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NCI―RTOG Translational Program Strategic Guidelines for the Early-Stage Development of Radiosensitizers
The addition of chemotherapeutic agents to ionizing radiation has improved survival in many malignancies. Cure rates may be further improved by adding novel targeted agents to current radiotherapy or radiochemotherapy regimens. Despite promising laboratory data, progress in the clinical development...
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Published in: | JNCI : Journal of the National Cancer Institute 2013-01, Vol.105 (1), p.11-24 |
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creator | LAWRENCE, Yaacov Richard VIKRAM, Bhadrasain COLEMAN, C. Norman DICKER, Adam P DIGNAM, James J CHAKRAVARTI, Arnab MACHTAY, Mitchell FREIDLIN, Boris TAKEBE, Naoko CURRAN, Walter J BENTZEN, Soren M OKUNIEFF, Paul |
description | The addition of chemotherapeutic agents to ionizing radiation has improved survival in many malignancies. Cure rates may be further improved by adding novel targeted agents to current radiotherapy or radiochemotherapy regimens. Despite promising laboratory data, progress in the clinical development of new drugs with radiation has been limited. To define and address the problems involved, a collaborative effort between individuals within the translational research program of the Radiation Oncology Therapy Group and the National Cancer Institute was established. We discerned challenges to drug development with radiation including: 1) the limited relevance of preclinical work, 2) the pharmaceutical industry's diminished interest, and 3) the important individual skills and institutional commitments required to ensure a successful program. The differences between early-phase trial designs with and without radiation are noted as substantial. The traditional endpoints for early-phase clinical trials-acute toxicity and maximum-tolerated dose-are of limited value when combining targeted agents with radiation. Furthermore, response rate is not a useful surrogate marker of activity in radiation combination trials.Consequently, a risk-stratified model for drug-dose escalation with radiation is proposed, based upon the known and estimated adverse effects. The guidelines discuss new clinical trial designs, such as the time-to-event continual reassessment method design for phase I trials, randomized phase II "screening" trials, and the use of surrogate endpoints, such as pathological response. It is hoped that by providing a clear pathway, this article will accelerate the rate of drug development with radiation. |
doi_str_mv | 10.1093/jnci/djs472 |
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Norman ; DICKER, Adam P ; DIGNAM, James J ; CHAKRAVARTI, Arnab ; MACHTAY, Mitchell ; FREIDLIN, Boris ; TAKEBE, Naoko ; CURRAN, Walter J ; BENTZEN, Soren M ; OKUNIEFF, Paul</creator><creatorcontrib>LAWRENCE, Yaacov Richard ; VIKRAM, Bhadrasain ; COLEMAN, C. Norman ; DICKER, Adam P ; DIGNAM, James J ; CHAKRAVARTI, Arnab ; MACHTAY, Mitchell ; FREIDLIN, Boris ; TAKEBE, Naoko ; CURRAN, Walter J ; BENTZEN, Soren M ; OKUNIEFF, Paul</creatorcontrib><description>The addition of chemotherapeutic agents to ionizing radiation has improved survival in many malignancies. Cure rates may be further improved by adding novel targeted agents to current radiotherapy or radiochemotherapy regimens. Despite promising laboratory data, progress in the clinical development of new drugs with radiation has been limited. To define and address the problems involved, a collaborative effort between individuals within the translational research program of the Radiation Oncology Therapy Group and the National Cancer Institute was established. We discerned challenges to drug development with radiation including: 1) the limited relevance of preclinical work, 2) the pharmaceutical industry's diminished interest, and 3) the important individual skills and institutional commitments required to ensure a successful program. The differences between early-phase trial designs with and without radiation are noted as substantial. The traditional endpoints for early-phase clinical trials-acute toxicity and maximum-tolerated dose-are of limited value when combining targeted agents with radiation. Furthermore, response rate is not a useful surrogate marker of activity in radiation combination trials.Consequently, a risk-stratified model for drug-dose escalation with radiation is proposed, based upon the known and estimated adverse effects. The guidelines discuss new clinical trial designs, such as the time-to-event continual reassessment method design for phase I trials, randomized phase II "screening" trials, and the use of surrogate endpoints, such as pathological response. It is hoped that by providing a clear pathway, this article will accelerate the rate of drug development with radiation.