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CANCER:

Gastrointestinal Cancer

1d
Trial completion • Enrollment change
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oxaliplatin
1d
Stereotactic Brain-directed Radiation With or Without Aguix Gadolinium-Based Nanoparticles in Brain Metastases (clinicaltrials.gov)
P2, N=134, Recruiting, Brigham and Women's Hospital | Active, not recruiting --> Recruiting
Enrollment open
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HER-2 (Human epidermal growth factor receptor 2)
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HER-2 positive
2d
New P1 trial
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KRAS (KRAS proto-oncogene GTPase) • NRAS (Neuroblastoma RAS viral oncogene homolog) • HRAS (Harvey rat sarcoma viral oncogene homolog) • HLA-DPB1 (Major Histocompatibility Complex, Class II, DP Beta 1)
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KRAS mutation • NRAS mutation • RAS mutation • HRAS mutation • KRAS G12 • NRAS G12
3d
The NIPA Study Naloxegol Administration to Prevent Opioids Induced Gastrointestinal Motility Disturbance in Brain Injured PAtients (clinicaltrials.gov)
P3, N=370, Suspended, University Hospital, Brest | Trial completion date: Sep 2026 --> Apr 2028 | Recruiting --> Suspended | Trial primary completion date: Mar 2026 --> Oct 2027
Trial completion date • Trial suspension • Trial primary completion date
3d
Clinicopathological features and immune checkpoint expression patterns in dMMR early gastric cancer: a retrospective pilot study. (PubMed, BMC Cancer)
These findings highlight the heterogeneity of immune checkpoint expression patterns and provide preliminary, hypothesis-generating insights into variability in response to PD-1/PD-L1 blockade.
Retrospective data • Journal • MSi-H Biomarker • PD(L)-1 Biomarker • IO biomarker • dMMR
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MSI (Microsatellite instability)
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MSI-H/dMMR
3d
NAT10 promotes colon cancer progression by enhancing predicted N4-acetylcytidine modification of Notch2 mRNA. (PubMed, Discov Oncol)
NAT10 promotes colon cancer progression in an enzymatic activity‑dependent manner by enhancing predicted ac4C modification of Notch2 mRNA to stabilize its expression. This study reveals a novel NAT10/ac4C/Notch2 regulatory axis and provides potential therapeutic targets for colon cancer.
Journal
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NOTCH2 (Notch 2)
3d
New trial
3d
AI for Onsite Cytology Evaluation in Endoscopic Ultrasound (clinicaltrials.gov)
P=N/A, N=136, Active, not recruiting, Orlando Health, Inc. | Recruiting --> Active, not recruiting | N=200 --> 136 | Trial completion date: Oct 2027 --> Dec 2026 | Trial primary completion date: Dec 2026 --> Apr 2026
Enrollment closed • Enrollment change • Trial completion date • Trial primary completion date
3d
Enhanced Outpatient Symptom Management to Reduce Acute Care Visits Due to Chemotherapy-Related Adverse Events (clinicaltrials.gov)
P=N/A, N=750, Active, not recruiting, M.D. Anderson Cancer Center | Trial completion date: Jan 2026 --> Jan 2028 | Trial primary completion date: Jan 2026 --> Jan 2028
Trial completion date • Trial primary completion date • Adverse events
3d
Crossover Trial of Systemic Chemotherapy in Patients With Metastatic Well-Differentiated Mucinous Appendiceal Adenocarcinomas With Pseudomyxoma Peritonei (clinicaltrials.gov)
P=N/A, N=30, Active, not recruiting, M.D. Anderson Cancer Center | Trial completion date: Jan 2026 --> Jan 2028 | Trial primary completion date: Jan 2026 --> Jan 2028
Trial completion date • Trial primary completion date
3d
Molecular mechanisms of KMT2C alterations in gastrointestinal cancers: enhancer network destabilization, lineage plasticity, and clinical translation. (PubMed, Front Immunol)
In this review, we integrate evidence from hepatocellular carcinoma, pancreatic ductal adenocarcinoma, cholangiocarcinoma, colorectal cancer, gastric cancer, esophageal cancer, and gallbladder cancer within a unified framework that links KMT2C domain architecture to enhancer-network destabilization, phenotypic state transitions, and clinical manifestations. We further propose a functional evaluation paradigm that reframes discrete KMT2C variants as graded states of epigenetic deficiency, coupled with a closed-loop validation strategy integrating tissue-based profiling, liquid biopsy monitoring, and spatial multi-omics analyses.
Review • Journal • Tumor mutational burden • PARP Biomarker
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TMB (Tumor Mutational Burden) • MSI (Microsatellite instability) • KMT2C (Lysine Methyltransferase 2C) • CHEK1 (Checkpoint kinase 1) • DRD (DNA Repair Deficiency)
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DDR