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This study investigates the feasibility of a 3-hour 3-weekly infusion versus the standard 24-hour infusion, and the approach with the best results is being further compared to 3-weekly doxorubicin in the phase III part of the study with PFS as primary endpoint.
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The models were further compared to other previously published models.
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The results are further compared to those of other published methods and are shown to be far more accurate.
The model is further compared to a similar published model and is shown to be far more accurate.
Our findings are further compared to experimental data obtained from measurements in aqueous solutions and ionic liquids.
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LGP models are further compared to the corresponding design code (Eurocode 3), reference values and several existing models.
Experimental results have been further compared to data in the open literature by authors with similar experimental investigations.
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