Loading…
Conditional survival of metastatic renal cell carcinoma patients treated with high-dose interleukin-2
Conditional survival (CS) is a clinically useful prediction measure which adjusts a patient's prognosis based on their duration of survival since initiation of therapy. CS has been described in numerous malignancies, and recently described in patients with metastatic renal cell carcinoma (mRCC)...
Saved in:
Published in: | Ecancermedicalscience 2016-09, Vol.10, p.676-676 |
---|---|
Main Authors: | , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | 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-c424t-9e2f55c95ab82015f981a9610f2705c6e6e1f8154f3a960f110c2f80c6c0c82c3 |
---|---|
cites | |
container_end_page | 676 |
container_issue | |
container_start_page | 676 |
container_title | Ecancermedicalscience |
container_volume | 10 |
creator | Gill, David M Stenehjem, David D Parikh, Kinjal Merriman, Joseph Sendilnathan, Arun Agarwal, Archana M Hahn, Andrew W Gupta, Sumati Tantravahi, Srinivas Kiran Samlowski, Wolfram E Agarwal, Neeraj |
description | Conditional survival (CS) is a clinically useful prediction measure which adjusts a patient's prognosis based on their duration of survival since initiation of therapy. CS has been described in numerous malignancies, and recently described in patients with metastatic renal cell carcinoma (mRCC) who received vascular endothelial growth factor tyrosine kinase inhibitor (VEGFTKI) therapy. However, CS has been not reported in the context of mRCC treated with high-dose interleukin-2 therapy (HDIL-2). A total of 176 patients with histologically confirmed metastatic clear cell RCC (mccRCC) treated with HDIL-2 at the University of Utah Huntsman Cancer Institute from 1988-2012 were evaluated. Using the Heng/IMDC model, they were stratified by performance status and prognostic risk groups. Two-year CS was defined as the probability of surviving an additional two years from initiation of HDIL-2 to 18 months after the start of HDIL-2 at three-month intervals. The median overall survival (OS) was 19.9 months. Stratifying patients into favourable (n = 35; 20%), intermediate (n = 110; 63%), and poor (n = 31; 18%) prognostic groups resulted in median OS of 47.5 (HR 0.57, 95% CI 0.35-0.88, p = 0.0106 versus intermediate), 19.6 (HR 0.33, 95% CI 0.10-0.33, p < 0.0001 versus poor), and 8.8 (HR 5.34, 95% CI 3.00-9.62, p < 0.0001 versus favourable) months respectively. Two-year overall CS increased from 43% at therapy initiation to 100% at 18 months. These results have significant ramifications in prognostication. Furthermore, it is important when counseling patients with mccRCC who have completed treatment with HDIL-2 and are in active follow-up. |
doi_str_mv | 10.3332/ecancer.2016.676 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5045298</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1952708248</sourcerecordid><originalsourceid>FETCH-LOGICAL-c424t-9e2f55c95ab82015f981a9610f2705c6e6e1f8154f3a960f110c2f80c6c0c82c3</originalsourceid><addsrcrecordid>eNpdUU1PJCEUJMaNX-vdk-nEi5eeBbqh4WJiJn4lJnvZPROGecyg3TACPcZ_v3Qcje4FXqh6lSoKoTOCZ03T0F9gtDcQZxQTPuMd30NHpGNtzTlm-1_mQ3Sc0hPGnEjKDtAh7ToqZUuOEMyDX7rsgtd9lca4ddsyBFsNkHXKOjtTRZhAA305dDTOh0FXmwKBz6nKEXSGZfXq8rpau9W6XoYElfMZYg_js_M1_Yl-WN0nON3dJ-jv7c2f-X39-PvuYX79WJuWtrmWQC1jRjK9ECUSs1IQLTnBlnaYGQ4ciBWEtbYpz9gSgg21AhtusBHUNCfo6l13My4GWJpiMOpebaIbdHxTQTv1HfFurVZhqxhuGZWiCFzuBGJ4GSFlNbg0JdcewpgUEQ1rcSNEV6gX_1GfwhjLTxWWZMWwoO0kiN9ZJoaUIthPMwSrqUO161BNHarSYVk5_xric-GjtOYfAUia8w</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1952708248</pqid></control><display><type>article</type><title>Conditional survival of metastatic renal cell carcinoma patients treated with high-dose interleukin-2</title><source>PubMed (Medline)</source><source>Publicly Available Content (ProQuest)</source><creator>Gill, David M ; Stenehjem, David D ; Parikh, Kinjal ; Merriman, Joseph ; Sendilnathan, Arun ; Agarwal, Archana M ; Hahn, Andrew W ; Gupta, Sumati ; Tantravahi, Srinivas Kiran ; Samlowski, Wolfram E ; Agarwal, Neeraj</creator><creatorcontrib>Gill, David