Who was studied?
Planned enrollment: 62 patients with HER2-expressing advanced refractory solid tumors.
What does the publication report?
The primary planned endpoint is objective response rate, with survival, safety and quality-of-life assessments.
Safety findings
No completed trial toxicity rates are provided in this protocol.
How should we interpret it?
This is a study protocol, not a report of treatment results. Planned enrollment and endpoints are not observed outcomes.
Read the original source
This independently written summary was checked against the publicly available abstract. It is not a translation of the full paper or a clinical recommendation.
Evaluation of RC48-ADC in Combination with PRaG Regimen: An Open-Label, Prospective, Multicentre Study Assessing Efficacy and Safety for Advanced Refractory HER2-Expressing Solid Tumors (PRaG3.0 Study Protocol) · DOI: 10.1177/15330338261432537 · PMID: 41823246
Educational reporting, not individualized medical advice. Discuss treatment decisions with your clinical team.