Copyright
©The Author(s) 2019.
World J Gastroenterol. Aug 7, 2019; 25(29): 3920-3928
Published online Aug 7, 2019. doi: 10.3748/wjg.v25.i29.3920
Published online Aug 7, 2019. doi: 10.3748/wjg.v25.i29.3920
Setting | Clinical trial | Drugs and regimen | n | ORR | PFS rate at 12 mo | Median PFS, mo | OS rate at 12 mo |
Neoadjuvant | [18] | Nivolumab (3) + Ipilimumab (1) | 7 | pCR 57% (4/7) | NR | NR | NR |
First line | CM-142[17] | Nivolumab (3) + Ipilimumab (1/6 wk) | 45 | 60% | 77% | NR | 83% |
≥ Second line | CM-142[14] | Nivolumab | 74 | 31% | 50% | 14.3 | 73% |
KN-164[16] | Pembrolizumab | 61 | 28% | 34% | 2.3 | 72% | |
CM-142[15] | Nivolumab (3) + Ipilimumab (1/3 wk) | 119 | 55% | 71% | NR | 85% |
- Citation: Tintelnot J, Stein A. Immunotherapy in colorectal cancer: Available clinical evidence, challenges and novel approaches. World J Gastroenterol 2019; 25(29): 3920-3928
- URL: https://www.wjgnet.com/1007-9327/full/v25/i29/3920.htm
- DOI: https://dx.doi.org/10.3748/wjg.v25.i29.3920