Tumor-Associated Lymphangiogenesis in the Development of Conjunctival Squamous Cell Carcinoma

Purpose To analyze whether tumor-associated lymphangiogenesis accompanies the development from premalignant conjunctival intraepithelial neoplasia (CIN) into invasive squamous cell carcinoma (SCC) of the conjunctiva and to study its association with prognosis and other tumor characteristics. Design...

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Veröffentlicht in:Ophthalmology (Rochester, Minn.) Minn.), 2010-04, Vol.117 (4), p.649-658
Hauptverfasser: Heindl, Ludwig M., MD, Hofmann-Rummelt, Carmen, MTA, Adler, Werner, PhD, Holbach, Leonard M., MD, Naumann, Gottfried O.H., MD, Kruse, Friedrich E., MD, Cursiefen, Claus, MD
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container_issue 4
container_start_page 649
container_title Ophthalmology (Rochester, Minn.)
container_volume 117
creator Heindl, Ludwig M., MD
Hofmann-Rummelt, Carmen, MTA
Adler, Werner, PhD
Holbach, Leonard M., MD
Naumann, Gottfried O.H., MD
Kruse, Friedrich E., MD
Cursiefen, Claus, MD
description Purpose To analyze whether tumor-associated lymphangiogenesis accompanies the development from premalignant conjunctival intraepithelial neoplasia (CIN) into invasive squamous cell carcinoma (SCC) of the conjunctiva and to study its association with prognosis and other tumor characteristics. Design Case-controlled, matched-pair cohort study. Participants Twenty patients with invasive SCC were closely matched with 20 patients with high-grade CIN and 20 patients with low-grade CIN regarding tumor size, tumor location, tumor extension, and patients' age. Methods Proliferating lymphatic vessels were identified using lymphatic vascular endothelial hyaluronan receptor-1 and podoplanin as specific lymphatic endothelial markers and Ki-67 as proliferation marker. Baseline tumor characteristics included tumor size, tumor-to-limbus distance, tumor-to-fornix distance, 2009 TNM classification, tumor cell type, mitotic rate, and Ki-67 proliferation index. Kaplan–Meier and Cox regression analyses of recurrence-free survival were performed. Main Outcome Measures Lymphatic vascular density (LVD) and relative lymphatic vascular area (RLVA) of proliferating lymphatic vessels within the tumor mass (intratumoral) and within an area ≤500 μm from the tumor border (peritumoral), and its association with tumor characteristics and recurrence-free survival. Results Intratumoral and peritumoral proliferating lymphatic vessels could be detected in all of the 60 conjunctival tumor samples. Invasive SCC revealed significantly higher values of intratumoral and peritumoral LVD and RLVA of proliferating lymphatics than high-grade or low-grade CIN ( P ≤0.001). Higher intratumoral lymphatic densities were significantly associated with larger tumor size ( P= 0.001), lower tumor-to-limbus distance ( P= 0.002), lower tumor-to-fornix distance ( P= 0.003), and higher TNM categories ( P< 0.001). Recurrence-free survival rates decreased significantly with higher intratumoral lymphatic densities ( P< 0.001). By multivariate Cox regression, large tumor size (hazard ratio 1.68, P= 0.002) and high intratumoral lymphatic density (hazard ratio 1.10, P= 0.046) were significant prognostic predictors of local recurrence. Conclusions Development of conjunctival SCC from premalignant lesions is accompanied by the outgrowth of new conjunctival lymphatic vessels. This active tumor-associated lymphangiogenesis seems to be associated with an increased risk of local recurrence in patients with CIN and conjunctival
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Design Case-controlled, matched-pair cohort study. Participants Twenty patients with invasive SCC were closely matched with 20 patients with high-grade CIN and 20 patients with low-grade CIN regarding tumor size, tumor location, tumor extension, and patients' age. Methods Proliferating lymphatic vessels were identified using lymphatic vascular endothelial hyaluronan receptor-1 and podoplanin as specific lymphatic endothelial markers and Ki-67 as proliferation marker. Baseline tumor characteristics included tumor size, tumor-to-limbus distance, tumor-to-fornix distance, 2009 TNM