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Regorafenib with or without a programmed cell death protein 1 antibody as third-line treatment for microsatellite
Wen-Zhuo He1, Lei Wang1,2, Chen-Xi Yin3
1VIP Region, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Guangzhou, P. R. China.
Background:
Although the use of regorafenib plus nivolumab demonstrates promising outcomes in patients with refractory microsatellite stable (MSS) metastatic colorectal cancer (mCRC), this effect has not been substantiated in other studies. Moreover, a comparison between the outcomes of regorafenib and programmed cell death protein 1 (PD-1) antibody combination therapy and regorafenib monotherapy remains unexplored. In this study, we aimed to assess whether regorafenib and PD-1 antibody combination therapy is superior to regorafenib monotherapy as a third-line treatment for MSS mCRC.
Methods:
Patients with MSS mCRC who received regorafenib and PD-1 antibody or regorafenib monotherapy as third-line treatment were eligible for inclusion.
Results:
In total, 179 patients were enrolled, of which 84 were administered regorafenib combined with a PD-1 antibody and 95 were administered regorafenib monotherapy. Patients administered regorafenib combined with a PD-1 antibody had similar progression-free survival (PFS) as those on regorafenib monotherapy (median PFS was 2.4 months and 1.9 months, respectively, p = 0.086). The administration of regorafenib combined with a PD-1 antibody resulted in significantly longer PFS than that seen with regorafenib monotherapy in both male (5.2 months vs. 2.4 months, p = 0.001) and female (3.9 months vs. 1.8 months, p = 0.037) patients without liver metastasis. Female patients with liver metastasis who were administered regorafenib combined with a PD-1 antibody had shorter PFS than those administered regorafenib monotherapy (1.8 months vs. 2.0 months, p = 0.030).
Conclusion:
Liver metastasis and sex are predictors of survival benefit following the addition of a PD-1 antibody to regorafenib in patients with MSS mCRC.
Insights
Regorafenib plus PD-1 antibody therapy showed similar progression-free survival as regorafenib monotherapy in refractory microsatellite stable metastatic colorectal cancer. However, benefits varied by sex and liver metastasis status.
Area of Science:
- Oncology
- Gastroenterology
- Immunotherapy
Background:
- Refractory microsatellite stable metastatic colorectal cancer (MSS mCRC) presents treatment challenges.
- Regorafenib plus nivolumab shows promise, but further validation is needed.
- Comparative outcomes of combination vs. monotherapy are underexplored.
Purpose of the Study:
- To compare the efficacy of regorafenib plus PD-1 antibody combination therapy versus regorafenib monotherapy.
- To evaluate third-line treatment options for MSS mCRC.
- To identify patient subgroups benefiting from combination therapy.
Main Methods:
- Retrospective study of 179 patients with MSS mCRC.
- Inclusion criteria: third-line regorafenib with PD-1 antibody or regorafenib monotherapy.
- Outcome assessment: progression-free survival (PFS).
Main Results:
- Overall PFS was similar between combination and monotherapy groups (2.4 vs. 1.9 months, p=0.086).
- Combination therapy significantly improved PFS in male and female patients without liver metastasis.
- Female patients with liver metastasis showed shorter PFS with combination therapy.
Conclusions:
- Liver metastasis and sex are key predictors of response to PD-1 antibody addition.
- Combination therapy may benefit specific MSS mCRC patient subgroups.
- Further research is warranted to optimize treatment strategies.
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