Time on Therapy for at Least Three Months Correlates with Overall Survival in Metastatic Renal Cell Carcinoma
With 15 drugs currently approved for the treatment of metastatic renal cell carcinoma (mRCC) and even more combination regimens with immunotherapy on the horizon, there remains a distinct lack of molecular biomarkers for therapeutic efficacy. Our study reports on real-world clinical outcomes of mRCC...
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Veröffentlicht in: | Cancers 2019-07, Vol.11 (7), p.1000 |
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creator | Chen, Viola J Hernandez-Meza, Gabriela Agrawal, Prashasti Zhang, Chiyuan A Xie, Lijia Gong, Cynthia L Hoerner, Christian R Srinivas, Sandy Oermann, Eric K Fan, Alice C |
description | With 15 drugs currently approved for the treatment of metastatic renal cell carcinoma (mRCC) and even more combination regimens with immunotherapy on the horizon, there remains a distinct lack of molecular biomarkers for therapeutic efficacy. Our study reports on real-world clinical outcomes of mRCC patients from a tertiary academic medical center treated with empirically selected standard-of-care therapy. We utilized the Stanford Renal Cell Carcinoma Database (RCCD) to report on various outcome measures, including overall survival (OS) and the median number of lines of targeted therapies received from the time of metastatic diagnosis. We found that most metastatic patients did not survive long enough to attempt even half of the available targeted therapies. We also noted that patients who failed to receive a clinical benefit within the first two lines of therapy could still go on to experience clinical benefit in later lines of therapy. The term, "clinical benefit" was assigned to a line of therapy if a patient remained on drug treatment for three months or longer. Moreover, patients with clinical benefit in at least one line of therapy experienced significantly longer OS compared to those who did not have clinical benefit in at least one line of therapy. Developing biomarkers that identify patients who will receive clinical benefit in individual lines of therapy is one potential strategy for achieving rational drug sequencing in mRCC. |
doi_str_mv | 10.3390/cancers11071000 |
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Our study reports on real-world clinical outcomes of mRCC patients from a tertiary academic medical center treated with empirically selected standard-of-care therapy. We utilized the Stanford Renal Cell Carcinoma Database (RCCD) to report on various outcome measures, including overall survival (OS) and the median number of lines of targeted therapies received from the time of metastatic diagnosis. We found that most metastatic patients did not survive long enough to attempt even half of the available targeted therapies. We also noted that patients who failed to receive a clinical benefit within the first two lines of therapy could still go on to experience clinical benefit in later lines of therapy. The term, "clinical benefit" was assigned to a line of therapy if a patient remained on drug treatment for three months or longer. Moreover, patients with clinical benefit in at least one line of therapy experienced significantly longer OS compared to those who did not have clinical benefit in at least one line of therapy. Developing biomarkers that identify patients who will receive clinical benefit in individual lines of therapy is one potential strategy for achieving rational drug sequencing in mRCC.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers11071000</identifier><identifier>PMID: 31319594</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Biomarkers ; Cell survival ; Consortia ; Drugs ; Immunotherapy ; Kidney cancer ; Ligands ; Medical prognosis ; Metastases ; Metastasis ; Patients ; Renal cell carcinoma</subject><ispartof>Cancers, 2019-07, Vol.11 (7), p.1000</ispartof><rights>2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 by the authors. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-62b8f72b2e5762cbf63799b9ffcbbaa43a3d1812d28f780857bb81c29b21f5243</citedby><cites>FETCH-LOGICAL-c421t-62b8f72b2e5762cbf63799b9ffcbbaa43a3d1812d28f780857bb81c29b21f5243</cites><orcidid>0000-0003-0159-1335 ; 0000-0003-3410-5292 ; 0000-0002-4813-5444</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678132/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678132/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31319594$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Viola J</creatorcontrib><creatorcontrib>Hernandez-Meza, Gabriela</creatorcontrib><creatorcontrib>Agrawal, Prashasti</creatorcontrib><creatorcontrib>Zhang, Chiyuan A</creatorcontrib><creatorcontrib>Xie, Lijia</creatorcontrib><creatorcontrib>Gong, Cynthia L</creatorcontrib><creatorcontrib>Hoerner, Christian R</creatorcontrib><creatorcontrib>Srinivas, Sandy</creatorcontrib><creatorcontrib>Oermann, Eric K</creatorcontrib><creatorcontrib>Fan, Alice C</creatorcontrib><title>Time on Therapy for at Least Three Months Correlates with Overall Survival in Metastatic Renal Cell Carcinoma</title><title>Cancers</title><addtitle>Cancers (Basel)</addtitle><description>With 15 drugs currently approved for the treatment of metastatic renal cell carcinoma (mRCC) and even more combination regimens with immunotherapy on the horizon, there remains a distinct lack of molecular biomarkers for therapeutic efficacy. 