M ; Stenehjem, David D ; Parikh, Kinjal ; Merriman, Joseph ; Sendilnathan, Arun ; Agarwal, Archana M ; Hahn, Andrew W ; Gupta, Sumati ; Tantravahi, Srinivas Kiran ; Samlowski, Wolfram E ; Agarwal, Neeraj</creatorcontrib><description>Conditional survival (CS) is a clinically useful prediction measure which adjusts a patient's prognosis based on their duration of survival since initiation of therapy. CS has been described in numerous malignancies, and recently described in patients with metastatic renal cell carcinoma (mRCC) who received vascular endothelial growth factor tyrosine kinase inhibitor (VEGFTKI) therapy. However, CS has been not reported in the context of mRCC treated with high-dose interleukin-2 therapy (HDIL-2). A total of 176 patients with histologically confirmed metastatic clear cell RCC (mccRCC) treated with HDIL-2 at the University of Utah Huntsman Cancer Institute from 1988-2012 were evaluated. Using the Heng/IMDC model, they were stratified by performance status and prognostic risk groups. Two-year CS was defined as the probability of surviving an additional two years from initiation of HDIL-2 to 18 months after the start of HDIL-2 at three-month intervals. The median overall survival (OS) was 19.9 months. Stratifying patients into favourable (n = 35; 20%), intermediate (n = 110; 63%), and poor (n = 31; 18%) prognostic groups resulted in median OS of 47.5 (HR 0.57, 95% CI 0.35-0.88, p = 0.0106 versus intermediate), 19.6 (HR 0.33, 95% CI 0.10-0.33, p < 0.0001 versus poor), and 8.8 (HR 5.34, 95% CI 3.00-9.62, p < 0.0001 versus favourable) months respectively. Two-year overall CS increased from 43% at therapy initiation to 100% at 18 months. These results have significant ramifications in prognostication. Furthermore, it is important when counseling patients with mccRCC who have completed treatment with HDIL-2 and are in active follow-up.</description><identifier>ISSN: 1754-6605</identifier><identifier>EISSN: 1754-6605</identifier><identifier>DOI: 10.3332/ecancer.2016.676</identifier><identifier>PMID: 27729941</identifier><language>eng</language><publisher>England: Cancer Intelligence</publisher><subject>Cancer therapies ; Clinical Study ; Consortia ; Counseling ; Decision making ; Immunotherapy ; Kidney cancer ; Laboratories ; Medical prognosis ; Metastasis ; Oncology ; Patients ; Studies</subject><ispartof>Ecancermedicalscience, 2016-09, Vol.10, p.676-676</ispartof><rights>the authors; licensee ecancermedicalscience. 2016. This work is licensed under the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>the authors; licensee ecancermedicalscience. 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c424t-9e2f55c95ab82015f981a9610f2705c6e6e1f8154f3a960f110c2f80c6c0c82c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1952708248/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1952708248?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27729941$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gill, David M</creatorcontrib><creatorcontrib>Stenehjem, David D</creatorcontrib><creatorcontrib>Parikh, Kinjal</creatorcontrib><creatorcontrib>Merriman, Joseph</creatorcontrib><creatorcontrib>Sendilnathan, Arun</creatorcontrib><creatorcontrib>Agarwal, Archana M</creatorcontrib><creatorcontrib>Hahn, Andrew W</creatorcontrib><creatorcontrib>Gupta, Sumati</creatorcontrib><creatorcontrib>Tantravahi, Srinivas Kiran</creatorcontrib><creatorcontrib>Samlowski, Wolfram E</creatorcontrib><creatorcontrib>Agarwal, Neeraj</creatorcontrib><title>Conditional survival of metastatic renal cell carcinoma patients treated with high-dose interleukin-2</title><title>Ecancermedicalscience</title><addtitle>Ecancermedicalscience</addtitle><description>Conditional survival (CS) is a clinically useful prediction measure which adjusts a patient's prognosis based on their duration of survival since initiation of therapy. CS has been described in numerous malignancies, and recently described in patients with metastatic renal cell carcinoma (mRCC) who received vascular endothelial growth factor tyrosine