ASCO Gastrointestinal Cancers Symposium 2026: key results and trends
What the 877 abstracts at ASCO Gastrointestinal Cancers Symposium 2026 reported, drug by drug: the readouts that stood out and the targets and modalities that dominated.
- abstracts
- 877
- drug-linked abstracts
- 381
- companies
- 109
- from Phase 3 studies
- 47
Drug-linked abstracts by phase
- Phase 1 34
- Phase 1/2 29
- Phase 2 129
- Phase 2/3 7
- Phase 3 47
Key results
Quotes are taken verbatim from each abstract's results; selection is automated. Report an issue
atezolizumab
Colorectal Cancer Metastatic dMMR Immunotherapy (COMMIT) study: A randomized phase III study of atezolizumab (atezo) monotherapy versus mFOLFOX6/bevacizumab/atezo (FFX/bev) in the first-line treatment of patients (pts) with deficient DNA mismatch repair (dMMR) or microsatellite instability-high (MSI-H) metastatic colorectal cancer (mCRC)— NRG-GI004/SWOG-S1610.
Read the abstract (opens in a new tab)Median PFS was 30.0 and 4.3 months, ORR was 80.6% v 46%, and DCR at 12 months was 62.9% v 32.4% in the FFX/bev+atezo arm compared to the atezo-only arm, respectively.
pembrolizumab
Adjuvant pembrolizumab for participants with hepatocellular carcinoma and complete radiologic response after surgical resection or local ablation: The phase 3 keynote-937 study.
Read the abstract (opens in a new tab)Median DMFS was NR (95% CI, 58.7 to NR) with pembrolizumab vs NR (95% CI, 59.0 to NR) with placebo (HR 0.98; 95% CI, 0.77-1.24), with 48 mo DMFS rate of 71% vs 70%.
durvalumab
Analysis of 5-fluorouracil, leucovorin, oxaliplatin, and docetaxel (FLOT) administration in MATTERHORN: A randomized, phase 3 study of durvalumab (D) plus FLOT in resectable gastric/gastroesophageal junction (G/GEJ) adenocarcinoma.
Read the abstract (opens in a new tab)EFS was improved with D + FLOT vs P + FLOT in pts who completed all FLOT (n=228 vs 243; hazard ratio [HR], 0.68; 95% confidence interval [CI], 0.49–0.94), stopped some FLOT (n=63 vs 60; HR, 0.35; 95% CI, 0.16–0.71) or stopped all FLOT (n=183 vs 167; HR, 0.72; 95% CI, 0.55–0.95).
fruquintinib
Matching-adjusted indirect comparison of fruquintinib versus ramucirumab in advanced gastric or gastroesophageal junction adenocarcinoma.
Read the abstract (opens in a new tab)The analysis showed that FRU plus paclitaxel had a numerical improvement in PFS compared to RAM plus paclitaxel (HR 0.78, 95% CI 0.58-1.04; p = 0.09), with a statistically significant RMST advantage of 1.18 months at 20 months (95% CI 0.08-2.27; p = 0.024).
zanidatamab
Zanidatamab + chemotherapy (CT) ± tislelizumab for first-line (1L) HER2-positive (HER2+) locally advanced, unresectable, or metastatic gastroesophageal adenocarcinoma (mGEA): Primary analysis from HERIZON-GEA-01.
Read the abstract (opens in a new tab)Grade ≥3 treatment-related AEs (TRAEs) occurred in 71.8% of pts with zanidatamab + tislelizumab + CT, 59.0% with zanidatamab + CT, and 59.6% with tras + CT.
oxaliplatin
Adjuvant oxaliplatin with S-1 (SOX) versus S-1 in patients with stage II-III gastric or gastro-oesophageal junction adenocarcinoma (CAPITAL): A randomised, open-label, phase 3 trial.
Read the abstract (opens in a new tab)The 3 and 5-year disease-free survival were 71.2% (66.5-76.3) and 66.2% (61.2-71.6) in the SOX group, as compared with 65.1% (60.2-70.5) and 55.6% (50.4-61.3) in the S-1 group.
regorafenib
Regorafenib combined with trifluridine/tipiracil versus regorafenib monotherapy in refractory metastatic colorectal cancer (FDZL-REGOT): A randomized phase 2 trial.
Read the abstract (opens in a new tab)The ORR was 11.0% (6/51) vs. 0 (0/51), and DCR was 66.7% (34/51) vs. 29.4% (15/51) in the combination group and the regorafenib group, separately, in the ITT analysis.
elraglusib
Results from the randomized phase 2 study (1801 Part 3B) of elraglusib plus gemcitabine/nab-paclitaxel (GnP) versus GnP in previously untreated metastatic pancreatic ductal adenocarcinoma (mPDAC).