</description><identifier>ISSN: 0027-8874</identifier><identifier>EISSN: 1460-2105</identifier><identifier>DOI: 10.1093/jnci/djs472</identifier><identifier>PMID: 23231975</identifier><identifier>CODEN: JNCIEQ</identifier><language>eng</language><publisher>Cary, NC: Oxford University Press</publisher><subject><![CDATA[Animals ; Antineoplastic agents ; Antineoplastic Agents - administration & dosage ; Antineoplastic Agents - pharmacology ; Biological and medical sciences ; Biomarkers, Tumor - metabolism ; Cancer ; Cell Hypoxia - drug effects ; Cell Hypoxia - radiation effects ; Chemotherapy ; Clinical trials ; Clinical Trials as Topic - methods ; Clinical Trials as Topic - standards ; Clinical Trials as Topic - trends ; Clinical Trials, Phase I as Topic - methods ; Clinical Trials, Phase II as Topic - methods ; Combined treatments (chemotherapy of immunotherapy associated with an other treatment) ; Cytostatic Agents - administration & dosage ; Cytostatic Agents - pharmacology ; Cytotoxins - administration & dosage ; Cytotoxins - pharmacology ; Disease Models, Animal ; DNA Damage - drug effects ; DNA Damage - radiation effects ; DNA Repair - drug effects ; DNA Repair - radiation effects ; Dose Fractionation, Radiation ; Drug Administration Schedule ; Drug Design ; Drugs ; ErbB Receptors - antagonists & inhibitors ; ErbB Receptors - metabolism ; Gene Expression Regulation, Neoplastic - drug effects ; Guidelines ; Humans ; Immunologic Factors - administration & dosage ; Immunologic Factors - pharmacology ; Ionizing radiation ; Medical sciences ; Molecular Targeted Therapy - methods ; Multiple tumors. Solid tumors. Tumors in childhood (general aspects) ; National Cancer Institute (U.S.) ; Neoplasms - drug therapy ; Neoplasms - metabolism ; Neoplasms - radiotherapy ; Oncology ; Pharmacology. Drug treatments ; Radiation ; Radiation therapy ; Radiation-Sensitizing Agents - administration & dosage ; Radiation-Sensitizing Agents - pharmacology ; radiotherapy ; Radiotherapy - adverse effects ; Research Design ; Side effects ; Signal Transduction - drug effects ; Survival ; Time Factors ; Toxicity ; Translational Research, Biomedical - methods ; Translational Research, Biomedical - standards ; Translational Research, Biomedical - trends ; Tumors ; United States]]></subject><ispartof>JNCI : Journal of the National Cancer Institute, 2013-01, Vol.105 (1), p.11-24</ispartof><rights>2014 INIST-CNRS</rights><rights>Copyright Oxford Publishing Limited(England) Jan 2, 2013</rights><rights>Published by Oxford University Press 2012. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4532-cad2be7ae01d6ccd308cd0772f6ea75bd933f6709d3a013524f5f72cf281bbd83</citedby><cites>FETCH-LOGICAL-c4532-cad2be7ae01d6ccd308cd0772f6ea75bd933f6709d3a013524f5f72cf281bbd83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27170682$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23231975$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LAWRENCE, Yaacov Richard</creatorcontrib><creatorcontrib>VIKRAM, Bhadrasain</creatorcontrib><creatorcontrib>COLEMAN, C. Norman</creatorcontrib><creatorcontrib>DICKER, Adam P</creatorcontrib><creatorcontrib>DIGNAM, James J</creatorcontrib><creatorcontrib>CHAKRAVARTI, Arnab</creatorcontrib><creatorcontrib>MACHTAY, Mitchell</creatorcontrib><creatorcontrib>FREIDLIN, Boris</creatorcontrib><creatorcontrib>TAKEBE, Naoko</creatorcontrib><creatorcontrib>CURRAN, Walter J</creatorcontrib><creatorcontrib>BENTZEN, Soren M</creatorcontrib><creatorcontrib>OKUNIEFF, Paul</creatorcontrib><title>NCI―RTOG Translational Program Strategic Guidelines for the Early-Stage Development of Radiosensitizers</title><title>JNCI : Journal of the National Cancer Institute</title><addtitle>J Natl Cancer Inst</addtitle><description>The addition of chemotherapeutic agents to ionizing radiation has improved survival in many malignancies. Cure rates may be further improved by adding novel targeted agents to current radiotherapy or radiochemotherapy regimens. Despite promising laboratory data, progress in the clinical development of new drugs with radiation has been limited. To define and address the problems