A Step Toward a Global Consensus on Gastric Cancer Resectability Integrating Artificial Intelligence-Based Consensus Modelling
Simple Summary
Abstract
1. Introduction
2. Materials and Methods
2.1. Study Design and Participants
2.2. Survey Instrument
- Definitions of resectability—including differentiation between technical and oncological resectability.
- Surgical strategy in borderline and advanced cases—covering lymphadenectomy extent, multivisceral resections, peritonectomy, and metastasectomy.
- Impact of preoperative therapies—evaluating how neoadjuvant chemotherapy or immunotherapy influences surgical decision-making.
- Surgical quality metrics—such as morbidity, mortality, hospital stay, and institutional volume.
- Resectability thresholds—exploring clinical scenarios with variable or controversial interpretations.
2.3. AI Model Preparation
- Primed using zero-shot prompting: without access to previous surgeon responses.
- Conditioned via structured prompts to mimic clinical reasoning by gastrointestinal oncology experts.
- Constrained to evidence-based frameworks, including NCCN, ESMO, Japanese Gastric Cancer Association (JGCA), and recent meta-analyses on GC resectability and multimodal therapy.
2.4. Two-Stage Comparative Design
2.5. Statistical Analysis
- Full concordance: Identical selection and reasoning between AI and majority surgeon response.
- Partial concordance: Responses differed in wording but reflected similar clinical logic or therapeutic intent.
- Discordance: Contradictory or opposing decisions.
3. Results
3.1. Respondent Characteristics
3.2. Concordance Between Surgeons and AI
3.3. Areas of Disagreement Between Surgeons and AI
3.4. Partial Concordance Between Surgeons and AI
3.5. Shift in Surgeon Responses Between Round 1 and Round 2
4. Discussion
4.1. Standardization Through AI: A New Pathway to Consensus
4.2. Concordance and Divergence: Evidence-Based vs. Contextual Judgment
4.3. Toward Hybrid Decision-Making Models
4.4. Strengths and Limitations
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
Appendix A
Question No. | Question | Answer Options |
---|---|---|
1 | Resectability is to be decided based on preoperative imaging, staging laparoscopy findings and intraoperative findings (clinical stages, cTNM, cStage). Do you think terms technical resectability & oncological resectability are different:(multiple choices are relevant) |
|
2 | Determining whether the surgical margins are clear of cancer cells by examining the resected tissue (frozen section) helps assess the oncological effectiveness of the procedure. Inability to achieve clear resection margins is a criterion of non-resectability: |
|
3 | Achieving R0 resection status is critical for optimizing survival outcomes, despite the inherent risks and complications associated with extensive surgical interventions. Therefore, monitoring the occurrence of postoperative complications (morbidity) and mortality provides insight into the quality of perioperative care. |
|
4 | Tracking the rate of morbidity/mortality following gastrectomy is an important measure of surgical quality and patient safety. Whether these outcome measures should influence a decision on performance of gastrectomy with multivisceral resection? |
|
5 | A shorter hospital stay is generally associated with better surgical outcomes and may indicate a more efficient recovery process. Therefore, duration of hospital stay for oncological gastrectomy should be below: |
|
6 | Is gastrectomy with multivisceral resection justified for cT4b tumours (that invades adjacent structures such as spleen, transverse colon, liver, diaphragm, pancreas, abdominal wall, adrenal gland, kidney, small intestine, or retroperitoneum): |
|
7 | Is gastrectomy with metastasectomy justified for cM1 tumours? |
|
8 | Is gastrectomy with peritonectomy justified for P1 tumours (with overt peritoneal metastasis): |
|
9 | Is gastrectomy with extensive peritoneal lavage justified for CY1 tumours (with positive peritoneal cytology): |
|
10 | Is gastrectomy with extended (D2plus/D3) lymphadenectomy justified for N3 bulky lymph node metastasis: |
|
11 | Evaluating the extent and thoroughness of lymph node dissection is important for staging and determining the prognosis of the patient. If a case is borderline resectable at your initial (after exploration) evaluation, should it modify the extent of ultimate lymphadenectomy: |
|
12 | Extensive nodal swelling along the major branched arteries or para-aortic lymph node swelling is called bulky-N disease. If large arteries are surrounded by bulky nodal metastatic tissue, do you consider the case resectable? Please indicate non-resectability (multiple choices are relevant): |
|
13 | Would you call it multivisceral resection? Gastrectomy with: (multiple choices are relevant) |
|
14 | Please indicate structures (that may be directly invaded; cT4b) to be resected if primary tumour is located at the esophago-gastric junction: (multiple choices are relevant) |
|
15 | Please indicate structures (that may be directly invaded; cT4b) to be resected if primary tumour is located at the proximal stomach (not invading esophago-gastric junction): (multiple choices are relevant) |
|
16 | Please indicate structures (that may be directly invaded; cT4b) to be resected if primary tumour is located at the middle third of the stomach: (multiple choices are relevant) |
|
17 | Please indicate structures (that may be directly invaded; cT4b) to be resected if primary tumour is located at the distal stomach: (multiple choices are relevant) |
|
18 | Gastric adenocarcinomas are considered unresectable if there is evidence of locally advanced disease with: |
|
19 | Gastric adenocarcinomas are considered unresectable if: |
|
20 | Would you consider all the above resectability criteria the same if a neoadjuvant systemic (chemo-/immuno) therapy had been used before? |
|
21 | Should staging laparoscopy be used for reliable resectability determination? |
|
22 | The (technical) resectability of the primary tumour by means of gastrectomy should be assessed during the staging laparoscopy by evaluation of the surrounding structures: |
|
23 | Structures for which otherwise no further dissection is necessary during standard gastrectomy include: |
|
24 | An expert opinion is to be formed on the nature of the operation. The operating surgeon should ascertain details about the extent of disease, including nodal involvement: |
|
25 | At what point during the surgical process should the operating surgeon report whether the gastric cancer surgery is intended to be curative or palliative? |
|
26 | Please describe your experience with performing gastrectomy as an 1st operator: |
|
27 | What is your experience in laparoscopic gastrectomy: |
|
28 | What is your experience in robotic gastrectomy: |
|
29 | Do you perform staging laparoscopy in patients with gastric cancer? |
|
30 | Do you perform extended D2plus/D3 lymphadenectomy with removal of extra-regional lymph nodes (i.e., para-aortic etc.)? (multiple choice) |
|
31 | Do you perform multivisceral resection for cT4B gastric cancer? |
|
32 | Do you extend gastrectomy with metastasectomy (liver, adrenalectomy, ovaries, other organs) for M1 gastric cancer? |
|
33 | Do you extend gastrectomy with peritonectomy for P1 gastric cancer (with overt peritoneal metastasis)? |
|
34 | Do you perform gastrectomy for positive cytology (CY1) gastric cancer without peritoneal metastases at preoperative staging? |
|
35 | What is your institution yearly gastrectomy volume? |
|
36 | What is your personal yearly gastrectomy volume? |
|
37 | What continent do you come from? |
|
References
- Sung, H.; Ferlay, J.; Siegel, R.L.; Laversanne, M.; Soerjomataram, I.; Jemal, A.; Bray, F. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J. Clin. 2021, 71, 209–249. [Google Scholar] [CrossRef]
- Ajani, J.A.; D’Amico, T.A.; Bentrem, D.J.; Chao, J.; Cooke, D.; Corvera, C.; Das, P.; Enzinger, P.C.; Enzler, T.; Fanta, P. Gastric cancer, version 2.2022, NCCN clinical practice guidelines in oncology. J. Natl. Compr. Cancer Netw. 2022, 20, 167–192. [Google Scholar] [CrossRef] [PubMed]
- Bray, F.; Laversanne, M.; Weiderpass, E.; Soerjomataram, I. The ever-increasing importance of cancer as a leading cause of premature death worldwide. Cancer 2021, 127, 3029–3030. [Google Scholar] [CrossRef] [PubMed]
