RecruitingPhase 3NCT06439225

Platinum and Taxane Chemo in Met Castration Resistant Prostate Cancer Patients With Alterations in DNA Damage Response Genes

A Randomized Phase III Trial Investigating Platinum and Taxane Chemotherapy in Metastatic Castration Resistant Prostate Cancer Patients With Alterations in DNA Damage Response Genes


Sponsor

Canadian Cancer Trials Group

Enrollment

236 participants

Start Date

Dec 30, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The usual approach for most patients who are not in a study is treatment with docetaxel. This study is being done to answer the following question: Can the chance of prostate cancer growing or spreading be lowered by adding a drug to the usual approach? This study is being done to find out if this approach is better or worse than the usual approach for prostate cancer. The usual approach is defined as the care most people get for prostate cancer.


Eligibility

Sex: MALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests whether platinum and taxane chemotherapy (a standard chemotherapy combination) works in patients with metastatic castration-resistant prostate cancer (cancer that continues to grow despite low testosterone) who have specific inherited or acquired DNA repair gene mutations, such as BRCA1, BRCA2, or ATM. **You may be eligible if...** - You have prostate cancer that is metastatic and no longer responding to hormone therapy (castration-resistant) - Your tumor or blood testing has confirmed a qualifying DNA repair gene mutation (e.g., BRCA1, BRCA2, ATM, CDK12, or similar) - You have previously received an advanced hormone therapy (ARPI) such as enzalutamide, abiraterone, or apalutamide - Your testosterone levels are below 50 ng/dL (castration levels) - Your cancer has progressed on imaging or via rising PSA levels **You may NOT be eligible if...** - Your cancer has neuroendocrine or small cell features - You have not yet recovered from prior treatment toxicities - You have not had adequate washout time from prior therapies Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGDocetaxel

75mg/m2 q21 days

DRUGCarboplatin

AUC5 q21 days


Locations(14)

Arthur J.E. Child Comprehensive Cancer Centre

Calgary, Alberta, Canada

Cross Cancer Institute

Edmonton, Alberta, Canada

BCCA - Vancouver

Vancouver, British Columbia, Canada

William Osler Health System

Brampton, Ontario, Canada

Waterloo Regional Health Network (WRHN)

Kitchener, Ontario, Canada

London Health Sciences Centre Research Inc.

London, Ontario, Canada

Ottawa Hospital Research Institute

Ottawa, Ontario, Canada

Odette Cancer Centre

Toronto, Ontario, Canada

University Health Network

Toronto, Ontario, Canada

CHUM-Centre Hospitalier de l'Universite de Montreal

Montreal, Quebec, Canada

The Jewish General Hospital

Montreal, Quebec, Canada

CHU de Quebec-Hopital l'Enfant-Jesus (HEJ)

Québec, Quebec, Canada

Allan Blair Cancer Centre

Regina, Saskatchewan, Canada

Saskatoon Cancer Centre

Saskatoon, Saskatchewan, Canada

View Full Details on ClinicalTrials.gov

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NCT06439225


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