Accelerating Drug Development in Hormone-Naïve Prostate Cancer through Multimodal Therapy Strategies: The MetaCURE Phase 2 Randomized Clinical Trial

MMT for newly diagnosed high-risk localized and low-volume metastatic prostate cancer is feasible, safe, and provides a rapid readout of efficacy. A significant proportion of patients, including those with oligometastatic disease, maintained an undetectable PSA following T-recovery at the 2-year endpoint. These results have informed the design of an adaptive trial using MMT on a continuous basis to prioritize effective approaches for further study.

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Publication Details

Journal
Clinical Cancer Research
Published
2025-11-20
DOI
https://doi.org/10.1158/1078-0432.ccr-25-2679
Primary Topic
Prostate Cancer Treatment and Research
Type
article
Field-Weighted Citation Impact
0.00
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article

Accelerating Drug Development in Hormone-Naïve Prostate Cancer through Multimodal Therapy Strategies: The MetaCURE Phase 2 Randomized Clinical Trial

Matthew C. Dallos, Eric A. Klein, Anuradha Gopalan, Christopher Gaffney et al.
Clinical Cancer Research
Prostate Cancer Treatment and Research
article

Accelerating Drug Development in Hormone-Naïve Prostate Cancer through Multimodal Therapy Strategies: The MetaCURE Phase 2 Randomized Clinical Trial

Matthew C. Dallos, Eric A. Klein, Anuradha Gopalan, Christopher Gaffney, Sean Matthew McBride, Paul Linh Nguyen, Shilpa Gupta, Hannah Benoliel, Deaglan Joseph McHugh, James Eastham, Mary‐Ellen Taplin, Sean Sachdev, Min Yuen Teo, Andres Martin Acosta, Patrick McCann, David Johnson Einstein, Andrew A. Wagner, Alvin C. Goh, Glenn J. Bubley, Scott E. Eggener, Andrea Arfè, Stanley L. Liauw, William J. Catàlona, Alicia Katherine Morgans, Adam S. Kibel, Howard I. Scher, David James VanderWeele, Russell Z. Szmulewitz, Rahul D. Tendulkar, Catherine Ryan, Karen A. Autio, Kevin M DeRudder, Irving Kaplan, Mehak Amjed
article en

Abstract

MMT for newly diagnosed high-risk localized and low-volume metastatic prostate cancer is feasible, safe, and provides a rapid readout of efficacy. A significant proportion of patients, including those with oligometastatic disease, maintained an undetectable PSA following T-recovery at the 2-year endpoint. These results have informed the design of an adaptive trial using MMT on a continuous basis to prioritize effective approaches for further study.

Clinical Cancer ResearchVol. 32(3)
Northwestern University (US), Brigham and Women's Hospital (US), Beth Israel Deaconess Medical Center (US), Cleveland Clinic (US), Memorial Sloan Kettering Cancer Center (US), University of Indianapolis (US), UCLA Health (US), Hadassah Medical Center (IL), Harvard University Press (US), Kettering University (US), University of Chicago (US), University of Chicago Medical Center (US), zuChem (United States) (US), Dana-Farber Cancer Institute (US), Grail (United States) (US), Dana-Farber Brigham Cancer Center (US), Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Indiana University – Purdue University Indianapolis (US)
Openalex Percentile: Top 49%
Prostate Cancer Treatment and Research
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