Clinicopathologic analysis of pancreatic adenocarcinoma in African Americans and Caucasians

African Americans have a higher incidence of pancreatic adenocarcinoma than do Caucasians for unknown reasons. Whether other clinicopathologic differences exist between these two groups is not known. This study was undertaken to compare the clinical, pathologic, and biologic findings for a group of...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Pancreas 2003, Vol.26 (1), p.28-32
Hauptverfasser: PERNICK, Nat L, SARKAR, Fazlul H, PHILIP, Philip A, ARLAUSKAS, Patricia, SHIELDS, Anthony F, VAITKEVICIUS, Vainutis K, DUGAN, Michael C, ADSAY, N. Volkan
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 32
container_issue 1
container_start_page 28
container_title Pancreas
container_volume 26
creator PERNICK, Nat L
SARKAR, Fazlul H
PHILIP, Philip A
ARLAUSKAS, Patricia
SHIELDS, Anthony F
VAITKEVICIUS, Vainutis K
DUGAN, Michael C
ADSAY, N. Volkan
description African Americans have a higher incidence of pancreatic adenocarcinoma than do Caucasians for unknown reasons. Whether other clinicopathologic differences exist between these two groups is not known. This study was undertaken to compare the clinical, pathologic, and biologic findings for a group of patients with a histologic diagnosis of pancreatic ductal adenocarcinoma of the usual type in a single institution. We studied 410 patients (166 African Americans and 244 Caucasians) with a histologic diagnosis of pancreatic ductal adenocarcinoma of the usual type and analyzed (a) the clinicopathologic characteristics of the tumors, (b) the immunohistochemical expression of biomarkers implicated in pancreatic carcinogenesis (Fas, Fas ligand, HER2, p21/waf-1, p27, and p53), and (c) the presence and types of K- mutations at codon 12 as determined by polymerase chain reaction-mediated amplification. All elements of data were not available for all patients. African Americans had significantly higher rates of K-ras mutations to valine than did Caucasians (58% versus 22%, respectively; p = 0.015) and were less likely to have received chemotherapy (45% versus 70%, respectively; p = 0.001) or radiation therapy (34% versus 57%, respectively; p = 0.003). African Americans also had more frequent positive surgical margins than did Caucasians (56% versus 25%, respectively; p = 0.001), although mean tumor size was similar between the two groups (African Americans, 3.4 cm; Caucasians, 3.5 cm). Other clinicopathologic variables were similar between the two groups, including median survival (African Americans, 8.5 months; Caucasians, 10.1 months), 5-year survival (African Americans, 3%; Caucasians, 6%), and stage at presentation. Differences in biomarker immunoreactivity included less frequent Fas expression (4% versus 24%, respectively; p = 0.048) and a trend toward more frequent strong HER2 expression (39% versus 18%, respectively p = 0.11) in African Americans than in Caucasians. Although African American and Caucasian patients had similar survival rates associated with usual type pancreatic ductal adenocarcinoma, there were differences in management and expression of biologic markers between these two groups. African Americans were significantly less likely to receive radiation therapy or chemotherapy than were Caucasians, which may assume more importance as treatment improves. At the molecular level, African Americans had more frequent K- mutations to valine than did Caucas
doi_str_mv 10.1097/00006676-200301000-00006