kinase inhibitor (VEGFTKI) therapy. However, CS has been not reported in the context of mRCC treated with high-dose interleukin-2 therapy (HDIL-2). A total of 176 patients with histologically confirmed metastatic clear cell RCC (mccRCC) treated with HDIL-2 at the University of Utah Huntsman Cancer Institute from 1988-2012 were evaluated. Using the Heng/IMDC model, they were stratified by performance status and prognostic risk groups. Two-year CS was defined as the probability of surviving an additional two years from initiation of HDIL-2 to 18 months after the start of HDIL-2 at three-month intervals. The median overall survival (OS) was 19.9 months. Stratifying patients into favourable (n = 35; 20%), intermediate (n = 110; 63%), and poor (n = 31; 18%) prognostic groups resulted in median OS of 47.5 (HR 0.57, 95% CI 0.35-0.88, p = 0.0106 versus intermediate), 19.6 (HR 0.33, 95% CI 0.10-0.33, p < 0.0001 versus poor), and 8.8 (HR 5.34, 95% CI 3.00-9.62, p < 0.0001 versus favourable) months respectively. Two-year overall CS increased from 43% at therapy initiation to 100% at 18 months. These results have significant ramifications in prognostication. Furthermore, it is important when counseling patients with mccRCC who have completed treatment with HDIL-2 and are in active follow-up.</description><subject>Cancer therapies</subject><subject>Clinical Study</subject><subject>Consortia</subject><subject>Counseling</subject><subject>Decision making</subject><subject>Immunotherapy</subject><subject>Kidney cancer</subject><subject>Laboratories</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Oncology</subject><subject>Patients</subject><subject>Studies</subject><issn>1754-6605</issn><issn>1754-6605</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpdUU1PJCEUJMaNX-vdk-nEi5eeBbqh4WJiJn4lJnvZPROGecyg3TACPcZ_v3Qcje4FXqh6lSoKoTOCZ03T0F9gtDcQZxQTPuMd30NHpGNtzTlm-1_mQ3Sc0hPGnEjKDtAh7ToqZUuOEMyDX7rsgtd9lca4ddsyBFsNkHXKOjtTRZhAA305dDTOh0FXmwKBz6nKEXSGZfXq8rpau9W6XoYElfMZYg_js_M1_Yl-WN0nON3dJ-jv7c2f-X39-PvuYX79WJuWtrmWQC1jRjK9ECUSs1IQLTnBlnaYGQ4ciBWEtbYpz9gSgg21AhtusBHUNCfo6l13My4GWJpiMOpebaIbdHxTQTv1HfFurVZhqxhuGZWiCFzuBGJ4GSFlNbg0JdcewpgUEQ1rcSNEV6gX_1GfwhjLTxWWZMWwoO0kiN9ZJoaUIthPMwSrqUO161BNHarSYVk5_xric-GjtOYfAUia8w</recordid><startdate>20160929</startdate><enddate>20160929</enddate><creator>Gill, David M</creator><creator>Stenehjem, David D</creator><creator>Parikh, Kinjal</creator><creator>Merriman, Joseph</creator><creator>Sendilnathan, Arun</creator><creator>Agarwal, Archana M</creator><creator>Hahn, Andrew W</creator><creator>Gupta, Sumati</creator><creator>Tantravahi, Srinivas Kiran</creator><creator>Samlowski, Wolfram E</creator><creator>Agarwal, Neeraj</creator><general>Cancer Intelligence</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160929</creationdate><title>Conditional survival of metastatic renal cell carcinoma patients treated with high-dose interleukin-2</title><author>Gill, David M ; Stenehjem, David D ; Parikh, Kinjal ; Merriman, Joseph ; Sendilnathan, Arun ; Agarwal, Archana M ; Hahn, Andrew W ; Gupta, Sumati ; Tantravahi, Srinivas Kiran ; Samlowski, Wolfram E ; Agarwal, Neeraj</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c424t-9e2f55c95ab82015f981a9610f2705c6e6e1f8154f3a960f110c2f80c6c0c82c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Cancer therapies</topic><topic>Clinical Study</topic><topic>Consortia</topic><topic>Counseling</topic><topic>Decision making</topic><topic>Immunotherapy</topic><topic>Kidney cancer</topic><topic>Laboratories</topic><topic>Medical prognosis</topic><topic>Metastasis</topic><topic>Oncology</topic><topic>Patients</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gill, David M</creatorcontrib><creatorcontrib>Stenehjem, David D</creatorcontrib><creatorcontrib>Parikh, Kinjal</creatorcontrib><creatorcontrib>Merriman, Joseph</creatorcontrib><creatorcontrib>Sendilnathan, Arun</creatorcontrib><creatorcontrib>Agarwal, Archana M</creatorcontrib><creatorcontrib>Hahn, Andrew W</creatorcontrib><creatorcontrib>Gupta, Sumati</creatorcontrib><creatorcontrib>Tantravahi, Srinivas