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A Multimarker Prognostic Assay for Primary Cutaneous Melanoma

Purpose: To determine the prognostic significance of a multimarker assay incorporating expression levels of three molecular markers in primary cutaneous melanoma. Experimental Design: We assessed expression levels of NCOA3, SPP1, and RGS1 using immunohistochemical analysis in a tissue microarray coh...

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Published in:Clinical cancer research 2009-11, Vol.15 (22), p.6987-6992
Main Authors: Kashani-Sabet, Mohammed, Venna, Suraj, Nosrati, Mehdi, Rangel, Javier, Sucker, Antje, Egberts, Friederike, Baehner, Frederick L, Simko, Jeff, Leong, Stanley P L, Haqq, Chris, Hauschild, Axel, Schadendorf, Dirk, Miller, 3rd, James R, Sagebiel, Richard W
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cites cdi_FETCH-LOGICAL-c389t-318a4aa503e1b36f4620cb801cd94a1dcadcf02a80fff6f73511b376e83a33cb3
container_end_page 6992
container_issue 22
container_start_page 6987
container_title Clinical cancer research
container_volume 15
creator Kashani-Sabet, Mohammed
Venna, Suraj
Nosrati, Mehdi
Rangel, Javier
Sucker, Antje
Egberts, Friederike
Baehner, Frederick L
Simko, Jeff
Leong, Stanley P L
Haqq, Chris
Hauschild, Axel
Schadendorf, Dirk
Miller, 3rd, James R
Sagebiel, Richard W
description Purpose: To determine the prognostic significance of a multimarker assay incorporating expression levels of three molecular markers in primary cutaneous melanoma. Experimental Design: We assessed expression levels of NCOA3, SPP1, and RGS1 using immunohistochemical analysis in a tissue microarray cohort of 395 patients. For each marker, we identified optimal cut-points for expression intensity to predict disease-specific survival (DSS) and, as a secondary endpoint, sentinel lymph node (SLN) status. The cumulative overexpression of all three markers was embodied in a multimarker index, and its prognostic effect on DSS and SLN status was assessed using Cox regression, Kaplan-Meier analysis, and logistic regression. The prognostic effect of this multimarker assay on DSS was assessed in an independent cohort of 141 patients, in which marker expression levels were scored using immunohistochemical analysis of stained tissue sections. Results: Increasing multimarker index scores were significantly predictive of reduced DSS and increased SLN metastasis in the 395-patient cohort. Multivariate logistic regression analysis revealed multimarker expression scores as an independent predictor of SLN status ( P = 0.001). Multivariate Cox regression analysis showed the independent effect of the multimarker index on DSS ( P < 0.001). The multimarker index was the most significant factor predicting DSS when compared with other clinical and histologic factors, including SLN status ( P = 0.002). Multimarker expression scores were also the most significantly predictive of DSS in the independent cohort ( P = 0.01). Conclusions: These results describe a multimarker assay with independent prognostic effect on the prediction of survival associated with melanoma in two distinct cohorts. (Clin Cancer Res 2009;15(22):6987–92)
doi_str_mv 10.1158/1078-0432.CCR-09-1777
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Experimental Design: We assessed expression levels of NCOA3, SPP1, and RGS1 using immunohistochemical analysis in a tissue microarray cohort of 395 patients. For each marker, we identified optimal cut-points for expression intensity to predict disease-specific survival (DSS) and, as a secondary endpoint, sentinel lymph node (SLN) status. The cumulative overexpression of all three markers was embodied in a multimarker index, and its prognostic effect on DSS and SLN status was assessed using Cox regression, Kaplan-Meier analysis, and logistic regression. The prognostic effect of this multimarker assay on DSS was assessed in an independent cohort of 141 patients, in which marker expression levels were scored using immunohistochemical analysis of stained tissue sections. Results: Increasing multimarker index scores were significantly predictive of reduced DSS and increased SLN metastasis in the 395-patient cohort. Multivariate logistic regression analysis revealed multimarker expression scores as an independent predictor of SLN status ( P = 0.001). Multivariate Cox regression analysis showed the independent effect of the multimarker index on DSS ( P &lt; 0.001). The multimarker index was the most significant factor predicting DSS when compared with other clinical and histologic factors, including SLN status ( P = 0.002). Multimarker expression scores were also the most significantly predictive of DSS in the independent cohort ( P = 0.01). Conclusions: These results describe a multimarker assay with independent prognostic effect on the prediction of survival associated with melanoma in two distinct cohorts. 