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_72885216</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>72885216</sourcerecordid><originalsourceid>FETCH-LOGICAL-c370t-81ce32de7179301b2871e5a44924cb95e3233561b5e9b7b4930b82690843df83</originalsourceid><addsrcrecordid>eNpFkTtPwzAUhS0EoqXwF1AW2AJ-JbbHKuIlVWLpxhDdOA4YJXGwk6H_HrcN1Mv1Pf7OtXyMUELwA8FKPOK48lzkKcWYYRK79CCdoSXJWJ5ySeU5WmIps5QRIRboKoRvjIlgmbpEC0K5UorwJfooWttb7QYYv1zrPq1OoId2F2xIXJMM0GtvYNzLtemdBq9t7zpIbJ-sG281xNqZwyZEa50UMGkINrbX6KKBNpibua7Q9vlpW7ymm_eXt2K9STUTeEwl0YbR2ggiVHxMRaUgJgPOFeW6Ulk8ZCzLSZUZVYmKR6iSNFdYclY3kq3Q_XHs4N3PZMJYdjZo07bQGzeFUtAYAyV5BOUR1N6F4E1TDt524HclweU-1_Iv1_I_16MUrbfzHVPVmfpknIOMwN0MQNDQNj4GZ8OJ45zFjyHsFxs1f44</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>72885216</pqid></control><display><type>article</type><title>Clinicopathologic analysis of pancreatic adenocarcinoma in African Americans and Caucasians</title><source>MEDLINE</source><source>Journals@Ovid Complete</source><creator>PERNICK, Nat L ; SARKAR, Fazlul H ; PHILIP, Philip A ; ARLAUSKAS, Patricia ; SHIELDS, Anthony F ; VAITKEVICIUS, Vainutis K ; DUGAN, Michael C ; ADSAY, N. Volkan</creator><creatorcontrib>PERNICK, Nat L ; SARKAR, Fazlul H ; PHILIP, Philip A ; ARLAUSKAS, Patricia ; SHIELDS, Anthony F ; VAITKEVICIUS, Vainutis K ; DUGAN, Michael C ; ADSAY, N. Volkan</creatorcontrib><description>African Americans have a higher incidence of pancreatic adenocarcinoma than do Caucasians for unknown reasons. Whether other clinicopathologic differences exist between these two groups is not known. This study was undertaken to compare the clinical, pathologic, and biologic findings for a group of patients with a histologic diagnosis of pancreatic ductal adenocarcinoma of the usual type in a single institution. We studied 410 patients (166 African Americans and 244 Caucasians) with a histologic diagnosis of pancreatic ductal adenocarcinoma of the usual type and analyzed (a) the clinicopathologic characteristics of the tumors, (b) the immunohistochemical expression of biomarkers implicated in pancreatic carcinogenesis (Fas, Fas ligand, HER2, p21/waf-1, p27, and p53), and (c) the presence and types of K- mutations at codon 12 as determined by polymerase chain reaction-mediated amplification. All elements of data were not available for all patients. African Americans had significantly higher rates of K-ras mutations to valine than did Caucasians (58% versus 22%, respectively; p = 0.015) and were less likely to have received chemotherapy (45% versus 70%, respectively; p = 0.001) or radiation therapy (34% versus 57%, respectively; p = 0.003). African Americans also had more frequent positive surgical margins than did Caucasians (56% versus 25%, respectively; p = 0.001), although mean tumor size was similar between the two groups (African Americans, 3.4 cm; Caucasians, 3.5 cm). Other clinicopathologic variables were similar between the two groups, including median survival (African Americans, 8.5 months; Caucasians, 10.1 months), 5-year survival (African Americans, 3%; Caucasians, 6%), and stage at presentation. Differences in biomarker immunoreactivity included less frequent Fas expression (4% versus 24%, respectively; p = 0.048) and a trend toward more frequent strong HER2 expression (39% versus 18%, respectively p = 0.11) in African Americans than in Caucasians. Although African American and Caucasian patients had similar survival rates associated with usual type pancreatic ductal adenocarcinoma, there were differences in management and expression of biologic markers between these two groups. African Americans were significantly less likely to receive radiation therapy or chemotherapy than were Caucasians, which may assume more importance as treatment improves. At the molecular level, African Americans had more frequent K- mutations to valine than did Caucasians.