Early On-treatment Changes in Circulating Tumor DNA Fraction and Response to Enzalutamide or Abiraterone in Metastatic Castration-Resistant Prostate Cancer

Author:

Tolmeijer Sofie H.1ORCID,Boerrigter Emmy2ORCID,Sumiyoshi Takayuki3ORCID,Kwan Edmond M.3ORCID,Ng Sarah W.S.3ORCID,Annala Matti4ORCID,Donnellan Gráinne3ORCID,Herberts Cameron3ORCID,Benoist Guillemette E.2ORCID,Hamberg Paul5ORCID,Somford Diederik M.6ORCID,van Oort Inge M.7ORCID,Schalken Jack A.7ORCID,Mehra Niven1ORCID,van Erp Nielka P.2ORCID,Wyatt Alexander W.38ORCID

Affiliation:

1. 1Department of Medical Oncology, Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, The Netherlands.

2. 2Department of Pharmacy, Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.

3. 3Vancouver Prostate Centre, Department of Urologic Sciences, University of British Columbia, Vancouver, British Columbia, Canada.

4. 4Prostate Cancer Research Center, Faculty of Medicine and Health Technology, Tampere University and Tays Cancer Center, Tampere, Finland.

5. 5Department of Medical Oncology, Franciscus Gasthuis & Vlietland, Rotterdam/Schiedam, the Netherlands.

6. 6Department of Urology, Canisius Wilhelmina Hospital, Nijmegen, the Netherlands.

7. 7Department of Urology, Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.

8. 8Michael Smith Genome Sciences Centre, BC Cancer, Vancouver, British of Columbia, Canada.

Abstract

Abstract Purpose: Androgen receptor pathway inhibitors (ARPI) are standard of care for treatment-naïve metastatic castration-resistant prostate cancer (mCRPC), but rapid resistance is common. Early identification of resistance will improve management strategies. We investigated whether changes in circulating tumor DNA (ctDNA) fraction during ARPI treatment are linked with mCRPC clinical outcomes. Experimental Design: Plasma cell-free DNA was collected from 81 patients with mCRPC at baseline and after 4 weeks of first-line ARPI treatment during two prospective multicenter observational studies (NCT02426333; NCT02471469). ctDNA fraction was calculated from somatic mutations in targeted sequencing and genome copy-number profiles. Samples were classified into detected versus undetected ctDNA. Outcome measurements were progression-free survival (PFS) and overall survival (OS). Nondurable treatment response was defined as PFS ≤6 months. Results: ctDNA was detected in 48/81 (59%) baseline and 29/81 (36%) 4-week samples. ctDNA fraction for samples with detected ctDNA was lower at 4 weeks versus baseline (median 5.0% versus 14.5%, P = 0.017). PFS and OS were shortest for patients with persistent ctDNA at 4 weeks (univariate HR, 4.79; 95% CI, 2.62–8.77 and univariate HR, 5.49; 95% CI, 2.76–10.91, respectively), independent of clinical prognostic factors. For patients exhibiting change from detected to undetected ctDNA by 4 weeks, there was no significant PFS difference versus patients with baseline undetected ctDNA. ctDNA change had a positive predictive value of 88% and negative predictive value of 92% for identifying nondurable responses. Conclusions: Early changes in ctDNA fraction are strongly linked to duration of first-line ARPI treatment benefit and survival in mCRPC and may inform early therapy switches or treatment intensification. See related commentary by Sartor, p. 2745

Funder

Canadian Cancer Society

Prostate Cancer Foundation

ZonMw

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

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