External multicentre validation of pseudomyxoma peritonei PSOGI-Ki67 classification
dc.contributor.author | Arjona-Sanchez, A. | |
dc.contributor.author | Martinez-López, A. | |
dc.contributor.author | Moreno-Montilla, M.T. | |
dc.contributor.author | Mulsow, J. | |
dc.contributor.author | Lozano-Lominchar, P. | |
dc.contributor.author | Martínez-Torres, B. | |
dc.contributor.author | Rau B. | |
dc.date.accessioned | 2024-05-19T14:34:28Z | |
dc.date.available | 2024-05-19T14:34:28Z | |
dc.date.issued | 2023 | |
dc.department | İstinye Üniversitesi | en_US |
dc.description.abstract | Background: Pseudomyxoma peritonei (PMP) is a rare malignant disease. Adding of the Ki67 proliferation index to the PSOGI PMP classification provided two different subcategories of the extensive HG-PMP group (HG-PMP ?15% and HG-PMP >15%) with different survival in a previous unicentric study. This study aims to carry out an external and multicentre validation of this new proposed classification. Method: It was a prospective analysis of samples from a historical and international cohort of patients. A representative area with higher cellular density was used to determine the Ki67%. The Ki67 proliferation index (%) was determined in all the HG-PMP patients. A Cox proportional hazard models and multivariable COX models were used. The Kaplan–Meier method and the two-tailed log-rank test were used to analyse the effect of different PSOGI-Ki67 categories on OS and DFS. Its predictive accuracy was analysed using Harrel's C-index and the ROC curve. The calibration was performed using the calibration plots matching. Results: After exclusions, 349 patients were available for analysis. The 5-years OS were 86% for LG-PMP, 59% for HG-PMP?15, 38% for HG-PMP>15 and 42% for SRC-PMP (p = 0.0001). The 5-years DFS were 49% for LG-PMP, 35% for HG-PMP?15, 16% for HG-PMP>15 and 18% SRC-PMP (p = 0.0001). The discrimination capability of PSOGI-Ki67 was validated. Conclusion: the PSOGI-Ki67 classification discriminates and predicts the OS and DFS in patients with PMP dividing the HG-PMP category into two well-defined sub-categories. The Ki67 proliferation index should be incorporated routinely in the pathology report for these patients. © 2023 Elsevier Ltd, BASO ~ The Association for Cancer Surgery, and the European Society of Surgical Oncology | en_US |
dc.identifier.doi | 10.1016/j.ejso.2023.03.206 | |
dc.identifier.endpage | 1488 | en_US |
dc.identifier.issn | 0748-7983 | |
dc.identifier.issue | 8 | en_US |
dc.identifier.pmid | 36935222 | en_US |
dc.identifier.scopus | 2-s2.0-85150308268 | en_US |
dc.identifier.scopusquality | N/A | en_US |
dc.identifier.startpage | 1481 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.ejso.2023.03.206 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12713/4494 | |
dc.identifier.volume | 49 | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | W.B. Saunders Ltd | en_US |
dc.relation.ispartof | European Journal of Surgical Oncology | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.snmz | 20240519_ka | en_US |
dc.subject | Antineoplastic Agent | en_US |
dc.subject | Ki 67 Antigen | en_US |
dc.subject | Ki 67 Antigen | en_US |
dc.subject | Adjuvant Chemotherapy | en_US |
dc.subject | Adult | en_US |
dc.subject | Aged | en_US |
dc.subject | Article | en_US |
dc.subject | Cancer Classification | en_US |
dc.subject | Cancer Patient | en_US |
dc.subject | Cancer Survival | en_US |
dc.subject | Cell Density | en_US |
dc.subject | Cohort Analysis | en_US |
dc.subject | Controlled Study | en_US |
dc.subject | Cytoreductive Surgery | en_US |
dc.subject | Disease Free Survival | en_US |
dc.subject | Female | en_US |
dc.subject | Follow Up | en_US |
dc.subject | Human | en_US |
dc.subject | Human Tissue | en_US |
dc.subject | Hyperthermic İntraperitoneal Chemotherapy | en_US |
dc.subject | Labeling İndex | en_US |
dc.subject | Major Clinical Study | en_US |
dc.subject | Male | en_US |
dc.subject | Median Survival Time | en_US |
dc.subject | Multicenter Study | en_US |
dc.subject | Neoadjuvant Chemotherapy | en_US |
dc.subject | Overall Survival | en_US |
dc.subject | Peritoneum Pseudomyxoma | en_US |
dc.subject | Predictive Value | en_US |
dc.subject | Proliferation İndex | en_US |
dc.subject | Prospective Study | en_US |
dc.subject | Receiver Operating Characteristic | en_US |
dc.subject | Survival Rate | en_US |
dc.subject | Systemic Therapy | en_US |
dc.subject | Tissue Section | en_US |
dc.subject | Validation Process | en_US |
dc.subject | Clinical Trial | en_US |
dc.subject | Pathology | en_US |
dc.subject | Peritoneum Pseudomyxoma | en_US |
dc.subject | Peritoneum Tumor | en_US |
dc.subject | Prognosis | en_US |
dc.subject | Proportional Hazards Model | en_US |
dc.subject | Retrospective Study | en_US |
dc.subject | Humans | en_US |
dc.subject | Ki-67 Antigen | en_US |
dc.subject | Peritoneal Neoplasms | en_US |
dc.subject | Prognosis | en_US |
dc.subject | Proportional Hazards Models | en_US |
dc.subject | Pseudomyxoma Peritonei | en_US |
dc.subject | Retrospective Studies | en_US |
dc.title | External multicentre validation of pseudomyxoma peritonei PSOGI-Ki67 classification | en_US |
dc.type | Article | en_US |