Read the abstract (opens in a new tab)The 1-yr OS rate was 44.1% with elraglusib/GnP vs 22.3% with GnP; the mOS was 10.1 mo with elraglusib/GnP vs 7.2 mo with GnP (HR, 0.62; p=0.01) with approximately 79% events recorded (25.8% of pts on elraglusib/GnP and 10.3% on GnP were censored with the majority at >12 mo OS).
benmelstobart
Preliminary results of benmelstobart (BEN) combined with concurrent chemoradiotherapy (cCRT) versus cCRT alone as neoadjuvant therapy for esophageal squamous cell carcinoma (ESCC): A multicentre, randomised study.
Read the abstract (opens in a new tab)pCR rates were 50% (9/18) versus 42% (10/24), and MPR rates were 78% (14/18) versus 63% (15/24), respectively.
trifluridine + tipiracil
The primary results of a randomized phase II trial of trifluridine/tipiracil (FTD/TPI) plus ramucirumab (RAM) versus FTD/TPI for previously treated patients with advanced gastric or gastroesophageal junction adenocarcinoma (RETRIEVE study, WJOG 15822G).
Read the abstract (opens in a new tab)There was no significant difference in ORR (5.4% vs 9.1%, P = 0.489) and DCR (50.0% vs 47.3%, P = 0.850) between both arms.
toripalimab
Perioperative PD-1 antibody toripalimab combined with chemotherapy versus chemotherapy alone in locally advanced gastric or gastroesophageal junction cancer: 3-year follow-up of the prospective, randomized, phase 2 NEOSUMMIT-01 trial.
Read the abstract (opens in a new tab)The 3-year EFS was 74.7% (95% CI: 63.6–87.7%) in the toripalimab plus chemotherapy group and 56.2% (95% CI: 43.3–73.0%) in the chemotherapy group, with a hazard ratio (HR) of 0.52 (95% CI: 0.27–1.00; P = 0.047).
anlotinib
Preliminary results of ALTER-PA-001 trial: A multicenter, open-label, randomized, phase II trial of anlotinib and benmelstobart in combination with AG versus AG as first-line treatment for metastatic pancreatic cancer.
Read the abstract (opens in a new tab)The most common TEAE were white blood cell decreased (51.9% vs. 50.0%), anemia (44.4% vs. 42.9%) and neutrophil count decreased (40.7% vs. 42.9%).
Trends at ASCO GI 2026
Small molecules were the most frequent modality (52% of drug-linked abstracts). PDCD1 was the most frequent target (16%). Colorectal cancer (CRC) was the most frequent disease (17%).
What the abstracts covered
Share of the 381 drug-linked abstracts, by the target, modality, disease and company of each drug. An abstract can count in more than one row, so a list can add up to more than 100%.
- Antibody-drug conjugates6%21 drug-linked abstracts
- Bispecific antibodies4%17 drug-linked abstracts
Top targets
- PDCD16216%
- TS5314%
- CD2744412%
- VEGFR2287%
- VEGFR4257%
- TUBB236%
- TOP1216%
- VEGFR-1205%
- SSTR2154%
- PDGFRA123%
Top modalities
- Small molecules19852%
- Monoclonal antibodies14939%
- Antibody-drug conjugates216%
- Radiopharmaceuticals195%
- Bispecific antibodies174%
- Peptides174%
- Non-antibody therapeutic proteins72%
- Carbohydrate, lipid and polymer therapeutics51%
Top diseases
- Colorectal cancer (CRC)6617%
- Metastatic colon cancer (mCRC)5314%
- Gastric cancer (GC)4712%
- Pancreatic adenocarcinoma (PDAC)4612%
- Hepatocellular carcinoma (HCC)4010%
- Gastroesophageal junction adenocarcinoma3910%
- Gastric adenocarcinoma277%
- Pancreatic cancer (PC)257%
- Esophageal Squamous Cell Carcinoma (ESCC)216%
- Biliary cancer205%
Most active companies
- AstraZeneca287%
- Bristol Myers Squibb246%
- Genentech205%
- Sanofi154%
- Taiho Pharmaceutical144%
- BeiGene133%
- Merck123%
- Eli Lilly113%
- HUTCHMED113%
- Pfizer113%
Explore every ASCO GI 2026 result in Gosset
All 381 drug-linked abstracts, joined to each drug’s trials, targets, developers and deals, with a source behind every line.
This page shows a sample of results. Gosset has the abstracts from this meeting and 100+ others; reach out for full access.