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Outcome of histologically node‐negative esophageal squamous cell carcinoma

The outcome of node‐negative esophageal carcinoma and the prognostic significance of lymph node micrometastasis remain unknown. The aim of this retrospective study was to clarify these two points. A series of 98 patients who underwent curative operation for histologically node‐negative (pNO in TNM c...

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Published in:World journal of surgery 2002-12, Vol.26 (12), p.1446-1451
Main Authors: Tabira, Yoichi, Yasunaga, Masahiro, Sakaguchi, Tomonori, Yamaguchi, Yuji, Okuma, Toshiyuki, Kawasuji, Michio
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Yasunaga, Masahiro
Sakaguchi, Tomonori
Yamaguchi, Yuji
Okuma, Toshiyuki
Kawasuji, Michio
description The outcome of node‐negative esophageal carcinoma and the prognostic significance of lymph node micrometastasis remain unknown. The aim of this retrospective study was to clarify these two points. A series of 98 patients who underwent curative operation for histologically node‐negative (pNO in TNM classification) esophageal carcinoma were enrolled in the study. We reviewed the cause of death of these patients. The survival curves were calculated and compared after stratifications according to clinicopathologic parameters. Lymph node micrometastasis in the patients with recurrences was examined using immunohistochemical staining of cytokeratin. Their ages ranged from 45 to 83 years (mean 64.3 years). There were 83 men and 15 women. Altogether, 54 patients were still alive, and 44 had died. A total of 9 patients died from recurrence of their esophageal carcinoma, 33 died from other causes (pneumonia 11, extraesophageal carcinoma 7, and so on), and 2 died from unknown causes. Eight patients had locoregionai recurrences, and two patients had distant recurrences. The overall survival rate for the 98 patients was 58.2%. The survival for patients with pT2 or pT3 tumors was significantly worse than for those with pTis or pTl tumors (p=0.02, log‐rank test). Other clinicopathologic factors did not affect the prognosis. Immunohistochemical study found no lymph node micrometastasis in 365 lymph nodes resected from the patients with recurrences. Only the depth of tumor invasion affected the outcome of patients with node‐negative esophageal carcinoma. Altogether, 75% of patients died of other causes without recurrence, with the two main causes of death being pulmonary complications and extraesophageal carcinoma in these patients. Lymph node micrometastasis was not associated with recurrence in this series. Résumé L’évolution des cancers de lœsophage NO et la signification des micrométastases ganglionnaires resent inconnues. Le but de cette étude rétrospective a été de clarifier ces deux problèmes. Nous avons inclus dans cette étude, 98 patients qui ont eu une résection à visée curative pour un cncer de l’œsophage (pNO selon la classificaton TNM). Nous avons revu les causes de mortalité chez ces patients. Les courbes de survie ont été calculées et comparées après stratification selon les données clinicopathologiques. Les micrométastases ganglionnaires chez les patients récidives ont été déterminées par une coloration immunohistochimique de la cytokératine. L’àge des pati
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The aim of this retrospective study was to clarify these two points. A series of 98 patients who underwent curative operation for histologically node‐negative (pNO in TNM classification) esophageal carcinoma were enrolled in the study. We reviewed the cause of death of these patients. The survival curves were calculated and compared after stratifications according to clinicopathologic parameters. Lymph node micrometastasis in the patients with recurrences was examined using immunohistochemical staining of cytokeratin. Their ages ranged from 45 to 83 years (mean 64.3 years). There were 83 men and 15 women. Altogether, 54 patients were still alive, and 44 had died. A total of 9 patients died from recurrence of their esophageal carcinoma, 33 died from other causes (pneumonia 