ARCTIC: Liquid Biomarkers in the Prospective Androgen Receptor Signaling Inhibitors (ARSI) Resistance Clinical Trials

Официальное название

Clinical Validation of a Circulating Tumor Cell AR Therapy Resistance Assay in Men With Metastatic Castration Resistant Prostate Cancer (ARCTIC)

Обзор

This study will follow men with metastatic castration resistant prostate cancer throughout their standard of care treatment for their disease to determine if the presence of different genes or proteins can predict which patients respond to the cancer treatment they receive. As tumors grow and begin to spread, they may release cells into patients' bloodstream. These cells are called "circulating tumor cells", or CTCs. CTCs can be used to look for differences in "biomarkers" (genes or proteins that may change based on how a person is or is not responding to treatment). The purpose of this research study is to learn whether scientists can use biomarkers from CTCs to predict which tumors will respond to certain hormonal therapies. Participants will have blood collected and provide an archival sample from a previous tumor biopsy. The researchers will compare biomarkers from participants who responded well to treatment to those who responded poorly in order to answer the research question.

Первичные конечные точки

• Comparison of progression-free survival (PFS) between biomarker positive and negative participants [Срок оценки: Through completion of participant participation, up to 3 years]

Вторичные конечные точки (5)

• Comparison of overall survival between biomarker positive and negative participants [Срок оценки: Through completion of participant participation, up to 3 years]
• Comparison of the proportion of participants that achieve a >50% PSA declines from baseline between biomarker positive and negative participants [Срок оценки: Through completion of participant participation, up to 3 years]
• Comparison of soft tissue response between biomarker positive and negative participants [Срок оценки: Through completion of participant participation, up to 3 years]
• Comparison of duration of therapy between biomarker positive and negative participants [Срок оценки: Through discontinuation of current therapy, up to 3 years]
• Number of emergent molecular lesions in CTCs that consistently emerge during subsequent AR therapy progression in men with mCRPC [Срок оценки: At disease progression, up to 3 years]

Критерии участия

Критерии включения

Patients will be eligible for inclusion in this study only if all of the following criteria apply:

• Histologically confirmed diagnosis of adenocarcinoma of the prostate. Patients with pure small cell/neuroendocrine tumors of the prostate are not permitted.
• Radiographic evidence of metastatic disease by CT, MRI, or PET imaging.
• Prior documented disease progression on one potent AR inhibitor (darolutamide, abiraterone, enzalutamide, or apalutamide or combinations of these) in any disease setting (mHSPC, nmCRPC, mCRPC) based on sequential PSA rises or radiographic progression.
• Planned therapy with either standard of care enzalutamide and/or abiraterone acetate or another potent AR inhibitor (darolutamide, apalutamide if available) within the coming 6 weeks
• Castrate levels of testosterone (<50 ng/dl) at most recent assessment and/or documented ongoing Androgen Deprivation Therapy.
• Evidence of disease progression based on a rising PSA on or following most recent therapy as evidenced by the following:

• Consecutive PSA rises at least 2 weeks apart
• Minimum PSA of 1.0 ng/dl prior to entry
• Age > 18 years.
• Ability to understand and the willingness to sign a written informed consent document.

Критерии исключения

A patient will not be eligible for inclusion in this study if any of the following criteria apply:

• History of intercurrent or past medical or psychiatric illness including active stage IV malignancy that would make participation in a blood drawing protocol difficult or not feasible at the discretion of the principal investigator or co-investigator(s).
• Unwillingness to be followed longitudinally for serial CTC biomarker studies.
• Life expectancy < 6 months
• Planned combination therapy with radiation or other systemic therapies other than ADT and bone health agents.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения

Когортное

Центры проведения

США · 3 центра

• Memorial Sloan Kettering Cancer Center — New York
• Duke University Medical Center — Durham
• University of Wisconsin-Madison — Madison

Идентификаторы

NCT: NCT06141993 · Pro00111532

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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