Evidence map›Paper›PMID 40700298›Full record

ReviewAntibodies (Basel, Switzerland)2025

Immunotherapy in GI Cancers: Lessons from Key Trials and Future Clinical Applications.

Supriya Peshin, Faizan Bashir, Naga Anvesh Kodali, Adit Dharia, Sajida Zaiter, Sakshi Singal, Nagaishwarya Moka

Abstract readReview
In one paragraph

Review in Antibodies (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Supriya PeshinNorton Community Hospital, Ballad Health, Norton, VA 24273, USA.ORCID 0000-0002-3895-9474
Faizan BashirSchool of Medicine, Shiraz University of Medical Sciences, Shiraz 71345-3119, Iran.ORCID 0009-0009-9634-613X
Naga Anvesh KodaliHCA Florida Ocala Hospital, University of Central Florida, Ocala, FL 34471, USA.
Adit DhariaHCA Florida West Hospital, Pensacola, FL 32514, USA.
Sajida ZaiterSchool of Medicine, Shiraz University of Medical Sciences, Shiraz 71345-3119, Iran.
Sakshi SingalMedical Oncology, East Tennessee State University, Johnson City, TN 37604, USA.
Nagaishwarya MokaDebusk College of Osteopathic Medicine, Lincoln Memorial University, Harrogate, TN 37752, USA.ORCID 0009-0004-1582-6320

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapy has emerged as a transformative approach in gastrointestinal (GI) cancers, addressing historically poor survival rates in advanced-stage disease. Immune checkpoint inhibitors (ICIs) targeting the PD-1/PD-L1 axis demonstrate remarkable efficacy in colorectal cancer with deficient mismatch repair (dMMR) or high microsatellite instability (MSI-H), exemplified by trials like NICHE-2 achieving exceptional pathological response rates. However, significant limitations persist, including resistance in some dMMR/MSI-H tumors, minimal efficacy in proficient mismatch repair (pMMR) tumors, and low overall response rates across most GI malignancies due to tumor heterogeneity and immune evasion mechanisms. Predictive biomarkers such as tumor mutational burden (TMB) and PD-L1 expression are crucial for optimizing patient selection, while hypermutated pMMR tumors with POLE mutations represent emerging therapeutic opportunities. In pancreatic adenocarcinoma, where survival remains dismal, combination strategies with chemotherapy and novel approaches like cancer vaccines show promise but lack transformative breakthroughs. Esophagogastric cancers benefit from ICIs combined with chemotherapy, particularly in MSI-H and HER2-positive tumors, while hepatocellular carcinoma has achieved significant progress with combinations like atezolizumab-bevacizumab and durvalumab-tremelimumab surpassing traditional therapies. Biliary tract cancers show modest improvements with durvalumab-chemotherapy combinations. Despite these advances, immunotherapy faces substantial challenges including immune-related adverse events, acquired resistance through cancer immunoediting, and the need for biomarker-driven approaches to overcome tumor microenvironment barriers. This review discusses key clinical trials, therapeutic progress, and emerging modalities including CAR T-cell therapies and combination strategies, emphasizing the critical need to address resistance mechanisms and refine precision medicine approaches to fully realize immunotherapy's potential in GI malignancies.

Indexed as

gastrointestinal cancersimmune checkpoint inhibitors (ICIs)immunotherapymicrosatellite instability-high (MSI-H) deficient mismatch repair (dMMR)PD-1/PD-L1 pathway

Identifiers

PMID40700298
PMCPMC12285940

What Socratic holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.