Efficacy and safety of radiotherapy combined with anti‐angiogenic therapy and immune checkpoint inhibitors in MSS/pMMR metastatic colorectal cancer

Author:

Zhai Menglan1,Zhang Zixuan2,Wang Haihong1,Ren Jinghua13,Zhang Sheng13,Li Mingjie1,Liu Lichao1,Li Lisha1,Zhang Lan4,Li Xin4,Zhang Tao135ORCID,Lin Zhenyu135ORCID

Affiliation:

1. Cancer Center, Union Hospital, Tongji Medical College Huazhong University of Science and Technology Wuhan China

2. Queen Mary School, Medical Department Nanchang University Nanchang Jiangxi China

3. Hubei Key Laboratory of Precision Radiation Oncology Wuhan China

4. Department of Radiology Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan China

5. Institute of Radiation Oncology Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan China

Abstract

AbstractPurposeSeveral studies have demonstrated the effectiveness of anti‐angiogenic drugs in combination with immune checkpoint inhibitors (ICIs) in patients with microsatellite stable (MSS) or mismatch repair proficient (pMMR) metastatic colorectal cancer (mCRC). However, whether combination radiotherapy (RT) can further improve the prognosis of mCRC patients after second‐line treatment remains to be explored.MethodsRetrospective analysis of data from mCRC patients who received anti‐angiogenic targeted therapy (TT) and immunotherapy (IT) with or without RT after the failure of standard therapy. Progression‐free survival (PFS), overall survival (OS), objective response rate (ORR), disease control rate (DCR), and safety were evaluated.ResultsA total of 82 patients who received TT + IT were analyzed. For RT group (n = 42) versus NRT group (n = 40), ORR was 21.4% (9/42) versus 5.0% (2/40); DCR was 83.8% (35/42) versus 65.0% (26/40). Compared with NRT group, RT improved PFS (median: 5.0 vs. 3.6 months; p = 0.04) and OS (median: 15.2 vs. 7.2 months; p = 0.01). In addition, in the population receiving RT, the PFS of RT sequential/simultaneous TT + IT was superior to TT + IT sequential RT (median: 7.1 vs. 6.2 vs. 3.5 months, p = 0.004). Multivariate analysis suggested RT was an independent prognostic factor for PFS and OS. No treatment‐related deaths were reported.ConclusionsCompared with TT + IT, RT combined with TT + IT improved survival outcomes in MSS/pMMR mCRC patients, with manageable toxicity. RT sequential/simultaneous TT + IT treatment is expected to be the optimal strategy for MSS/PMMR mCRC.

Funder

Chinese Society of Clinical Oncology

Publisher

Wiley

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology

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