- Lumish, M.A.; Ku, G.Y. Approach to resectable gastric cancer: Evolving paradigm of neoadjuvant and adjuvant treatment. Curr. Treat. Options Oncol. 2022, 23, 1044–1058. [Google Scholar] [CrossRef]
- Al-Batran, S.-E.; Homann, N.; Pauligk, C.; Goetze, T.O.; Meiler, J.; Kasper, S.; Kopp, H.-G.; Mayer, F.; Haag, G.M.; Luley, K. Perioperative chemotherapy with fluorouracil plus leucovorin, oxaliplatin, and docetaxel versus fluorouracil or capecitabine plus cisplatin and epirubicin for locally advanced, resectable gastric or gastro-oesophageal junction adenocarcinoma (FLOT4): A randomised, phase 2/3 trial. Lancet 2019, 393, 1948–1957. [Google Scholar] [CrossRef]
- Bang, Y.-J.; Van Cutsem, E.; Feyereislova, A.; Chung, H.C.; Shen, L.; Sawaki, A.; Lordick, F.; Ohtsu, A.; Omuro, Y.; Satoh, T. Trastuzumab in combination with chemotherapy versus chemotherapy alone for treatment of HER2-positive advanced gastric or gastro-oesophageal junction cancer (ToGA): A phase 3, open-label, randomised controlled trial. Lancet 2010, 376, 687–697. [Google Scholar] [CrossRef]
- Kelly, R.J.; Ajani, J.A.; Kuzdzal, J.; Zander, T.; Van Cutsem, E.; Piessen, G.; Mendez, G.; Feliciano, J.; Motoyama, S.; Lièvre, A. Adjuvant nivolumab in resected esophageal or gastroesophageal junction cancer. N. Engl. J. Med. 2021, 384, 1191–1203. [Google Scholar] [CrossRef]
- Strong, V.E.; Song, K.Y.; Park, C.H.; Jacks, L.M.; Gonen, M.; Shah, M.; Coit, D.G.; Brennan, M.F. Comparison of gastric cancer survival following R0 resection in the United States and Korea using an internationally validated nomogram. Ann. Surg. 2010, 251, 640–646. [Google Scholar] [CrossRef]
- Lordick, F.; Carneiro, F.; Cascinu, S.; Fleitas, T.; Haustermans, K.; Piessen, G.; Vogel, A.; Smyth, E.; Committee, E.G. Gastric cancer: ESMO Clinical Practice Guideline for diagnosis, treatment and follow-up. Ann. Oncol. 2022, 33, 1005–1020. [Google Scholar] [CrossRef] [PubMed]
- Smyth, E.; Verheij, M.; Allum, W.; Cunningham, D.; Cervantes, A.; Arnold, D.; Committee, E.G. Gastric cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann. Oncol. 2016, 27, v38–v49. [Google Scholar] [CrossRef]
- Dejeu, V.; Dejeu, P.; Muresan, A.; Bradea, P.; Dejeu, D. Analysis of patient outcomes following curative R0 multiorgan resections for locally advanced gastric cancer: A systematic review and meta-analysis. J. Clin. Med. 2024, 13, 3010. [Google Scholar] [CrossRef]
- Giampieri, R.; Del Prete, M.; Cantini, L.; Baleani, M.G.; Bittoni, A.; Maccaroni, E.; Berardi, R. Optimal management of resected gastric cancer. Cancer Manag. Res. 2018, 10, 1605–1618. [Google Scholar] [CrossRef] [PubMed]
- Ellison, L.M.; Man, Y.; Stojadinovic, A.; Xin, H.; Avital, I. Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy in treatment of gastric cancer with peritoneal carcinomatosis. Chin. J. Cancer Res. 2017, 29, 86–92. [Google Scholar] [CrossRef]
- Goetze, T.O.; Al-Batran, S.-E. Perspectives on the Management of Oligometastatic Disease in Esophago-Gastric Cancer. Cancers 2022, 14, 5200. [Google Scholar] [CrossRef]
- European Chapter Congress of the International Gastric Cancer Association (IGCA). Available online: https://egcc2024.org (accessed on 7 January 2025).
- He, J.; Baxter, S.L.; Xu, J.; Xu, J.; Zhou, X.; Zhang, K. The practical implementation of artificial intelligence technologies in medicine. Nat. Med. 2019, 25, 30–36. [Google Scholar] [CrossRef]
- Topol, E.J. High-performance medicine: The convergence of human and artificial intelligence. Nat. Med. 2019, 25, 44–56. [Google Scholar] [CrossRef]
- Kelly, C.J.; Karthikesalingam, A.; Suleyman, M.; Corrado, G.; King, D. Key challenges for delivering clinical impact with artificial intelligence. BMC Med. 2019, 17, 195. [Google Scholar] [CrossRef]
- Sendak, M.P.; D’Arcy, J.; Kashyap, S.; Gao, M.; Nichols, M.; Corey, K.; Ratliff, W.; Balu, S. A path for translation of machine learning products into healthcare delivery. EMJ Innov. 2020, 10, 19–00172. [Google Scholar]
- Raghu, M.; Schmidt, E. A survey of deep learning for scientific discovery. arXiv 2020, arXiv:2003.11755. [Google Scholar] [CrossRef]
- Yu, K.-H.; Kohane, I.S. Framing the challenges of artificial intelligence in medicine. BMJ Qual. Saf. 2019, 28, 238–241. [Google Scholar] [CrossRef]
- Jha, S.; Topol, E.J. Adapting to artificial intelligence: Radiologists and pathologists as information specialists. JAMA 2016, 316, 2353–2354. [Google Scholar] [CrossRef]
- Morley, J. Thinking Critically About AI in Healthcare; University of Oxford: Oxford, UK, 2023. [Google Scholar]
- Shreve, J.T.; Khanani, S.A.; Haddad, T.C. Artificial intelligence in oncology: Current capabilities, future opportunities, and ethical considerations. In Proceedings of the American Society of Clinical Oncology Educational Book American Society of Clinical Oncology Annual Meeting, Alexandria, VA, USA, 3–7 June 2022; pp. 1–10. [Google Scholar]
- Joshi, S.S.; Badgwell, B.D. Current treatment and recent progress in gastric cancer. CA Cancer J. Clin. 2021, 71, 264–279. [Google Scholar] [CrossRef] [PubMed]
- Network, C.G.A.R. Comprehensive molecular characterization of gastric adenocarcinoma. Nature 2014, 513, 202. [Google Scholar] [CrossRef] [PubMed]
- Chao, J.; Fuchs, C.S.; Shitara, K.; Tabernero, J.; Muro, K.; Van Cutsem, E.; Bang, Y.-J.; De Vita, F.; Landers, G.; Yen, C.-J. Assessment of pembrolizumab therapy for the treatment of microsatellite instability–high gastric or gastroesophageal junction cancer among patients in the KEYNOTE-059, KEYNOTE-061, and KEYNOTE-062 clinical trials. JAMA Oncol. 2021, 7, 895–902. [Google Scholar] [CrossRef] [PubMed]
- Gretton, C. Trust and transparency in machine learning-based clinical decision support. In Human and Machine Learning: Visible, Explainable, Trustworthy and Transparent; Springer: Berlin/Heidelberg, Germany, 2018; pp. 279–292. [Google Scholar]
- Goddard, K.; Roudsari, A.; Wyatt, J.C. Automation bias: A systematic review of frequency, effect mediators, and mitigators. J. Am. Med. Inform. Assoc. 2012, 19, 121–127. [Google Scholar] [CrossRef]
- Langer, M.; König, C.J.; Back, C.; Hemsing, V. Trust in artificial intelligence: Comparing trust processes between human and automated trustees in light of unfair bias. J. Bus. Psychol. 2023, 38, 493–508. [Google Scholar] [CrossRef]
- Bussone, A.; Stumpf, S.; O’Sullivan, D. The role of explanations on trust and reliance in clinical decision support systems. In Proceedings of the 2015 International Conference on Healthcare Informatics, Dallas, TX, USA, 21–23 October 2015; IEEE: Piscataway, NJ, USA, 2015; pp. 160–169. [Google Scholar]
- Jacobs, M.; Pradier, M.F.; McCoy, T.H., Jr.; Perlis, R.H.; Doshi-Velez, F.; Gajos, K.Z. How machine-learning recommendations influence clinician treatment selections: The example of the antidepressant selection. Transl. Psychiatry 2021, 11, 108. [Google Scholar] [CrossRef]
Answer | Before AI (First Round) | |
---|---|---|
N | (%) | |
Question 26: Please describe your experience with performing gastrectomy as an 1st operator: (n = 56) | ||
Less than 5 years | 20 | 35.71% |
5–10 years | 6 | 10.71% |
10–15 years | 9 | 16.07% |
15–20 years | 8 | 14.29% |
More than 20 years | 13 | 23.21% |
Question 27: What is your experience in laparoscopic gastrectomy: (n = 57) | ||
No experience | 8 | 14.04% |
Less than 5 years | 16 | 28.07% |
5–10 years | 18 | 31.58% |
10–15 years | 9 | 15.79% |
15–20 years | 3 | 5.26% |
More than 20 years | 3 | 5.26% |
Question 28: What is your experience in robotic gastrectomy: (n = 57) | ||
No experience | 28 | 49.12% |
Less than 1 year | 12 | 21.05% |
1–5 years | 8 | 14.04% |
5–10 years | 7 | 12.28% |
10–20 years | 2 | 3.51% |
More than 20 years | 0 | 0.00% |
Question 29: Do you perform staging laparoscopy in patients with gastric cancer? (n = 57) | ||
Yes, routinely in patients with “non-early” GC who are not amenable to endoscopic treatment and who do not have clinically (imaging) detectable distant metastases (cM0) | 31 | 54.39% |
Yes, but only when non-resectability is suspected | 10 | 17.54% |
Yes, I start every gastrectomy for advanced GC with laparoscopy | 5 | 8.77% |
Yes, twice: as a staging procedure (before creation of treatment plan by the MDT), and after preoperative (neo-adjuvant) therapy–re-staging | 11 | 19.30% |
No, never | 0 | 0.00% |
Question 30: Do you perform extended D2plus/D3 lymphadenectomy with removal of extra-regional lymph nodes (i.e., para-aortic etc.)? (multiple choice) (n = 57) | ||
Yes | 7 | 12.28% |
