Local Ablative Therapy For Hormone Sensitive Oligometastatic Prostate Cancer

Prostate Cancer Metastatic Clinical Trial

— PLATON  

Official title:

A Randomized Phase III Trial of Local Ablative Therapy For Hormone Sensitive Oligometastatic Prostate Cancer [PLATON]

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03784755
• Other study ID #: PR20
• Status: Recruiting
• Phase: N/A
• Start date: November 15, 2019
• Est. completion date: July 30, 2027

Study information

• Verified date: April 2024
• Source: Canadian Cancer Trials Group
• Contact: Wendy Parulekar
• Phone: 613-533-6430
• Email: wparulekar[@]ctg.queensu.ca
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to compare the effects of ablative therapy (radiation or surgery) to all sites of disease combined with standard treatments on prostate cancer, compared to the standard or usual treatments used to treat this disease.

Description:

The standard or usual treatment for this disease is systemic therapy, which includes androgen deprivation therapy (ADT) with or without chemotherapy or hormone therapy. Additionally, for some patients with specific disease features, standard treatment may also include ablative treatment (radiation or surgery) of the prostate gland if this was not completed prior to enrolling into this study.

Ablative Therapy is a procedure used to destroy cancer cells and tissue. In this study Stereotactic Body Radiation Therapy (SBRT) or surgery will be used to destroy prostate cancer metastases. It is not clear if ablative therapy (SBRT or surgery) to all sites of disease used in combination with standard systemic therapy can offer better results than standard treatment alone.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 410
• Est. completion date: July 30, 2027
• Est. primary completion date: December 31, 2026
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologic diagnosis/confirmation of prostate adenocarcinoma and no evidence of small cell cancer.

• Stage IV at presentation or relapse after curative intent therapy, classification per AJCC 8th edition: M1 disease with = 5 metastases

• = 3 metastases in any non-bone organ system

• Zoladex must commence within 12 weeks prior to randomization or within 12 weeks after randomization.

• Radiology (CT/MRI chest/abdomen/pelvis) within 42 days of randomization

• Bone scan within 42 days of randomization

• All tumours (Primary prostate and metastases) must be amenable to local ablative therapy (radiation and/or surgery).

• Age = 18

• ECOG performance 0-2

• Patient is able (i.e. sufficiently fluent) and willing to complete the quality of life and economics questionnaires in either English or French

• Patient consent must be appropriately obtained in accordance with applicable local and regulatory requirements. Each patient must sign a consent form prior to enrollment in the trial to document their willingness to participate

• Patients must be medically suitable for study treatments as assessed by the appropriate specialties: medical, radiation, and surgical

• Patients with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen

• Patients must be accessible for treatment and follow-up. Investigators must assure themselves the patients randomized on this trial will be available for complete documentation of the treatment, adverse events, and follow-up

• In accordance with CCTG policy, ablative therapy to metastases is to begin within 6 weeks after patient randomization

• Men of childbearing potential must have agreed to use a highly effective contraceptive method to prevent pregnancy while on study

• Patient must consent to provision of, and Investigator must confirm location of and commit to obtain a representative formalin fixed paraffin block of tumour tissue in order that the specific correlative studies described in the protocol may be conducted. Where tissue exists but local centre regulations prohibit submission of blocks of tumour tissue, the approval of the CCTG must be sought prior to randomization of the first patient to allow cores (two 2 mm cores of tumour from the block) and slides (20 x 5 micron thick unstained slides) of representative tumour tissue to be substituted

• Patient must consent to provision of samples of whole blood (for cfDNA) in order that the specific correlative studies described in the protocol may be conducted.

Exclusion Criteria:

• Prior treatment with ADT in the neoadjuvant or adjuvant setting, unless treatment was discontinued = 12 months prior to randomization AND total duration of treatment was = 36 months (including expiry of last depot injection).

• Previously diagnosed recurrent/metastatic disease which has been already treated with any systemic therapy or radiotherapy with palliative intent.

• Castration resistant prostate cancer, defined as rising PSA (per PCWG3) or radiographic progression in the setting of castrate levels of serum testosterone (< 1.7 nmol/L).

