Loading…

Does endogenous immune response determine the outcome of surgical therapy for metastatic melanoma?

Although the presence of tumor cells in the blood of patients with metastatic melanoma suggests widely disseminated disease, many of these patients enjoy prolonged survival or cure after surgical resection. Our previous study of adjuvant vaccine therapy after complete resection of metastatic melanom...

Full description

Saved in:
Bibliographic Details
Published in:Annals of surgical oncology 2000-04, Vol.7 (3), p.232-238
Main Authors: Hsueh, E C, Gupta, R K, Yee, R, Leopoldo, Z C, Qi, K, Morton, D L
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c341t-e5cff5080b0193b7f97bd79867679d3d6780a89c147c005942befc2a3d0599253
cites cdi_FETCH-LOGICAL-c341t-e5cff5080b0193b7f97bd79867679d3d6780a89c147c005942befc2a3d0599253
container_end_page 238
container_issue 3
container_start_page 232
container_title Annals of surgical oncology
container_volume 7
creator Hsueh, E C
Gupta, R K
Yee, R
Leopoldo, Z C
Qi, K
Morton, D L
description Although the presence of tumor cells in the blood of patients with metastatic melanoma suggests widely disseminated disease, many of these patients enjoy prolonged survival or cure after surgical resection. Our previous study of adjuvant vaccine therapy after complete resection of metastatic melanoma revealed a strong correlation between postoperative survival and elevated antibody titers to a 90-kDa tumor-associated antigen (TA90) expressed by melanoma cells of the vaccine. We hypothesized a similar correlation between postoperative survival and endogenous anti-TA90 antibody titers induced by the patient's melanoma in the absence of postoperative adjuvant immunotherapy. From 1970 to 1996, 64 patients underwent complete resection of distant melanoma metastases and did not receive postoperative adjuvant immunotherapy. Serum collected within 4 months after surgery was tested in a coded and blinded fashion for anti-TA90 IgG and IgM by enzyme-linked immunosorbent assay, and for total IgG and IgM (controls) by radial immunodiffusion. Median follow-up for the study population was 19 months (range, 3-147 months). There was no significant correlation between anti-TA90 IgG titer and total IgG level (P = .4785), or between anti-TA90 IgM and total IgM (P = .0989). Univariate analysis showed that postoperative anti-TA90 IgM titer as a continuous variable was significantly associated with overall survival (OS); i.e., the higher the anti-TA90 IgM titer, the longer the OS. Using an established cutoff titer of 800, median OS was 42 months for patients with high anti-TA90 IgM titers (n = 28) vs. 9 months for patients with low titers (n = 36) (P = .0001). There was no significant correlation between total IgG/IgM and survival (P = .4107 and .4044, respectively). Multivariate analysis identified anti-TA90 IgM as the most significant independent variable influencing OS after complete resection of distant melanoma metastases (P = .0001). We conclude that the endogenous immune response to metastatic melanoma determines the outcome after surgical therapy. Enhancement of this specific immune response may prolong the survival of patients with distant melanoma metastases.
doi_str_mv 10.1007/BF02523659
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_71087836</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>71087836</sourcerecordid><originalsourceid>FETCH-LOGICAL-c341t-e5cff5080b0193b7f97bd79867679d3d6780a89c147c005942befc2a3d0599253</originalsourceid><addsrcrecordid>eNqFkUtLxDAUhYMoOj42_gApLlwI1ZukaZKV-BoVBtzouqTp7ViZNGPSLubfm2EGFDeu7oOPwz33EHJK4YoCyOu7KTDBeCn0DplQwYu8KBXdTT2UKtesFAfkMMZPACo5iH1yQEFqqoSYkPrBY8ywb_wcez_GrHNu7DELGJe-j5g1OGBwXVoNH5j5cbDepdpmcQzzzprFeh_McpW1PmQOBxMHM3Q2tQvTe2dujsleaxYRT7b1iLxPH9_un_PZ69PL_e0st7ygQ47Ctq0ABTVQzWvZalk3UqtSllI3vCmlAqO0pYW0AEIXrMbWMsObNGgm-BG52Ogug_8aMQ6V66LFRToDk7NKUlBS8fJfkFEopOY0ged_wE8_hj6ZqBiTPH1arqHLDWSDjzFgWy1D50xYVRSqdT7VTz4JPtsqjrXD5he6CYR_A7eYie0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>227353471</pqid></control><display><type>article</type><title>Does endogenous immune response determine the outcome of surgical therapy for metastatic melanoma?