • Eastern Cooperative Oncology Group Performance Status (ECOG PS) >2 and metastatic burden (≥3 organs) were associated with poorer outcomes. Grade 3-4 adverse events occurred in 22.2% of patients.

Conclusions:

  • The BRICS regimen demonstrates clinically meaningful efficacy and manageable toxicity in refractory pMMR/MSS metastatic CRC.
  • ECOG PS >2 and high metastatic burden predict limited benefit, suggesting the need for prospective validation in biomarker-selected populations.