• Patients who present with de novo stage IV disease with pelvic lymphadenopathy as their only site of metastases (N1 M0), where the primary prostate has never been treated with curative intent prostate surgery or radiotherapy in the past.

• Inability to treat all sites of disease with local ablative therapy

• Patients with parenchymal brain metastases

Related Conditions & MeSH terms

• Prostate Cancer Metastatic
• Prostatic Neoplasms

Intervention

Radiation:
• Ablative Radiation Therapy
Undergo stereotactic radiotherapy and/or surgery to all sites of disease (oligometastases and primary prostate if previously untreated).

Other:
• Standard of care
Patients continue to receive their current planned systemic therapy at the discretion of the treating physician

Locations

Country	Name	City	State
Canada	Royal Victoria Regional Health Centre	Barrie	Ontario
Canada	QEII Health Sciences Centre	Halifax	Nova Scotia
Canada	Juravinski Cancer Centre at Hamilton Health Sciences	Hamilton	Ontario
Canada	Trillium Health Partners - Credit Valley Hospital	Mississauga	Ontario
Canada	CHUM-Centre Hospitalier de l'Universite de Montreal	Montreal	Quebec
Canada	CIUSSS de l'Est-de-I'lle-de-Montreal	Montreal	Quebec
Canada	The Jewish General Hospital	Montreal	Quebec
Canada	Ottawa Hospital Research Institute	Ottawa	Ontario
Canada	Hotel-Dieu de Quebec	Quebec City	Quebec
Canada	Allan Blair Cancer Centre	Regina	Saskatchewan
Canada	Saskatoon Cancer Centre	Saskatoon	Saskatchewan
Canada	Algoma District Cancer Program	Sault Ste. Marie	Ontario
Canada	Health Sciences North	Sudbury	Ontario
Canada	Odette Cancer Centre	Toronto	Ontario
Canada	University Health Network	Toronto	Ontario
Canada	BCCA - Victoria	Victoria	British Columbia
Canada	CancerCare Manitoba	Winnipeg	Manitoba

Sponsors (2)

Lead Sponsor	Collaborator
Canadian Cancer Trials Group	Canadian Cancer Society (CCS)

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Failure-free Survival	defined as the time from randomization to the time of the first occurrence.	6 years
Secondary	Radiographic Progression-free Survival	the comparison of these outcomes between the two treatment arms will be tested by the log-rank test	6 years
Secondary	Incidence of new metastases as first event	the comparison of these outcomes between the two treatment arms will be tested by the log-rank test	6 years
Secondary	Overall Survival	the comparison of these outcomes between the two treatment arms will be tested by the log-rank test	6 years
Secondary	Ablative treatment related adverse events (>/= grade 3) using CTCAE v5.0		6 years
Secondary	Quality of Life measured by EORTC QLQ-C30	It consists of both multi-item scales and single item measures, including five functioning domains, a global quality of life domain, three symptom domains and six single items. For each domain or single item measure a linear transformation will be applied to standardize the raw score to range between 0 and 100	6 years
Secondary	Quality of Life measured by Bone Metastases module (BM22)	The BM22 has 22 questions consisting of the 4 subscales (painful sites (PS) and pain characteristics (PC) on the symptom scale and functional interference (FI) and psychosocial aspects (PA) on the functional scale). Modules, relevant subscales will also be linear transformed to standardize the raw score to range between 0 and 100 in accordance with the EORTC scoring manuals.	6 years
Secondary	Quality of Life measured by prostate (PR25) questionnaire module	has 25 questions in four domains (urinary, bowel, sexual, and hormonal). Modules, relevant subscales will also be linear transformed to standardize the raw score to range between 0 and 100 in accordance with the EORTC scoring manuals.	6 years
Secondary	Economic analysis measured by EQ-5D-5L	The robustness of the model results will be assessed using one-way and multi-way sensitivity analyses. Major drivers of medical care costs, namely hospitalization, chemotherapy and survival, will be varied ± 20%, to examine the impact on the base-case incremental cost effectiveness ratios (ICERs). Bootstrapping and the development of a cost-effectiveness acceptability curve will also be conducted.	6 years
Secondary	Economic analysis by determining an incremental cost-effectiveness ratio reported as a difference in cost per FFS-year between the 2 arms		6 years