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Experimental Design: We assessed expression levels of NCOA3, SPP1, and RGS1 using immunohistochemical analysis in a tissue microarray cohort of 395 patients. For each marker, we identified optimal cut-points for expression intensity to predict disease-specific survival (DSS) and, as a secondary endpoint, sentinel lymph node (SLN) status. The cumulative overexpression of all three markers was embodied in a multimarker index, and its prognostic effect on DSS and SLN status was assessed using Cox regression, Kaplan-Meier analysis, and logistic regression. The prognostic effect of this multimarker assay on DSS was assessed in an independent cohort of 141 patients, in which marker expression levels were scored using immunohistochemical analysis of stained tissue sections. Results: Increasing multimarker index scores were significantly predictive of reduced DSS and increased SLN metastasis in the 395-patient cohort. Multivariate logistic regression analysis revealed multimarker expression scores as an independent predictor of SLN status ( P = 0.001). Multivariate Cox regression analysis showed the independent effect of the multimarker index on DSS ( P &lt; 0.001). The multimarker index was the most significant factor predicting DSS when compared with other clinical and histologic factors, including SLN status ( P = 0.002). Multimarker expression scores were also the most significantly predictive of DSS in the independent cohort ( P = 0.01). Conclusions: These results describe a multimarker assay with independent prognostic effect on the prediction of survival associated with melanoma in two distinct cohorts. (Clin Cancer Res 2009;15(22):6987–92)</description><subject>biomarkers</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Cohort Studies</subject><subject>Disease-Free Survival</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Immunohistochemistry - methods</subject><subject>Lymphatic Metastasis</subject><subject>Medical Oncology - methods</subject><subject>melanoma</subject><subject>Melanoma - diagnosis</subject><subject>Melanoma - metabolism</subject><subject>Neoplasm Metastasis</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Prognosis</subject><subject>Regression Analysis</subject><subject>Skin Neoplasms - diagnosis</subject><subject>Skin Neoplasms - metabolism</subject><subject>Treatment Outcome</subject><issn>1078-0432</issn><issn>1557-3265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNpFkE1PwzAMhiMEYmPwE0C9IQ4dcdM06YHDVPElbQIhOEdummyFdh1JK7R_T6sOcbLlPHZePYRcAp0DcHkLVMiQxiyaZ9lbSNMQhBBHZAqci5BFCT_u-z9mQs68_6QUYqDxKZlAKqWIRTIld4tg1VVtWaP7Mi54dc162_i21MHCe9wHthmGw_M-yLoWt6bpfLAyFW6bGs_JicXKm4tDnZGPh_v37Clcvjw-Z4tlqJlM25CBxBiRU2YgZ4mNk4jqXFLQRRojFBoLbWmEklprEysYh54TiZEMGdM5m5Hr8e7ONd-d8a2qS69NVY15lGBMpBBJ0ZN8JLVrvHfGqt2YXgFVgzg1SFGDFNWLUzRVg7h-7-rwQ5fXpvjfOpjqgZsR2JTrzU_pjNK41cY54w06vVHAVRSpJO1D_ALCZnd4</recordid><startdate>20091115</startdate><enddate>20091115</enddate><creator>Kashani-Sabet, Mohammed</creator><creator>Venna, Suraj</creator><creator>Nosrati, Mehdi</creator><creator>Rangel, Javier</creator><creator>Sucker, Antje</creator><creator>Egberts, Friederike</creator><creator>Baehner, Frederick L</creator><creator>Simko, Jeff</creator><creator>Leong, Stanley P L</creator><creator>Haqq, Chris</creator><creator>Hauschild, Axel</creator><creator>Schadendorf, Dirk</creator><creator>Miller, 3rd, James R</creator><creator>Sagebiel, Richard W</creator><general>American Association for Cancer Research</general><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>20091115</creationdate><title>A Multimarker Prognostic Assay for Primary Cutaneous Melanoma</title><author>Kashani-Sabet, Mohammed ; 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Experimental Design: We assessed expression levels of NCOA3, SPP1, and RGS1 using immunohistochemical analysis in a tissue microarray cohort of 395 patients. For each marker, we identified optimal cut-points for expression intensity to predict disease-specific survival (DSS) and, as a secondary endpoint, sentinel lymph node (SLN) status. The cumulative overexpression of all three markers was embodied in a multimarker index, and its prognostic effect on DSS and SLN status was assessed using Cox regression, Kaplan-Meier analysis, and logistic regression. The prognostic effect of this multimarker assay on DSS was assessed in an independent cohort of 141 patients, in which marker expression levels were scored using immunohistochemical analysis of stained tissue sections. Results: Increasing multimarker index scores were significantly predictive of reduced DSS and increased SLN metastasis in the 395-patient cohort. Multivariate logistic regression analysis revealed multimarker expression scores as an independent predictor of SLN status ( P = 0.001). Multivariate Cox regression analysis showed the independent effect of the multimarker index on DSS ( P &lt; 0.001). The multimarker index was the most significant factor predicting DSS when compared with other clinical and histologic factors, including SLN status ( P = 0.002). Multimarker expression scores were also the most significantly predictive of DSS in the independent cohort ( P = 0.01). Conclusions: These results describe a multimarker assay with independent prognostic effect on the prediction of survival associated with melanoma in two distinct cohorts. (Clin Cancer Res 2009;15(22):6987–92)</abstract><cop>United States</cop><pub>American Association for Cancer Research</pub><pmid>19887476</pmid><doi>10.1158/1078-0432.CCR-09-1777</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source Freely Accessible Science Journals
subjects biomarkers
Biomarkers, Tumor - metabolism
Cohort Studies
Disease-Free Survival
Gene Expression Regulation, Neoplastic
Humans
Immunohistochemistry - methods
Lymphatic Metastasis
Medical Oncology - methods
melanoma
Melanoma - diagnosis
Melanoma - metabolism
Neoplasm Metastasis
Oligonucleotide Array Sequence Analysis
Prognosis
Regression Analysis
Skin Neoplasms - diagnosis
Skin Neoplasms - metabolism
Treatment Outcome
title A Multimarker Prognostic Assay for Primary Cutaneous Melanoma
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