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Moreover, patients with clinical benefit in at least one line of therapy experienced significantly longer OS compared to those who did not have clinical benefit in at least one line of therapy. Developing biomarkers that identify patients who will receive clinical benefit in individual lines of therapy is one potential strategy for achieving rational drug sequencing in mRCC.</description><subject>Biomarkers</subject><subject>Cell survival</subject><subject>Consortia</subject><subject>Drugs</subject><subject>Immunotherapy</subject><subject>Kidney cancer</subject><subject>Ligands</subject><subject>Medical prognosis</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Patients</subject><subject>Renal cell carcinoma</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkc1LHTEUxUOpVFHX3UnATTdP8zGTTDZCGaoWngjt6zokeXd8kZnkNcm84n9vxA-sq4Sb3znck4PQV0rOOFfk3JngIGVKiaSEkE_ogBHJFkKo5vO7-z46zvm-AoRzKoX8gvY55VS1qjlA08pPgGPAqw0ks33AQ0zYFLwEk0sdJgB8E0PZZNzHlGA0BTL-58sG3-6qYhzx7znt_M6M2Ad8A6XqTPEO_4JQZz1UojfJ-RAnc4T2BjNmOH45D9Gfyx-r_nqxvL362X9fLlzDaFkIZrtBMsuglYI5OwgulbJqGJy1xjTc8DXtKFuzinWka6W1HXVMWUaHljX8EF08-25nO8HaQSh1Vb1NfjLpQUfj9f8vwW_0XdxpIWRHOasG314MUvw7Qy568tnVLCZAnLNmTFBWv5M9oacf0Ps4p5q9Um0jG0UooZU6f6ZcijknGN6WoUQ_tak_tFkVJ-8zvPGv3fFH-bGctg</recordid><startdate>20190717</startdate><enddate>20190717</enddate><creator>Chen, Viola J</creator><creator>Hernandez-Meza, Gabriela</creator><creator>Agrawal, Prashasti</creator><creator>Zhang, Chiyuan A</creator><creator>Xie, Lijia</creator><creator>Gong, Cynthia L</creator><creator>Hoerner, Christian R</creator><creator>Srinivas, Sandy</creator><creator>Oermann, Eric K</creator><creator>Fan, Alice C</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-0159-1335</orcidid><orcidid>https://orcid.org/0000-0003-3410-5292</orcidid><orcidid>https://orcid.org/0000-0002-4813-5444</orcidid></search><sort><creationdate>20190717</creationdate><title>Time on Therapy for at Least Three Months Correlates with Overall Survival in Metastatic Renal Cell Carcinoma</title><author>Chen, Viola J ; Hernandez-Meza, Gabriela ; Agrawal, Prashasti ; Zhang, Chiyuan A ; Xie, Lijia ; Gong, Cynthia L ; Hoerner, Christian R ; Srinivas, Sandy ; Oermann, Eric K ; Fan, Alice C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-62b8f72b2e5762cbf63799b9ffcbbaa43a3d1812d28f780857bb81c29b21f5243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Biomarkers</topic><topic>Cell survival</topic><topic>Consortia</topic><topic>Drugs</topic><topic>Immunotherapy</topic><topic>Kidney cancer</topic><topic>Ligands</topic><topic>Medical prognosis</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Patients</topic><topic>Renal cell carcinoma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Viola J</creatorcontrib><creatorcontrib>Hernandez-Meza, Gabriela</creatorcontrib><creatorcontrib>Agrawal, Prashasti</creatorcontrib><creatorcontrib>Zhang, Chiyuan A</creatorcontrib><creatorcontrib>Xie, Lijia</creatorcontrib><creatorcontrib>Gong, Cynthia L</creatorcontrib><creatorcontrib>Hoerner, Christian R</creatorcontrib><creatorcontrib>Srinivas, Sandy</creatorcontrib><creatorcontrib>Oermann, Eric K</creatorcontrib><creatorcontrib>Fan, Alice C</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>Biological Sciences</collection><collection>ProQuest Research Library</collection><collection>ProQuest Biological Science Journals</collection><collection>Research Library (Corporate)</collection><collection>Access via ProQuest (Open Access)</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Viola J</au><au>Hernandez-Meza, Gabriela</au><au>Agrawal, Prashasti</au><au>Zhang, Chiyuan A</au><au>Xie, Lijia</au><au>Gong, Cynthia L</au><au>Hoerner, Christian R</au><au>Srinivas, Sandy</au><au>Oermann, Eric K</au><au>Fan, Alice C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Time on Therapy for at Least Three Months Correlates with Overall Survival in Metastatic Renal Cell Carcinoma</atitle><jtitle>Cancers</jtitle><addtitle>Cancers (Basel)</addtitle><date>2019-07-17</date><risdate>2019</risdate><volume>11</volume><issue>7</issue><spage>1000</spage><pages>1000-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>With 15 drugs currently approved for the treatment of metastatic renal cell carcinoma (mRCC) and even more combination regimens with immunotherapy on the horizon, there remains a distinct lack of molecular biomarkers for therapeutic efficacy. 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Moreover, patients with clinical benefit in at least one line of therapy experienced significantly longer OS compared to those who did not have clinical benefit in at least one line of therapy. Developing biomarkers that identify patients who will receive clinical benefit in individual lines of therapy is one potential strategy for achieving rational drug sequencing in mRCC.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>31319594</pmid><doi>10.3390/cancers11071000</doi><orcidid>https://orcid.org/0000-0003-0159-1335</orcidid><orcidid>https://orcid.org/0000-0003-3410-5292</orcidid><orcidid>https://orcid.org/0000-0002-4813-5444</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biomarkers Cell survival Consortia Drugs Immunotherapy Kidney cancer Ligands Medical prognosis Metastases Metastasis Patients Renal cell carcinoma |
title | Time on Therapy for at Least Three Months Correlates with Overall Survival in Metastatic Renal Cell Carcinoma |
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