Kidney cancer: the Cytokine Working Group experience (1986-2001): part II. Management of IL-2 toxicity and studies with other cytokines
The Cytokine Working Group (CWG) was initially established in 1986 as the Extramural IL-2/LAK Working Group. With funding from the National Cancer Institute (NCI), the CWG was mandated to confirming data regarding the efficacy of the high-dose interleukin-2 (IL2)/lymphokine-activated killer cell (LA...
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Veröffentlicht in: | Medical oncology (Northwood, London, England) London, England), 2001-01, Vol.18 (3), p.209-220 |
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description | The Cytokine Working Group (CWG) was initially established in 1986 as the Extramural IL-2/LAK Working Group. With funding from the National Cancer Institute (NCI), the CWG was mandated to confirming data regarding the efficacy of the high-dose interleukin-2 (IL2)/lymphokine-activated killer cell (LAK cell) regimen piloted at the NCI in the treatment of renal cell cancer. Since those initial studies, the CWG has conducted a series of clinical trials, often with correlative immunologic investigations, to evaluate combination immunotherapy in attempts to enhance the efficacy of IL-2 or to reduce toxicity. Subsequently, the CWG conducted trials to demonstrate the activity of lower-dose outpatient combination cytokine regimens to help determine their role in the armamentarium of treatment for metastatic renal cell cancer. This has culminated in a phase III randomized trial comparing the activity of high-dose IL-2 with the activity of outpatient IL-2 plus interferon-alpha. The CWG also has honed the management of both high-dose IL-2 and outpatient IL-2 regimens to make these safer in the hands of experienced clinicians. In addition, the CWG has produced a series of carefully conducted clinical trials of new cytokines, again attempting to define their clinical efficacy as anticancer agents. These include studies of IL-4, IL-6, and IL-12. Currently, the CWG is conducting studies with new approaches to IL-2 therapy, as well as planning trials with new agents for treatment of renal cell cancer. This review describes these efforts conducted over the past 15 yr. |
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Management of IL-2 toxicity and studies with other cytokines</title><source>MEDLINE</source><source>SpringerLink Journals</source><creator>Dutcher, J ; Atkins, M B ; Margolin, K ; Weiss, G ; Clark, J ; Sosman, J ; Logan, T ; Aronson, F ; Mier, J</creator><creatorcontrib>Dutcher, J ; Atkins, M B ; Margolin, K ; Weiss, G ; Clark, J ; Sosman, J ; Logan, T ; Aronson, F ; Mier, J ; Cytokine Working Group</creatorcontrib><description>The Cytokine Working Group (CWG) was initially established in 1986 as the Extramural IL-2/LAK Working Group. With funding from the National Cancer Institute (NCI), the CWG was mandated to confirming data regarding the efficacy of the high-dose interleukin-2 (IL2)/lymphokine-activated killer cell (LAK cell) regimen piloted at the NCI in the treatment of renal cell cancer. Since those initial studies, the CWG has conducted a series of clinical trials, often with correlative immunologic investigations, to evaluate combination immunotherapy in attempts to enhance the efficacy of IL-2 or to reduce toxicity. Subsequently, the CWG conducted trials to demonstrate the activity of lower-dose outpatient combination cytokine regimens to help determine their role in the armamentarium of treatment for metastatic renal cell cancer. This has culminated in a phase III randomized trial comparing the activity of high-dose IL-2 with the activity of outpatient IL-2 plus interferon-alpha. The CWG also has honed the management of both high-dose IL-2 and outpatient IL-2 regimens to make these safer in the hands of experienced clinicians. In addition, the CWG has produced a series of carefully conducted clinical trials of new cytokines, again attempting to define their clinical efficacy as anticancer agents. These include studies of IL-4, IL-6, and IL-12. Currently, the CWG is conducting studies with new approaches to IL-2 therapy, as well as planning trials with new agents for treatment of renal cell cancer. This review describes these efforts conducted over the past 15 yr.