Sometimes | 13 | 22.81% |
If a positive para-aortic node is found (longest axis at least 10 mm) at preoperative radiological examination | 5 | 8.77% |
In patients who have radiological evidence of positive para-aortic nodes before preoperative chemotherapy and then show clinical response at restaging examinations | 24 | 42.11% |
Only when lymph node metastases are proved (intraoperative pathology counselling) | 1 | 1.75% |
Even if these lymph nodes are not suspected for metastases | 1 | 1.75% |
Even if these lymph nodes are not suspected for metastases, but the patient shows clinical response to preoperative chemotherapy | 1 | 1.75% |
No, never | 5 | 8.77% |
Question 31: Do you perform multivisceral resection for cT4B gastric cancer? (n = 57) | ||
Yes | 9 | 15.79% |
Sometimes | 20 | 35.09% |
Only when direct invasion of adjacent organ is proved (intraoperative pathology counselling) | 16 | 28.07% |
Even when direct invasion of adjacent organ is not suspected (preoperative imaging), but I have such a suspicion during gastrectomy | 10 | 17.54% |
No, never. It is not justified | 2 | 3.51% |
Question 32: Do you extend gastrectomy with metastasectomy (liver, adrenalectomy, ovaries, other organs) for M1 gastric cancer? (n = 56) | ||
Yes | 6 | 10.71% |
Sometimes | 17 | 30.36% |
Only when M1 is proved by intraoperative pathology | 1 | 1.79% |
Only if it fulfils criteria of oligometastatic disease (OMEC definition) | 31 | 55.36% |
No, never. It is not justified | 1 | 1.79% |
Question 33: Do you extend gastrectomy with peritonectomy for P1 gastric cancer (with overt peritoneal metastasis)? (n = 57) | ||
Yes, but only within a clinical trial | 10 | 17.54% |
Only when PCI is no more than 6 | 14 | 24.56% |
Only when PCI is no more than 12 for non-poorly cohesive tumours | 1 | 1.75% |
Only if the procedure can be supplemented with the HIPEC | 21 | 36.84% |
No, never. It is not justified | 11 | 19.30% |
Question 34: Do you perform gastrectomy for positive cytology (CY1) gastric cancer without peritoneal metastases at preoperative staging? (n = 58) | ||
Yes always, but only within a clinical trial | 6 | 10.34% |
Only when positive cytology is reversed to negative by preoperative (induction) systemic therapy | 24 | 41.38% |
Even when peritoneal cytology still positive after preoperative systemic therapy | 7 | 12.07% |
Only if the procedure can be supplemented with the HIPEC | 20 | 34.48% |
No, never. It is not justified | 1 | 1.72% |
Question 35: What is your institution yearly gastrectomy volume? (n = 58) | ||
<20 | 5 | 8.62% |
20–30 | 12 | 20.69% |
31–50 | 19 | 32.76% |
51–100 | 14 | 24.14% |
>100 | 8 | 13.79% |
Question 36: What is your personal yearly gastrectomy volume? (n = 58) | ||
<10 | 26 | 44.83% |
10–20 | 13 | 22.41% |
21–30 | 5 | 8.62% |
31–50 | 11 | 18.97% |
>50 | 3 | 5.17% |
Question 37: What continent do you come from? (n = 58) | ||
Asia | 2 | 3.45% |
North America | 1 | 1.72% |
South America | 2 | 3.45% |
Europe | 53 | 91.38% |
other | 0 | 0.00% |
No | Question | Surgeons | AI |
---|---|---|---|
1 | Resectability is to be decided based on preoperative imaging, staging laparoscopy findings and intraoperative findings (clinical stages, cTNM, cStage). Do you think terms technical resectability & oncological resectability are different:(multiple choices are relevant) | 1—Yes, they are—79% 3—Curative gastrectomy refers only to oncological resectability—64% 4—Palliative gastrectomy is for symptom relief only when safe – 64% 6—Reduction gastrectomy after response to preoperative chemotherapy—24% | 1—Yes, they are (technical resectability & oncological resectability are different) 3—Curative gastrectomy (performed with the intention of cure) refers only to oncological resectability 4—Palliative gastrectomy (when cure is not possible) is performed to relieve patients (serious) symptoms only when it may be done safely 6—Reduction gastrectomy should be performed for oligometastatic disease with partial response to preoperative chemotherapy |
4 | Tracking the rate of morbidity/mortality following gastrectomy is an important measure of surgical quality and patient safety. Whether these outcome measures should influence a decision on performance of gastrectomy with multivisceral resection? | 3—Multivisceral resections for locally advanced gastric cancer should only be undertaken in centres that carefully monitor their own results and can demonstrate acceptably low morbidity/mortality associated with gastrectomy and multivisceral resection—61% | 3—Multivisceral resections for locally advanced gastric cancer should only be undertaken in centres that carefully monitor their own results and can demonstrate acceptably low morbidity/mortality associated with gastrectomy and multivisceral resection |
7 | Is gastrectomy with metastasectomy justified for cM1 tumours | 3—Only if R0 or complete cytoreduction group (CCR 0–1) is anticipated to achieve—47% 4—Only if the stage does not exceed (generally accepted) definition of the oligometastatic disease—44% | 3—Only if R0 or complete cytoreduction group (CCR 0–1) is anticipated to achieve Reason: R0 resection or complete cytoreduction (CCR 0–1) is essential for considering gastrectomy with metastasectomy in cM1 tumors. Achieving complete removal of all visible disease significantly improves prognosis in selected cases. This aligns with the principle that surgery is justified only if it contributes meaningfully to disease control. |
9 | Is gastrectomy with extensive peritoneal lavage justified for CY1 tumours (with positive peritoneal cytology): | 5—Only if the resection is preceded by conversion to negative peritoneal cytology under the induction (neoadjuvant) systemic [with/without intraperitoneal therapy (i.p. normothermic paclitaxel/PIPAC)] therapy –54% | 5—Only if the resection is preceded by conversion to negative peritoneal cytology under the induction (neoadjuvant) systemic [with/without intraperitoneal therapy (i.p. normothermic paclitaxel/PIPAC)] therapy Reason: Positive peritoneal cytology (CY1) is a marker of poor prognosis. Conversion to negative cytology after neoadjuvant systemic or intraperitoneal therapy significantly improves the likelihood of achieving long-term survival. Gastrectomy with peritoneal lavage is justified in this context as part of a comprehensive treatment strategy aimed at achieving R0 resection. |
10 | Is gastrectomy with extended (D2plus/D3) lymphadenectomy justified for N3 bulky lymph node metastasis: | 2—Only if the resection is preceded by major regression under the induction (neoadjuvant) systemic (immuno-)therapy—63% | 2—Only if the resection is preceded by major regression under the induction (neoadjuvant) systemic (immuno-)therapy Reason: N3 bulky lymph node metastasis represents advanced nodal disease and is often associated with poor prognosis. Significant regression after neoadjuvant systemic or immunotherapy improves the feasibility of achieving an R0 resection and may justify an extended lymphadenectomy. Without such regression, surgery is unlikely to provide meaningful survival benefits and carries higher risks of morbidity. |
11 | Evaluating the extent and thoroughness of lymph node dissection is important for staging and determining the prognosis of the patient. If a case is borderline resectable at your initial (after exploration) evaluation, should it modify the extent of ultimate lymphadenectomy: | 6—Yes, it should be D2 plus (extraregional lymph nodes) if there is a good response to preoperative therapy—53% | 6—Yes, it should be D2 plus (extraregional lymph nodes) if there is a good response to preoperative therapy Reason: In borderline resectable cases, the response to preoperative therapy is a critical determinant for the extent of lymphadenectomy. If there is a favorable response (e.g., significant tumor regression), an extended lymphadenectomy (D2 plus) may improve staging accuracy and potentially enhance survival outcomes. However, the decision must be weighed against the patient’s condition and perioperative risks. |
13 | Would you call it multivisceral resection? Gastrectomy with:(multiple choices are relevant) | 3—Right and/or left diaphragmatic crus—25% 4—Splenectomy– 79% 5—Distal pancreatectomy– 91% 6—Liver resection with one/two liver segments—86% 7—Liver resection with three or more liver segments—63% 8—Pancreatoduodenectomy—86% 9—Colonic resection (hemicolectomy or transversectomy)—96% 10—Salpingo-oophorectomy with or without hysterectomy—71% | 3—Right and/or left diaphragmatic crus 4—Splenectomy 5—Distal pancreatectomy 6—Liver resection with one/two liver segments 7—Liver resection with three or more liver segments 8—Pancreatoduodenectomy 9—Colonic resection (hemicolectomy or transversectomy) 10—Salpingo-oophorectomy with or without hysterectomy |
