Gastrointestinal Neoplasms
Recent clinical, regulatory, research and industry developments relating to this disease.
Emerging IO checkpoints in gastrointestinal oncology.
Targeted therapy guided by circulating tumor DNA analysis in advanced gastrointestinal tumors.
Recent developments in immunotherapy for gastrointestinal tract cancers.
Cancer-derived exosomes as novel biomarkers in metastatic gastrointestinal cancer.
Endoscopic submucosal dissection: European Society of Gastrointestinal Endoscopy (ESGE) Guideline.
Efficacy and safety of imatinib mesylate in advanced gastrointestinal stromal tumors.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
- 4 clinical trials expected to report results, the earliest in Q1 2027.
- Q1 2027A FIRST-IN-HUMAN (FIH) STUDY OF IDRX-42 IN PARTICIPANTS WITH METASTATIC AND/OR UNRESECTABLE GASTROINTESTINAL STROMAL TUMORS (GIST)
- Q4 2027A Phase 1b/2, Multicenter, Open-label Study to Evaluate the Efficacy and Safety of GSK5764227 Alone and in Combination in Participants With Previously Treated Advanced Unresectable or Metastatic Gastrointestinal Solid Tumors
- Q2 2028A Phase 3, Randomized, Multicenter, Open-Label Study of IDRX-42 (GSK6042981) Versus Sunitinib in Participants With Metastatic and/or Unresectable Gastrointestinal Stromal Tumors (GIST) After Imatinib Therapy (StrateGIST 3)
- Q1 2030AN INTERVENTIONAL, PHASE 3, DOUBLE-BLIND, RANDOMIZED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF PF-08634404 IN COMBINATION WITH CHEMOTHERAPY VERSUS BEVACIZUMAB IN COMBINATION WITH CHEMOTHERAPY IN TREATMENT-NAÏVE PARTICIPANTS WITH METASTATIC COLORECTAL CANCER
Clinical MilestonesViewHide
- 2026-07-06AN INTERVENTIONAL, PHASE 3, DOUBLE-BLIND, RANDOMIZED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF PF-08634404 IN COMBINATION WITH CHEMOTHERAPY VERSUS BEVACIZUMAB IN COMBINATION WITH CHEMOTHERAPY IN TREATMENT-NAÏVE PARTICIPANTS WITH METASTATIC COLORECTAL CANCERResults expected Q1 2030
- 2026-07-02A FIRST-IN-HUMAN (FIH) STUDY OF IDRX-42 IN PARTICIPANTS WITH METASTATIC AND/OR UNRESECTABLE GASTROINTESTINAL STROMAL TUMORS (GIST)Results expected Q1 2027
- 2026-06-12A Phase 3, Randomized, Multicenter, Open-Label Study of IDRX-42 (GSK6042981) Versus Sunitinib in Participants With Metastatic and/or Unresectable Gastrointestinal Stromal Tumors (GIST) After Imatinib Therapy (StrateGIST 3)Results expected Q2 2028
- 2025-11-18A Phase 1b/2, Multicenter, Open-label Study to Evaluate the Efficacy and Safety of GSK5764227 Alone and in Combination in Participants With Previously Treated Advanced Unresectable or Metastatic Gastrointestinal Solid TumorsResults expected Q4 2027
- 2026-07-06ClinicalAN INTERVENTIONAL, PHASE 3, DOUBLE-BLIND, RANDOMIZED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF PF-08634404 IN COMBINATION WITH CHEMOTHERAPY VERSUS BEVACIZUMAB IN COMBINATION WITH CHEMOTHERAPY IN TREATMENT-NAÏVE PARTICIPANTS WITH METASTATIC COLORECTAL CANCERResults expected Q1 2030
- 2026-07-02ClinicalA FIRST-IN-HUMAN (FIH) STUDY OF IDRX-42 IN PARTICIPANTS WITH METASTATIC AND/OR UNRESECTABLE GASTROINTESTINAL STROMAL TUMORS (GIST)Results expected Q1 2027
- 2026-06-12ClinicalA Phase 3, Randomized, Multicenter, Open-Label Study of IDRX-42 (GSK6042981) Versus Sunitinib in Participants With Metastatic and/or Unresectable Gastrointestinal Stromal Tumors (GIST) After Imatinib Therapy (StrateGIST 3)Results expected Q2 2028
- 2025-11-18ClinicalA Phase 1b/2, Multicenter, Open-label Study to Evaluate the Efficacy and Safety of GSK5764227 Alone and in Combination in Participants With Previously Treated Advanced Unresectable or Metastatic Gastrointestinal Solid TumorsResults expected Q4 2027
Clinical trials
The current development programme across all trial phases.
