Prostate Cancer Clinical Trials

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Towards Optimal Treatment for High Risk Prostate Cancer; Stereotactic Pelvic Radiotherapy with Focal Boost to the Primary Tumour

Status: Recruiting
Location: See location...
Intervention Type: Radiation
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to combine several optimized treatments of high risk prostate cancer. The main question to answer is: is it safe to combine these optimized treatments. * patients will be irradiated on the prostate and (elective) lymph nodes more concentrated but with fewer hospital visits (hypofractionation) * the tumor will get a higher dose * androgen deprivation therapy will be reduced as much al possible preventing side effects Researchers will compare oncological outcome and toxicity.

Eligibility
Participation Requirements
Sex: Male
Minimum Age: 18
Healthy Volunteers: f
View:

• Men (aged ≥18 years of age) diagnosed within 6 months before inclusion with high risk prostate cancer:

‣ T3 based on digital rectal examination AND/OR

⁃ Grade \>= 4 AND/OR

⁃ PSA \>=20 ug/L

• Indication for elective lymph node irradiation (based on current clinical guidelines) OR N1 on imaging (with a maximum of 4 suspect lymph nodes)

Locations
Other Locations
Netherlands
Haaglanden Medical Centre
RECRUITING
Leidschendam
Contact Information
Primary
Ursula J Fisscher, PhD
u.fisscher@haaglandenmc.nl
0031889792357
Backup
Mirjam E Mast, PhD
m.mast@haaglandenmc.nl
+31 88 9792357
Time Frame
Start Date: 2024-01-02
Estimated Completion Date: 2032-12-18
Participants
Target number of participants: 207
Treatments
Experimental: HYPOPRIME treatment
Hypo fractionated pelvic radiotherapy with boost to primary tumour in the prostate with elective lymph node irradiation and minimized androgen deprivation therapy
Related Therapeutic Areas
Sponsors
Leads: Haaglanden Medical Centre
Collaborators: Tata Memorial Centre

This content was sourced from clinicaltrials.gov