classification, tumor cell type, mitotic rate, and Ki-67 proliferation index. Kaplan–Meier and Cox regression analyses of recurrence-free survival were performed. Main Outcome Measures Lymphatic vascular density (LVD) and relative lymphatic vascular area (RLVA) of proliferating lymphatic vessels within the tumor mass (intratumoral) and within an area ≤500 μm from the tumor border (peritumoral), and its association with tumor characteristics and recurrence-free survival. Results Intratumoral and peritumoral proliferating lymphatic vessels could be detected in all of the 60 conjunctival tumor samples. Invasive SCC revealed significantly higher values of intratumoral and peritumoral LVD and RLVA of proliferating lymphatics than high-grade or low-grade CIN ( P ≤0.001). Higher intratumoral lymphatic densities were significantly associated with larger tumor size ( P= 0.001), lower tumor-to-limbus distance ( P= 0.002), lower tumor-to-fornix distance ( P= 0.003), and higher TNM categories ( P&lt; 0.001). Recurrence-free survival rates decreased significantly with higher intratumoral lymphatic densities ( P&lt; 0.001). By multivariate Cox regression, large tumor size (hazard ratio 1.68, P= 0.002) and high intratumoral lymphatic density (hazard ratio 1.10, P= 0.046) were significant prognostic predictors of local recurrence. Conclusions Development of conjunctival SCC from premalignant lesions is accompanied by the outgrowth of new conjunctival lymphatic vessels. This active tumor-associated lymphangiogenesis seems to be associated with an increased risk of local recurrence in patients with CIN and conjunctival invasive SCC. Financial Disclosure(s) The author(s) have no proprietary or commercial interest in any materials discussed in this article.</description><identifier>ISSN: 0161-6420</identifier><identifier>EISSN: 1549-4713</identifier><identifier>DOI: 10.1016/j.ophtha.2010.01.032</identifier><identifier>PMID: 20346821</identifier><identifier>CODEN: OPHTDG</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Biological and medical sciences ; Carcinoma in Situ - metabolism ; Carcinoma in Situ - pathology ; Carcinoma, Squamous Cell - pathology ; Case-Control Studies ; Conjunctival Neoplasms - metabolism ; Conjunctival Neoplasms - pathology ; Dermatology ; Female ; Humans ; Image Processing, Computer-Assisted ; Immunoenzyme Techniques ; Ki-67 Antigen - metabolism ; Lymphangiogenesis ; Lymphatic Vessels - metabolism ; Lymphatic Vessels - pathology ; Male ; Matched-Pair Analysis ; Medical sciences ; Membrane Glycoproteins - metabolism ; Middle Aged ; Miscellaneous ; Neoplasm Invasiveness ; Ophthalmology ; Precancerous Conditions ; Proportional Hazards Models ; Retrospective Studies ; Tumors of the skin and soft tissue. 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All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c427t-ff4f2a99e57f791dd79d61459657c56ef6fb328e4929f1971d40f04cd5ab998b3</citedby><cites>FETCH-LOGICAL-c427t-ff4f2a99e57f791dd79d61459657c56ef6fb328e4929f1971d40f04cd5ab998b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ophtha.2010.01.032$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=22763487$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20346821$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Heindl, Ludwig M., MD</creatorcontrib><creatorcontrib>Hofmann-Rummelt, Carmen, MTA</creatorcontrib><creatorcontrib>Adler, Werner, PhD</creatorcontrib><creatorcontrib>Holbach, Leonard M., MD</creatorcontrib><creatorcontrib>Naumann, Gottfried O.H., MD</creatorcontrib><creatorcontrib>Kruse, Friedrich E., MD</creatorcontrib><creatorcontrib>Cursiefen, Claus, MD</creatorcontrib><title>Tumor-Associated Lymphangiogenesis in the Development of Conjunctival Squamous Cell Carcinoma</title><title>Ophthalmology (Rochester, Minn.)