11, extraesophageal carcinoma 7, and so on), and 2 died from unknown causes. Eight patients had locoregionai recurrences, and two patients had distant recurrences. The overall survival rate for the 98 patients was 58.2%. The survival for patients with pT2 or pT3 tumors was significantly worse than for those with pTis or pTl tumors (p=0.02, log‐rank test). Other clinicopathologic factors did not affect the prognosis. Immunohistochemical study found no lymph node micrometastasis in 365 lymph nodes resected from the patients with recurrences. Only the depth of tumor invasion affected the outcome of patients with node‐negative esophageal carcinoma. Altogether, 75% of patients died of other causes without recurrence, with the two main causes of death being pulmonary complications and extraesophageal carcinoma in these patients. Lymph node micrometastasis was not associated with recurrence in this series. Résumé L’évolution des cancers de lœsophage NO et la signification des micrométastases ganglionnaires resent inconnues. Le but de cette étude rétrospective a été de clarifier ces deux problèmes. Nous avons inclus dans cette étude, 98 patients qui ont eu une résection à visée curative pour un cncer de l’œsophage (pNO selon la classificaton TNM). Nous avons revu les causes de mortalité chez ces patients. Les courbes de survie ont été calculées et comparées après stratification selon les données clinicopathologiques. Les micrométastases ganglionnaires chez les patients récidives ont été déterminées par une coloration immunohistochimique de la cytokératine. L’àge des patients allait de 45 à 83 ans (moyenne: 65.3 ans). Il y avait 83 hommes et 15 femmes. Cinquante‐quatre patients étaient en vie et 44 patients étaient décédés. Neuf patients sont décédés d’une récidive de leur cancer le l’œsophage, 33 sont décédés d’autres causes (principalement une infection pulmonaire:n=11, ou un cancer extra‐esophagien: n=7) alors que deux patients sont décédés de cause inconnue. Huit patients ont eu une récidive locorégionale et deux, une récidive à distance. La survie globale pour les 98 patients a été de 58.2%. La survie des patients ayant des tumeurs pT2 ou pT3 a été significativement moins bonne que pour les tumeurs pTis ou pT1 (p=0.02, test du log‐rank). Les autres facteurs clinicopathologiques n’ont pas affecté le pronostic. Par l’étude immunohistochimique aucune micrométastase n’a été retrouvée parmi 365 ganglions réséqués chez des patients ayant eu une récidive. Seule la profondeur d’invasion tumorale a influené l’évolution de la maladie chez les patients NO. Parmi les patients décédés, 75% étaient sans récidive; les deux causes principales étant des complications pulmonaires et un cancer extra‐esophagien. Dans cette série, les micrométastases n’ont jamais été la cause de récidive. Resumen No están bien establecidos ni la evolución ni el resultado final del carcinoma escamocelular del esófago con ganglios negativos, tampoco el significado pronóstico de las micrometástasis ganglionares. El propósito de este estudio retrospectivo fue aclarar estos interrogantes. Noventa y ocho pacientes sometidos a operación curativa por carcinoma esofágico con ganglios histológicmente negativos (pNO en la clasificación TNM) fueron incorporados en el estudio. Se revisaron las causas de muerte y se calcularon las curvas de supervivencia para compararlas luego de la estratificación según parámetros clínico patológicos. El estudio de los ganglios para determinar micrometástasis fue hecho en los pacientes que desarrollaron recurrencia mediante coloración immunohistológica de queratina. Las edades oscilaron entre 45 y 83 años (promedio: 65.3); hubo 83 hombres y 15 mujeres. Cincuenta y dos pacientes están vivos, 44 murieron. Nueve murieron por carcinoma recurrente, 33 por otras causas (neumonía 11, carcinoma extraesofágico 7, etc.) y dos por causa desconocida. Ocho presentaron recurrencia local‐regional y dos metástasis distantes. La tasa global de supervivencia para los 98 pacientes fue 58.2%. La supervivencia en los pacientes con neoplasmas pT2 o pT3 fue significativamente peor que en los pTis o pT1 (p=0.02). Otros factores clínicos