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Comprehensive Approaches in Gastrointestinal Oncology: Focus on Colorectal, Gastric, and Pancreatic Cancer Treatment

A Special Issue of Journal of Clinical Medicine (ISSN 2077-0383) belonging to the section "Oncology".

Deadline for manuscript submissions: 15 October 2026 | Viewed by 1083

Editors


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Guest Editor
General Surgery Unit, Department of Surgery, Cittiglio-Angera Hospital, ASST SetteLaghi, 21100 Varese, Italy
Interests: surgical oncology; gastric cancer; colon cancer; minimally invasive surgery; emergency surgery
Special Issues, Collections and Topics in MDPI journals

E-Mail Website
Guest Editor
Department of Surgery, University of Ioannina, Ioannina, Greece
Interests: surgical oncology; gastric cancer; colon cancer; minimally invasive surgery; emergency surgery
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Gastrointestinal oncology increasingly relies on a translational framework that connects molecular discoveries to clinical decision-making. Particularly, in colorectal, gastric, and pancreatic cancer, a coordinated multidisciplinary and translational strategy represents the most effective road to improving patients' prognosis. Preclinical findings are rapidly translated into clinical trials with a biomarker-driven approach, converting biological complexity into personalized therapeutic strategies.

On the other hand, clinical management requires a multidisciplinary team including surgeons, oncologists, gastroenterologists, radiologists, as well as molecular pathologists. Necessarily, this team will be able to integrate all the info about the patient's disease in order to identify the most correct solution to cure it, both for its microscopic and macroscopic aspects.

Certainly, the complexity of these topics requires a lot of different competencies. International collaborations lead to the definition of guidelines and enable data sharing across diverse populations. Scientific publishing diffuses knowledge and in turn stimulates new research and new project.

This Special Issue aims to present and disseminate the most recent advances related to the management of colorectal, gastric, and pancreatic cancer. We consider contributions addressing translational research with clear clinical implications, new insights about staging modalities and multidisciplinary and multimodal treatment strategies, and future perspectives of surgical approaches. Contributions about technological innovations without potential direct patient benefit will be discouraged.   

Topics of interest for publication include, but are not limited to, the following:

Colorectal cancer, gastric cancer, pancreatic cancer, biological staging, clinical staging, early tumors, locally advanced tumors, oligometastatic tumors, neoadjuvant approach, chemotherapy, radiotherapy, immunotherapy, radical surgery, conservative treatment, and targeted therapy.

Prof. Dr. Stefano Rausei
Dr. Georgios D. Lianos
Guest Editors

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Keywords

  • colorectal cancer
  • gastric cancer
  • pancreatic cancer
  • biological staging
  • clinical staging
  • early tumors
  • locally advanced tumors
  • oligometastatic tumor
  • neoadjuvant approach
  • chemotherapy
  • radiotherapy
  • immunotherapy
  • radical surgery
  • conservative treatment
  • targeted therapy

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Published Papers (2 papers)