15 | Please indicate structures (that may be directly invaded; cT4b) to be resected if primary tumour is located at the proximal stomach (not invading esophago-gastric junction): (multiple choices are relevant) | 1—Lower esophagus (transhiatally)—58% 2—Whole stomach—67% 3—Distal pancreas—62% 4—Spleen—71% 6—Proximal two/thirds of the stomach—24% 7—Left liver lobe—58% | 2—Whole stomach Reason: In some cases, resection of the entire stomach may be necessary for oncological clearance, especially if the tumor extensively involves the proximal stomach and other regions. 3—Distal pancreas Reason: Tumors located in the proximal stomach may invade the distal pancreas, particularly if they are in the posterior wall or near the greater curvature. 4—Spleen Reason: Due to its proximity to the proximal stomach, the spleen may be invaded by tumors extending laterally or posteriorly. 6—Proximal two/thirds of the stomach Reason: This is a common extent of resection for tumors confined to the proximal stomach that do not require total gastrectomy. 7—Left liver lobe Reason: Tumors in the proximal stomach, particularly those near the lesser curvature, may invade the left lobe of the liver. |
16 | Please indicate structures (that may be directly invaded; cT4b) to be resected if primary tumour is located at the middle third of the stomach: (multiple choices are relevant): | 2—Whole stomach—80% 3—Distal pancreas—73% 4—Spleen—76% 6—Left liver lobe—60% | 2—Whole stomach Reason: Tumors in the middle third of the stomach often require total gastrectomy for adequate oncological clearance if they extend significantly proximally or distally. 3—Distal pancreas Reason: The tumor’s location near the posterior wall or greater curvature can lead to invasion of the distal pancreas, necessitating resection. 4—Spleen Reason: Tumors involving the posterior or lateral portions of the middle third of the stomach may invade the spleen, especially near the greater curvature. 5—Proximal one/third of the stomach Reason: Tumors extending proximally may require resection of the proximal stomach to achieve clear margins. 6—Left liver lobe Reason: Tumors on the lesser curvature of the stomach can invade the left liver lobe, particularly with posterior extension. |
19 | Gastric adenocarcinomas are considered unresectable if: | 1—The primary tumor shows extensive invasion to adjacent structures and cannot be separated from the surrounding normal tissues—53% 2—The primary tumor has encased major vascular structures—75% 4—Presence of metastatic lymph nodes outside the scope of surgery—47% 5—Presence of distant metastasis or intraperitoneal implantation (including positive peritoneal lavage fluid cytology—40% 6—presence of distant metastasis or intraperitoneal implantation (excluding positive peritoneal lavage fluid cytology) –45% | 1—The primary tumor shows extensive invasion to adjacent structures and cannot be separated from the surrounding normal tissues Reason: Extensive invasion into adjacent structures that cannot be separated indicates technical non-resectability due to the impossibility of achieving R0 resection without compromising critical structures. 2—The primary tumor has encased major vascular structures Reason: Encasing major vascular structures (e.g., aorta, celiac axis) makes the tumor technically non-resectable and increases the risk of incomplete resection (R2) or patient morbidity/mortality. 4—Presence of metastatic lymph nodes outside the scope of surgery Reason: Metastatic lymph nodes outside the planned surgical field (e.g., para-aortic nodes) suggest systemic disease, making the tumor oncologically unresectable. 5—Presence of distant metastasis or intraperitoneal implantation (including positive peritoneal lavage fluid cytology) Reason: Distant metastases or peritoneal involvement indicate systemic disease, which precludes curative resection. |
23 | Structures for which otherwise no further dissection is necessary during standard gastrectomy include: | 1—Intrathoracic esophagus—39% 2—Diaphragmatic crura—37% 3—Liver—52% 4—Spleen– 50% 5—Pancreas—50% 6—Colon—48% 7—Para-aortic lymph nodes– 44% 8—Ovaries—46% 9—Greater omentum– 30% 10—Parietal peritoneum—43% | 1—Intrathoracic esophagus Reason: Dissection of the intrathoracic esophagus is not part of a standard gastrectomy unless the tumor involves the esophago-gastric junction. 2—Diaphragmatic crura Reason: The diaphragmatic crura are not dissected during a standard gastrectomy unless there is evidence of tumor invasion or proximity to the esophago-gastric junction. 3—Liver Reason: The liver is not typically dissected during standard gastrectomy unless there is direct tumor invasion or metastatic disease requiring resection. 5—Pancreas Reason: The pancreas is not dissected in a standard gastrectomy unless there is tumor involvement or extension near the posterior gastric wall. 6—Colon Reason: The colon is not dissected unless there is direct tumor invasion requiring en bloc resection. 7—Para-aortic lymph nodes Reason: Dissection of para-aortic lymph nodes is not part of standard gastrectomy. It may be performed as part of an extended lymphadenectomy or if these nodes are involved. 8—Ovaries Reason: Ovaries are not routinely addressed during standard gastrectomy unless there are suspected or confirmed metastatic lesions (e.g., Krukenberg tumor). 10—Parietal peritoneum Reason: The parietal peritoneum is not typically dissected unless there is evidence of tumor invasion or peritoneal metastases. |
No | Question | Surgeons | AI |
---|---|---|---|
20 | Would you consider all the above resectability criteria the same if a neoadjuvant systemic (chemo-/immuno) therapy had been used before? | 1—Yes, no matter preoperative treatment—31% 3—Yes, but with cautious use of intraoperative pathology counselling—36% | 4—More conservative approach is justified if clinical response had been achieved Reason: Neoadjuvant systemic therapy can downstage tumors, reducing the extent of disease and potentially converting some cases previously deemed unresectable to resectable. A conservative surgical approach may be justified to balance the benefits of surgery against the risks, especially in patients demonstrating a good clinical response. This approach prioritizes achieving R0 resection without excessive morbidity. |
25 | At what point during the surgical process should the operating surgeon report whether the gastric cancer surgery is intended to be curative or palliative? | 1—At the beginning of the procedure—45% 4—Only after evaluation of the final pathology report of the resection specimen, irrespectively of the peritoneal (lavage) cytology findings—25% | 3—During the procedure, usually immediately following the resection Reason: The decision on whether the surgery is curative or palliative is most accurately determined during the procedure, particularly after the resection is performed. At this point, the surgeon has the most comprehensive intraoperative information, including the extent of tumor invasion, feasibility of achieving R0 margins, and findings from staging evaluations such as frozen section results or peritoneal lavage cytology. This allows for a real-time, informed decision. |
No | Question | Surgeons | AI |
---|---|---|---|
2 | Determining whether the surgical margins are clear of cancer cells by examining the resected tissue (frozen section) helps assess the oncological effectiveness of the procedure. Inability to achieve clear resection margins is a criterion of non-resectability. | 1—Yes, but only macroscopically positive margins (R2)—24% 2—Yes, but only when you prove it with an intraoperative frozen section—32% 3—No, even when intraoperative frozen section is positive, because final pathology of the resection specimen may be different (clear margins)– 18% 5—Resections margins should be clear at every cost, and they are not a non-resectability criterion—18% | 1—Yes, but only macroscopically positive margins (R2) 2—Yes, but only when you prove it with an intraoperative frozen section 4—No, even R2 resection is justified if it may eliminate symptoms |