y patológicos no demostraron efecto sobre el pronóstico. El estudio immunohistoquímico no reveló micrometástasis ganglionares en 365 ganglios resecados de pacientes con recurrencias. Sólo la profundidad de la invasión tumoral afectó la evolución final en estos carcinomas esofágicos con ganglios negativos. Setenta y cinco por ciento de los pacientes murieron por causas diferentes de la recurrencia tumoral, y las dos causas principales de muerte fueron la complicación pulmonar y el carcinoma extraesofágico en los pacientes libres de recurrencia. La presencia de micrometástasis ganglionares no apareció asociada con recurrencia en esta serie.</description><identifier>ISSN: 0364-2313</identifier><identifier>EISSN: 1432-2323</identifier><identifier>DOI: 10.1007/s00268-002-6415-4</identifier><identifier>PMID: 12297913</identifier><identifier>CODEN: WJSUDI</identifier><language>eng</language><publisher>New York: Springer‐Verlag</publisher><subject>Adult ; Age Distribution ; Aged ; Biological and medical sciences ; Biopsy, Needle ; Carcinoma, Squamous Cell - mortality ; Carcinoma, Squamous Cell - pathology ; Carcinoma, Squamous Cell - therapy ; Chemosensitivity Testing ; Cohort Studies ; Combined Modality Therapy - methods ; Esophageal Cancer ; Esophageal Carcinoma ; Esophageal Neoplasms - mortality ; Esophageal Neoplasms - pathology ; Esophageal Neoplasms - therapy ; Esophageal Squamous Cell Carcinoma ; Esophagus ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Incidence ; Lymph Nodes - pathology ; Male ; Medical sciences ; Middle Aged ; Neoplasm Invasiveness - pathology ; Neoplasm Recurrence, Local - mortality ; Neoplasm Recurrence, Local - pathology ; Neoplasm Recurrence, Local - therapy ; Neoplasm Staging ; Preoperative Chemotherapy ; Probability ; Prognosis ; Retrospective Studies ; Risk Assessment ; Sex Distribution ; Statistics, Nonparametric ; Survival Rate ; Treatment Outcome ; Tumors</subject><ispartof>World journal of surgery, 2002-12, Vol.26 (12), p.1446-1451</ispartof><rights>2002 International Society of Surgery</rights><rights>2003 INIST-CNRS</rights><rights>by the Société Internationale de Chirurgie 2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4114-ed565780561bae5b5989d58d6290eab8dab1c01dd66958b441a558d2fffe3e373</citedby><cites>FETCH-LOGICAL-c4114-ed565780561bae5b5989d58d6290eab8dab1c01dd66958b441a558d2fffe3e373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=14447695$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12297913$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tabira, Yoichi</creatorcontrib><creatorcontrib>Yasunaga, Masahiro</creatorcontrib><creatorcontrib>Sakaguchi, Tomonori</creatorcontrib><creatorcontrib>Yamaguchi, Yuji</creatorcontrib><creatorcontrib>Okuma, Toshiyuki</creatorcontrib><creatorcontrib>Kawasuji, Michio</creatorcontrib><title>Outcome of histologically node‐negative esophageal squamous cell carcinoma</title><title>World journal of surgery</title><addtitle>World J Surg</addtitle><description>The outcome of node‐negative esophageal carcinoma and the prognostic significance of lymph node micrometastasis remain unknown. The aim of this retrospective study was to clarify these two points. A series of 98 patients who underwent curative operation for histologically node‐negative (pNO in TNM classification) esophageal carcinoma were enrolled in the study. We reviewed the cause of death of these patients. The survival curves were calculated and compared after stratifications according to clinicopathologic parameters. Lymph node micrometastasis in the patients with recurrences was examined using immunohistochemical staining of cytokeratin. Their ages ranged from 45 to 83 years (mean 64.3 years). There were 83 men and 15 women. Altogether, 54 patients were still alive, and 44 had died. A total of 9 patients died from recurrence of their esophageal carcinoma, 33 died from other causes (pneumonia 11, extraesophageal carcinoma 7, and so on), and 2 died from unknown causes. Eight patients had locoregionai recurrences, and two patients had distant recurrences. The overall survival rate for the 98 patients was 58.2%. The survival for patients