</title><addtitle>Ophthalmology</addtitle><description>Purpose To analyze whether tumor-associated lymphangiogenesis accompanies the development from premalignant conjunctival intraepithelial neoplasia (CIN) into invasive squamous cell carcinoma (SCC) of the conjunctiva and to study its association with prognosis and other tumor characteristics. Design Case-controlled, matched-pair cohort study. Participants Twenty patients with invasive SCC were closely matched with 20 patients with high-grade CIN and 20 patients with low-grade CIN regarding tumor size, tumor location, tumor extension, and patients' age. Methods Proliferating lymphatic vessels were identified using lymphatic vascular endothelial hyaluronan receptor-1 and podoplanin as specific lymphatic endothelial markers and Ki-67 as proliferation marker. Baseline tumor characteristics included tumor size, tumor-to-limbus distance, tumor-to-fornix distance, 2009 TNM classification, tumor cell type, mitotic rate, and Ki-67 proliferation index. Kaplan–Meier and Cox regression analyses of recurrence-free survival were performed. Main Outcome Measures Lymphatic vascular density (LVD) and relative lymphatic vascular area (RLVA) of proliferating lymphatic vessels within the tumor mass (intratumoral) and within an area ≤500 μm from the tumor border (peritumoral), and its association with tumor characteristics and recurrence-free survival. Results Intratumoral and peritumoral proliferating lymphatic vessels could be detected in all of the 60 conjunctival tumor samples. Invasive SCC revealed significantly higher values of intratumoral and peritumoral LVD and RLVA of proliferating lymphatics than high-grade or low-grade CIN ( P ≤0.001). Higher intratumoral lymphatic densities were significantly associated with larger tumor size ( P= 0.001), lower tumor-to-limbus distance ( P= 0.002), lower tumor-to-fornix distance ( P= 0.003), and higher TNM categories ( P&lt; 0.001). Recurrence-free survival rates decreased significantly with higher intratumoral lymphatic densities ( P&lt; 0.001). By multivariate Cox regression, large tumor size (hazard ratio 1.68, P= 0.002) and high intratumoral lymphatic density (hazard ratio 1.10, P= 0.046) were significant prognostic predictors of local recurrence. Conclusions Development of conjunctival SCC from premalignant lesions is accompanied by the outgrowth of new conjunctival lymphatic vessels. This active tumor-associated lymphangiogenesis seems to be associated with an increased risk of local recurrence in patients with CIN and conjunctival invasive SCC. Financial Disclosure(s) The author(s) have no proprietary or commercial interest in any materials discussed in this article.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>Carcinoma in Situ - metabolism</subject><subject>Carcinoma in Situ - pathology</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Case-Control Studies</subject><subject>Conjunctival Neoplasms - metabolism</subject><subject>Conjunctival Neoplasms - pathology</subject><subject>Dermatology</subject><subject>Female</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted</subject><subject>Immunoenzyme Techniques</subject><subject>Ki-67 Antigen - metabolism</subject><subject>Lymphangiogenesis</subject><subject>Lymphatic Vessels - metabolism</subject><subject>Lymphatic Vessels - pathology</subject><subject>Male</subject><subject>Matched-Pair Analysis</subject><subject>Medical sciences</subject><subject>Membrane Glycoproteins - metabolism</subject><subject>Middle Aged</subject><subject>Miscellaneous</subject><subject>Neoplasm Invasiveness</subject><subject>Ophthalmology</subject><subject>Precancerous Conditions</subject><subject>Proportional Hazards Models</subject><subject>Retrospective Studies</subject><subject>Tumors of the skin and soft tissue. 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Premalignant lesions</topic><topic>Vesicular Transport Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Heindl, Ludwig M., MD</creatorcontrib><creatorcontrib>Hofmann-Rummelt, Carmen, MTA</creatorcontrib><creatorcontrib>Adler, Werner, PhD</creatorcontrib><creatorcontrib>Holbach, Leonard M., MD</creatorcontrib><creatorcontrib>Naumann, Gottfried O.H., MD</creatorcontrib><creatorcontrib>Kruse, Friedrich E., MD</creatorcontrib><creatorcontrib>Cursiefen, Claus, MD</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>Ophthalmology (Rochester, Minn.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Heindl, Ludwig M., MD</au><au>Hofmann-Rummelt, Carmen, MTA</au><au>Adler, Werner, PhD</au><au>Holbach, Leonard M., MD</au><au>Naumann, Gottfried O.H., MD</au><au>Kruse, Friedrich E., MD</au><au>Cursiefen, Claus, MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tumor-Associated Lymphangiogenesis in the Development of Conjunctival Squamous Cell Carcinoma</atitle><jtitle>Ophthalmology (Rochester, Minn.)