</description><identifier>ISSN: 1357-0560</identifier><identifier>EISSN: 1357-0560</identifier><identifier>EISSN: 1559-131X</identifier><identifier>DOI: 10.1385/MO:18:3:209</identifier><identifier>PMID: 11917945</identifier><identifier>CODEN: MONCEZ</identifier><language>eng</language><publisher>United States: Springer Nature B.V</publisher><subject>Antineoplastic Agents - adverse effects ; Antineoplastic Agents - pharmacology ; Antineoplastic Agents - therapeutic use ; Antitumor agents ; Carcinoma, Renal Cell - drug therapy ; Carcinoma, Renal Cell - immunology ; Cytokines - pharmacology ; Cytokines - therapeutic use ; Dose-Response Relationship, Drug ; Humans ; Interferon-alpha - pharmacology ; Interleukin-2 - adverse effects ; Interleukin-2 - pharmacology ; Interleukin-2 - therapeutic use ; Kidney Neoplasms - drug therapy ; Kidney Neoplasms - immunology ; Multicenter Studies as Topic ; Oncology ; Randomized Controlled Trials as Topic</subject><ispartof>Medical oncology (Northwood, London, England), 2001-01, Vol.18 (3), p.209-220</ispartof><rights>Humana Press Inc. 2001</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c345t-e64903e90c969b97435f5d97ca79b8c9a5e7801409b593e0fa2b87e75cd91a0e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11917945$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dutcher, J</creatorcontrib><creatorcontrib>Atkins, M B</creatorcontrib><creatorcontrib>Margolin, K</creatorcontrib><creatorcontrib>Weiss, G</creatorcontrib><creatorcontrib>Clark, J</creatorcontrib><creatorcontrib>Sosman, J</creatorcontrib><creatorcontrib>Logan, T</creatorcontrib><creatorcontrib>Aronson, F</creatorcontrib><creatorcontrib>Mier, J</creatorcontrib><creatorcontrib>Cytokine Working Group</creatorcontrib><title>Kidney cancer: the Cytokine Working Group experience (1986-2001): part II. Management of IL-2 toxicity and studies with other cytokines</title><title>Medical oncology (Northwood, London, England)</title><addtitle>Med Oncol</addtitle><description>The Cytokine Working Group (CWG) was initially established in 1986 as the Extramural IL-2/LAK Working Group. With funding from the National Cancer Institute (NCI), the CWG was mandated to confirming data regarding the efficacy of the high-dose interleukin-2 (IL2)/lymphokine-activated killer cell (LAK cell) regimen piloted at the NCI in the treatment of renal cell cancer. Since those initial studies, the CWG has conducted a series of clinical trials, often with correlative immunologic investigations, to evaluate combination immunotherapy in attempts to enhance the efficacy of IL-2 or to reduce toxicity. Subsequently, the CWG conducted trials to demonstrate the activity of lower-dose outpatient combination cytokine regimens to help determine their role in the armamentarium of treatment for metastatic renal cell cancer. This has culminated in a phase III randomized trial comparing the activity of high-dose IL-2 with the activity of outpatient IL-2 plus interferon-alpha. The CWG also has honed the management of both high-dose IL-2 and outpatient IL-2 regimens to make these safer in the hands of experienced clinicians. In addition, the CWG has produced a series of carefully conducted clinical trials of new cytokines, again attempting to define their clinical efficacy as anticancer agents. These include studies of IL-4, IL-6, and IL-12. Currently, the CWG is conducting studies with new approaches to IL-2 therapy, as well as planning trials with new agents for treatment of renal cell cancer. This review describes these efforts conducted over the past 15 yr.