with pT2 or pT3 tumors was significantly worse than for those with pTis or pTl tumors (p=0.02, log‐rank test). Other clinicopathologic factors did not affect the prognosis. Immunohistochemical study found no lymph node micrometastasis in 365 lymph nodes resected from the patients with recurrences. Only the depth of tumor invasion affected the outcome of patients with node‐negative esophageal carcinoma. Altogether, 75% of patients died of other causes without recurrence, with the two main causes of death being pulmonary complications and extraesophageal carcinoma in these patients. Lymph node micrometastasis was not associated with recurrence in this series. Résumé L’évolution des cancers de lœsophage NO et la signification des micrométastases ganglionnaires resent inconnues. Le but de cette étude rétrospective a été de clarifier ces deux problèmes. Nous avons inclus dans cette étude, 98 patients qui ont eu une résection à visée curative pour un cncer de l’œsophage (pNO selon la classificaton TNM). Nous avons revu les causes de mortalité chez ces patients. Les courbes de survie ont été calculées et comparées après stratification selon les données clinicopathologiques. Les micrométastases ganglionnaires chez les patients récidives ont été déterminées par une coloration immunohistochimique de la cytokératine. L’àge des patients allait de 45 à 83 ans (moyenne: 65.3 ans). Il y avait 83 hommes et 15 femmes. Cinquante‐quatre patients étaient en vie et 44 patients étaient décédés. Neuf patients sont décédés d’une récidive de leur cancer le l’œsophage, 33 sont décédés d’autres causes (principalement une infection pulmonaire:n=11, ou un cancer extra‐esophagien: n=7) alors que deux patients sont décédés de cause inconnue. Huit patients ont eu une récidive locorégionale et deux, une récidive à distance. La survie globale pour les 98 patients a été de 58.2%. La survie des patients ayant des tumeurs pT2 ou pT3 a été significativement moins bonne que pour les tumeurs pTis ou pT1 (p=0.02, test du log‐rank). Les autres facteurs clinicopathologiques n’ont pas affecté le pronostic. Par l’étude immunohistochimique aucune micrométastase n’a été retrouvée parmi 365 ganglions réséqués chez des patients ayant eu une récidive. Seule la profondeur d’invasion tumorale a influené l’évolution de la maladie chez les patients NO. Parmi les patients décédés, 75% étaient sans récidive; les deux causes principales étant des complications pulmonaires et un cancer extra‐esophagien. Dans cette série, les micrométastases n’ont jamais été la cause de récidive. Resumen No están bien establecidos ni la evolución ni el resultado final del carcinoma escamocelular del esófago con ganglios negativos, tampoco el significado pronóstico de las micrometástasis ganglionares. El propósito de este estudio retrospectivo fue aclarar estos interrogantes. Noventa y ocho pacientes sometidos a operación curativa por carcinoma esofágico con ganglios histológicmente negativos (pNO en la clasificación TNM) fueron incorporados en el estudio. Se revisaron las causas de muerte y se calcularon las curvas de supervivencia para compararlas luego de la estratificación según parámetros clínico patológicos. El estudio de los ganglios para determinar micrometástasis fue hecho en los pacientes que desarrollaron recurrencia mediante coloración immunohistológica de queratina. Las edades oscilaron entre 45 y 83 años (promedio: 65.3); hubo 83 hombres y 15 mujeres. Cincuenta y dos pacientes están vivos, 44 murieron. Nueve murieron por carcinoma recurrente, 33 por otras causas (neumonía 11, carcinoma extraesofágico 7, etc.) y dos por causa desconocida. Ocho presentaron recurrencia local‐regional y dos metástasis distantes. La tasa global de supervivencia para los 98 pacientes fue 58.2%. La supervivencia en los pacientes con neoplasmas pT2 o pT3 fue significativamente peor que en los pTis o pT1 (p=0.02). Otros factores clínicos y patológicos no demostraron efecto sobre el pronóstico. El estudio immunohistoquímico no reveló micrometástasis ganglionares en 365 ganglios resecados de pacientes con recurrencias. Sólo la profundidad de la invasión tumoral afectó la evolución final en estos carcinomas esofágicos con ganglios negativos. Setenta y cinco por ciento de los pacientes murieron por causas diferentes de la recurrencia tumoral, y las dos causas principales de muerte fueron la complicación pulmonar y el carcinoma extraesofágico en los pacientes libres de recurrencia. La presencia de micrometástasis ganglionares no apareció asociada con recurrencia en esta serie.