Ensuring the safety of new drugs is critically important to regulators, pharmaceutical researchers and patients alike. Even so, unexpected toxicities still account for 20–30% of clinical trial failure
The purpose of this study is to determine if the addition of apalutamide to ADT provides superior efficacy in improving radiographic progression-free survival (rPFS) or overall survival (OS) for par
Pass rates calculated for the gamma evaluation in the tumor target and OARs compared with a reference TPS dose with the calculated dose in 3DVH and compass (C-Recal.: Compass Recalculation, C-Recon.:
Objective: The occurrence, development, and prognosis of serious adverse events (SAEs) associated with anticancer drugs in clinical trials have important guiding significance for real-world clinical a