About this trial
HER2 overexpression is observed in approximately 20% of gastric cancers and gastroesophageal junction (GEJ) cancers, making it a validated target for anti-tumor therapy . In advanced-stage systemic therapy, trastuzumab combined with chemotherapy has demonstrated clinical benefits for HER2-positive gastric and GEJ cancers . However, the combination of trastuzumab and pertuzumab plus chemotherapy did not significantly improve overall survival (OS) compared to trastuzumab monotherapy in HER2-expressed gastric/GEJ cancers .
In neoadjuvant therapy for early-stage or locally advanced gastric cancer, there is currently no standardized perioperative regimen for HER2-positive gastric or GEJ cancers, and effective treatment remains challenging .
Zanidatamab, a humanized bispecific IgG1-like antibody targeting HER2's ECD4 and ECD2 epitopes, exhibits unique enhanced functionality . Phase II studies (NCT03929666) showed that zanidatamab combined with chemotherapy as first-line therapy for HER2-positive advanced gastroesophageal adenocarcinoma (GEA) demonstrated superior survival benefits and durable responses compared to standard therapy (trastuzumab plus chemotherapy) . A Phase III study (HERIZON-GEA-01, NCT05152147) is now underway to further validate its efficacy when combined with chemotherapy ± tislelizumab versus trastuzumab-based chemotherapy .
For previously untreated stage II/III locally advanced gastroesophageal junction adenocarcinoma (cT1-2N+M0, cT3-4aNanyM0) with confirmed HER2 high expression (HER2 3+/2+ FISH+), neoadjuvant zanidatamab combined with chemotherapy (FLOT/SOX/CAPOX) is being explored to evaluate safety and efficacy, potentially offering a new treatment option for HER2-positive GEJ cancers in perioperative settings .
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Signed informed consent.
Histologically/radiologically confirmed Stage II/III (cT1-2N+M0 or cT3-4aNanyM0) Siewert II/III GEJ/gastric adenocarcinoma.
HER2-high (IHC 3+/2+FISH+); HER2 2+ requires FISH (no time restriction).
Age 18-75, any gender.
Disqualifiers
Unresectable/metastatic (Stage IV) disease.
Prior systemic GC therapy.
Other malignancies within 5 years (except those with >90% 5-year survival).
Cardiopulmonary dysfunction.
Trial design
Single group
Treatments tested in this trial
Zanidatamab Combined with Chemotherapy
DrugZanidatamab Combined with Chemotherapy as Neoadjuvant Therapy
Treatment groups
Trial outcomes
Primary outcomes
Major pathological response rate (MPR)
MPR is defined as 10% or fewer viable cancer cells from the resected tumor following neoadjuvant treatment
Secondary outcomes
Pathological complete response rate(pCR)
R0 Resection
Recurrence Free Survival (RFS)
Treatment-Emergent Adverse Events
Locations
Sponsors and contacts
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