Copyright
©The Author(s) 2024.
World J Gastrointest Oncol. Feb 15, 2024; 16(2): 273-286
Published online Feb 15, 2024. doi: 10.4251/wjgo.v16.i2.273
Published online Feb 15, 2024. doi: 10.4251/wjgo.v16.i2.273
Limitations | Solution |
Most clinical trials do not take into account the etiology of HCC | Subgroup analysis according on real-world causes |
Insufficient exploratory analysis of subgroups during safety evaluation | Further analysis will be performed based on the subject's characteristics (e.g., height, weight, underlying disease) or the subject's population (e.g., sex, age) |
The sample size of some studies was too small and easy to shift the results | Strict adherence to the inclusion and exclusion criteria, increasing the sample size |
Assessing QOL after treatment could help assess the negative impact and clinical decisions of appropriate treatment, but the primary endpoint of most experiments does not include QOL | The primary endpoint, in addition to tumor treatment response and imaging assessment |
- Citation: Pan D, Liu HN, Qu PF, Ma X, Ma LY, Chen XX, Wang YQ, Qin XB, Han ZX. Progress in the treatment of advanced hepatocellular carcinoma with immune combination therapy. World J Gastrointest Oncol 2024; 16(2): 273-286
- URL: https://www.wjgnet.com/1948-5204/full/v16/i2/273.htm
- DOI: https://dx.doi.org/10.4251/wjgo.v16.i2.273