</description><subject>Adult</subject><subject>Age Distribution</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Biopsy, Needle</subject><subject>Carcinoma, Squamous Cell - mortality</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Carcinoma, Squamous Cell - therapy</subject><subject>Chemosensitivity Testing</subject><subject>Cohort Studies</subject><subject>Combined Modality Therapy - methods</subject><subject>Esophageal Cancer</subject><subject>Esophageal Carcinoma</subject><subject>Esophageal Neoplasms - mortality</subject><subject>Esophageal Neoplasms - pathology</subject><subject>Esophageal Neoplasms - therapy</subject><subject>Esophageal Squamous Cell Carcinoma</subject><subject>Esophagus</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Incidence</subject><subject>Lymph Nodes - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neoplasm Invasiveness - pathology</subject><subject>Neoplasm Recurrence, Local - mortality</subject><subject>Neoplasm Recurrence, Local - pathology</subject><subject>Neoplasm Recurrence, Local - therapy</subject><subject>Neoplasm Staging</subject><subject>Preoperative Chemotherapy</subject><subject>Probability</subject><subject>Prognosis</subject><subject>Retrospective Studies</subject><subject>Risk Assessment</subject><subject>Sex Distribution</subject><subject>Statistics, Nonparametric</subject><subject>Survival Rate</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><issn>0364-2313</issn><issn>1432-2323</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNqFkE1u2zAQhYmgQeK4PUA2gVCg2Snh8E_iroGRtAkMeOEWXRIUNbIVSKItWim86xFyxp4kdG3AQDfZPBLDb2YeHyGXQG-A0uw2UMpUnkZNlQCZihMyAsFZyjjjH8iIciXiHfg5uQjhmVLIFFVn5BwY05kGPiLT2bBxvsXEV8myDhvf-EXtbNNsk86X-PfPa4cLu6lfMMHgV0u7QNskYT3Y1g8hcdg0ibO9qzvf2o_ktLJNwE-Hc0x-Ptz_mHxPp7Nvj5O7aeoEgEixlEpmOZUKCouykDrXpcxLxTRFW-SlLcBRKEultMwLIcDK-MyqqkKOPONjcr2fu-r9esCwMW0ddlZsh9GVyVgmeK7zCH7-D3z2Q99Fb4aB1lKCoBGCPeR6H0KPlVn1dWv7rQFqdjmbfc4mqtnlbETsuToMHooWy2PHIdgIfDkANsQ4q952rg5HTgiRxd9F7uue-103uH1_s_n1NJ__K-4klgR_A71SmIE</recordid><startdate>200212</startdate><enddate>200212</enddate><creator>Tabira, Yoichi</creator><creator>Yasunaga, Masahiro</creator><creator>Sakaguchi, Tomonori</creator><creator>Yamaguchi, Yuji</creator><creator>Okuma, Toshiyuki</creator><creator>Kawasuji, Michio</creator><general>Springer‐Verlag</general><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QO</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>200212</creationdate><title>Outcome of histologically node‐negative esophageal squamous cell carcinoma</title><author>Tabira, Yoichi ; Yasunaga, Masahiro ; Sakaguchi, Tomonori ; Yamaguchi, Yuji ; Okuma, Toshiyuki ; Kawasuji, Michio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4114-ed565780561bae5b5989d58d6290eab8dab1c01dd66958b441a558d2fffe3e373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adult</topic><topic>Age Distribution</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Biopsy, Needle</topic><topic>Carcinoma, Squamous Cell - mortality</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Carcinoma, Squamous Cell - therapy</topic><topic>Chemosensitivity Testing</topic><topic>Cohort Studies</topic><topic>Combined Modality Therapy - methods</topic><topic>Esophageal Cancer</topic><topic>Esophageal Carcinoma</topic><topic>Esophageal Neoplasms - mortality</topic><topic>Esophageal Neoplasms - pathology</topic><topic>Esophageal Neoplasms - therapy</topic><topic>Esophageal Squamous Cell Carcinoma</topic><topic>Esophagus</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Incidence</topic><topic>Lymph Nodes - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neoplasm Invasiveness - pathology</topic><topic>Neoplasm Recurrence, Local - mortality</topic><topic>Neoplasm Recurrence, Local - pathology</topic><topic>Neoplasm Recurrence, Local - therapy</topic><topic>Neoplasm Staging</topic><topic>Preoperative Chemotherapy</topic><topic>Probability</topic><topic>Prognosis</topic><topic>Retrospective Studies</topic><topic>Risk Assessment</topic><topic>Sex Distribution</topic><topic>Statistics, Nonparametric</topic><topic>Survival Rate</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tabira, Yoichi</creatorcontrib><creatorcontrib>Yasunaga, Masahiro</creatorcontrib><creatorcontrib>Sakaguchi, Tomonori</creatorcontrib><creatorcontrib>Yamaguchi, Yuji</creatorcontrib><creatorcontrib>Okuma, Toshiyuki</creatorcontrib><creatorcontrib>Kawasuji, Michio</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>World journal of surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tabira, Yoichi</au><au>Yasunaga, Masahiro</au><au>Sakaguchi, Tomonori</au><au>Yamaguchi, Yuji</au><au>Okuma, Toshiyuki</au><au>Kawasuji, Michio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Outcome of histologically node‐negative esophageal squamous cell carcinoma</atitle><jtitle>World journal of surgery</jtitle><addtitle>World J Surg</addtitle><date>2002-12</date><risdate>2002</risdate><volume>26</volume><issue>12</issue><spage>1446</spage><epage>1451</epage><pages>1446-1451</pages><issn>0364-2313</issn><eissn>1432-2323</eissn><coden>WJSUDI</coden><abstract>The outcome of node‐negative esophageal carcinoma and the prognostic significance of lymph node micrometastasis remain unknown. The aim of this retrospective study was to clarify these two points. A series of 98 patients who underwent curative operation for histologically node‐negative (pNO in TNM classification) esophageal carcinoma were enrolled in the study. We reviewed the cause of death of these patients. The survival curves were calculated and compared after stratifications according to clinicopathologic parameters. Lymph node micrometastasis in the patients with recurrences was examined using immunohistochemical staining of cytokeratin. Their ages ranged from 45 to 83 years (mean 64.3 years). There were 83 men and 15 women. Altogether, 54 patients were still alive, and 44 had died. A total of 9 patients died from recurrence of their esophageal carcinoma, 33 died from other causes (pneumonia 11, extraesophageal carcinoma 7, and so on), and 2 died from unknown causes. Eight patients had locoregionai recurrences, and two patients had distant recurrences. The overall survival rate for the 98 patients was 58.2%. The survival for patients with pT2 or pT3 tumors was significantly worse than for those with pTis or pTl tumors (p=0.02, log‐rank test). Other clinicopathologic factors did not affect the prognosis. Immunohistochemical study found no lymph node micrometastasis in 365 lymph nodes resected from the patients with recurrences. Only the depth of tumor invasion affected the outcome of patients with node‐negative esophageal carcinoma. Altogether, 75% of patients died of other causes without recurrence, with the two main causes of death being pulmonary complications and extraesophageal carcinoma in these patients. Lymph node micrometastasis was not associated with recurrence in this series. Résumé L’évolution des cancers de lœsophage NO et la signification des micrométastases ganglionnaires resent inconnues. Le but de cette étude rétrospective a été de clarifier ces deux problèmes. Nous avons inclus dans cette étude, 98 patients qui ont eu une résection à visée curative pour un cncer de l’œsophage (pNO selon la classificaton TNM). Nous avons revu les causes de mortalité chez ces patients. Les courbes de survie ont été calculées et comparées après stratification selon les données clinicopathologiques. Les micrométastases ganglionnaires chez les patients récidives ont été déterminées par une coloration immunohistochimique de la cytokératine. L’àge des patients allait de 45 à 83 ans (moyenne: 65.3 ans). Il y avait 83 hommes et 15 femmes. Cinquante‐quatre patients étaient en vie et 44 patients étaient décédés. Neuf patients sont décédés d’une récidive de leur cancer le l’œsophage, 33 sont décédés d’autres causes (principalement une infection pulmonaire:n=11, ou