
Practice-changing ESMO 2026 GI oncology highlights, including zanidatamab-based regimens that extend survival in HER2-positive gastroesophageal cancer, even in PD-L1–negative patients.
Experts in gastrointestinal oncology review key data from the ESMO Congress across gastroesophageal, pancreatic and rectal cancers, discussing what each finding means for practice now and where the field is heading. In HER2-positive gastroesophageal adenocarcinoma, final analyses of HERIZON-GEA-01 show an overall survival benefit for zanidatamab-based regimens over trastuzumab plus chemotherapy. The panel sees this as support for the triplet with tislelizumab as a first-line option. In pancreatic cancer, subgroup analyses of RASolute 302 reinforce daraxonrasib as a standard of care in previously treated metastatic disease. The panel covers how to interpret the RAS wild-type results and gives practical advice on managing skin toxicity. AMPLIFY-7P did not meet its primary end point but still offers lessons on how well the vaccine triggers an immune response, how well circulating tumor DNA predicts outcomes, and the need for combination strategies after surgery. Finally, AZUR-1 highlights the promise of neoadjuvant dostarlimab for organ preservation in mismatch repair-deficient rectal cancer. It also raises the challenges of standardizing how clinical complete response is defined and how patients are monitored.

Practice-changing ESMO 2026 GI oncology highlights, including zanidatamab-based regimens that extend survival in HER2-positive gastroesophageal cancer, even in PD-L1–negative patients.

Additional analyses from the RASolute 302 trial offer further insight into daraxonrasib, a pan-RAS inhibitor, compared with chemotherapy in patients with previously treated metastatic pancreatic adenocarcinoma.

AMPLIFY-7P evaluated a lymph node-targeting mutant KRAS amphiphile vaccine versus observation as adjuvant therapy for patients with resected pancreatic ductal adenocarcinoma.

The AZUR-1 trial builds on earlier single-institution data showing that single-agent anti-PD-1 therapy could spare select patients with mismatch repair-deficient rectal cancer from surgery and radiation.