</description><subject>Antineoplastic Agents - adverse effects</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Antitumor agents</subject><subject>Carcinoma, Renal Cell - drug therapy</subject><subject>Carcinoma, Renal Cell - immunology</subject><subject>Cytokines - pharmacology</subject><subject>Cytokines - therapeutic use</subject><subject>Dose-Response Relationship, Drug</subject><subject>Humans</subject><subject>Interferon-alpha - pharmacology</subject><subject>Interleukin-2 - adverse effects</subject><subject>Interleukin-2 - pharmacology</subject><subject>Interleukin-2 - therapeutic use</subject><subject>Kidney Neoplasms - drug therapy</subject><subject>Kidney Neoplasms - immunology</subject><subject>Multicenter Studies as Topic</subject><subject>Oncology</subject><subject>Randomized Controlled Trials as Topic</subject><issn>1357-0560</issn><issn>1357-0560</issn><issn>1559-131X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpdkUFv1DAQhS0EoqVw4o5GnIpQyjiO4zg3tIKyYld7AXG0HGfSuuzGwXZE9xfwtwnqSiBObw6f3hvpY-wlxysuGvluu2t504q2RP2InXMhVYGyxsf_3GfsWUp3iCWXpX7KzjjXXOlKnrNfn30_0hGcHR3FFvItweqYw3c_EnwLcckbuI5hnoDuJ4qeFg4uuW7qokTkb1qYbMywXl_B1o72hg40ZggDrDdFCTnce-fzEezYQ8pz7ynBT59vISxLEdxpKj1nTwa7T_TilBfs68cPX1afis3uer16vymcqGQuqK40CtLodK07rSohB9lr5azSXeO0laQa5BXqTmpBONiyaxQp6XrNLZK4YJcPvVMMP2ZK2Rx8crTf25HCnAyv6kqi4ogL-vo_9C7McVy-M42SspSy4gv09gFyMaQUaTBT9Acbj4aj-aPHbHeGN0aYRc9CvzpVzt2B-r_syYf4DVk3iDo</recordid><startdate>20010101</startdate><enddate>20010101</enddate><creator>Dutcher, J</creator><creator>Atkins, M B</creator><creator>Margolin, K</creator><creator>Weiss, G</creator><creator>Clark, J</creator><creator>Sosman, J</creator><creator>Logan, T</creator><creator>Aronson, F</creator><creator>Mier, J</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>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>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>20010101</creationdate><title>Kidney cancer: the Cytokine Working Group experience (1986-2001): part II. 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Management of IL-2 toxicity and studies with other cytokines</atitle><jtitle>Medical oncology (Northwood, London, England)</jtitle><addtitle>Med Oncol</addtitle><date>2001-01-01</date><risdate>2001</risdate><volume>18</volume><issue>3</issue><spage>209</spage><epage>220</epage><pages>209-220</pages><issn>1357-0560</issn><eissn>1357-0560</eissn><eissn>1559-131X</eissn><coden>MONCEZ</coden><abstract>The Cytokine Working Group (CWG) was initially established in 1986 as the Extramural IL-2/LAK Working Group. With funding from the National Cancer Institute (NCI), the CWG was mandated to confirming data regarding the efficacy of the high-dose interleukin-2 (IL2)/lymphokine-activated killer cell (LAK cell) regimen piloted at the NCI in the treatment of renal cell cancer. Since those initial studies, the CWG has conducted a series of clinical trials, often with correlative immunologic investigations, to evaluate combination immunotherapy in attempts to enhance the efficacy of IL-2 or to reduce toxicity. Subsequently, the CWG conducted trials to demonstrate the activity of lower-dose outpatient combination cytokine regimens to help determine their role in the armamentarium of treatment for metastatic renal cell cancer. This has culminated in a phase III randomized trial comparing the activity of high-dose IL-2 with the activity of outpatient IL-2 plus interferon-alpha. The CWG also has honed the management of both high-dose IL-2 and outpatient IL-2 regimens to make these safer in the hands of experienced clinicians. In addition, the CWG has produced a series of carefully conducted clinical trials of new cytokines, again attempting to define their clinical efficacy as anticancer agents. These include studies of IL-4, IL-6, and IL-12. 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subjects | Antineoplastic Agents - adverse effects Antineoplastic Agents - pharmacology Antineoplastic Agents - therapeutic use Antitumor agents Carcinoma, Renal Cell - drug therapy Carcinoma, Renal Cell - immunology Cytokines - pharmacology Cytokines - therapeutic use Dose-Response Relationship, Drug Humans Interferon-alpha - pharmacology Interleukin-2 - adverse effects Interleukin-2 - pharmacology Interleukin-2 - therapeutic use Kidney Neoplasms - drug therapy Kidney Neoplasms - immunology Multicenter Studies as Topic Oncology Randomized Controlled Trials as Topic |
title | Kidney cancer: the Cytokine Working Group experience (1986-2001): part II. Management of IL-2 toxicity and studies with other cytokines |
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