Copyright
©The Author(s) 2019.
World J Gastroenterol. May 28, 2019; 25(20): 2416-2429
Published online May 28, 2019. doi: 10.3748/wjg.v25.i20.2416
Published online May 28, 2019. doi: 10.3748/wjg.v25.i20.2416
NCT number | Institution | Phase | Disease | Intervention | Estimated enrollment | Primary endpoint |
NCT03482102 | United States (MGH) | II | Locally advanced/ unresectable or metastatic disease HCC or biliary tract cancer | Experimental: Tremelimumab + Durvalumab + EBRT | 70 | Best overall response rate |
NCT03203304 | United States (UCh) | I | HCC | SBRT Nivolumab → +/- ipilimumab + SBRT (8 Gy × 5) | 50 | Number of participants with adverse events |
NCT03316872 | Canada (UHN) | II | HCC showing progression after sorafenib | Pembrolizumab + SBRT | 30 | Overall response rate |
NCT03812562 | United States (NU) | I | HCC intended to be resected | 90Y SIRT → Nivolumab | 12 | Recurrence rate |
NCT03033446 | Singapore (NCC) | II | HCC not suitable for resection or transplant | 90Y SIRT → Nivolumab | 40 | Response rate |
NCT02837029 | United States (NU) | I/Ib | HCC stage IIIA - IVB | 90Y SIRT → Nivolumab | 35 | Maximum tolerated dose |
NCT03099564 | United States (UNC) | I | HCC | 90Y SIRT + Pembrolizumab | 30 | Progression-free survival |
- Citation: Choi C, Yoo GS, Cho WK, Park HC. Optimizing radiotherapy with immune checkpoint blockade in hepatocellular carcinoma. World J Gastroenterol 2019; 25(20): 2416-2429
- URL: https://www.wjgnet.com/1007-9327/full/v25/i20/2416.htm
- DOI: https://dx.doi.org/10.3748/wjg.v25.i20.2416