Which classification system defines best prognosis of mucinous neoplasms of the appendix with peritoneal dissemination: TNM vs PSOGI?

AimsSeveral classification systems are used for pseudomyxoma peritonei. The four-tiered classification system proposed by Peritoneal Surface Oncology Group International (PSOGI) and the two-tiered proposed by the eighth edition of the American Joint Committee on Cancer (AJCC) result from evolution i...

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Veröffentlicht in:Journal of clinical pathology 2023-04, Vol.76 (4), p.266-273
Hauptverfasser: Martín-Román, Lorena, Lozano, Pablo, Gómez, Yesica, Fernández-Aceñero, María Jesús, Vasquez, Wenceslao, Palencia, Natividad, González-Bayón, Luis
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container_end_page 273
container_issue 4
container_start_page 266
container_title Journal of clinical pathology
container_volume 76
creator Martín-Román, Lorena
Lozano, Pablo
Gómez, Yesica
Fernández-Aceñero, María Jesús
Vasquez, Wenceslao
Palencia, Natividad
González-Bayón, Luis
description AimsSeveral classification systems are used for pseudomyxoma peritonei. The four-tiered classification system proposed by Peritoneal Surface Oncology Group International (PSOGI) and the two-tiered proposed by the eighth edition of the American Joint Committee on Cancer (AJCC) result from evolution in terminology and pathological insight. The aim is to evaluate the impact of PSOGI and eighth edition of the AJCC classifications on survival.MethodsPathological slides were reviewed from a prospectively maintained database including patients treated with cytoreductive surgery and hyperthermic intraperitoneal chemotherapy for an appendiceal mucinous neoplasm with peritoneal dissemination between January 2009 and December 2019. Patients were reclassified according to PSOGI and AJCC eighth edition criteria. Survival analysis evaluated the impact of each classification system on overall survival (OS) and disease-free survival (DFS) while the concordance-index evaluated their predictive power.Results95 patients were identified; 21.1% were reclassified as acellular mucin, 55.8% as low-grade mucinous carcinoma peritonei, 8.4% as high-grade MCP (HGMCP) and 14 as HGMCP with signet ring cells. Median OS was not reached, 5-year OS and DFS were 86.1% and 51.5%, respectively. Multivariate analysis revealed significant associations with OS (PSOGI: HR 10.2, p=0.039; AJCC: HR 7.7, p=0.002) and DFS (PSOGI: HR 12.7, p=0.001; AJCC: HR 3.7, p
doi_str_mv 10.1136/jclinpath-2021-207883
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The four-tiered classification system proposed by Peritoneal Surface Oncology Group International (PSOGI) and the two-tiered proposed by the eighth edition of the American Joint Committee on Cancer (AJCC) result from evolution in terminology and pathological insight. The aim is to evaluate the impact of PSOGI and eighth edition of the AJCC classifications on survival.MethodsPathological slides were reviewed from a prospectively maintained database including patients treated with cytoreductive surgery and hyperthermic intraperitoneal chemotherapy for an appendiceal mucinous neoplasm with peritoneal dissemination between January 2009 and December 2019. Patients were reclassified according to PSOGI and AJCC eighth edition criteria. Survival analysis evaluated the impact of each classification system on overall survival (OS) and disease-free survival (DFS) while the concordance-index evaluated their predictive power.Results95 patients were identified; 21.1% were reclassified as acellular mucin, 55.8% as low-grade mucinous carcinoma peritonei, 8.4% as high-grade MCP (HGMCP) and 14 as HGMCP with signet ring cells. Median OS was not reached, 5-year OS and DFS were 86.1% and 51.5%, respectively. Multivariate analysis revealed significant associations with OS (PSOGI: HR 10.2, p=0.039; AJCC: HR 7.7, p=0.002) and DFS (PSOGI: HR 12.7, p=0.001; AJCC: HR 3.7, p&lt;0.001). The predictive capacity of both classification systems was unacceptable for OS and DFS (concordance-index values &lt;0.7).ConclusionsBoth classification systems behaved similarly when stratifying our series into prognostic groups. The PSOGI classification provides better histopathological description, but histology alone is insufficient for adequate patient prognostication.</description><identifier>ISSN: 0021-9746</identifier><identifier>EISSN: 1472-4146</identifier><identifier>DOI: 10.1136/jclinpath-2021-207883</identifier><identifier>PMID: 34725195</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd and Association of Clinical Pathologists</publisher><subject>Antigens ; Appendiceal Neoplasms - pathology ; Appendiceal Neoplasms - therapy ; appendix ; Appendix - pathology ; Cancer ; Chemotherapy ; Classification ; Histology ; Humans ; Medical prognosis ; Missing data ; neoplasms ; Neoplasms, Cystic, Mucinous, and Serous ; Oncology ; Original research ; Pathology ; Peritoneal Neoplasms - pathology ; Peritoneal Neoplasms - therapy ; peritoneum ; Prognosis ; Pseudomyxoma Peritonei - therapy ; regional perfusion ; Retrospective Studies ; Statistical analysis ; Surgical outcomes ; Survival analysis ; Survival Rate ; Terminology ; Tumors</subject><ispartof>Journal of clinical pathology, 2023-04, Vol.76 (4), p.266-273</ispartof><rights>Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2023 Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b379t-d4d55b75e1cf61698b52d8742e6989a4a6a6d5b0a2fa1712c346b0ebe2d8818d3</citedby><cites>FETCH-LOGICAL-b379t-d4d55b75e1cf61698b52d8742e6989a4a6a6d5b0a2fa1712c346b0ebe2d8818d3</cites><orcidid>0000-0003-0423-910X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34725195$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Martín-Román, Lorena</creatorcontrib><creatorcontrib>Lozano, Pablo</creatorcontrib><creatorcontrib>Gómez, Yesica</creatorcontrib><creatorcontrib>Fernández-Aceñero, María Jesús</creatorcontrib><creatorcontrib>Vasquez, Wenceslao</creatorcontrib><creatorcontrib>Palencia, Natividad</creatorcontrib><creatorcontrib>González-Bayón, Luis</creatorcontrib><title>Which classification system defines best prognosis of mucinous neoplasms of the appendix with peritoneal dissemination: TNM vs PSOGI?