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The ACR 20/50/70 response assesses the treatment of symptoms and signs in subjects with active RA.
The ACR20/ACR50/ACR70 response assesses the treatment of symptoms and signs in patients with active PsA.
Vaccine response rate was chosen as the primary endpoint to evaluate the immunogenicity of the vaccines as vaccine response assesses the ability of participants to respond to the vaccine regardless of their serostatus at pre-vaccination.
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Few reports are available documenting survival outcomes according to response assessed using different response-assessment schemes.
The second potential predictive factor of response assessed was TS.
Primary outcome was objective response (assessed by RECIST).
The significance of response assessed using paired t-test.
By contrast, the response assessed using RECIST, mRECIST, and EASL criteria did not correlate with survival.
Physician global response assessed by a blinded evaluator should be considered in future studies.
Treatment was repeated every 2 weeks, with response assessed every six cycles.
Tumour thickness also correlated with pathologic response assessed according to the Blazer classification.
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