Evidence map›Paper›PMID 24803583›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2014

Toward a drug development path that targets metastatic progression in osteosarcoma.

Chand Khanna, Timothy M Fan, Richard Gorlick, Lee J Helman, Eugenie S Kleinerman, Peter C Adamson, Peter J Houghton, William D Tap, Danny R Welch, Patricia S Steeg and 22 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed
11.6field-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

94 citing papers in PubMed, 199 citations in OpenAlex.

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34 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

32 authors at 20 institutions in 4 countries.

Chand KhannaMolecular Oncology Section, Metastasis Biology; Center for Cancer Research; National Cancer Institute, NIH, Bethesda, Maryland;
Timothy M FanDepartment of Veterinary Clinical Medicine, University of Illinois at Urbana-Champaign, Urbana, Illinois; t-fan@illinois.edu.
Richard GorlickDepartment of Pediatrics and Molecular Pharmacology, The Albert Einstein College of Medicine of Yeshiva University; Division of Hematology/Oncology, Department of Pediatrics, The Children's Hospital at Montefiore, Bronx;
Lee J HelmanCenter for Cancer Research; National Cancer Institute, NIH, Bethesda, Maryland;
Eugenie S KleinermanCancer Biology and.
Peter C AdamsonDivision of Clinical Pharmacology & Therapeutics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania;
Peter J HoughtonCenter for Childhood Cancer, The Research Institute, Nationwide Children's Hospital, Columbus, Ohio;
William D TapSarcoma Oncology, Melanoma and Sarcoma Service, Memorial Sloan-Kettering Cancer Center, Weill Cornell Medical College, New York, New York; Departments of.
Danny R WelchKansas University Medical Center, Kansas City, Kansas;
Patricia S SteegLaboratory of Molecular Pharmacology; Center for Cancer Research; National Cancer Institute, NIH, Bethesda, Maryland;
Glenn MerlinoLaboratory of Cancer Biology and Genetics; Center for Cancer Research; National Cancer Institute, NIH, Bethesda, Maryland;
Poul H B SorensenDepartment of Pathology, University of British Columbia; BC Cancer Research Centre, Vancouver, British Columbia; and.
Paul MeltzerGenetics Branch; Center for Cancer Research; National Cancer Institute, NIH, Bethesda, Maryland;
David G KirschPharmacology & Cancer Biology, Duke University Medical Center, Durham, North Carolina;
Katherine A JanewayDepartment of Pediatrics, Harvard Medical School; Pediatric Oncology, Dana-Farber Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts;
Brenda WeigelDepartment of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota;
Lor RandallHuntsman Cancer Institute & Primary Children's Medical Center, University of Utah, Salt Lake City, Utah;
Stephen J WithrowFlint Animal Cancer Center, Colorado State University, Fort Collins, Colorado; Departments of.
Melissa PaoloniComparative Oncology Program; Center for Cancer Research; National Cancer Institute, NIH, Bethesda, Maryland;
Rosandra KaplanTumor Microenvironment Section, Pediatric Oncology Branch; Center for Cancer Research; National Cancer Institute, NIH, Bethesda, Maryland;
Beverly A TeicherMolecular Pharmacology Branch; Center for Cancer Research; National Cancer Institute, NIH, Bethesda, Maryland;
Nita L SeibelCancer Therapy Evaluations Program; Center for Cancer Research; National Cancer Institute, NIH, Bethesda, Maryland;
Malcolm SmithNational Cancer Institute, NIH, Bethesda, Maryland;
Aykut UrenOncology and Biochemistry and Molecular & Cellular Biology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, District of Columbia;
Shreyaskumar R PatelSarcoma Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas;
Jeffrey TrentTranslational Genomics Research Institute (TGen), Phoenix, Arizona;
Sharon A SavageClinical Genetics Branch; Center for Cancer Research; National Cancer Institute, NIH, Bethesda, Maryland;
Lisa MirabelloGenetic Epidemiology Branch, Division of Cancer Epidemiology and Genetics; Center for Cancer Research; National Cancer Institute, NIH, Bethesda, Maryland;
Denise ReinkeUniversity of Michigan Comprehensive Cancer Center, Ann Arbor, Michigan;
Donald A BarkaukasChildren's Oncology Group, QuadW-COG Childhood Sarcoma Biostatistics and Annotation Office, Monrovia;
Mark KrailoDepartment of Preventive Medicine, Keck School of Medicine at the University of Southern California, Los Angeles, California;
Mark BernsteinDepartment of Pediatrics, IWK Health Centre, Dalhousie University, Halifax, Nova Scotia, Canada.
National Cancer Institute · USAlbert Einstein College of Medicine · USChildren's Hospital of Philadelphia · USChildren's Oncology Group · CHColorado State University · USDalhousie University · CADuke Medical Center · USGeorgetown University · USHarvard University · USLaboratory of Molecular Genetics · PLMemorial Sloan Kettering Cancer Center · USNationwide Children's Hospital · USPrimary Children's Hospital · USThe University of Texas MD Anderson Cancer Center · USTranslational Genomics Research Institute · USUniversity Medical Center · USUniversity of British Columbia · CAUniversity of Illinois Urbana-Champaign · USUniversity of Michigan · USUniversity of Minnesota Medical Center · US