3 | Achieving R0 resection status is critical for optimizing survival outcomes, despite the inherent risks and complications associated with extensive surgical interventions. Therefore, monitoring the occurrence of postoperative complications (morbidity) and mortality provides insight into the quality of perioperative care. | 1—Risk of morbidity/mortality should always be in mind before decision of multivisceral resection—65% 3—Risk of morbidity/mortality associated with multivisceral resection may be outweighed by the benefits of improved survival after curative gastrectomy—32% | 3—Risk of morbidity/mortality associated with multivisceral resection may be outweighed by the benefits of improved survival after curative gastrectomy |
5 | A shorter hospital stay is generally associated with better surgical outcomes and may indicate a more efficient recovery process. Therefore, duration of hospital stay for oncological gastrectomy should be below: | 1—10 days—26% 6—Depends on total, distal or proximal gastrectomy—16% 7—Depends on splenectomy, pancreatectomy, any multivisceral resection, or HIPEC—35% | 6—Depends on total, distal or proximal gastrectomy |
6 | Is gastrectomy with multivisceral resection justified for cT4b tumours (that invades adjacent structures such as spleen, transverse colon, liver, diaphragm, pancreas, abdominal wall, adrenal gland, kidney, small intestine, or retroperitoneum): | 3—Only if R0 is anticipated to achieve—37% 5—Only if surgical team can prove low morbidity/mortality, as well as the multidisciplinary team can ensure that all aspects of the patient’s condition are considered—46% | 5—Only if surgical team can prove low morbidity/mortality, as well as the multidisciplinary team can ensure that all aspects of the patient’s condition are considered |
8 | Is gastrectomy with peritonectomy justified for P1 tumours (with overt peritoneal metastasis): | 1—Yes, but only for P1a (previous P1—i.e., disseminating metastasis to the region directly adjacent to the peritoneum of the stomach, including the greater omentum; not distant peritoneum or ovarian metastases)—16% 3—Yes, but only for PCI below 12, with poorly cohesive type below 7—16% 7—Only if the resection is preceded by major regression under the induction (neoadjuvant) systemic [with/without intraperitoneal therapy (i.p. normothermic paclitaxel/PIPAC)] therapy—37% | 5—Only if complete cytoreduction (CC0/CC1) is to be achieved Reason: Achieving complete cytoreduction (CC0/CC1) is a prerequisite for considering gastrectomy with peritonectomy in patients with P1 tumors. Without complete cytoreduction, the procedure does not confer significant survival benefits and exposes patients to unnecessary surgical morbidity. AI considers response 5 to be the most appropriate overall, although responses 3 and 7 are also relevant in the context of specific clinical scenarios. If required to select a single option, AI would identify response 5 as the optimal choice. |
12 | Extensive nodal swelling along the major branched arteries or para-aortic lymph node swelling is called bulky-N disease. If large arteries are surrounded by bulky nodal metastatic tissue, do you consider the case resectable? Please indicate non-resectability (multiple choices are relevant): | 1—Coeliac axis—46% 2—Common hepatic a.—30% 5—any of the above—22% | 5—Any of the above Reason: If bulky-N disease involves extensive nodal swelling surrounding any of the major branched arteries (coeliac axis, common hepatic artery, left gastric artery, or proximal portion of the splenic artery), it typically renders the case non-resectable due to the high risk of incomplete resection (R2) and the technical challenges associated with safely dissecting these vessels. Such involvement also indicates an advanced stage of disease with poor prognosis, where surgery is unlikely to provide meaningful survival benefit. |
14 | Please indicate structures (that may be directly invaded; cT4b) to be resected if primary tumour is located at the esophago-gastric junction: (multiple choices are relevant): | 1—Intrathoracic esophagus (below carina)—56% 2—Lower esophagus (transhiatally)– 73% 3—Whole stomach—46% 4—Distal pancreas—44% 5—Spleen—55% 6—Proximal one/third of the stomach—40% 7—Proximal two/thirds of the stomach—26% 8—Left liver lobe—55% | 1—Intrathoracic esophagus (below carina): Reason: Tumors at the esophago-gastric junction (EGJ) often extend into the lower thoracic esophagus. If directly invaded, resection of this segment is necessary. 2—Lower esophagus (transhiatally): Reason: Transhiatal resection of the lower esophagus is a standard part of surgery for EGJ tumors with esophageal invasion. 3—Whole stomach: Reason: Depending on the extent of the tumor and gastric involvement, resection of the entire stomach may be required for oncological clearance. 5—Spleen: Reason: The spleen may be involved in cases of advanced tumors extending posteriorly or laterally. Resection may be necessary if invaded. 6—Proximal one/third of the stomach: Reason: If the tumor is localized to the EGJ and proximal stomach, resection of this portion is sufficient. 7—Proximal two/thirds of the stomach: Reason: In cases where the tumor involves a larger portion of the stomach but spares the distal part, this extent of resection may be warranted. |
17 | Please indicate structures (that may be directly invaded; cT4b) to be resected if primary tumour is located at the distal stomach:(multiple choices are relevant): | 1—Whole stomach, if poorly cohesive carcinoma—65% 2—Distal pancreas—42% 3—Spleen– 36% 4—Distal three/thirds of the stomach (small remnant)—58% 5—Distal stomach—42% 6—Antrum of the stomach—31% 7—Colon—73% 8—Head of pancreas—53% | 1—Whole stomach, if poorly cohesive carcinoma Reason: Poorly cohesive carcinomas (e.g., signet-ring cell carcinoma) often exhibit diffuse spread, making total gastrectomy necessary even for distal tumors to achieve R0 resection. 2—Distal pancreas Reason: Tumors in the distal stomach, particularly those involving the posterior wall or greater curvature, can invade the distal pancreas, necessitating resection. 4—Distal three/thirds of the stomach (small remnant) Reason: When oncological clearance requires resecting most of the stomach, leaving only a small remnant may be appropriate for proximal margin control. 5—Distal stomach Reason: This is the standard resection for tumors confined to the distal stomach that do not require total gastrectomy. 7—Colon Reason: Tumors in the distal stomach, particularly near the greater curvature or posterior wall, may invade the transverse colon, necessitating colonic resection. |
21 | Should staging laparoscopy be used for reliable resectability determination? | 2—Yes, reliable determination of the resectability is possible using staging laparoscopy—34% 3—Yes, all surrounding structures should be assessed during staging laparoscopy—27% 4—Yes, all surrounding structures should be assessed only (!) in case of preoperative suspicion of infiltration/metastases—20% | 3—Yes, all surrounding structures should be assessed during staging laparoscopy Reason: Staging laparoscopy is a crucial tool for determining resectability, especially in advanced gastric cancer. It allows for direct visualization of peritoneal surfaces, surrounding structures, and ascites, providing valuable information about peritoneal metastases or invasion of adjacent structures. Comprehensive assessment of all surrounding structures during the procedure increases the reliability of the resectability evaluation. |
22 | The (technical) resectability of the primary tumour by means of gastrectomy should be assessed during the staging laparoscopy by evaluation of the surrounding structures: | 1—Yes, all surrounding structures should be assessed during staging laparoscopy—39% 2—Yes, all surrounding structures should be assessed only (!) in case of preoperative suspicion of infiltration/metastases on imaging—34% | 1—Yes, all surrounding structures should be assessed during staging laparoscopy Reason: Staging laparoscopy is a crucial tool for assessing the technical resectability of the primary tumor. A thorough evaluation of all surrounding structures allows for a comprehensive determination of local invasion, peritoneal metastases, or other factors affecting resectability. This ensures that no potentially resectable tumor is overlooked and that unnecessary laparotomies for unresectable cases are avoided. |