Research activity
Key research shaping understanding of this disease, combining the latest publications with the most influential evidence.
Major themes8
- Gastrointestinal Neoplasms7
- Dysbiosis2
- Gastrointestinal Microbiome2
- Immune Checkpoint Inhibitors2
- Biomarkers, Tumor1
- Circulating Tumor DNA1
- Digestive System Physiological Phenomena1
- Exosomes1
Leading journals6
- Endoscopy2
- Frontiers in immunology2
- The New England journal of medicine2
- Advances in anatomic pathology1
- International journal of clinical oncology1
- JAMA oncology1
Leading researchers8
- Wang Y3
- Deprez PH2
- Komatsu Y2
- Pimentel-Nunes P2
- Vieth M2
- Wang Z2
- Adams S1
- Ah Kang S1
Affiliations (unnormalised)6
- Cancer Institute Hospital of Japanese Foundation for Cancer Research2
- Erasmus Medical Center2
- National Cancer Center Hospital2
- National Cancer Center Hospital East2
- Bispebjerg Hospital1
- Cancer Center Amsterdam1
Related conditions
Diseases frequently studied alongside this one. Number shows shared papers.
Disease profile
A grounded synthesis of the condition — overview, causes, mechanism, risk factors and current standard of care.
Gastrointestinal neoplasms are tumors or cancers arising anywhere in the gastrointestinal tract, from the mouth to the anal canal. The literature grounding here spans diagnosis, pathology, immunology, metabolism, microbiology, genetics, complications, blood, and therapy, reflecting the broad clinical and biological heterogeneity of these cancers.
The supplied grounding does not support a specific cause or aetiology for gastrointestinal neoplasms overall. It only indicates that genetics, microbiology, and metabolism are studied in relation to these tumors, without defining a single causal pathway.
The grounding supports several biological themes rather than one unified mechanism. Tumor immune response is important, including the prognostic and predictive value of tumor-infiltrating lymphocytes, and the gastrointestinal microbiome is a co-studied mechanism. The literature also reflects pathology-focused staging and characterization of lesions, including the need for accurate histologic assessment in superficial disease.
The supplied grounding does not support general risk factors for gastrointestinal neoplasms overall. It does indicate that immune-related biomarkers such as tumor-infiltrating lymphocytes and prognostic nutritional index have been studied in relation to outcomes, but these are not established risk factors in the provided material.
Management in the supplied grounding includes endoscopic resection approaches for selected superficial gastrointestinal cancers, with endoscopic submucosal dissection used to achieve en bloc resection and accurate pathology staging. For advanced gastrointestinal tract cancers, immune checkpoint inhibitors, particularly anti-PD-1 and anti-PD-L1 therapies, are described as increasingly important, often in combination with chemotherapy in specific settings. The grounding also mentions cell therapy such as claudin18.2-redirected CAR-T therapy in later-line disease.
AI-generated summary grounded in MeSH and 6 peer-reviewed sources. Informational only — not medical advice. Generated 2026-07-07.
Reference
Authoritative identity, definition & identifiers.
Tumors or cancer of the GASTROINTESTINAL TRACT, from the MOUTH to the ANAL CANAL.
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Clinical trials — ClinicalTrials.gov (U.S. National Library of Medicine)
- Research activity — Europe PMC (EMBL-EBI) + OpenAlex-derived paper links
- Related entities are derived from literature co-mention (studied together) — associative, not causal.