Prostate cancer is the most common cancer in men in the United States, with about one in eight men diagnosed during their lifetime. Many prostate cancers grow slowly and may never cause problems, while others are aggressive and require immediate treatment. Current options include surgery, radiation, hormone therapy, and chemotherapy, with treatment decisions depending on how fast the cancer is growing and whether it has spread.
What's actually going on in research
Trials are testing PARP inhibitors for men with specific DNA repair gene mutations, new hormonal agents that work after standard hormone therapy stops working, radiopharmaceuticals that deliver radiation directly to cancer cells, and immunotherapies including CAR-T cells and checkpoint inhibitors. Researchers are also studying ways to identify which slow-growing cancers can be safely watched rather than immediately treated.
PARP inhibitors
Olaparib and rucaparib are FDA-approved for advanced prostate cancer with BRCA mutations. Trials are testing whether these drugs work earlier in treatment and in men with other DNA repair gene changes.
Radiopharmaceuticals
Lutetium-177-PSMA-617 was FDA-approved in 2022 and delivers radiation directly to prostate cancer cells. Studies are testing whether it works earlier in treatment and in combination with other drugs.
Tumor-targeting immunotherapy
Trials are testing CAR-T cells engineered to attack PSMA, a protein found on most prostate cancer cells. Other studies combine checkpoint inhibitors with vaccines or DNA-damaging drugs to help the immune system recognize the cancer.
What to know before you search
Eligibility typically depends on whether the cancer is localized or has spread, PSA level, prior treatments, specific gene mutations like BRCA1 or BRCA2, and performance status.
What types of trials are currently open
- Hormonal therapy trials — Testing new drugs that block testosterone in different ways, often for men whose cancer has stopped responding to standard hormone therapy.
- Targeted therapy trials — Testing drugs aimed at specific mutations, like PARP inhibitors for BRCA mutations or drugs targeting the PI3K pathway.
- Immunotherapy trials — Testing treatments that help the immune system attack prostate cancer, including vaccines, checkpoint inhibitors, and CAR-T cells.
- Radiation trials — Testing new forms of radiation therapy, including radiopharmaceuticals that travel through the bloodstream to reach cancer cells throughout the body.
- Active surveillance studies — Following men with slow-growing prostate cancer closely with PSA tests and biopsies to determine who can safely delay treatment.
Recently added Prostate Cancer trials
Receive imaging scans during prostate cancer surgery to detect remaining cancer cells
Radical prostatectomy (RP) is currently one of the gold standard of care in managing localized prostate cancer (Pca). However, despite advances in Robot-Assisted RP (RARP), cancer cells may still be found (up to 42%) at the edge of the removed prostate specimen, commonly referred as Positive Surgical Margins (PSM). PSM are well-known risk factors of adverse oncological outcomes (biochemical recurrence). It is therefore essential to characterize intraoperatively the tumor extent. In RARP, the leading intraoperative margin assessment (IMA) technique, NeuroSAFE is based on Intra-operative frozen section (IFS) of both prostate lateral sides sampled at 3-5 mm intervals. However, despite proven oncological benefit, adoption is still limited to expert centers due to a prolonged operative time, loss of integrity of the surgical specimen for definitive histopathological analysis, omission of regions (apex, base), and logistical complexity (trained uropathologist, cryostat…). With this prospective single-center project, we wish to explore the use of non-invasive optical imaging technology, HyperSpectral Imaging (HSI), as a reliable alternative for examination of the ex-vivo prostate specimen to 1. Distinguish normal versus tumor tissue at the surgical margin in fresh specimen. 2. Quantify whether HSI can be integrated into the intraoperative workflow (feasibility), thus, image acquisition time and inference time should then be evaluated.
Donate a blood sample to help develop personalized tumor models
This is a study : * Single-center * Prospective * Translational * Based on data and blood samples. In this context, the aim is to collect approximately 10 ml of blood from each patient included in the 3D tumoroid development project. The main objective is to establish and validate a panel of vascularized and perfused 3D tumoroids for personalized medicine based on patient tumors for urological cancers, incorporating autologous immune cells. Translated with DeepL.com (free version)
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