24 | An expert opinion is to be formed on the nature of the operation. The operating surgeon should ascertain details about the extent of disease, including nodal involvement: | 1—Curative—46% 4—Resection technically possible, but oncologically not justified due to substantial risk of R1/2 resection—26% | 4—Resection technically possible, but oncologically not justified due to substantial risk of R1/2 resection Reason: This choice reflects a nuanced understanding of surgical decision-making. Even if resection is technically possible, the oncological outcome must be the priority. If achieving R0 resection (curative intent) is unlikely due to extensive disease or nodal involvement, surgery may not be justified, as R1/2 resection provides limited survival benefit and exposes the patient to unnecessary risks. |
Question 1: Resectability is to be decided based on preoperative imaging, staging laparoscopy findings and intraoperative findings (clinical stages, cTNM, cStage). Do you think terms technical resectability & oncological resectability are different:(multiple choices are relevant) | |||
Answers | Before AI (first round) N = 59 | After AI (second round) N = 48 | p |
Yes, they are | 47 (79.66%) | 38 (79.17%) | 1.0000 |
No, they are not | 4 (6.78%) | 4 (8.33%) | 1.0000 |
Curative gastrectomy (performed with the intention of cure) refers only to oncological resectability. | 38 (64.41%) | 23 (47.92%) | 0.1163 |
Palliative gastrectomy (when cure is not possible) is performed to relieve patients (serious) symptoms only when it may be done safely | 38 (64.41%) | 28 (58.33%) | 0.5536 |
Reduction gastrectomy should be performed for oligometastatic disease | 1 (1.69%) | 2 (4.17%) | 0.5862 |
Reduction gastrectomy should be performed for oligometastatic disease with partial response to preoperative chemotherapy | 14 (23.73%) | 11 (22.92%) | 1.0000 |
Other (please specify) | 1 (1.69%) | 0 (0%) | 1.0000 |
Question 2: Determining whether the surgical margins are clear of cancer cells by examining the resected tissue (frozen section) helps assess the oncological effectiveness of the procedure. Inability to achieve clear resection margins is a criterion of non-resectability: | |||
Answers | Before AI (first round) N = 58 | After AI (second round) N = 48 | p |
Yes, but only macroscopically positive margins (R2) | 14 (24.14%) | 19 (39.58%) | 0.0967 |
Yes, but only when you prove it with an intraoperative frozen section | 18 (31.03%) | 12 (25.00%) | 0.5235 |
No, even when intraoperative frozen section is positive, because final pathology of the resection specimen may be different (clear margins) | 10 (17.24%) | 6 (12.50%) | 0.5912 |
No, even R2 resection is justified if it may eliminate symptoms | 3 (5.17%) | 3 (6.25%) | 1.0000 |
Resections margins should be clear at every cost, and they are not a non-resectability criterion | 10 (17.24%) | 8 (16.67%) | 1.0000 |
Other (please specify) | 3 (5.17%) | 0 (0%) | 0.2496 |
Question 3: Achieving R0 resection status is critical for optimizing survival outcomes, despite the inherent risks and complications associated with extensive surgical interventions. Therefore, monitoring the occurrence of postoperative complications (morbidity) and mortality provides insight into the quality of perioperative care. | |||
Answers | Before AI (first round) N = 58 | After AI (second round) N = 48 | p |
Risk of morbidity/mortality should always be in mind before decision of multivisceral resection | 37 (63.79%) | 30 (62.50%) | 1.0000 |
Risk of morbidity/mortality is independent of multivisceral resection | 1 (1.72%) | 2 (4.17%) | 0.5887 |
Risk of morbidity/mortality associated with multivisceral resection may be outweighed by the benefits of improved survival after curative gastrectomy | 19 (32.76%) | 16 (33.33%) | 1.0000 |
Risk of morbidity/mortality associated with multivisceral resection is so high that it cannot outweighed by the benefits of improved survival after R0 resection | 1 (1.72%) | 0 (0.00%) | 1.0000 |
Question 4: Tracking the rate of morbidity/mortality following gastrectomy is an important measure of surgical quality and patient safety. Whether these outcome measures should influence a decision on performance of gastrectomy with multivisceral resection? | |||
Answers | Before AI (first round) N = 58 | After AI (second round) N = 48 | p |
Multivisceral resections for locally advanced gastric cancer should only be undertaken in centres that carefully monitor their morbidity/mortality associated with gastrectomy and multivisceral resection | 14 (24.14%) | 5 (10.42%) | 0.0791 |
Multivisceral resections for locally advanced gastric cancer should only be undertaken in centres that demonstrate acceptably low morbidity/mortality associated with gastrectomy and multivisceral resection | 6 (10.34%) | 4 (8.33%) | 1.0000 |
Multivisceral resections for locally advanced gastric cancer should only be undertaken in centres that carefully monitor their own results and can demonstrate acceptably low morbidity/mortality associated with gastrectomy and multivisceral resection | 35 (60.34%) | 37 (77.08%) | 0.0941 |
Multivisceral resections for locally advanced gastric cancer should only be undertaken in large volume centres irrespectively of their own results | 2 (3.45%) | 2 (4.17%) | 1.0000 |
Multivisceral resections are not justified in the surgical treatment of locally advanced gastric cancer | 0 (0.00%) | 0 (0.00%) | N/a |
Other (please specify) | 1 (1.72%) | 0 (0.00%) | 1.0000 |
Question 5: A shorter hospital stay is generally associated with better surgical outcomes and may indicate a more efficient recovery process. Therefore, duration of hospital stay for oncological gastrectomy should be below: | |||
Answers | Before AI (first round) N = 58 | After AI (second round) N = 48 | p |
10 days | 15 (25.86%) | 16 (33.33%) | 0.5203 |
11 days | 1 (1.72%) | 0 (0.00%) | 1.0000 |
12 days | 3 (5.17%) | 0 (0.00%) | 0.2496 |
14 days | 3 (5.17%) | 1 (2.08%) | 0.6247 |
75th percentile by year | 0 (0.00%) | 3 (6.25%) | 0.0897 |
Depends on total, distal or proximal gastrectomy | 10 (17.24%) | 19 (39.58%) | 0.0155 * |
Depends on splenectomy, pancreatectomy, any multivisceral resection, or HIPEC | 20 (34.48%) | 9 (18.75%) | 0.0829 |
Other (please specify) | 6 (10.34%) | 0 (0%) | 0.0309 * |
Question 6: Is gastrectomy with multivisceral resection justified for cT4b tumours (that invades adjacent structures such as spleen, transverse colon, liver, diaphragm, pancreas, abdominal wall, adrenal gland, kidney, small intestine, or retroperitoneum): | |||
Answers | Before AI (first round) N = 58 | After AI (second round) N = 48 | p |
Yes, it is always justified | 0 (0.00%) | 1 (2.08%) | 0.4528 |
No, never | 3 (5.17%) | 0 (0.00%) | 0.2496 |
Only if R0 is anticipated to achieve | 22 (37.93%) | 15 (31.25%) | 0.5417 |
Only if the patient’s general condition allows for the success of the operation | 4 (6.90%) | 4 (8.33%) | 1.0000 |
Only if surgical team can prove low morbidity/mortality, as well as the multidisciplinary team can ensure that all aspects of the patient’s condition are considered. | 26 (44.83%) | 28 (58.33%) | 0.1783 |
Other (please specify) | 3 (5.17%) | 0 (0.00%) | 0.2496 |
Answers | Before AI (first round) N = 58 | After AI (second round) N = 48 | p |
Question 7: Is gastrectomy with metastasectomy justified for cM1 tumours: | |||
Yes, it is always justified | 0 (0.00%) | 0 (0.00%) | N/a |
No, never | 0 (0.00%) | 2 (4.17%) | 0.2027 |
Only if R0 or complete cytoreduction group (CCR 0–1) is anticipated to achieve | 27 (46.55%) | 25 (52.08%) | 0.6966 |
Only if the stage does not exceed (generally accepted) definition of the oligometastatic disease | 26 (44.83%) | 21 (43.75%) | 1.0000 |
Only if the resection can be done on one stage | 0 (0.00%) | 0 (0.00%) | N/a |
Other (please specify) | 5 (8.62%) | 0 (0.00%) | 0.0621 |
Answers | Before AI (first round) N = 58 | After AI (second round) N = 48 | p |
Question 8: Is gastrectomy with peritonectomy justified for P1 tumours (with overt peritoneal metastasis): | |||
Yes, but only for P1a (previous P1—i.e., disseminating metastasis to the region directly adjacent to the peritoneum of the stomach, including the greater omentum; not distant peritoneum or ovarian metastases) | 9 (15.52%) | 4 (8.33%) | 0.3746 |
Yes, but only for PCI below 7, irrespectively of histologic type | 5 (8.62%) | 2 (4.17%) | 0.4525 |