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
COG FOREIGN ACCRUALU10CA098543 · NCI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI ADAMSON, PETER C. · 2003 to 2013
$335.5M
Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
Characterization of the Osteosarcoma GenomeZIABC011328 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MELTZER, PAUL S. · 2010 to 2025
$28.0M
Genetic Modifiers of Cancer RiskZIACP010142 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI MIRABELLO, LISA · 2009 to 2025
$17.1M
Support for Human Specimen Banking in NCI-Supported Cancer Clinical TrialsU24CA114766 · NCI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI RAMIREZ MILAN, NILSA DEL CARMEN · 2005 to 2014
$14.5M
Molecular Biology of Pediatric TumorsZIASC006892 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI HELMAN, LEE J. · 2009 to 2017
$6.3M
Tumor and Metastasis BiologyZIABC010566 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HELMAN, LEE J. · 2009 to 2017
$4.6M
Independent Scientist Award for Radiation ResearchK02AI093866 · NIAID · DUKE UNIVERSITY · PI KIRSCH, DAVID GUY · 2011 to 2015
$501k
Intramural NIH HHS ZIA BC010566NCI NIH HHS P30 CA016672NCI NIH HHS U10 CA098543NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899NCI NIH HHS U10 CA98543NCI NIH HHS U24 CA114766NIAID NIH HHS K02 AI093866
6 · The paper itself

Abstract

Despite successful primary tumor treatment, the development of pulmonary metastasis continues to be the most common cause of mortality in patients with osteosarcoma. A conventional drug development path requiring drugs to induce regression of established lesions has not led to improvements for patients with osteosarcoma in more than 30 years. On the basis of our growing understanding of metastasis biology, it is now reasonable and essential that we focus on developing therapeutics that target metastatic progression. To advance this agenda, a meeting of key opinion leaders and experts in the metastasis and osteosarcoma communities was convened in Bethesda, Maryland. The goal of this meeting was to provide a "Perspective" that would establish a preclinical translational path that could support the early evaluation of potential therapeutic agents that uniquely target the metastatic phenotype. Although focused on osteosarcoma, the need for this perspective is shared among many cancer types. The consensus achieved from the meeting included the following: the biology of metastatic progression is associated with metastasis-specific targets/processes that may not influence grossly detectable lesions; targeting of metastasis-specific processes is feasible; rigorous preclinical data are needed to support translation of metastasis-specific agents into human trials where regression of measurable disease is not an expected outcome; preclinical data should include an understanding of mechanism of action, validation of pharmacodynamic markers of effective exposure and response, the use of several murine models of effectiveness, and where feasible the inclusion of the dog with naturally occurring osteosarcoma to define the activity of new drugs in the micrometastatic disease setting.

Indexed as

Disease Models, AnimalDrug Evaluation, PreclinicalAnimalsAntineoplastic AgentsBone NeoplasmsDisease ProgressionDogsHumansOsteosarcomaAntineoplastic Agents

Identifiers

PMID24803583
PMCPMC4134738
OpenAlexW1974879801

What OpenQuestion holds

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Registered trials

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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.