| Literature DB >> 32816849 |
Qu Zhang1, Jia Luo2, Han Si1, Shaad E Abdullah3, Brandon W Higgs1, Todd Hembrough1, Song Wu1, Chen Gao4, Wenjing Xu4, Phillip A Dennis3, Michiel S van der Heijden5, Neil H Segal6, Jamie E Chaft2,7, J Carl Barrett1, Matthew D Hellmann8,7,9.
Abstract
The utility of circulating tumor DNA (ctDNA) as a biomarker in patients with advanced cancers receiving immunotherapy is uncertain. We therefore analyzed pretreatment (n = 978) and on-treatment (n = 171) ctDNA samples across 16 advanced-stage tumor types from three phase I/II trials of durvalumab (± the anti-CTLA4 therapy tremelimumab). Higher pretreatment variant allele frequencies (VAF) were associated with poorer overall survival (OS) and other known prognostic factors, but not objective response, suggesting a prognostic role for patient outcomes. On-treatment reductions in VAF and lower on-treatment VAF were independently associated with longer progression-free survival and OS and increased objective response rate, but not prognostic variables, suggesting that on-treatment ctDNA dynamics are predictive of benefit from immune checkpoint blockade. Accordingly, we propose a concept of "molecular response" using ctDNA, incorporating both pretreatment and on-treatment VAF, that predicted long-term survival similarly to initial radiologic response while also permitting early differentiation of responders among patients with initially radiologically stable disease. SIGNIFICANCE: In a pan-cancer analysis of immune checkpoint blockade, pretreatment ctDNA levels appeared prognostic and on-treatment dynamics predictive. A "molecular response" metric identified long-term responders and adjudicated benefit among patients with initially radiologically stable disease. Changes in ctDNA may be more dynamic than radiographic changes and could complement existing trial endpoints.This article is highlighted in the In This Issue feature, p. 1775. ©2020 American Association for Cancer Research.Entities:
Year: 2020 PMID: 32816849 DOI: 10.1158/2159-8290.CD-20-0047
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 39.397