</description><identifier>ISSN: 0885-3177</identifier><identifier>ISSN: 1536-4828</identifier><identifier>EISSN: 1536-4828</identifier><identifier>DOI: 10.1097/00006676-200301000-00006</identifier><identifier>PMID: 12499914</identifier><identifier>CODEN: PANCE4</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams &amp; Wilkins</publisher><subject>Aged ; Biological and medical sciences ; Black or African American ; Black People ; Carcinoma, Pancreatic Ductal - diagnosis ; Carcinoma, Pancreatic Ductal - ethnology ; Carcinoma, Pancreatic Ductal - pathology ; Demography ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Genes, ras ; Humans ; Immunohistochemistry ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Medical sciences ; Middle Aged ; Mutation ; Pancreatic Neoplasms - diagnosis ; Pancreatic Neoplasms - ethnology ; Pancreatic Neoplasms - pathology ; Survival Analysis ; Tumors ; White People</subject><ispartof>Pancreas, 2003, Vol.26 (1), p.28-32</ispartof><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-81ce32de7179301b2871e5a44924cb95e3233561b5e9b7b4930b82690843df83</citedby><cites>FETCH-LOGICAL-c370t-81ce32de7179301b2871e5a44924cb95e3233561b5e9b7b4930b82690843df83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=14435361$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12499914$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>PERNICK, Nat L</creatorcontrib><creatorcontrib>SARKAR, Fazlul H</creatorcontrib><creatorcontrib>PHILIP, Philip A</creatorcontrib><creatorcontrib>ARLAUSKAS, Patricia</creatorcontrib><creatorcontrib>SHIELDS, Anthony F</creatorcontrib><creatorcontrib>VAITKEVICIUS, Vainutis K</creatorcontrib><creatorcontrib>DUGAN, Michael C</creatorcontrib><creatorcontrib>ADSAY, N. Volkan</creatorcontrib><title>Clinicopathologic analysis of pancreatic adenocarcinoma in African Americans and Caucasians</title><title>Pancreas</title><addtitle>Pancreas</addtitle><description>African Americans have a higher incidence of pancreatic adenocarcinoma than do Caucasians for unknown reasons. Whether other clinicopathologic differences exist between these two groups is not known. This study was undertaken to compare the clinical, pathologic, and biologic findings for a group of patients with a histologic diagnosis of pancreatic ductal adenocarcinoma of the usual type in a single institution. We studied 410 patients (166 African Americans and 244 Caucasians) with a histologic diagnosis of pancreatic ductal adenocarcinoma of the usual type and analyzed (a) the clinicopathologic characteristics of the tumors, (b) the immunohistochemical expression of biomarkers implicated in pancreatic carcinogenesis (Fas, Fas ligand, HER2, p21/waf-1, p27, and p53), and (c) the presence and types of K- mutations at codon 12 as determined by polymerase chain reaction-mediated amplification. All elements of data were not available for all patients. African Americans had significantly higher rates of K-ras mutations to valine than did Caucasians (58% versus 22%, respectively; p = 0.015) and were less likely to have received chemotherapy (45% versus 70%, respectively; p = 0.001) or radiation therapy (34% versus 57%, respectively; p = 0.003). African Americans also had more frequent positive surgical margins than did Caucasians (56% versus 25%, respectively; p = 0.001), although mean tumor size was similar between the two groups (African Americans, 3.4 cm; Caucasians, 3.5 cm). Other clinicopathologic variables were similar between the two groups, including median survival (African Americans, 8.5 months; Caucasians, 10.1 months), 5-year survival (African Americans, 3%; Caucasians, 6%), and stage at presentation. Differences in biomarker immunoreactivity included less frequent Fas expression (4% versus 24%, respectively; p = 0.048) and a trend toward more frequent strong HER2 expression (39% versus 18%, respectively p = 0.11) in African Americans than in Caucasians. Although African American and Caucasian patients had similar survival rates associated with usual type pancreatic ductal adenocarcinoma, there were differences in management and expression of biologic markers between these two groups. African Americans were significantly less likely to receive radiation therapy or chemotherapy than were Caucasians, which may assume more importance as treatment improves. At the molecular level, African Americans had more frequent K- mutations to valine than did Caucasians.