</title><source>Springer Link</source><creator>Hsueh, E C ; Gupta, R K ; Yee, R ; Leopoldo, Z C ; Qi, K ; Morton, D L</creator><creatorcontrib>Hsueh, E C ; Gupta, R K ; Yee, R ; Leopoldo, Z C ; Qi, K ; Morton, D L</creatorcontrib><description>Although the presence of tumor cells in the blood of patients with metastatic melanoma suggests widely disseminated disease, many of these patients enjoy prolonged survival or cure after surgical resection. Our previous study of adjuvant vaccine therapy after complete resection of metastatic melanoma revealed a strong correlation between postoperative survival and elevated antibody titers to a 90-kDa tumor-associated antigen (TA90) expressed by melanoma cells of the vaccine. We hypothesized a similar correlation between postoperative survival and endogenous anti-TA90 antibody titers induced by the patient's melanoma in the absence of postoperative adjuvant immunotherapy. From 1970 to 1996, 64 patients underwent complete resection of distant melanoma metastases and did not receive postoperative adjuvant immunotherapy. Serum collected within 4 months after surgery was tested in a coded and blinded fashion for anti-TA90 IgG and IgM by enzyme-linked immunosorbent assay, and for total IgG and IgM (controls) by radial immunodiffusion. Median follow-up for the study population was 19 months (range, 3-147 months). There was no significant correlation between anti-TA90 IgG titer and total IgG level (P = .4785), or between anti-TA90 IgM and total IgM (P = .0989). Univariate analysis showed that postoperative anti-TA90 IgM titer as a continuous variable was significantly associated with overall survival (OS); i.e., the higher the anti-TA90 IgM titer, the longer the OS. Using an established cutoff titer of 800, median OS was 42 months for patients with high anti-TA90 IgM titers (n = 28) vs. 9 months for patients with low titers (n = 36) (P = .0001). There was no significant correlation between total IgG/IgM and survival (P = .4107 and .4044, respectively). Multivariate analysis identified anti-TA90 IgM as the most significant independent variable influencing OS after complete resection of distant melanoma metastases (P = .0001). We conclude that the endogenous immune response to metastatic melanoma determines the outcome after surgical therapy. Enhancement of this specific immune response may prolong the survival of patients with distant melanoma metastases.</description><identifier>ISSN: 1068-9265</identifier><identifier>EISSN: 1534-4681</identifier><identifier>DOI: 10.1007/BF02523659</identifier><identifier>PMID: 10791855</identifier><language>eng</language><publisher>United States: Springer Nature B.V</publisher><subject>Antigens, Neoplasm - blood ; Enzyme-Linked Immunosorbent Assay ; Female ; Follow-Up Studies ; Humans ; Immunoglobulin G - blood ; Immunoglobulin M - blood ; Male ; Melanoma - immunology ; Melanoma - secondary ; Melanoma - surgery ; Middle Aged ; Proportional Hazards Models ; Skin Neoplasms - immunology ; Skin Neoplasms - secondary ; Skin Neoplasms - surgery ; Survival Analysis ; Treatment Outcome</subject><ispartof>Annals of surgical oncology, 2000-04, Vol.7 (3), p.232-238</ispartof><rights>The Society of Surgical Oncology, Inc. 2000</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c341t-e5cff5080b0193b7f97bd79867679d3d6780a89c147c005942befc2a3d0599253</citedby><cites>FETCH-LOGICAL-c341t-e5cff5080b0193b7f97bd79867679d3d6780a89c147c005942befc2a3d0599253</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10791855$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hsueh, E C</creatorcontrib><creatorcontrib>Gupta, R K</creatorcontrib><creatorcontrib>Yee, R</creatorcontrib><creatorcontrib>Leopoldo, Z C</creatorcontrib><creatorcontrib>Qi, K</creatorcontrib><creatorcontrib>Morton, D L</creatorcontrib><title>Does endogenous immune response determine the outcome of surgical therapy for metastatic melanoma?</title><title>Annals of surgical oncology</title><addtitle>Ann Surg Oncol</addtitle><description>Although the presence of tumor cells in the blood of patients with metastatic melanoma suggests widely disseminated disease, many of these patients enjoy prolonged survival or cure after surgical resection. Our previous study of adjuvant vaccine therapy after complete resection of metastatic melanoma revealed a strong correlation between postoperative survival and elevated antibody titers to a 90-kDa tumor-associated antigen (TA90) expressed by melanoma cells of the vaccine. We hypothesized a similar correlation between postoperative survival and endogenous anti-TA90 antibody titers induced by the patient's melanoma in the absence of postoperative adjuvant immunotherapy. From 1970 to 1996, 64 patients underwent complete resection of distant