</title><title>Journal of clinical pathology</title><addtitle>J Clin Pathol</addtitle><addtitle>J Clin Pathol</addtitle><description>AimsSeveral classification systems are used for pseudomyxoma peritonei. The four-tiered classification system proposed by Peritoneal Surface Oncology Group International (PSOGI) and the two-tiered proposed by the eighth edition of the American Joint Committee on Cancer (AJCC) result from evolution in terminology and pathological insight. The aim is to evaluate the impact of PSOGI and eighth edition of the AJCC classifications on survival.MethodsPathological slides were reviewed from a prospectively maintained database including patients treated with cytoreductive surgery and hyperthermic intraperitoneal chemotherapy for an appendiceal mucinous neoplasm with peritoneal dissemination between January 2009 and December 2019. Patients were reclassified according to PSOGI and AJCC eighth edition criteria. Survival analysis evaluated the impact of each classification system on overall survival (OS) and disease-free survival (DFS) while the concordance-index evaluated their predictive power.Results95 patients were identified; 21.1% were reclassified as acellular mucin, 55.8% as low-grade mucinous carcinoma peritonei, 8.4% as high-grade MCP (HGMCP) and 14 as HGMCP with signet ring cells. Median OS was not reached, 5-year OS and DFS were 86.1% and 51.5%, respectively. Multivariate analysis revealed significant associations with OS (PSOGI: HR 10.2, p=0.039; AJCC: HR 7.7, p=0.002) and DFS (PSOGI: HR 12.7, p=0.001; AJCC: HR 3.7, p&lt;0.001). The predictive capacity of both classification systems was unacceptable for OS and DFS (concordance-index values &lt;0.7).ConclusionsBoth classification systems behaved similarly when stratifying our series into prognostic groups. 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The four-tiered classification system proposed by Peritoneal Surface Oncology Group International (PSOGI) and the two-tiered proposed by the eighth edition of the American Joint Committee on Cancer (AJCC) result from evolution in terminology and pathological insight. The aim is to evaluate the impact of PSOGI and eighth edition of the AJCC classifications on survival.MethodsPathological slides were reviewed from a prospectively maintained database including patients treated with cytoreductive surgery and hyperthermic intraperitoneal chemotherapy for an appendiceal mucinous neoplasm with peritoneal dissemination between January 2009 and December 2019. Patients were reclassified according to PSOGI and AJCC eighth edition criteria. Survival analysis evaluated the impact of each classification system on overall survival (OS) and disease-free survival (DFS) while the concordance-index evaluated their predictive power.Results95 patients were identified; 21.1% were reclassified as acellular mucin, 55.8% as low-grade mucinous carcinoma peritonei, 8.4% as high-grade MCP (HGMCP) and 14 as HGMCP with signet ring cells. Median OS was not reached, 5-year OS and DFS were 86.1% and 51.5%, respectively. Multivariate analysis revealed significant associations with OS (PSOGI: HR 10.2, p=0.039; AJCC: HR 7.7, p=0.002) and DFS (PSOGI: HR 12.7, p=0.001; AJCC: HR 3.7, p&lt;0.001). The predictive capacity of both classification systems was unacceptable for OS and DFS (concordance-index values &lt;0.7).ConclusionsBoth classification systems behaved similarly when stratifying our series into prognostic groups. The PSOGI classification provides better histopathological description, but histology alone is insufficient for adequate patient prognostication.</abstract><cop>England</cop><pub>BMJ Publishing Group Ltd and Association of Clinical Pathologists</pub><pmid>34725195</pmid><doi>10.1136/jclinpath-2021-207883</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-0423-910X</orcidid></addata></record>
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subjects Antigens
Appendiceal Neoplasms - pathology
Appendiceal Neoplasms - therapy
appendix
Appendix - pathology
Cancer
Chemotherapy
Classification
Histology
Humans
Medical prognosis
Missing data
neoplasms
Neoplasms, Cystic, Mucinous, and Serous
Oncology
Original research
Pathology
Peritoneal Neoplasms - pathology
Peritoneal Neoplasms - therapy
peritoneum
Prognosis
Pseudomyxoma Peritonei - therapy
regional perfusion
Retrospective Studies
Statistical analysis
Surgical outcomes
Survival analysis
Survival Rate
Terminology
Tumors
title Which classification system defines best prognosis of mucinous neoplasms of the appendix with peritoneal dissemination: TNM vs PSOGI?
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