Evidence map›Paper›PMID 23812271›Full record

ReviewNature reviews. Drug discovery2013

Strategies for optimizing the response of cancer and normal tissues to radiation.

Everett J Moding, Michael B Kastan, David G Kirsch

Abstract readReview
In one paragraph

Review in Nature reviews. Drug discovery, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 221 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
221citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

221 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Monitoring early response to chemoradiotherapy withEuropean journal of nuclear medicine and molecular imaging · 2017
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161 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Everett J ModingDepartment of Pharmacology and Cancer Biology, Duke University Medical Center, Durham 27710, North Carolina, USA.
Michael B Kastan
David G Kirsch

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007171 · NIGMS · DUKE UNIVERSITY · PI KONTOS, CHRISTOPHER D · 1985 to 2021
$31.2M
ROLE OF P53 IN THE CELLULAR RESPONSE TO DNA DAMAGER01ES005777 · NIEHS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI KASTAN, MICHAEL B · 1992 to 2017
$2.3M
Chromatin Modulation Associated with DNA Breakage and Repair in Human CellsR01CA159826 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI KASTAN, MICHAEL B · 2011 to 2014
$1.4M
Independent Scientist Award for Radiation ResearchK02AI093866 · NIAID · DUKE UNIVERSITY · PI KIRSCH, DAVID GUY · 2011 to 2015
$501k
Defining the cellular target of radiotherapy in primary mouse models of cancerF30CA177220 · NCI · DUKE UNIVERSITY · PI MODING, EVERETT JAMES · 2013 to 2014
$79k
NCI NIH HHS F30 CA177220NCI NIH HHS R01 CA159826NIAID NIH HHS K02 AI093866NIEHS NIH HHS R01 ES005777NIGMS NIH HHS T32 GM007171
6 · The paper itself

Abstract

Approximately 50% of all patients with cancer receive radiation therapy at some point during the course of their treatment, and the majority of these patients are treated with curative intent. Despite recent advances in the planning of radiation treatment and the delivery of image-guided radiation therapy, acute toxicity and potential long-term side effects often limit the ability to deliver a sufficient dose of radiation to control tumours locally. In the past two decades, a better understanding of the hallmarks of cancer and the discovery of specific signalling pathways by which cells respond to radiation have provided new opportunities to design molecularly targeted therapies to increase the therapeutic window of radiation therapy. Here, we review efforts to develop approaches that could improve outcomes with radiation therapy by increasing the probability of tumour cure or by decreasing normal tissue toxicity.

Indexed as

Radiotherapy, Image-GuidedRadiotherapy, Intensity-ModulatedAnimalsAntineoplastic AgentsChemoradiotherapyDose-Response Relationship, RadiationHumansNeoplasmsRadiation DosageRadiation-Protective AgentsRadiation-Sensitizing AgentsAntineoplastic AgentsRadiation-Protective AgentsRadiation-Sensitizing Agents

Identifiers

PMID23812271
PMCPMC3906736

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.