melanoma metastases and did not receive postoperative adjuvant immunotherapy. Serum collected within 4 months after surgery was tested in a coded and blinded fashion for anti-TA90 IgG and IgM by enzyme-linked immunosorbent assay, and for total IgG and IgM (controls) by radial immunodiffusion. Median follow-up for the study population was 19 months (range, 3-147 months). There was no significant correlation between anti-TA90 IgG titer and total IgG level (P = .4785), or between anti-TA90 IgM and total IgM (P = .0989). Univariate analysis showed that postoperative anti-TA90 IgM titer as a continuous variable was significantly associated with overall survival (OS); i.e., the higher the anti-TA90 IgM titer, the longer the OS. Using an established cutoff titer of 800, median OS was 42 months for patients with high anti-TA90 IgM titers (n = 28) vs. 9 months for patients with low titers (n = 36) (P = .0001). There was no significant correlation between total IgG/IgM and survival (P = .4107 and .4044, respectively). Multivariate analysis identified anti-TA90 IgM as the most significant independent variable influencing OS after complete resection of distant melanoma metastases (P = .0001). We conclude that the endogenous immune response to metastatic melanoma determines the outcome after surgical therapy. Enhancement of this specific immune response may prolong the survival of patients with distant melanoma metastases.</description><subject>Antigens, Neoplasm - blood</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Immunoglobulin G - blood</subject><subject>Immunoglobulin M - blood</subject><subject>Male</subject><subject>Melanoma - immunology</subject><subject>Melanoma - secondary</subject><subject>Melanoma - surgery</subject><subject>Middle Aged</subject><subject>Proportional Hazards Models</subject><subject>Skin Neoplasms - immunology</subject><subject>Skin Neoplasms - secondary</subject><subject>Skin Neoplasms - surgery</subject><subject>Survival Analysis</subject><subject>Treatment Outcome</subject><issn>1068-9265</issn><issn>1534-4681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqFkUtLxDAUhYMoOj42_gApLlwI1ZukaZKV-BoVBtzouqTp7ViZNGPSLubfm2EGFDeu7oOPwz33EHJK4YoCyOu7KTDBeCn0DplQwYu8KBXdTT2UKtesFAfkMMZPACo5iH1yQEFqqoSYkPrBY8ywb_wcez_GrHNu7DELGJe-j5g1OGBwXVoNH5j5cbDepdpmcQzzzprFeh_McpW1PmQOBxMHM3Q2tQvTe2dujsleaxYRT7b1iLxPH9_un_PZ69PL_e0st7ygQ47Ctq0ABTVQzWvZalk3UqtSllI3vCmlAqO0pYW0AEIXrMbWMsObNGgm-BG52Ogug_8aMQ6V66LFRToDk7NKUlBS8fJfkFEopOY0ged_wE8_hj6ZqBiTPH1arqHLDWSDjzFgWy1D50xYVRSqdT7VTz4JPtsqjrXD5he6CYR_A7eYie0</recordid><startdate>20000401</startdate><enddate>20000401</enddate><creator>Hsueh, E C</creator><creator>Gupta, R K</creator><creator>Yee, R</creator><creator>Leopoldo, Z C</creator><creator>Qi, K</creator><creator>Morton, D L</creator><general>Springer Nature B.V</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>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7T5</scope><scope>7X8</scope></search><sort><creationdate>20000401</creationdate><title>Does endogenous immune response determine the outcome of surgical therapy for metastatic melanoma?</title><author>Hsueh, E C ; Gupta, R K ; Yee, R ; Leopoldo, Z C ; Qi, K ; Morton, D L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c341t-e5cff5080b0193b7f97bd79867679d3d6780a89c147c005942befc2a3d0599253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Antigens, Neoplasm - blood</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Immunoglobulin G - blood</topic><topic>Immunoglobulin M - blood</topic><topic>Male</topic><topic>Melanoma - immunology</topic><topic>Melanoma - secondary</topic><topic>Melanoma - surgery</topic><topic>Middle Aged</topic><topic>Proportional Hazards Models</topic><topic>Skin Neoplasms - immunology</topic><topic>Skin Neoplasms - secondary</topic><topic>Skin Neoplasms - surgery</topic><topic>Survival Analysis</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hsueh, E C</creatorcontrib><creatorcontrib>Gupta, R K</creatorcontrib><creatorcontrib>Yee, R</creatorcontrib><creatorcontrib>Leopoldo, Z C</creatorcontrib><creatorcontrib>Qi, K</creatorcontrib><creatorcontrib>Morton, D L</creatorcontrib><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>Oncogenes and Growth Factors 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>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</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</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>PML(ProQuest Medical Library)</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>Immunology Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of surgical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hsueh, E C</au><au>Gupta, R K</au><au>Yee, R</au><au>Leopoldo, Z C</au><au>Qi, K</au><au>Morton, D L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Does endogenous immune response determine the outcome of surgical therapy for metastatic melanoma?