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Research

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21 pages, 2434 KB  
Article
Days Alive and out of Hospital at 30 Days After Curative Gastrectomy for Gastric Adenocarcinoma: Complication-Severity Gradient and Readmission Burden
by Adem Ozcan, Gizem Gunes, Ali Bal and Abdulkadir Unsal
J. Clin. Med. 2026, 15(17), 6811; https://doi.org/10.3390/jcm15176811 - 2 Sep 2026
Abstract
Background/Objectives: Days alive and out of the hospital at 30 days (DAOH30) integrates survival, index hospitalization, and readmission. We characterized DAOH30 after gastrectomy, assessed its complication-severity gradient and readmission burden, and explored its association with an index-cancer-excluded Charlson Comorbidity Index (CCI). Methods: This [...] Read more.
Background/Objectives: Days alive and out of the hospital at 30 days (DAOH30) integrates survival, index hospitalization, and readmission. We characterized DAOH30 after gastrectomy, assessed its complication-severity gradient and readmission burden, and explored its association with an index-cancer-excluded Charlson Comorbidity Index (CCI). Methods: This single-center retrospective analysis included adults undergoing R0 total gastrectomy or subtotal distal gastrectomy for non-metastatic gastric adenocarcinoma between January 2020 and April 2026. DAOH30 was derived from the index postoperative length of stay, readmission days, and 30-day mortality. Rank-based tests and median quantile regression were used. Results: Among 123 patients, median DAOH30 was 21 days (interquartile range, 18–22; range, 4–26). No 30-day deaths occurred; eight patients (6.5%) were readmitted. Median DAOH30 decreased from 22 days without complications to 21 days after Clavien–Dindo grade I–II complications and 17 days after grade ≥ III complications (Kruskal–Wallis p < 0.001; one-sided Jonckheere–Terpstra p < 0.001; two-sided permutation sensitivity p < 0.001). After adjustment, grade ≥ III complications were associated with 4.00 fewer median DAOH30 days (bootstrap 95% confidence interval, −7.31 to −2.25; model-based p < 0.001). Readmissions contributed 73 additional inpatient days, with a median decrement of 9.5 days per readmitted patient. No statistically significant independent association was detected between the index-cancer-excluded CCI and DAOH30 (adjusted median difference, −0.17 days per point; bootstrap 95% confidence interval, −1.34 to 0.40; model-based p = 0.640). Conclusions: DAOH30 summarized early hospital burden, but in this no-mortality, low-readmission cohort it was largely determined by index length of stay. Multicenter validation with patient-reported anchoring is warranted. Full article
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Review

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36 pages, 1175 KB  
Review
Circulating Tumor DNA for Minimal Residual Disease Detection and Recurrence Prediction in Upper Gastrointestinal Cancers: A Scoping Review
by Loizos Hadjigeorgiou, Melina Yerolatsite, Nanteznta Torounidou, George Zarkavelis, Dimitrios Schizas, Vasileios Tatsis, Stefano Rausei, Konstantinos Vlachos and Georgios D. Lianos
J. Clin. Med. 2026, 15(16), 6222; https://doi.org/10.3390/jcm15166222 - 11 Aug 2026
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Abstract
Circulating tumor DNA (ctDNA) is a promising non-invasive biomarker for detecting minimal residual disease (MRD) and predicting recurrence after curative treatment, yet evidence in esophageal squamous cell carcinoma (ESCC), esophageal adenocarcinoma (EAC), and gastric cancer has largely been examined within individual tumor types. [...] Read more.
Circulating tumor DNA (ctDNA) is a promising non-invasive biomarker for detecting minimal residual disease (MRD) and predicting recurrence after curative treatment, yet evidence in esophageal squamous cell carcinoma (ESCC), esophageal adenocarcinoma (EAC), and gastric cancer has largely been examined within individual tumor types. In this scoping review, we mapped this evidence across all three malignancies and clarified key methodological and clinical considerations. Following the PRISMA-ScR guidelines, we searched PubMed, Scopus, and the Cochrane Library (3 April 2026) for studies linking ctDNA to disease-free, recurrence-free, or overall survival after curative-intent treatment. Twenty-seven studies (1746 patients; 10 ESCC, 4 EAC, 8 gastric, and 5 mixed) were included. Across every tumor type, postoperative ctDNA MRD was the most informative timepoint, with independent multivariable hazard ratios for disease-free, recurrence-free, or event-free survival of 2.8 to 21.8, whereas preoperative ctDNA was seldom prognostic. Serial monitoring further improved performance and flagged recurrence 78 to 278 days before imaging. Tumor-informed assays showed higher sensitivity than tumor-agnostic ones (80% vs. 35%), though direct comparisons were limited; correction for clonal hematopoiesis was essential for tumor-agnostic assays, and blood-based assays performed poorly in diffuse-type and peritoneal disease. Postoperative ctDNA MRD is a consistent, independent prognostic biomarker across upper gastrointestinal cancers that adds prognostic information beyond conventional staging and pathological response, supporting prospective interventional trials of ctDNA-guided management. Full article
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