Advances in the Treatment of Gastrointestinal (GI) Cancers

A special issue of Cancers (ISSN 2072-6694). This special issue belongs to the section "Cancer Therapy".

Deadline for manuscript submissions: 27 February 2026 | Viewed by 99

Special Issue Editor


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Guest Editor
Department of Gastroenterology and Hepatology, Okayama University Hospital, Okayama 700-8558, Japan
Interests: gastrointestinal cancer; gastric cancer

Special Issue Information

Dear Colleagues,

This Special Issue aims to present recent advances in the treatment of gastrointestinal (GI) cancers, including esophageal, gastric, colorectal, pancreatic, and hepatobiliary malignancies. We welcome original research articles and reviews focusing on novel therapeutic strategies, biomarker-driven approaches, immunotherapy, targeted therapy, and emerging molecular mechanisms underlying GI tumor progression and resistance. Studies addressing translational research, clinical trials, and precision oncology are particularly encouraged. Through this Collection, we seek to provide a platform for sharing cutting-edge findings that can contribute to improved outcomes and personalized treatment approaches in GI oncology.

Dr. Yoshiyasu Kono
Guest Editor

Manuscript Submission Information

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Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2900 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • gastrointestinal cancers
  • targeted therapy
  • immunotherapy
  • precision oncology
  • biomarkers
  • molecular mechanisms
  • tumor microenvironment
  • resistance to therapy
  • translational research
  • clinical trials

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Published Papers (1 paper)

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Research

13 pages, 1252 KiB  
Article
Prognostic Impact of Gastrointestinal Immune-Related Adverse Events Depends on Nutritional Status in Cancer Patients Treated with Immune Checkpoint Inhibitors
by Shoichiro Hirata, Yoshiyasu Kono, Emi Tanaka, Masahiko Sue, Yasuto Takeuchi, Tomoki Yoshikawa, Yoshie Maki, Tomohiro Kamio, Daisuke Kametaka, Katsunori Matsueda, Chihiro Sakaguchi, Kenta Hamada, Masaya Iwamuro, Seiji Kawano, Yoshiro Kawahara and Motoyuki Otsuka
Cancers 2025, 17(16), 2634; https://doi.org/10.3390/cancers17162634 - 12 Aug 2025
Abstract
Background: Gastrointestinal immune-related adverse events (GI-irAEs) are recognized complications of immune checkpoint inhibitors (ICIs), but their prognostic relevance and associated risk factors remain unclear. This study aimed to assess whether baseline nutritional status, measured using the prognostic nutritional index (PNI), modifies the prognostic [...] Read more.
Background: Gastrointestinal immune-related adverse events (GI-irAEs) are recognized complications of immune checkpoint inhibitors (ICIs), but their prognostic relevance and associated risk factors remain unclear. This study aimed to assess whether baseline nutritional status, measured using the prognostic nutritional index (PNI), modifies the prognostic impact of GI-irAEs, and to identify clinical factors associated with their occurrence. Methods: We retrospectively analyzed 1104 cancer patients treated with ICIs at a single institution. GI-irAEs were defined as gastrointestinal symptoms requiring clinical intervention. Patients were stratified by irAE type and PNI (≥40 vs. <40), and differences in survival and treatment response were evaluated. Potential risk factors for developing GI-irAEs were also examined. Results: GI-irAEs occurred in 2.7% of patients and were associated with prolonged overall survival (median: 28.7 vs. 14.0 months) among those with PNI ≥ 40. This survival advantage was not observed in patients with PNI < 40. The PNI-dependent prognostic pattern was specific to GI-irAEs and not observed for non-GI irAEs. Similar trends were confirmed in 4- and 8-week landmark analyses. Differences in objective response rate and disease control rate by PNI status were most pronounced in patients with GI-irAEs. The use of anti-CTLA-4 antibodies was significantly associated with GI-irAE development (odds ratio 4.24; 95% confidence interval 1.73–10.39). Conclusions: GI-irAEs appear to confer a survival benefit primarily in patients with preserved nutritional status. PNI may serve as a useful tool to contextualize the clinical relevance of GI-irAEs and help identify patients most likely to benefit from immune activation during ICI therapy. Full article
(This article belongs to the Special Issue Advances in the Treatment of Gastrointestinal (GI) Cancers)
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