Prediction of plasma ctDNA fraction and prognostic implications of liquid biopsy in advanced prostate cancer
Fonseca, Nicolette M.; Maurice-Dror, Corinne; Herberts, Cameron; Tu, Wilson; Fan, William; Murtha, Andrew J.; Kollmannsberger, Catarina; Kwan, Edmond M.; Parekh, Karan; Schönlau, Elena; Bernales, Cecily Q.; Donnellan, Gráinne; Ng, Sarah W.S.; Sumiyoshi, Takayuki; Vergidis, Joanna; Noonan, Krista; Finch, Daygen L.; Zulfiqar, Muhammad; Miller, Stacy; Parimi, Sunil; Lavoie, Jean Michel; Hardy, Edward; Soleimani, Maryam; Nappi, Lucia; Eigl, Bernhard J.; Kollmannsberger, Christian; Taavitsainen, Sinja; Nykter, Matti; Tolmeijer, Sofie H.; Boerrigter, Emmy; Mehra, Niven; van Erp, Nielka P.; De Laere, Bram; Lindberg, Johan; Grönberg, Henrik; Khalaf, Daniel J.; Annala, Matti; Chi, Kim N.; Wyatt, Alexander W. (2024)
Fonseca, Nicolette M.
Maurice-Dror, Corinne
Herberts, Cameron
Tu, Wilson
Fan, William
Murtha, Andrew J.
Kollmannsberger, Catarina
Kwan, Edmond M.
Parekh, Karan
Schönlau, Elena
Bernales, Cecily Q.
Donnellan, Gráinne
Ng, Sarah W.S.
Sumiyoshi, Takayuki
Vergidis, Joanna
Noonan, Krista
Finch, Daygen L.
Zulfiqar, Muhammad
Miller, Stacy
Parimi, Sunil
Lavoie, Jean Michel
Hardy, Edward
Soleimani, Maryam
Nappi, Lucia
Eigl, Bernhard J.
Kollmannsberger, Christian
Taavitsainen, Sinja
Nykter, Matti
Tolmeijer, Sofie H.
Boerrigter, Emmy
Mehra, Niven
van Erp, Nielka P.
De Laere, Bram
Lindberg, Johan
Grönberg, Henrik
Khalaf, Daniel J.
Annala, Matti
Chi, Kim N.
Wyatt, Alexander W.
2024
1828
Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-202407197683
https://urn.fi/URN:NBN:fi:tuni-202407197683
Kuvaus
Peer reviewed
Tiivistelmä
No consensus strategies exist for prognosticating metastatic castration-resistant prostate cancer (mCRPC). Circulating tumor DNA fraction (ctDNA%) is increasingly reported by commercial and laboratory tests but its utility for risk stratification is unclear. Here, we intersect ctDNA%, treatment outcomes, and clinical characteristics across 738 plasma samples from 491 male mCRPC patients from two randomized multicentre phase II trials and a prospective province-wide blood biobanking program. ctDNA% correlates with serum and radiographic metrics of disease burden and is highest in patients with liver metastases. ctDNA% strongly predicts overall survival, progression-free survival, and treatment response independent of therapeutic context and outperformed established prognostic clinical factors. Recognizing that ctDNA-based biomarker genotyping is limited by low ctDNA% in some patients, we leverage the relationship between clinical prognostic factors and ctDNA% to develop a clinically-interpretable machine-learning tool that predicts whether a patient has sufficient ctDNA% for informative ctDNA genotyping (available online: https://www.ctDNA.org). Our results affirm ctDNA% as an actionable tool for patient risk stratification and provide a practical framework for optimized biomarker testing.
Kokoelmat
- TUNICRIS-julkaisut [19236]