Yes, but only for PCI below 12, with poorly cohesive type below 7 | 9 (15.52%) | 7 (14.58%) | 1.0000 |
Only if R0 is anticipated to achieve | 2 (3.45%) | 3 (6.25%) | 0.6566 |
Only if complete cytoreduction (CC0/CC1) is to be achieved | 5 (8.62%) | 10 (20.83%) | 0.0949 |
Only if the resection can be supplemented with HIPEC | 1 (1.72%) | 0 (0.00%) | 1.0000 |
Only if the resection is preceded by major regression under the induction (neoadjuvant) systemic [with/without intraperitoneal therapy (i.p. normothermic paclitaxel/PIPAC)] therapy | 21 (36.21%) | 22 (45.83%) | 0.3287 |
Other (please specify) | 6 (10.34%) | 0 (0.00%) | 0.0309 * |
Answers | Before AI (first round) N = 58 | After AI (second round) N = 48 | p |
Question 9: Is gastrectomy with extensive peritoneal lavage justified for CY1 tumours (with positive peritoneal cytology): | |||
No, never | 2 (3.45%) | 5 (10.42%) | 0.2404 |
No, extensive peritoneal lavage is justified only for CY0 and positive molecular cytology (CEA, OSNA etc.) | 4 (6.90%) | 2 (4.17%) | 0.6872 |
Yes, but only if R0 is anticipated to achieve | 8 (13.79%) | 9 (18.75%) | 0.5974 |
Only if the resection can be supplemented with HIPEC | 10 (17.24%) | 6 (12.50%) | 0.5912 |
Only if the resection is preceded by conversion to negative peritoneal cytology under the induction (neoadjuvant) systemic [with/without intraperitoneal therapy (i.p. normothermic paclitaxel/PIPAC)] therapy | 32 (55.17%) | 26 (54.17%) | 1.0000 |
Other (please specify) | 2 (3.45%) | 0 (0.00%) | 0.4997 |
Answers | Before AI (first round) N = 58 | After AI (second round) N = 48 | p |
Question 10: Is gastrectomy with extended (D2plus/D3) lymphadenectomy justified for N3 bulky lymph node metastasis: | |||
No, never | 3 (5.17%) | 3 (6.25%) | 1.0000 |
Only if the resection is preceded by major regression under the induction (neoadjuvant) systemic (immuno-)therapy | 36 (62.07%) | 32 (66.67%) | 0.6867 |
Yes, but only if R0 is anticipated to achieve | 8 (13.79%) | 7 (14.58%) | 1.0000 |
Yes, but only if para-aortic lymph nodes (station #16) can be removed electively | 1 (1.72%) | 3 (6.25%) | 0.3265 |
Yes, but only if enlarged para-aortic lymph nodes (station #16) can be effectively removed | 5 (8.62%) | 3 (6.25%) | 0.7263 |
Only if the resection can be supplemented with HIPEC | 1 (1.72%) | 0 (0.00%) | 1.0000 |
Other (please specify) | 4 (6.90%) | 0 (0.00%) | 0.1246 |
Answers | Before AI (first round) N = 56 | After AI (second round) N = 47 | p |
Question 11: Evaluating the extent and thoroughness of lymph node dissection is important for staging and determining the prognosis of the patient. If a case is borderline resectable at your initial (after exploration) evaluation, should it modify the extent of ultimate lymphadenectomy: | |||
No, it should be reduction gastrectomy (D0) | 1 (1.79%) | 0 (0.00%) | 1.0000 |
No, it should be D1 (perigastric lymph nodes) | 0 (0.00%) | 0 (0.00%) | N/a |
No, it should be D1 plus (depends on localisation of the primary tumour) | 0 (0.00%) | 0 (0.00%) | N/a |
No, it should be always just D2 | 12 (21.43%) | 12 (25.53%) | 0.6470 |
Yes, it should be D2 plus (extraregional lymph nodes) | 9 (16.07%) | 4 (8.51%) | 0.3730 |
Yes, it should be D2 plus (extraregional lymph nodes) if there is a good response to preoperative therapy | 30 (53.57%) | 31 (65.96%) | 0.2313 |
Other (please specify) | 4 (7.14%) | 0 (0.00%) | 0.1234 |
Answers | Before AI (first round) N = 55 | After AI (second round) N = 42 | p |
Question 12: Extensive nodal swelling along the major branched arteries or para-aortic lymph node swelling is called bulky-N disease. If large arteries are surrounded by bulky nodal metastatic tissue, do you consider the case resectable? Please indicate non-resectability (multiple choices are relevant): | |||
Coeliac axis | 26 (47.27%) | 24 (57.14%) | 0.4132 |
Common hepatic a. | 17 (30.91%) | 19 (45.24%) | 0.2032 |
Left gastric a. | 6 (10.91%) | 3 (7.14%) | 0.7275 |
Proximal portion of splenic a. | 4 (7.27%) | 3 (7.14%) | 1.0000 |
any of the above | 12 (21.82%) | 10 (23.81%) | 0.8124 |
Other (please specify) | 17 (30.91%) | 0 (0%) | <0.0001 * |
Answers | Before AI (first round) N = 57 | After AI (second round) N = 48 | p |
Question 13: Would you call it multivisceral resection? Gastrectomy with:(multiple choices are relevant) | |||
Omentectomy (both, major and minor omentum) | 2 (3.51%) | 1 (2.08%) | 1.0000 |
Bursectomy | 2 (3.51%) | 2 (4.17%) | 1.0000 |
Right and/or left diaphragmatic crus | 14 (24.56%) | 15 (31.25%) | 0.5138 |
Splenectomy | 45 (78.95%) | 37 (77.08%) | 0.8180 |
Distal pancreatectomy | 52 (91.23%) | 48 (100.00%) | 0.0611 |
Liver resection with one/two liver segments | 49 (85.96%) | 45 (93.75%) | 0.2212 |
Liver resection with three or more liver segments | 36 (63.16%) | 37 (77.08%) | 0.1407 |
Pancreatoduodenectomy | 49 (85.96%) | 45 (93.75%) | 0.2212 |
Colonic resection (hemicolectomy or transversectomy) | 55 (96.49%) | 48 (100.00%) | 0.4989 |
Salpingo-oophorectomy with or without hysterectomy | 41 (71.93%) | 38 (79.17%) | 0.4973 |
Other (please specify) | 1 (1.75%) | 0 (0.00%) | 1.0000 |
Answers | Before AI (first round) N = 56 | After AI (second round) N = 47 | p |
Question 14: Please indicate structures (that may be directly invaded; cT4b) to be resected if primary tumour is located at the esophago-gastric junction:(multiple choices are relevant) | |||
Intrathoracic esophagus (below carina) | 32 (57.14%) | 33 (70.21%) | 0.2196 |
Lower esophagus (transhiatally) | 41 (73.21%) | 36 (76.60%) | 0.8207 |
Whole stomach | 26 (46.43%) | 32 (68.09%) | 0.0305 * |
Distal pancreas | 25 (44.64%) | 26 (55.32%) | 0.3254 |
Spleen | 31 (55.36%) | 30 (63.83%) | 0.4253 |
Proximal one/third of the stomach | 23 (41.07%) | 26 (55.32%) | 0.1696 |
Proximal two/thirds of the stomach | 14 (25.00%) | 20 (42.55%) | 0.0917 |
Left liver lobe | 31 (55.36%) | 33 (70.21%) | 0.1545 |
Other (please specify) | 5 (8.93%) | 0 (0.00%) | 0.0612 |
Answers | Before AI (first round) N = 56 | After AI (second round) N = 48 | p |
Question 15: Please indicate structures (that may be directly invaded; cT4b) to be resected if primary tumour is located at the proximal stomach (not invading esophago-gastric junction): (multiple choices are relevant) | |||
Lower esophagus (transhiatally) | 33 (58.93%) | 31 (64.58%) | 0.6863 |
Whole stomach | 38 (67.86%) | 38 (79.17%) | 0.2678 |
Distal pancreas | 35 (62.50%) | 37 (77.08%) | 0.1372 |
Spleen | 40 (71.43%) | 36 (75.00%) | 0.8250 |
Proximal one/third of the stomach | 10 (17.86%) | 16 (33.33%) | 0.1108 |
Proximal two/thirds of the stomach | 14 (25.00%) | 19 (39.58%) | 0.1403 |
Left liver lobe | 33 (58.93%) | 34 (70.83%) | 0.2246 |
Other (please specify) | 6 (10.71%) | 0 (0.00%) | 0.0295 * |
Answers | Before AI (first round) N = 56 | After AI (second round) N = 48 | p |
Question 16: Please indicate structures (that may be directly invaded; cT4b) to be resected if primary tumour is located at the middle third of the stomach:(multiple choices are relevant) | |||
Lower esophagus (transhiatally) | 9 (16.07%) | 18 (37.50%) | 0.0150 * |
Whole stomach | 45 (80.36%) | 41 (85.42%) | 0.6063 |
Distal pancreas | 41 (73.21%) | 39 (81.25%) | 0.3606 |
Spleen | 43 (76.79%) | 36 (75.00%) | 1.0000 |
Proximal one/third of the stomach | 10 (17.86%) | 18 (37.50%) | 0.0284 * |
Left liver lobe | 34 (60.71%) | 36 (75.00%) | 0.1451 |
Distal stomach (antrectomy) | 10 (17.86%) | 12 (25.00%) | 0.4715 |
Other (please specify) | 4 (7.14%) | 0 (0.00%) | 0.1222 |
Answers | Before AI (first round) N = 56 | After AI (second round) N = 48 | p |
Question 17: Please indicate structures (that may be directly invaded; cT4b) to be resected if primary tumour is located at the distal stomach:(multiple choices are relevant) | |||
Whole stomach, if poorly cohesive carcinoma | 36 (64.29%) | 32 (66.67%) | 0.8385 |
Distal pancreas | 23 (41.07%) | 26 (54.17%) | 0.2375 |
Spleen | 20 (35.71%) | 24 (50.00%) | 0.1663 |
Distal three/thirds of the stomach (small remnant) | 33 (58.93%) | 33 (68.75%) | 0.3160 |
Distal stomach | 24 (42.86%) | 20 (41.67%) | 1.0000 |
Antrum of the stomach | 18 (32.14%) | 17 (35.42%) | 0.8356 |
Colon | 41 (73.21%) | 42 (87.50%) | 0.0884 |
Head of a pancreas | 30 (53.57%) | 32 (66.67%) | 0.2295 |
Other (please specify) | 6 (10.71%) | 0 (0.00%) | 0.0295 * |
Answers | Before AI (first round) N = 57 | After AI (second round) N = 48 | p |