un cancer extra‐esophagien: n=7) alors que deux patients sont décédés de cause inconnue. Huit patients ont eu une récidive locorégionale et deux, une récidive à distance. La survie globale pour les 98 patients a été de 58.2%. La survie des patients ayant des tumeurs pT2 ou pT3 a été significativement moins bonne que pour les tumeurs pTis ou pT1 (p=0.02, test du log‐rank). Les autres facteurs clinicopathologiques n’ont pas affecté le pronostic. Par l’étude immunohistochimique aucune micrométastase n’a été retrouvée parmi 365 ganglions réséqués chez des patients ayant eu une récidive. Seule la profondeur d’invasion tumorale a influené l’évolution de la maladie chez les patients NO. Parmi les patients décédés, 75% étaient sans récidive; les deux causes principales étant des complications pulmonaires et un cancer extra‐esophagien. Dans cette série, les micrométastases n’ont jamais été la cause de récidive. Resumen No están bien establecidos ni la evolución ni el resultado final del carcinoma escamocelular del esófago con ganglios negativos, tampoco el significado pronóstico de las micrometástasis ganglionares. El propósito de este estudio retrospectivo fue aclarar estos interrogantes. Noventa y ocho pacientes sometidos a operación curativa por carcinoma esofágico con ganglios histológicmente negativos (pNO en la clasificación TNM) fueron incorporados en el estudio. Se revisaron las causas de muerte y se calcularon las curvas de supervivencia para compararlas luego de la estratificación según parámetros clínico patológicos. El estudio de los ganglios para determinar micrometástasis fue hecho en los pacientes que desarrollaron recurrencia mediante coloración immunohistológica de queratina. Las edades oscilaron entre 45 y 83 años (promedio: 65.3); hubo 83 hombres y 15 mujeres. Cincuenta y dos pacientes están vivos, 44 murieron. Nueve murieron por carcinoma recurrente, 33 por otras causas (neumonía 11, carcinoma extraesofágico 7, etc.) y dos por causa desconocida. Ocho presentaron recurrencia local‐regional y dos metástasis distantes. La tasa global de supervivencia para los 98 pacientes fue 58.2%. La supervivencia en los pacientes con neoplasmas pT2 o pT3 fue significativamente peor que en los pTis o pT1 (p=0.02). Otros factores clínicos y patológicos no demostraron efecto sobre el pronóstico. El estudio immunohistoquímico no reveló micrometástasis ganglionares en 365 ganglios resecados de pacientes con recurrencias. Sólo la profundidad de la invasión tumoral afectó la evolución final en estos carcinomas esofágicos con ganglios negativos. Setenta y cinco por ciento de los pacientes murieron por causas diferentes de la recurrencia tumoral, y las dos causas principales de muerte fueron la complicación pulmonar y el carcinoma extraesofágico en los pacientes libres de recurrencia. La presencia de micrometástasis ganglionares no apareció asociada con recurrencia en esta serie.</abstract><cop>New York</cop><pub>Springer‐Verlag</pub><pmid>12297913</pmid><doi>10.1007/s00268-002-6415-4</doi><tpages>6</tpages></addata></record>
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subjects Adult
Age Distribution
Aged
Biological and medical sciences
Biopsy, Needle
Carcinoma, Squamous Cell - mortality
Carcinoma, Squamous Cell - pathology
Carcinoma, Squamous Cell - therapy
Chemosensitivity Testing
Cohort Studies
Combined Modality Therapy - methods
Esophageal Cancer
Esophageal Carcinoma
Esophageal Neoplasms - mortality
Esophageal Neoplasms - pathology
Esophageal Neoplasms - therapy
Esophageal Squamous Cell Carcinoma
Esophagus
Female
Gastroenterology. Liver. Pancreas. Abdomen
Humans
Incidence
Lymph Nodes - pathology
Male
Medical sciences
Middle Aged
Neoplasm Invasiveness - pathology
Neoplasm Recurrence, Local - mortality
Neoplasm Recurrence, Local - pathology
Neoplasm Recurrence, Local - therapy
Neoplasm Staging
Preoperative Chemotherapy
Probability
Prognosis
Retrospective Studies
Risk Assessment
Sex Distribution
Statistics, Nonparametric
Survival Rate
Treatment Outcome
Tumors
title Outcome of histologically node‐negative esophageal squamous cell carcinoma
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