</jtitle><addtitle>Ophthalmology</addtitle><date>2010-04</date><risdate>2010</risdate><volume>117</volume><issue>4</issue><spage>649</spage><epage>658</epage><pages>649-658</pages><issn>0161-6420</issn><eissn>1549-4713</eissn><coden>OPHTDG</coden><abstract>Purpose To analyze whether tumor-associated lymphangiogenesis accompanies the development from premalignant conjunctival intraepithelial neoplasia (CIN) into invasive squamous cell carcinoma (SCC) of the conjunctiva and to study its association with prognosis and other tumor characteristics. Design Case-controlled, matched-pair cohort study. Participants Twenty patients with invasive SCC were closely matched with 20 patients with high-grade CIN and 20 patients with low-grade CIN regarding tumor size, tumor location, tumor extension, and patients' age. Methods Proliferating lymphatic vessels were identified using lymphatic vascular endothelial hyaluronan receptor-1 and podoplanin as specific lymphatic endothelial markers and Ki-67 as proliferation marker. Baseline tumor characteristics included tumor size, tumor-to-limbus distance, tumor-to-fornix distance, 2009 TNM classification, tumor cell type, mitotic rate, and Ki-67 proliferation index. Kaplan–Meier and Cox regression analyses of recurrence-free survival were performed. Main Outcome Measures Lymphatic vascular density (LVD) and relative lymphatic vascular area (RLVA) of proliferating lymphatic vessels within the tumor mass (intratumoral) and within an area ≤500 μm from the tumor border (peritumoral), and its association with tumor characteristics and recurrence-free survival. Results Intratumoral and peritumoral proliferating lymphatic vessels could be detected in all of the 60 conjunctival tumor samples. Invasive SCC revealed significantly higher values of intratumoral and peritumoral LVD and RLVA of proliferating lymphatics than high-grade or low-grade CIN ( P ≤0.001). Higher intratumoral lymphatic densities were significantly associated with larger tumor size ( P= 0.001), lower tumor-to-limbus distance ( P= 0.002), lower tumor-to-fornix distance ( P= 0.003), and higher TNM categories ( P&lt; 0.001). Recurrence-free survival rates decreased significantly with higher intratumoral lymphatic densities ( P&lt; 0.001). By multivariate Cox regression, large tumor size (hazard ratio 1.68, P= 0.002) and high intratumoral lymphatic density (hazard ratio 1.10, P= 0.046) were significant prognostic predictors of local recurrence. Conclusions Development of conjunctival SCC from premalignant lesions is accompanied by the outgrowth of new conjunctival lymphatic vessels. This active tumor-associated lymphangiogenesis seems to be associated with an increased risk of local recurrence in patients with CIN and conjunctival invasive SCC. Financial Disclosure(s) The author(s) have no proprietary or commercial interest in any materials discussed in this article.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>20346821</pmid><doi>10.1016/j.ophtha.2010.01.032</doi><tpages>10</tpages></addata></record>
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subjects Adult
Aged
Aged, 80 and over
Biological and medical sciences
Carcinoma in Situ - metabolism
Carcinoma in Situ - pathology
Carcinoma, Squamous Cell - pathology
Case-Control Studies
Conjunctival Neoplasms - metabolism
Conjunctival Neoplasms - pathology
Dermatology
Female
Humans
Image Processing, Computer-Assisted
Immunoenzyme Techniques
Ki-67 Antigen - metabolism
Lymphangiogenesis
Lymphatic Vessels - metabolism
Lymphatic Vessels - pathology
Male
Matched-Pair Analysis
Medical sciences
Membrane Glycoproteins - metabolism
Middle Aged
Miscellaneous
Neoplasm Invasiveness
Ophthalmology
Precancerous Conditions
Proportional Hazards Models
Retrospective Studies
Tumors of the skin and soft tissue. Premalignant lesions
Vesicular Transport Proteins - metabolism
title Tumor-Associated Lymphangiogenesis in the Development of Conjunctival Squamous Cell Carcinoma
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