Question 18: Gastric adenocarcinomas are considered unresectable if there is evidence of locally advanced disease with: | |||
Disease infiltration of the root of the mesentery | 46 (80.70%) | 43 (89.58%) | 0.2784 |
Para-aortic lymph nodes highly suspicious on imaging or confirmed by biopsy | 14 (24.56%) | 14 (29.17%) | 0.6607 |
Invasion or encasement of major vascular structures (excluding the splenic vessels) | 41 (71.93%) | 35 (72.92%) | 1.0000 |
N3 lymph node involvement | 8 (14.04%) | 9 (18.75%) | 0.5983 |
Peritoneal involvement (including positive peritoneal cytology) | 27 (47.37%) | 26 (54.17%) | 0.5585 |
Ovarian metastases | 16 (28.07%) | 14 (29.17%) | 1.0000 |
Other (please specify) | 4 (7.02%) | 0 (0.00%) | 0.1233 |
Answers | Before AI (first round) N = 56 | After AI (second round) N = 48 | p |
Question 19: Gastric adenocarcinomas are considered unresectable if: | |||
the primary tumour shows extensive invasion to adjacent structures and cannot be separated from the surrounding normal tissues | 30 (53.57%) | 31 (64.58%) | 0.3190 |
the primary tumour has encased major vascular structures | 42 (75.00%) | 37 (77.08%) | 0.8226 |
the regional lymph nodes are fixed and fused into clusters | 8 (14.29%) | 12 (25.00%) | 0.2142 |
presence of metastatic lymph nodes outside the scope of surgery | 26 (46.43%) | 36 (75.00%) | 0.0048 * |
presence of distant metastasis or intraperitoneal implantation (including positive peritoneal lavage fluid cytology) | 23 (41.07%) | 25 (52.08%) | 0.3248 |
presence of distant metastasis or intraperitoneal implantation (excluding positive peritoneal lavage fluid cytology) | 26 (46.43%) | 26 (54.17%) | 0.5554 |
Other (please specify) | 4 (7.14%) | 0 (0.00%) | 0.1222 |
Answers | Before AI (first round) N = 56 | After AI (second round) N = 48 | p |
Question 20: Would you consider all the above resectability criteria the same if a neoadjuvant systemic (chemo-/immuno) therapy had been used before? | |||
Yes, no matter preoperative treatment | 18 (32.14%) | 19 (39.58%) | 0.5382 |
No, if preoperative immuno(chemo-)therapy was used | 8 (14.29%) | 9 (18.75%) | 0.6011 |
Yes, but with cautious use of intraoperative pathology counselling | 20 (35.71%) | 8 (16.67%) | 0.0450 * |
More conservative approach is justified if clinical response had been achieved | 5 (8.93%) | 12 (25.00%) | 0.0344 * |
Just gastrectomy with adequate lymphadenectomy is required (for staging purposes) | 4 (7.14%) | 0 (0.00%) | 0.1222 |
Other (please specify) | 1 (1.79%) | 0 (0.00%) | 1.0000 |
Answers | Before AI (first round) N = 57 | After AI (second round) N = 48 | p |
Question 21: Should staging laparoscopy be used for reliable resectability determination? | |||
No, reliable determination of the resectability is not possible using staging laparoscopy | 8 (14.04%) | 5 (10.42%) | 0.7676 |
Yes, reliable determination of the resectability is possible using staging laparoscopy | 19 (33.33%) | 13 (27.08%) | 0.5291 |
Yes, all surrounding structures should be assessed during staging laparoscopy | 16 (28.07%) | 12 (25.00%) | 0.8258 |
Yes, all surrounding structures should be assessed only (!) in case of preoperative suspicion of infiltration/metastases for determining stage of the disease | 11 (19.30%) | 14 (29.17%) | 0.2585 |
Reliable determination of neoplastic infiltration of surrounding structures can be decided only based on pathologic findings of the resected specimen | 1 (1.75%) | 4 (8.33%) | 0.1760 |
Other (please specify) | 2 (3.51%) | 0 (0.00%) | 0.4989 |
Answers | Before AI (first round) N = 57 | After AI (second round) N = 47 | p |
Question 22: The (technical) resectability of the primary tumour by means of gastrectomy should be assessed during the staging laparoscopy by evaluation of the surrounding structures: | |||
Yes, all surrounding structures should be assessed during staging laparoscopy | 23 (40.35%) | 16 (34.04%) | 0.5468 |
Yes, all surrounding structures should be assessed only (!) in case of preoperative suspicion of infiltration/metastases on imaging | 19 (33.33%) | 18 (38.30%) | 0.6821 |
No, reliable determination of direct invasion of the surrounding structures is not possible during staging laparoscopy | 10 (17.54%) | 5 (10.64%) | 0.4054 |
Anatomical structures for which otherwise no further dissection is necessary during standard gastrectomy (not multivisceral resection) should be inspected for direct invasion | 5 (8.77%) | 5 (10.64%) | 0.7520 |
Reliable determination of neoplastic infiltration of surrounding structures can be decided only based on pathologic findings of the resected specimen | 0 (0.00%) | 3 (6.38%) | 0.0890 |
Other (please specify) | 0 (0.00%) | 0 (0.00%) | N/a |
Answers | Before AI (first round) N = 55 | After AI (second round) N = 47 | p |
Question 23: Structures for which otherwise no further dissection is necessary during standard gastrectomy include: | |||
intrathoracic esophagus | 22 (40.00%) | 29 (61.70%) | 0.0466 * |
diaphragmatic crura | 21 (38.18%) | 24 (51.06%) | 0.2319 |
liver | 29 (52.73%) | 35 (74.47%) | 0.0260 * |
spleen | 28 (50.91%) | 26 (55.32%) | 0.6943 |
pancreas | 28 (50.91%) | 36 (76.60%) | 0.0083 * |
colon | 27 (49.09%) | 32 (68.09%) | 0.0705 |
para-aortic lymph nodes | 25 (45.45%) | 33 (70.21%) | 0.0161 * |
ovaries | 26 (47.27%) | 35 (74.47%) | 0.0081 * |
greater omentum | 16 (29.09%) | 8 (17.02%) | 0.1685 |
parietal peritoneum | 24 (43.64%) | 34 (72.34%) | 0.0049 * |
Other (please specify) | 6 (10.91%) | 0 (0.00%) | 0.0295 * |
Answers | Before AI (first round) N = 55 | After AI (second round) N = 46 | p |
Question 24: An expert opinion is to be formed on the nature of the operation. The operating surgeon should ascertain details about the extent of disease, including nodal involvement: | |||
curative | 25 (45.45%) | 13 (28.26%) | 0.0995 |
borderline curative | 4 (7.27%) | 5 (10.87%) | 0.7282 |
palliative | 0 (0.00%) | 0 (0.00%) | N/a |
resection technically possible, but oncologically not justified due to substantial risk of R1/2 resection | 14 (25.45%) | 21 (45.65%) | 0.5466 |
resection technically not possible, even by means of extended multivisceral resection | 5 (9.09%) | 7 (15.22%) | 0.3722 |
Other (please specify) | 7 (12.73%) | 0 (0.00%) | 0.0149 * |
Answers | Before AI (first round) N = 57 | After AI (second round) N = 48 | p |
Question 25: At what point during the surgical process should the operating surgeon report whether the gastric cancer surgery is intended to be curative or palliative? | |||
At the beginning of the procedure | 25 (43.86%) | 21 (43.75%) | 1.0000 |
After completion of the procedure (at the end) | 7 (12.28%) | 4 (8.33%) | 0.7506 |
During the procedure, usually immediately following the resection | 7 (12.28%) | 9 (18.75%) | 0.4200 |
Only after evaluation of the final pathology report of the resection specimen, irrespectively of the peritoneal (lavage) cytology findings | 1 (1.75%) | 3 (6.25%) | 0.3296 |
Only after evaluation of the final pathology report of the resection specimen, including the peritoneal (lavage) cytology findings | 14 (24.56%) | 11 (22.92%) | 1.0000 |
Other (please specify) | 3 (5.26%) | 0 (0.00%) | 0.2484 |
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
© 2025 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
Gęca, K.; Roviello, F.; Skórzewska, M.; Mlak, R.; Polkowski, W.P.; ICRGC Collaborators. A Step Toward a Global Consensus on Gastric Cancer Resectability Integrating Artificial Intelligence-Based Consensus Modelling. Cancers 2025, 17, 2664. https://doi.org/10.3390/cancers17162664
Gęca K, Roviello F, Skórzewska M, Mlak R, Polkowski WP, ICRGC Collaborators. A Step Toward a Global Consensus on Gastric Cancer Resectability Integrating Artificial Intelligence-Based Consensus Modelling. Cancers. 2025; 17(16):2664. https://doi.org/10.3390/cancers17162664
Chicago/Turabian StyleGęca, Katarzyna, Franco Roviello, Magdalena Skórzewska, Radosław Mlak, Wojciech P. Polkowski, and ICRGC Collaborators. 2025. "A Step Toward a Global Consensus on Gastric Cancer Resectability Integrating Artificial Intelligence-Based Consensus Modelling" Cancers 17, no. 16: 2664. https://doi.org/10.3390/cancers17162664
APA StyleGęca, K., Roviello, F., Skórzewska, M., Mlak, R., Polkowski, W. P., & ICRGC Collaborators. (2025). A Step Toward a Global Consensus on Gastric Cancer Resectability Integrating Artificial Intelligence-Based Consensus Modelling. Cancers, 17(16), 2664. https://doi.org/10.3390/cancers17162664