</description><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Black or African American</subject><subject>Black People</subject><subject>Carcinoma, Pancreatic Ductal - diagnosis</subject><subject>Carcinoma, Pancreatic Ductal - ethnology</subject><subject>Carcinoma, Pancreatic Ductal - pathology</subject><subject>Demography</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Genes, ras</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Pancreatic Neoplasms - diagnosis</subject><subject>Pancreatic Neoplasms - ethnology</subject><subject>Pancreatic Neoplasms - pathology</subject><subject>Survival Analysis</subject><subject>Tumors</subject><subject>White People</subject><issn>0885-3177</issn><issn>1536-4828</issn><issn>1536-4828</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkTtPwzAUhS0EoqXwF1AW2AJ-JbbHKuIlVWLpxhDdOA4YJXGwk6H_HrcN1Mv1Pf7OtXyMUELwA8FKPOK48lzkKcWYYRK79CCdoSXJWJ5ySeU5WmIps5QRIRboKoRvjIlgmbpEC0K5UorwJfooWttb7QYYv1zrPq1OoId2F2xIXJMM0GtvYNzLtemdBq9t7zpIbJ-sG281xNqZwyZEa50UMGkINrbX6KKBNpibua7Q9vlpW7ymm_eXt2K9STUTeEwl0YbR2ggiVHxMRaUgJgPOFeW6Ulk8ZCzLSZUZVYmKR6iSNFdYclY3kq3Q_XHs4N3PZMJYdjZo07bQGzeFUtAYAyV5BOUR1N6F4E1TDt524HclweU-1_Iv1_I_16MUrbfzHVPVmfpknIOMwN0MQNDQNj4GZ8OJ45zFjyHsFxs1f44</recordid><startdate>2003</startdate><enddate>2003</enddate><creator>PERNICK, Nat L</creator><creator>SARKAR, Fazlul H</creator><creator>PHILIP, Philip A</creator><creator>ARLAUSKAS, Patricia</creator><creator>SHIELDS, Anthony F</creator><creator>VAITKEVICIUS, Vainutis K</creator><creator>DUGAN, Michael C</creator><creator>ADSAY, N. Volkan</creator><general>Lippincott Williams &amp; Wilkins</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>7X8</scope></search><sort><creationdate>2003</creationdate><title>Clinicopathologic analysis of pancreatic adenocarcinoma in African Americans and Caucasians</title><author>PERNICK, Nat L ; SARKAR, Fazlul H ; PHILIP, Philip A ; ARLAUSKAS, Patricia ; SHIELDS, Anthony F ; VAITKEVICIUS, Vainutis K ; DUGAN, Michael C ; ADSAY, N. Volkan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-81ce32de7179301b2871e5a44924cb95e3233561b5e9b7b4930b82690843df83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Black or African American</topic><topic>Black People</topic><topic>Carcinoma, Pancreatic Ductal - diagnosis</topic><topic>Carcinoma, Pancreatic Ductal - ethnology</topic><topic>Carcinoma, Pancreatic Ductal - pathology</topic><topic>Demography</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Genes, ras</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Mutation</topic><topic>Pancreatic Neoplasms - diagnosis</topic><topic>Pancreatic Neoplasms - ethnology</topic><topic>Pancreatic Neoplasms - pathology</topic><topic>Survival Analysis</topic><topic>Tumors</topic><topic>White People</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>PERNICK, Nat L</creatorcontrib><creatorcontrib>SARKAR, Fazlul H</creatorcontrib><creatorcontrib>PHILIP, Philip A</creatorcontrib><creatorcontrib>ARLAUSKAS, Patricia</creatorcontrib><creatorcontrib>SHIELDS, Anthony F</creatorcontrib><creatorcontrib>VAITKEVICIUS, Vainutis K</creatorcontrib><creatorcontrib>DUGAN, Michael C</creatorcontrib><creatorcontrib>ADSAY, N. Volkan</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>MEDLINE - Academic</collection><jtitle>Pancreas</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>PERNICK, Nat L</au><au>SARKAR, Fazlul H</au><au>PHILIP, Philip A</au><au>ARLAUSKAS, Patricia</au><au>SHIELDS, Anthony F</au><au>VAITKEVICIUS, Vainutis K</au><au>DUGAN, Michael C</au><au>ADSAY, N. Volkan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinicopathologic analysis of pancreatic adenocarcinoma in African Americans and Caucasians</atitle><jtitle>Pancreas</jtitle><addtitle>Pancreas</addtitle><date>2003</date><risdate>2003</risdate><volume>26</volume><issue>1</issue><spage>28</spage><epage>32</epage><pages>28-32</pages><issn>0885-3177</issn><issn>1536-4828</issn><eissn>1536-4828</eissn><coden>PANCE4</coden><abstract>African Americans have a higher incidence of pancreatic adenocarcinoma than do Caucasians for unknown reasons. Whether other