involved, a collaborative effort between individuals within the translational research program of the Radiation Oncology Therapy Group and the National Cancer Institute was established. We discerned challenges to drug development with radiation including: 1) the limited relevance of preclinical work, 2) the pharmaceutical industry's diminished interest, and 3) the important individual skills and institutional commitments required to ensure a successful program. The differences between early-phase trial designs with and without radiation are noted as substantial. The traditional endpoints for early-phase clinical trials-acute toxicity and maximum-tolerated dose-are of limited value when combining targeted agents with radiation. Furthermore, response rate is not a useful surrogate marker of activity in radiation combination trials.Consequently, a risk-stratified model for drug-dose escalation with radiation is proposed, based upon the known and estimated adverse effects. The guidelines discuss new clinical trial designs, such as the time-to-event continual reassessment method design for phase I trials, randomized phase II "screening" trials, and the use of surrogate endpoints, such as pathological response. It is hoped that by providing a clear pathway, this article will accelerate the rate of drug development with radiation.</description><subject>Animals</subject><subject>Antineoplastic agents</subject><subject>Antineoplastic Agents - administration & dosage</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Cancer</subject><subject>Cell Hypoxia - drug effects</subject><subject>Cell Hypoxia - radiation effects</subject><subject>Chemotherapy</subject><subject>Clinical trials</subject><subject>Clinical Trials as Topic - methods</subject><subject>Clinical Trials as Topic - standards</subject><subject>Clinical Trials as Topic - trends</subject><subject>Clinical Trials, Phase I as Topic - methods</subject><subject>Clinical Trials, Phase II as Topic - methods</subject><subject>Combined treatments (chemotherapy of immunotherapy associated with an other treatment)</subject><subject>Cytostatic Agents - administration & dosage</subject><subject>Cytostatic Agents - pharmacology</subject><subject>Cytotoxins - administration & dosage</subject><subject>Cytotoxins - pharmacology</subject><subject>Disease Models, Animal</subject><subject>DNA Damage - drug effects</subject><subject>DNA Damage - radiation effects</subject><subject>DNA Repair - drug effects</subject><subject>DNA Repair - radiation effects</subject><subject>Dose Fractionation, Radiation</subject><subject>Drug Administration Schedule</subject><subject>Drug Design</subject><subject>Drugs</subject><subject>ErbB Receptors - antagonists & inhibitors</subject><subject>ErbB Receptors - metabolism</subject><subject>Gene Expression Regulation, Neoplastic - drug effects</subject><subject>Guidelines</subject><subject>Humans</subject><subject>Immunologic Factors - administration & dosage</subject><subject>Immunologic Factors - pharmacology</subject><subject>Ionizing radiation</subject><subject>Medical sciences</subject><subject>Molecular Targeted Therapy - methods</subject><subject>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</subject><subject>National Cancer Institute (U.S.)</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - metabolism</subject><subject>Neoplasms - radiotherapy</subject><subject>Oncology</subject><subject>Pharmacology. Drug treatments</subject><subject>Radiation</subject><subject>Radiation therapy</subject><subject>Radiation-Sensitizing Agents - administration & dosage</subject><subject>Radiation-Sensitizing Agents - pharmacology</subject><subject>radiotherapy</subject><subject>Radiotherapy - adverse effects</subject><subject>Research Design</subject><subject>Side effects</subject><subject>Signal Transduction - drug effects</subject><subject>Survival</subject><subject>Time Factors</subject><subject>Toxicity</subject><subject>Translational Research, Biomedical - methods</subject><subject>Translational Research, Biomedical - standards</subject><subject>Translational Research, Biomedical - trends</subject><subject>Tumors</subject><subject>United