Evidence map›Paper›PMID 28993414›Full record

ReviewCancer research2017

A Collaborative Model for Accelerating the Discovery and Translation of Cancer Therapies.

Ophélia Maertens, Mila E McCurrach, Benjamin S Braun, Thomas De Raedt, Inbal Epstein, Tannie Q Huang, Jennifer O Lauchle, Hyerim Lee, Jianqiang Wu, Timothy P Cripe and 4 more

Open access · greenAbstract readReview
In one paragraph

Review in Cancer research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. A Comprehensive Review on Schisandrin B and Its Biological Properties.Oxidative medicine and cellular longevity · 2020
    Review
  12. Article
  13. Article
  14. Review
  15. Emerging therapeutic targets for neurofibromatosis type 1.Expert opinion on therapeutic targets · 2018
    Review
  16. Article
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

14 authors at 3 institutions in 1 country.

Ophélia MaertensGenetics Division, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Mila E McCurrachChildren's Tumor Foundation, New York, New York.
Benjamin S BraunDepartment of Pediatrics and Comprehensive Cancer Center, University of California, San Francisco, California.
Thomas De RaedtGenetics Division, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Inbal EpsteinDepartment of Pediatrics and Comprehensive Cancer Center, University of California, San Francisco, California.
Tannie Q HuangDepartment of Pediatrics and Comprehensive Cancer Center, University of California, San Francisco, California.
Jennifer O LauchleDepartment of Pediatrics and Comprehensive Cancer Center, University of California, San Francisco, California.
Hyerim LeeChildren's Tumor Foundation, New York, New York.
Jianqiang WuDivision of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Dept. of Pediatrics, University of Cincinnati, Cincinnati, Ohio.
Timothy P CripeNationwide Children's Hospital, Hematology & Oncology, Columbus, Ohio.
D Wade ClappHerman Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana.
Nancy RatnerDivision of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Dept. of Pediatrics, University of Cincinnati, Cincinnati, Ohio.
Kevin ShannonDepartment of Pediatrics and Comprehensive Cancer Center, University of California, San Francisco, California.
Karen CichowskiGenetics Division, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts. kcichowski@rics.bwh.harvard.edu.
Harvard University · USDana-Farber/Harvard Cancer Center · USGenentech

Funding

Translational InformaticsP30CA082103 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Kate Taylor Shumate · 1999 to 2026
$209.7M
Project 4: Secondary Cancers Among NF1 Cancer SurvivorsU54CA196519 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI Yunlong Liu · 2015 to 2026
$26.9M
MITOGENIC ACTIVITIES IN NEUROFIBROMATOSISR01NS028840 · NINDS · UNIVERSITY OF CINCINNATI · PI NANCY RATNER · 1990 to 2026
$10.1M
Elucidating the Regulation and Function of the NF1 tumor suppressorR01CA111754 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI KAREN M CICHOWSKI · 2005 to 2026
$7.4M
Xenograft Core for NF1 Experimental TherapeuticsP50NS057531 · NINDS · CINCINNATI CHILDRENS HOSP MED CTR · PI CRIPE, TIMOTHY P · 2008 to 2012
$6.8M
Research Training in Childhood CancerT32CA128583 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Eric Alejandro Sweet-Cordero · 2007 to 2026
$6.0M
Translational Investigation of KRas & NF1 in Myeloid LeukemiaR37CA072614 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SHANNON, KEVIN M. · 2007 to 2016
$3.4M
Preclinical Testing of Targeted Therapies for NeurofibromasU01NS055849 · NINDS · INDIANA UNIVERSITY INDIANAPOLIS · PI CLAPP, DAVID W · 2008 to 2011
$2.4M
Elucidating the role of new RasGAP tumor suppressors in cancerR01CA188659 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI CICHOWSKI, KAREN M · 2014 to 2018
$1.7M
Mechanisms linking RAS signals to disordered hematopoiesis and myeloid neoplasiaR01CA173085 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BRAUN, BENJAMIN · 2013 to 2017
$1.6M
NCI NIH HHS P30 CA082103NCI NIH HHS R01 CA111754NCI NIH HHS R01 CA173085NCI NIH HHS R01 CA188659NCI NIH HHS R37 CA072614NCI NIH HHS T32 CA128583NCI NIH HHS U54 CA196519NINDS NIH HHS P50 NS057531NINDS NIH HHS R01 NS028840NINDS NIH HHS U01 NS055849
6 · The paper itself

Abstract

Preclinical studies using genetically engineered mouse models (GEMM) have the potential to expedite the development of effective new therapies; however, they are not routinely integrated into drug development pipelines. GEMMs may be particularly valuable for investigating treatments for less common cancers, which frequently lack alternative faithful models. Here, we describe a multicenter cooperative group that has successfully leveraged the expertise and resources from philanthropic foundations, academia, and industry to advance therapeutic discovery and translation using GEMMs as a preclinical platform. This effort, known as the Neurofibromatosis Preclinical Consortium (NFPC), was established to accelerate new treatments for tumors associated with neurofibromatosis type 1 (NF1). At its inception, there were no effective treatments for NF1 and few promising approaches on the horizon. Since 2008, participating laboratories have conducted 95 preclinical trials of 38 drugs or combinations through collaborations with 18 pharmaceutical companies. Importantly, these studies have identified 13 therapeutic targets, which have inspired 16 clinical trials. This review outlines the opportunities and challenges of building this type of consortium and highlights how it can accelerate clinical translation. We believe that this strategy of foundation-academic-industry partnering is generally applicable to many diseases and has the potential to markedly improve the success of therapeutic development.

Indexed as

Disease Models, AnimalAnimalsDrug DiscoveryHumansMiceMolecular Targeted TherapyNeoplasmsNeurofibromatosis 1Translational Research, Biomedical

Identifiers

PMID28993414
PMCPMC5668167
OpenAlexW2762643060

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.