Evidence map›Paper›PMID 24485463›Full record

ArticleCell2014

Mathematical modeling of PDGF-driven glioblastoma reveals optimized radiation dosing schedules.

Kevin Leder, Ken Pitter, Quincey LaPlant, Dolores Hambardzumyan, Brian D Ross, Timothy A Chan, Eric C Holland, Franziska Michor

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 137 papers.

0numbers the graph read from it
0cells of the map it votes in
137citing papers in PubMed
20.2field-weighted citation impact, top 1% of its field
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

137 citing papers in PubMed, 279 citations in OpenAlex.

  1. Review
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  8. 75 Years of Mathematical Oncology.bioRxiv : the preprint server for biology · 2026
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77 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 1 country.

Kevin Leder *Department of Industrial and Systems Engineering, University of Minnesota, Minneapolis, MN 55455, USA.
Ken Pitter *Brain Tumor Center, Department of Cancer Biology and Genetics, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
Quincey LaPlantBrain Tumor Center, Department of Cancer Biology and Genetics, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
Dolores HambardzumyanDepartments of Neurosciences and Molecular Medicines, Cleveland, OH 44195, USA.
Brian D RossCenter for Molecular Imaging and Department of Radiology, University of Michigan, Ann Arbor, MI 48109, USA.
Timothy A ChanHuman Oncology and Pathogenesis Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
Eric C HollandDivision of Human Biology, Alvord Brain Tumor Center, University of Washington, Seattle, WA 98109, USA.
Franziska MichorDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Memorial Sloan Kettering Cancer Center · USHarvard University · USUniversity of Michigan–Ann Arbor · USUniversity of Minnesota · USUniversity of Washington · US

Funding

Weill Cornell/Rockefeller/Sloan-Kettering MST ProgramT32GM007739 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI HSU, KATHARINE C · 1985 to 2023
$51.1M
QUANTITATION OF HUMAN BRAIN TUMOR THERAPY RESPONSE BY MRP01CA085878 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ROSS, BRIAN D. · 2001 to 2017
$31.9M
The Cell-Of-Origin of Human CancersU54CA143798 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI MICHOR, FRANZISKA · 2009 to 2014
$11.2M
The Proneural Perivascular Niche and Therapeutic ResponseU54CA163167 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI HUSE, JASON · 2011 to 2015
$4.6M
P3IK Signaling and Biology of Therapeutic Response in Brain and Prostate TumorsU01CA141502 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI HOLLAND, ERIC C. · 2009 to 2013
$4.2M
The Role of Signaling Pathways in Brain Tumors in MiceR01CA100688 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI HOLLAND, ERIC C. · 2003 to 2013
$3.8M
Characterizing the functional stem-like properties of primary and recurrent gliomF31NS076028 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI PITTER, KENNETH L · 2011 to 2013
$141k
NCI NIH HHS P01 CA085878NCI NIH HHS R01 CA100688NCI NIH HHS U01 CA141502NCI NIH HHS U01 CA141502-01NCI NIH HHS U54 CA143798NCI NIH HHS U54 CA163167NIGMS NIH HHS T32 GM007739NINDS NIH HHS F31 NS076028
6 · The paper itself

Abstract

Glioblastomas (GBMs) are the most common and malignant primary brain tumors and are aggressively treated with surgery, chemotherapy, and radiotherapy. Despite this treatment, recurrence is inevitable and survival has improved minimally over the last 50 years. Recent studies have suggested that GBMs exhibit both heterogeneity and instability of differentiation states and varying sensitivities of these states to radiation. Here, we employed an iterative combined theoretical and experimental strategy that takes into account tumor cellular heterogeneity and dynamically acquired radioresistance to predict the effectiveness of different radiation schedules. Using this model, we identified two delivery schedules predicted to significantly improve efficacy by taking advantage of the dynamic instability of radioresistance. These schedules led to superior survival in mice. Our interdisciplinary approach may also be applicable to other human cancer types treated with radiotherapy and, hence, may lay the foundation for significantly increasing the effectiveness of a mainstay of oncologic therapy. PAPERCLIP:

Indexed as

Radiation DosageAnimalsBrain NeoplasmsGlioblastomaHumansMiceModels, Biological

Identifiers

PMID24485463
PMCPMC3923371
OpenAlexW2139183953

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.