Xenograft models for pediatric cancer therapies

Fac Rev. 2021 Feb 2:10:11. doi: 10.12703/r/10-11. eCollection 2021.

Abstract

The prognosis for childhood cancer has improved considerably over the past 50 years. This improvement is attributed to well-designed clinical trials which have incorporated chemotherapy, surgery, and radiation. With an increased understanding of cancer biology and genetics, we have entered an era of precision medicine and immunotherapy that provides potential for improved cure rates. However, preclinical evaluation of these therapies is more nuanced, requiring more robust animal models. Evaluation of targeted treatments requires molecularly defined xenograft models that can capture the diversity within pediatric cancer. The development of novel immunotherapies ideally involves the use of animal models that can accurately recapitulate the human immune response. In this review, we provide an overview of xenograft models for childhood cancers, review successful examples of novel therapies translated from xenograft models to the clinic, and describe the modern tools of xenograft biobanks and humanized xenograft models for the study of immunotherapies.

Keywords: Xenograft; immunotherapy; pediatric cancer; precision medicine; preclinical model.

Publication types

  • Review

Grants and funding

David Teachey was supported by funds from the National Institutes of Health (NIH) grant RO1 CA193776/CA/NCI NIH HHS/United States. Kevin McNerney was supported by the National Center for Advancing Translational Sciences of the NIH under award number TL1TR001880. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.