Evidence Level:Sensitive: C2 – Inclusion Criteria
Title:
Disitamab Vedotin Combined With SOX Regimen Versus SOX Alone as Adjuvant Therapy for HER2-Moderate/High Expressing Stage Ⅲ Gastric Cancer: A Prospective, Multicenter, Randomized, Phase Ⅱ Clinical Trial
Evidence Level:Sensitive: C2 – Inclusion Criteria
Title:
Clinical studies on the efficacy and safety of RC148 injection monotherapy and combination regimens in patients with locally advanced unresectable or metastatic malignant solid tumors.
More C2 evidence

Evidence Level:Sensitive: C2 – Inclusion Criteria
Title:
A Study of RC48-ADC Combination Therapies as First-line Treatment in Advanced Metastatic Gastric Cancer
Excerpt:...- HER2-expressing status determined by laboratory to be IHC 1+, 2+ or 3+....
Evidence Level:Sensitive: C2 – Inclusion Criteria
Title:
Disitamab Vedotin Combined With PD-1 and Neoadjuvant Chemotherapy for Locally Advanced Gastric Cancer(RC48-C018)
Excerpt:...Use pre-treatment endoscopic biopsy samples for HER2 detection in the local laboratory: HER2 high expression confirmed after IHC results (defined as: IHC 2+ 3+); 7....
Evidence Level:Sensitive: C2 – Inclusion Criteria
Title:
This study aims to evaluate the efficacy and safety of Disitamab Vedotin combined with Cisplatin and Candelinib in the treatment of patients with locally advanced cervical cancer.
Less C2 evidence

Evidence Level:Sensitive: C3 – Early Trials
Title:
From AVATAR Mice to Patients: RC48-ADC Exerted Promising Efficacy in Advanced Gastric Cancer With HER2 Expression
Excerpt:The preliminary results show that RC48-ADC has satisfactory efficacy in HER2-positive or HER2-moderate expressed GC patients, and the adverse effects are tolerable. In addition, RC48-ADC has also shown promising antitumor effects in HER2-positive patients who have progressed after receiving anti-HER2 therapy....In conclusion, RC48-ADC exerted promising antitumor activity in HER2-positive as well as score of 2+ in IHC and ISH-negative AGC patients after progression of systematic treatment.
DOI:10.3389/fphar.2021.757994