Zanidatamab Combined With Chemotherapy as Neoadjuvant Therapy for HER2-high Expression G/GEJC

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorXijing Hospital

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 volunteers

Qualifiers

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

Design model

Single group

Treatments tested in this trial

  • Zanidatamab Combined with Chemotherapy

    Drug

    Zanidatamab Combined with Chemotherapy as Neoadjuvant Therapy

Treatment groups

30 Participants
are divided into 1 treatment group
Group A: Experimental: Zanidatamab Combined with ChemotherapyExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Major pathological response rate (MPR)

MPR is defined as 10% or fewer viable cancer cells from the resected tumor following neoadjuvant treatment

Time frame
24 months

Secondary outcomes

1

Pathological complete response rate(pCR)

Time frame
24 months
2

R0 Resection

Time frame
24 months
3

Recurrence Free Survival (RFS)

Time frame
5 years
4

Treatment-Emergent Adverse Events

Time frame
24 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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