</atitle><jtitle>Annals of surgical oncology</jtitle><addtitle>Ann Surg Oncol</addtitle><date>2000-04-01</date><risdate>2000</risdate><volume>7</volume><issue>3</issue><spage>232</spage><epage>238</epage><pages>232-238</pages><issn>1068-9265</issn><eissn>1534-4681</eissn><abstract>Although the presence of tumor cells in the blood of patients with metastatic melanoma suggests widely disseminated disease, many of these patients enjoy prolonged survival or cure after surgical resection. Our previous study of adjuvant vaccine therapy after complete resection of metastatic melanoma revealed a strong correlation between postoperative survival and elevated antibody titers to a 90-kDa tumor-associated antigen (TA90) expressed by melanoma cells of the vaccine. We hypothesized a similar correlation between postoperative survival and endogenous anti-TA90 antibody titers induced by the patient's melanoma in the absence of postoperative adjuvant immunotherapy. From 1970 to 1996, 64 patients underwent complete resection of distant melanoma metastases and did not receive postoperative adjuvant immunotherapy. Serum collected within 4 months after surgery was tested in a coded and blinded fashion for anti-TA90 IgG and IgM by enzyme-linked immunosorbent assay, and for total IgG and IgM (controls) by radial immunodiffusion. Median follow-up for the study population was 19 months (range, 3-147 months). There was no significant correlation between anti-TA90 IgG titer and total IgG level (P = .4785), or between anti-TA90 IgM and total IgM (P = .0989). Univariate analysis showed that postoperative anti-TA90 IgM titer as a continuous variable was significantly associated with overall survival (OS); i.e., the higher the anti-TA90 IgM titer, the longer the OS. Using an established cutoff titer of 800, median OS was 42 months for patients with high anti-TA90 IgM titers (n = 28) vs. 9 months for patients with low titers (n = 36) (P = .0001). There was no significant correlation between total IgG/IgM and survival (P = .4107 and .4044, respectively). Multivariate analysis identified anti-TA90 IgM as the most significant independent variable influencing OS after complete resection of distant melanoma metastases (P = .0001). We conclude that the endogenous immune response to metastatic melanoma determines the outcome after surgical therapy. Enhancement of this specific immune response may prolong the survival of patients with distant melanoma metastases.</abstract><cop>United States</cop><pub>Springer Nature B.V</pub><pmid>10791855</pmid><doi>10.1007/BF02523659</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1068-9265
ispartof Annals of surgical oncology, 2000-04, Vol.7 (3), p.232-238
issn 1068-9265
1534-4681
language eng
recordid cdi_proquest_miscellaneous_71087836
source Springer Link
subjects Antigens, Neoplasm - blood
Enzyme-Linked Immunosorbent Assay
Female
Follow-Up Studies
Humans
Immunoglobulin G - blood
Immunoglobulin M - blood
Male
Melanoma - immunology
Melanoma - secondary
Melanoma - surgery
Middle Aged
Proportional Hazards Models
Skin Neoplasms - immunology
Skin Neoplasms - secondary
Skin Neoplasms - surgery
Survival Analysis
Treatment Outcome
title Does endogenous immune response determine the outcome of surgical therapy for metastatic melanoma?
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T20%3A03%3A51IST&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=Does%20endogenous%20immune%20response%20determine%20the%20outcome%20of%20surgical%20therapy%20for%20metastatic%20melanoma?&rft.jtitle=Annals%20of%20surgical%20oncology&rft.au=Hsueh,%20E%20C&rft.date=2000-04-01&rft.volume=7&rft.issue=3&rft.spage=232&rft.epage=238&rft.pages=232-238&rft.issn=1068-9265&rft.eissn=1534-4681&rft_id=info:doi/10.1007/BF02523659&rft_dat=%3Cproquest_cross%3E71087836%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c341t-e5cff5080b0193b7f97bd79867679d3d6780a89c147c005942befc2a3d0599253%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=227353471&rft_id=info:pmid/10791855&rfr_iscdi=true