4.8 Article

Molecular Features of Cancers Exhibiting Exceptional Responses to Treatment

Journal

CANCER CELL
Volume 39, Issue 1, Pages 38-+

Publisher

CELL PRESS
DOI: 10.1016/j.ccell.2020.10.015

Keywords

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Funding

  1. Intramural Research Program of the NIH, National Cancer Institute, Center for Cancer Research
  2. Center for Cancer Genomics, National Cancer Institute
  3. NCI, NIH
  4. LEIDOS [HHSN261200800001E/17X184TO1]
  5. Nationwide Children's Hospital on LEIDOS [HHSN261200800001E/14X242TO1]
  6. NCI [HHSN261201700005I/TO1]
  7. IMS on NCI [HHSN26120150002B/TO10]
  8. University of Chicago (Genomic Data Center) on NCI [HHSN261200800001E/17X147TO2]
  9. NIH/NCI [U24 CA210969]
  10. NIH (Program in Translational Medicine) [T32 GM122741]
  11. [5U24CA143843]
  12. [5 U24 CA210988]

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Genomic analysis has identified molecular mechanisms for exceptional responses to cancer therapy in a small fraction of patients with advanced disease, including DNA damage response, intracellular signaling, immune engagement, and genetic alterations. These analyses have revealed synthetic lethal relationships and rare genetic lesions that favor therapeutic success, providing valuable insights into oncogenic mechanisms influencing the response to cancer therapy.
A small fraction of cancer patients with advanced disease survive significantly longer than patients with clinically comparable tumors. Molecular mechanisms for exceptional responses to therapy have been identified by genomic analysis of tumor biopsies from individual patients. Here, we analyzed tumor biopsies from an unbiased cohort of 111 exceptional responder patients using multiple platforms to profile genetic and epigenetic aberrations as well as the tumor microenvironment. Integrative analysis uncovered plausible mechanisms for the therapeutic response in nearly a quarter of the patients. The mechanisms were assigned to four broad categories-DNA damage response, intracellular signaling, immune engagement, and genetic alterations characteristic of favorable prognosis- with many tumors falling into multiple categories. These analyses revealed synthetic lethal relationships that may be exploited therapeutically and rare genetic lesions that favor therapeutic success, while also providing a wealth of testable hypotheses regarding oncogenic mechanisms that may influence the response to cancer therapy.

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