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Establishing a Preclinical Multidisciplinary Board for Brain Tumors.
Nimmervoll, Birgit V; Boulos, Nidal; Bianski, Brandon; Dapper, Jason; DeCuypere, Michael; Shelat, Anang; Terranova, Sabrina; Terhune, Hope E; Gajjar, Amar; Patel, Yogesh T; Freeman, Burgess B; Onar-Thomas, Arzu; Stewart, Clinton F; Roussel, Martine F; Guy, R Kipling; Merchant, Thomas E; Calabrese, Christopher; Wright, Karen D; Gilbertson, Richard J.
Affiliation
  • Nimmervoll BV; Cancer Research UK Cambridge Institute and Department of Oncology, University of Cambridge, Cambridge, England, United Kingdom.
  • Boulos N; Department of Hematology, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Bianski B; Department of Radiological Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Dapper J; Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • DeCuypere M; Department of Surgery, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Shelat A; Department of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Terranova S; Cancer Research UK Cambridge Institute and Department of Oncology, University of Cambridge, Cambridge, England, United Kingdom.
  • Terhune HE; Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Gajjar A; Department of Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Patel YT; Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Freeman BB; Preclinical Pharmacokinetics Core, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Onar-Thomas A; Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Stewart CF; Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Roussel MF; Department of Tumor Cell Biology, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Guy RK; Department of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Merchant TE; University of Kentucky College of Pharmacy, Lexington, Kentucky.
  • Calabrese C; Department of Radiological Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Wright KD; Preclinical Imaging Core, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Gilbertson RJ; Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts. richard.gilbertson@cruk.cam.ac.uk karenD_wright@dfci.harvard.edu.
Clin Cancer Res ; 24(7): 1654-1666, 2018 04 01.
Article in En | MEDLINE | ID: mdl-29301833
ABSTRACT

Purpose:

Curing all children with brain tumors will require an understanding of how each subtype responds to conventional treatments and how best to combine existing and novel therapies. It is extremely challenging to acquire this knowledge in the clinic alone, especially among patients with rare tumors. Therefore, we developed a preclinical brain tumor platform to test combinations of conventional and novel therapies in a manner that closely recapitulates clinic trials.Experimental

Design:

A multidisciplinary team was established to design and conduct neurosurgical, fractionated radiotherapy and chemotherapy studies, alone or in combination, in accurate mouse models of supratentorial ependymoma (SEP) subtypes and choroid plexus carcinoma (CPC). Extensive drug repurposing screens, pharmacokinetic, pharmacodynamic, and efficacy studies were used to triage active compounds for combination preclinical trials with "standard-of-care" surgery and radiotherapy.

Results:

Mouse models displayed distinct patterns of response to surgery, irradiation, and chemotherapy that varied with tumor subtype. Repurposing screens identified 3-hour infusions of gemcitabine as a relatively nontoxic and efficacious treatment of SEP and CPC. Combination neurosurgery, fractionated irradiation, and gemcitabine proved significantly more effective than surgery and irradiation alone, curing one half of all animals with aggressive forms of SEP.

Conclusions:

We report a comprehensive preclinical trial platform to assess the therapeutic activity of conventional and novel treatments among rare brain tumor subtypes. It also enables the development of complex, combination treatment regimens that should deliver optimal trial designs for clinical testing. Postirradiation gemcitabine infusion should be tested as new treatments of SEP and CPC. Clin Cancer Res; 24(7); 1654-66. ©2018 AACR.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Neoplasms Limits: Animals / Humans Language: En Journal: Clin Cancer Res Journal subject: NEOPLASIAS Year: 2018 Document type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Neoplasms Limits: Animals / Humans Language: En Journal: Clin Cancer Res Journal subject: NEOPLASIAS Year: 2018 Document type: Article Affiliation country: United kingdom