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The oncolytic virus Delta-24-RGD elicits an antitumor effect in pediatric glioma and DIPG mouse models.

Naiara Martínez-VélezMarc Garcia-MoureMiguel MarigilMarisol González-HuarrizMontse PuigdellosesJaime Gállego Pérez-LarrayaMarta ZalacaínLucía MarrodánMaider Varela-GuruceagaVirginia LaspideaJose Javier AristuLuis Isaac RamosSonia Tejada-SolísRicardo Díez-ValleChris JonesAlan MackayJose A Martínez-ClimentMaria Jose García-BarchinoEric H RaabeMichelle MonjeOren J BecherMarie Pierre JunierElias A El-HabrHervé ChneiweissGuillermo AldaveHong JiangJuan FueyoAna Patiño-GarcíaCandelaria Gomez-ManzanoMarta Marija Alonso
Published in: Nature communications (2019)
Pediatric high-grade glioma (pHGG) and diffuse intrinsic pontine gliomas (DIPGs) are aggressive pediatric brain tumors in desperate need of a curative treatment. Oncolytic virotherapy is emerging as a solid therapeutic approach. Delta-24-RGD is a replication competent adenovirus engineered to replicate in tumor cells with an aberrant RB pathway. This virus has proven to be safe and effective in adult gliomas. Here we report that the administration of Delta-24-RGD is safe in mice and results in a significant increase in survival in immunodeficient and immunocompetent models of pHGG and DIPGs. Our results show that the Delta-24-RGD antiglioma effect is mediated by the oncolytic effect and the immune response elicited against the tumor. Altogether, our data highlight the potential of this virus as treatment for patients with these tumors. Of clinical significance, these data have led to the start of a phase I/II clinical trial at our institution for newly diagnosed DIPG (NCT03178032).
Keyphrases
  • high grade
  • clinical trial
  • immune response
  • low grade
  • newly diagnosed
  • electronic health record
  • big data
  • metabolic syndrome
  • risk assessment
  • inflammatory response
  • adipose tissue
  • deep learning
  • rectal cancer
  • phase iii