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...
Saved in:
Published in: | Annals of surgical oncology 2000-04, Vol.7 (3), p.232-238 |
---|---|
Main Authors: | , , , , , |
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 & 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 & Medical Complete (Alumni)</collection><collection>Health & 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 |