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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
Main Authors: 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
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cited_by cdi_FETCH-LOGICAL-c4532-cad2be7ae01d6ccd308cd0772f6ea75bd933f6709d3a013524f5f72cf281bbd83
cites cdi_FETCH-LOGICAL-c4532-cad2be7ae01d6ccd308cd0772f6ea75bd933f6709d3a013524f5f72cf281bbd83
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container_title JNCI : Journal of the National Cancer Institute
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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. 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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. 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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&amp;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. 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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. 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identifier ISSN: 0027-8874
ispartof JNCI : Journal of the National Cancer Institute, 2013-01, Vol.105 (1), p.11-24
issn 0027-8874
1460-2105
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3536642
source Oxford Journals Online
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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