States</subject><issn>0027-8874</issn><issn>1460-2105</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNpdkV1rFDEUhoModq1eeS8BEQQZm4_JZOZGkLWuhWKlXa9DJjnZZslMtslsoV75J_yD_hKz7Fo_zs25OA8vL-dB6Dklbynp-Ml6NP7ErnMt2QM0o3VDKkaJeIhmhDBZta2sj9CTnNekTMfqx-iIccZpJ8UM-c_zs5_ff1wuLxZ4mfSYg558HHXAX1JcJT3gqynpCVbe4MXWWwh-hIxdTHi6BnyqU7irria9AvwBbiHEzQDjhKPDl9r6mGHMfvLfIOWn6JHTIcOzwz5GXz-eLuefqvOLxdn8_XllasFZZbRlPUgNhNrGGMtJayyRkrkGtBS97Th3jSSd5ZpQLljthJPMONbSvrctP0bv9rmbbT-ANaVO0kFtkh90ulNRe_XvZfTXahVvFRe8aWpWAl4fAlK82UKe1OCzgRD0CHGbFWWtIB3teF3Ql_-h67hN5Xs7SpYPN0LIQr3ZUybFnBO4-zKUqJ1CtVOo9goL_eLv_vfsb2cFeHUAdDY6uGLN-PyHk1SSpmX8FzdvqB8</recordid><startdate>20130102</startdate><enddate>20130102</enddate><creator>LAWRENCE, Yaacov Richard</creator><creator>VIKRAM, Bhadrasain</creator><creator>COLEMAN, C. Norman</creator><creator>DICKER, Adam P</creator><creator>DIGNAM, James J</creator><creator>CHAKRAVARTI, Arnab</creator><creator>MACHTAY, Mitchell</creator><creator>FREIDLIN, Boris</creator><creator>TAKEBE, Naoko</creator><creator>CURRAN, Walter J</creator><creator>BENTZEN, Soren M</creator><creator>OKUNIEFF, Paul</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>IQODW</scope><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>7TO</scope><scope>7U7</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7U1</scope><scope>7U2</scope><scope>5PM</scope></search><sort><creationdate>20130102</creationdate><title>NCI―RTOG Translational Program Strategic Guidelines for the Early-Stage Development of Radiosensitizers</title><author>LAWRENCE, Yaacov Richard ; VIKRAM, Bhadrasain ; COLEMAN, C. Norman ; DICKER, Adam P ; DIGNAM, James J ; CHAKRAVARTI, Arnab ; MACHTAY, Mitchell ; FREIDLIN, Boris ; TAKEBE, Naoko ; CURRAN, Walter J ; BENTZEN, Soren M ; OKUNIEFF, Paul</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4532-cad2be7ae01d6ccd308cd0772f6ea75bd933f6709d3a013524f5f72cf281bbd83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Antineoplastic agents</topic><topic>Antineoplastic Agents - administration & dosage</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Cancer</topic><topic>Cell Hypoxia - drug effects</topic><topic>Cell Hypoxia - radiation effects</topic><topic>Chemotherapy</topic><topic>Clinical trials</topic><topic>Clinical Trials as Topic - methods</topic><topic>Clinical Trials as Topic - standards</topic><topic>Clinical Trials as Topic - trends</topic><topic>Clinical Trials, Phase I as Topic - methods</topic><topic>Clinical Trials, Phase II as Topic - methods</topic><topic>Combined treatments (chemotherapy of immunotherapy associated with an other treatment)</topic><topic>Cytostatic Agents - administration & dosage</topic><topic>Cytostatic Agents - pharmacology</topic><topic>Cytotoxins - administration & dosage</topic><topic>Cytotoxins - pharmacology</topic><topic>Disease Models, Animal</topic><topic>DNA Damage - drug effects</topic><topic>DNA Damage - radiation effects</topic><topic>DNA Repair - drug effects</topic><topic>DNA Repair - radiation effects</topic><topic>Dose Fractionation, Radiation</topic><topic>Drug Administration Schedule</topic><topic>Drug Design</topic><topic>Drugs</topic><topic>ErbB Receptors - antagonists & inhibitors</topic><topic>ErbB Receptors - metabolism</topic><topic>Gene Expression Regulation, Neoplastic - drug effects</topic><topic>Guidelines</topic><topic>Humans</topic><topic>Immunologic Factors - administration & dosage</topic><topic>Immunologic Factors - pharmacology</topic><topic>Ionizing radiation</topic><topic>Medical sciences</topic><topic>Molecular Targeted Therapy - methods</topic><topic>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</topic><topic>National Cancer Institute (U.S.)</topic><topic>Neoplasms - drug therapy</topic><topic>Neoplasms - metabolism</topic><topic>Neoplasms - radiotherapy</topic><topic>Oncology</topic><topic>Pharmacology. Drug treatments</topic><topic>Radiation</topic><topic>Radiation therapy</topic><topic>Radiation-Sensitizing Agents - administration & dosage</topic><topic>Radiation-Sensitizing Agents - pharmacology</topic><topic>radiotherapy</topic><topic>Radiotherapy - adverse effects</topic><topic>Research Design</topic><topic>Side effects</topic><topic>Signal Transduction - drug effects</topic><topic>Survival</topic><topic>Time Factors</topic><topic>Toxicity</topic><topic>Translational Research, Biomedical - methods</topic><topic>Translational Research, Biomedical - standards</topic><topic>Translational Research, Biomedical - trends</topic><topic>Tumors</topic><topic>United States</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LAWRENCE, Yaacov Richard</creatorcontrib><creatorcontrib>VIKRAM, Bhadrasain</creatorcontrib><creatorcontrib>COLEMAN, C. 