clinicopathologic differences exist between these two groups is not known. This study was undertaken to compare the clinical, pathologic, and biologic findings for a group of patients with a histologic diagnosis of pancreatic ductal adenocarcinoma of the usual type in a single institution. We studied 410 patients (166 African Americans and 244 Caucasians) with a histologic diagnosis of pancreatic ductal adenocarcinoma of the usual type and analyzed (a) the clinicopathologic characteristics of the tumors, (b) the immunohistochemical expression of biomarkers implicated in pancreatic carcinogenesis (Fas, Fas ligand, HER2, p21/waf-1, p27, and p53), and (c) the presence and types of K- mutations at codon 12 as determined by polymerase chain reaction-mediated amplification. All elements of data were not available for all patients. African Americans had significantly higher rates of K-ras mutations to valine than did Caucasians (58% versus 22%, respectively; p = 0.015) and were less likely to have received chemotherapy (45% versus 70%, respectively; p = 0.001) or radiation therapy (34% versus 57%, respectively; p = 0.003). African Americans also had more frequent positive surgical margins than did Caucasians (56% versus 25%, respectively; p = 0.001), although mean tumor size was similar between the two groups (African Americans, 3.4 cm; Caucasians, 3.5 cm). Other clinicopathologic variables were similar between the two groups, including median survival (African Americans, 8.5 months; Caucasians, 10.1 months), 5-year survival (African Americans, 3%; Caucasians, 6%), and stage at presentation. Differences in biomarker immunoreactivity included less frequent Fas expression (4% versus 24%, respectively; p = 0.048) and a trend toward more frequent strong HER2 expression (39% versus 18%, respectively p = 0.11) in African Americans than in Caucasians. Although African American and Caucasian patients had similar survival rates associated with usual type pancreatic ductal adenocarcinoma, there were differences in management and expression of biologic markers between these two groups. African Americans were significantly less likely to receive radiation therapy or chemotherapy than were Caucasians, which may assume more importance as treatment improves. At the molecular level, African Americans had more frequent K- mutations to valine than did Caucasians.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams &amp; Wilkins</pub><pmid>12499914</pmid><doi>10.1097/00006676-200301000-00006</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0885-3177
ispartof Pancreas, 2003, Vol.26 (1), p.28-32
issn 0885-3177
1536-4828
1536-4828
language eng
recordid cdi_proquest_miscellaneous_72885216
source MEDLINE; Journals@Ovid Complete
subjects Aged
Biological and medical sciences
Black or African American
Black People
Carcinoma, Pancreatic Ductal - diagnosis
Carcinoma, Pancreatic Ductal - ethnology
Carcinoma, Pancreatic Ductal - pathology
Demography
Female
Gastroenterology. Liver. Pancreas. Abdomen
Genes, ras
Humans
Immunohistochemistry
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Male
Medical sciences
Middle Aged
Mutation
Pancreatic Neoplasms - diagnosis
Pancreatic Neoplasms - ethnology
Pancreatic Neoplasms - pathology
Survival Analysis
Tumors
White People
title Clinicopathologic analysis of pancreatic adenocarcinoma in African Americans and Caucasians
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T11%3A54%3A32IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Clinicopathologic%20analysis%20of%20pancreatic%20adenocarcinoma%20in%20African%20Americans%20and%20Caucasians&rft.jtitle=Pancreas&rft.au=PERNICK,%20Nat%20L&rft.date=2003&rft.volume=26&rft.issue=1&rft.spage=28&rft.epage=32&rft.pages=28-32&rft.issn=0885-3177&rft.eissn=1536-4828&rft.coden=PANCE4&rft_id=info:doi/10.1097/00006676-200301000-00006&rft_dat=%3Cproquest_cross%3E72885216%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=72885216&rft_id=info:pmid/12499914&rfr_iscdi=true