Kiran</creatorcontrib><creatorcontrib>Samlowski, Wolfram E</creatorcontrib><creatorcontrib>Agarwal, Neeraj</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content (ProQuest)</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Ecancermedicalscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gill, David M</au><au>Stenehjem, David D</au><au>Parikh, Kinjal</au><au>Merriman, Joseph</au><au>Sendilnathan, Arun</au><au>Agarwal, Archana M</au><au>Hahn, Andrew W</au><au>Gupta, Sumati</au><au>Tantravahi, Srinivas Kiran</au><au>Samlowski, Wolfram E</au><au>Agarwal, Neeraj</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Conditional survival of metastatic renal cell carcinoma patients treated with high-dose interleukin-2</atitle><jtitle>Ecancermedicalscience</jtitle><addtitle>Ecancermedicalscience</addtitle><date>2016-09-29</date><risdate>2016</risdate><volume>10</volume><spage>676</spage><epage>676</epage><pages>676-676</pages><issn>1754-6605</issn><eissn>1754-6605</eissn><abstract>Conditional survival (CS) is a clinically useful prediction measure which adjusts a patient's prognosis based on their duration of survival since initiation of therapy. CS has been described in numerous malignancies, and recently described in patients with metastatic renal cell carcinoma (mRCC) who received vascular endothelial growth factor tyrosine kinase inhibitor (VEGFTKI) therapy. However, CS has been not reported in the context of mRCC treated with high-dose interleukin-2 therapy (HDIL-2). A total of 176 patients with histologically confirmed metastatic clear cell RCC (mccRCC) treated with HDIL-2 at the University of Utah Huntsman Cancer Institute from 1988-2012 were evaluated. Using the Heng/IMDC model, they were stratified by performance status and prognostic risk groups. Two-year CS was defined as the probability of surviving an additional two years from initiation of HDIL-2 to 18 months after the start of HDIL-2 at three-month intervals. The median overall survival (OS) was 19.9 months. Stratifying patients into favourable (n = 35; 20%), intermediate (n = 110; 63%), and poor (n = 31; 18%) prognostic groups resulted in median OS of 47.5 (HR 0.57, 95% CI 0.35-0.88, p = 0.0106 versus intermediate), 19.6 (HR 0.33, 95% CI 0.10-0.33, p < 0.0001 versus poor), and 8.8 (HR 5.34, 95% CI 3.00-9.62, p < 0.0001 versus favourable) months respectively. Two-year overall CS increased from 43% at therapy initiation to 100% at 18 months. These results have significant ramifications in prognostication. Furthermore, it is important when counseling patients with mccRCC who have completed treatment with HDIL-2 and are in active follow-up.</abstract><cop>England</cop><pub>Cancer Intelligence</pub><pmid>27729941</pmid><doi>10.3332/ecancer.2016.676</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1754-6605 |
ispartof | Ecancermedicalscience, 2016-09, Vol.10, p.676-676 |
issn | 1754-6605 1754-6605 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5045298 |
source | PubMed (Medline); Publicly Available Content (ProQuest) |
subjects | Cancer therapies Clinical Study Consortia Counseling Decision making Immunotherapy Kidney cancer Laboratories Medical prognosis Metastasis Oncology Patients Studies |
title | Conditional survival of metastatic renal cell carcinoma patients treated with high-dose interleukin-2 |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T06%3A36%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Conditional%20survival%20of%20metastatic%20renal%20cell%20carcinoma%20patients%20treated%20with%20high-dose%20interleukin-2&rft.jtitle=Ecancermedicalscience&rft.au=Gill,%20David%20M&rft.date=2016-09-29&rft.volume=10&rft.spage=676&rft.epage=676&rft.pages=676-676&rft.issn=1754-6605&rft.eissn=1754-6605&rft_id=info:doi/10.3332/ecancer.2016.676&rft_dat=%3Cproquest_pubme%3E1952708248%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c424t-9e2f55c95ab82015f981a9610f2705c6e6e1f8154f3a960f110c2f80c6c0c82c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1952708248&rft_id=info:pmid/27729941&rfr_iscdi=true |