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Norman</au><au>DICKER, Adam P</au><au>DIGNAM, James J</au><au>CHAKRAVARTI, Arnab</au><au>MACHTAY, Mitchell</au><au>FREIDLIN, Boris</au><au>TAKEBE, Naoko</au><au>CURRAN, Walter J</au><au>BENTZEN, Soren M</au><au>OKUNIEFF, Paul</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>NCI―RTOG Translational Program Strategic Guidelines for the Early-Stage Development of Radiosensitizers</atitle><jtitle>JNCI : Journal of the National Cancer Institute</jtitle><addtitle>J Natl Cancer Inst</addtitle><date>2013-01-02</date><risdate>2013</risdate><volume>105</volume><issue>1</issue><spage>11</spage><epage>24</epage><pages>11-24</pages><issn>0027-8874</issn><eissn>1460-2105</eissn><coden>JNCIEQ</coden><abstract>The addition of chemotherapeutic agents to ionizing radiation has improved survival in many malignancies. Cure rates may be further improved by adding novel targeted agents to current radiotherapy or radiochemotherapy regimens. Despite promising laboratory data, progress in the clinical development of new drugs with radiation has been limited. To define and address the problems involved, a collaborative effort between individuals within the translational research program of the Radiation Oncology Therapy Group and the National Cancer Institute was established. We discerned challenges to drug development with radiation including: 1) the limited relevance of preclinical work, 2) the pharmaceutical industry's diminished interest, and 3) the important individual skills and institutional commitments required to ensure a successful program. The differences between early-phase trial designs with and without radiation are noted as substantial. The traditional endpoints for early-phase clinical trials-acute toxicity and maximum-tolerated dose-are of limited value when combining targeted agents with radiation. Furthermore, response rate is not a useful surrogate marker of activity in radiation combination trials.Consequently, a risk-stratified model for drug-dose escalation with radiation is proposed, based upon the known and estimated adverse effects. The guidelines discuss new clinical trial designs, such as the time-to-event continual reassessment method design for phase I trials, randomized phase II "screening" trials, and the use of surrogate endpoints, such as pathological response. It is hoped that by providing a clear pathway, this article will accelerate the rate of drug development with radiation.</abstract><cop>Cary, NC</cop><pub>Oxford University Press</pub><pmid>23231975</pmid><doi>10.1093/jnci/djs472</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antineoplastic agents Antineoplastic Agents - administration & dosage Antineoplastic Agents - pharmacology Biological and medical sciences Biomarkers, Tumor - metabolism Cancer Cell Hypoxia - drug effects Cell Hypoxia - radiation effects Chemotherapy Clinical trials Clinical Trials as Topic - methods Clinical Trials as Topic - standards Clinical Trials as Topic - trends Clinical Trials, Phase I as Topic - methods Clinical Trials, Phase II as Topic - methods Combined treatments (chemotherapy of immunotherapy associated with an other treatment) Cytostatic Agents - administration & dosage Cytostatic Agents - pharmacology Cytotoxins - administration & dosage Cytotoxins - pharmacology Disease Models, Animal DNA Damage - drug effects DNA Damage - radiation effects DNA Repair - drug effects DNA Repair - radiation effects Dose Fractionation, Radiation Drug Administration Schedule Drug Design Drugs ErbB Receptors - antagonists & inhibitors ErbB Receptors - metabolism Gene Expression Regulation, Neoplastic - drug effects Guidelines Humans Immunologic Factors - administration & dosage Immunologic Factors - pharmacology Ionizing radiation Medical sciences Molecular Targeted Therapy - methods Multiple tumors. Solid tumors. Tumors in childhood (general aspects) National Cancer Institute (U.S.) Neoplasms - drug therapy Neoplasms - metabolism Neoplasms - radiotherapy Oncology Pharmacology. Drug treatments Radiation Radiation therapy Radiation-Sensitizing Agents - administration & dosage Radiation-Sensitizing Agents - pharmacology radiotherapy Radiotherapy - adverse effects Research Design Side effects Signal Transduction - drug effects Survival Time Factors Toxicity Translational Research, Biomedical - methods Translational Research, Biomedical - standards Translational Research, Biomedical - trends Tumors United States |
title | NCI―RTOG Translational Program Strategic Guidelines for the Early-Stage Development of Radiosensitizers |
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