№ files_lp_3_process_7_017084
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Public funding announcement outlining eligibility, financial conditions, reporting obligations, and application procedures for prostate cancer research grants in Newfoundland and Labrador for 2026.
Year:
2026
Region:
Newfoundland and Labrador
Subject:
Prostate cancer research funding
Document Type:
Call for research proposals
Issuing Organization:
Prostate Cancer Fight Foundation (PCFF)
Partner Organization:
Ride For Dad (Avalon and Gander Chapters)
Total Funding Available:
$29,000
Typical Grant Value:
$20,000–$50,000
Grant Duration:
12 months
Application Deadline:
February 28, 2026
Eligible Applicants:
Individuals, academics, institutions, affiliated foundations
Purpose:
Support research or seed funding for new clinical initiatives related to prostate cancer
Prohibited Expenses:
Administration or overhead costs, equipment purchases, travel, sabbatical leaves, conferences, seminars, living expenses, general information pamphlets, for-profit projects
Reporting Requirements:
Public announcement within one month; 100-word public update every 6 months; final lay summary
Review Process:
Peer review by Medical Advisory Board
Fund Disbursement Period:
Within 12 months of award
Contact Person:
Peter Wallace, Co-Chair
Contact Email:
[email protected]
Website:
www.ridefordad.ca
Price: 8 / 10 USD
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Year:
2026
Region / City:
N/A
Topic:
Prostate Brachytherapy Post-Treatment Care
Document Type:
Medical Instruction
Institution:
N/A
Author:
N/A
Target Audience:
Patients undergoing prostate HDR brachytherapy
Effective Period:
N/A
Approval Date:
N/A
Modification Date:
N/A
Year:
2011
Region / City:
United States
Topic:
Prostate Cancer, Disability Benefits
Document Type:
Questionnaire
Author:
REDACTED
Target Audience:
Veterans, Healthcare Providers
Period of Validity:
Not specified
Approval Date:
11/02/2010
Revision Date:
4/1/2011, 4/7/2011
Year:
2023
Region / City:
UK
Subject:
Decision Aid, BPH
Document Type:
Report
Organization / Institution:
NHS England
Author:
Winton Centre for Risk & Evidence Communication
Target Audience:
Clinicians, patients
Period of validity:
Not specified
Approval Date:
Not specified
Date of modifications:
Not specified
Year:
2024
Region:
Greater Manchester, UK
Topic:
Prostate cancer management
Document type:
Clinical protocol
Organization:
GM Cancer Urology Pathway Board
Author:
A Webber, GM Trusts subgroup
Target audience:
Healthcare professionals in urology and oncology
Date of review:
April 2024
Next review date:
April 2025
Version:
1.2
References:
NICE NG131 guidelines, BAUS guidelines, NHS Long Term Plan for Cancer, NHSE Personalised Care for Cancer Initiative, GM Cancer Plan
Year:
2026
Region / city:
N/A
Topic:
Prostate cancer trials
Document type:
Call for proposals
Organization / institution:
N/A
Author:
N/A
Target audience:
Researchers and healthcare professionals
Action period:
Until 13 February 2026
Approval date:
N/A
Date of amendments:
N/A
Organisation:
Canberra Health Services
Department:
Radiation Oncology Department
Document Type:
Clinical Procedure
Clinical Focus:
Prostate Fiducial Marker Implant
Patient Group:
Adult patients
Professional Scope:
Registered Nurses (RNs)
Standards Referenced:
Australian College of Perioperative Nurses (ACORN) Standards
Related Facility:
Canberra Hospital
Procedure Context:
Radiation therapy preparation
Setting:
Brachytherapy bunker theatre
Type:
Educational assessment
Subject:
Prostate cancer staging, pathology, and clinical management
Medical focus:
Oncology; Urology
Content format:
Multiple-choice questions and case-based scenarios
Key topics:
Gleason score; PSA testing; Clinical staging (cT); CS Extension codes; SSF codes; Prostatectomy findings; Active surveillance; Imaging modalities
Referenced source:
http://cancerbulletin.facs.org/forums/showthread.php?6644-SSF-12-amp-13-Prostate
Year:
2026
Organization:
Prostate Cancer Fight Foundation/Ride For Dad
Document Type:
Grant Application Form
Subject:
Prostate Cancer Research Funding
Application Deadline:
February 28, 2026
Submission Method:
Email submission of completed form
Contact Person:
Peter Wallace
Contact Email:
[email protected]
Eligible Applicants:
Principal Investigators and research teams
Geographic Scope:
Canada
Funding Restrictions:
No administrative costs permitted
Reporting Requirements:
Semi-annual and final project reports required for previous recipients
Public Disclosure:
Lay and scientific abstracts agreed to be publicly available
Additional Requirements:
Photo and brief bio sketch to be submitted separately
Year:
2025
Region / City:
United States
Subject:
Prostate cancer biomarker test coverage
Document Type:
Guidelines
Organization:
Health Evidence Review Commission (HERC)
Author:
Health Evidence Review Commission (HERC)
Target Audience:
Healthcare providers, policymakers
Period of Validity:
2025 and ongoing
Approval Date:
December 2021
Date of Changes:
January 2025
Year:
2021
Region / city:
India
Topic:
Prostate Cancer Radiation Therapy
Document type:
Survey
Organization / institution:
N/A
Author:
N/A
Target audience:
Radiation Therapists
Effective period:
N/A
Approval date:
N/A
Date of amendments:
N/A
Year:
Not specified
Region / City:
Not specified
Topic:
Medical procedure, prostate biopsy
Document Type:
Consent form
Author:
Not specified
Target Audience:
Patients undergoing prostate biopsy
Period of Validity:
Not specified
Approval Date:
Not specified
Modification Date:
Not specified
Context:
A medical consent form outlining the risks, benefits, and procedure of transrectal ultrasound and prostate biopsy.
Year:
2026
Region / City:
Not specified
Topic:
Cancer genomics, epigenetics, prostate cancer
Document type:
Supplementary material
Institution:
Not specified
Authors:
Chennan Li et al.
Target audience:
Researchers in oncology and molecular biology
Sample type:
Plasma and buffy coat
Methods:
ctDNA sequencing, 5mC/5hmC methylomics, clonal reconstruction
Timepoints:
Baseline, restaging, progression, off-study
Genes analyzed:
AR, BRCA2, erythroid markers, platelet/megakaryocyte markers, globins
Data included:
Sequencing metrics, methylation percentages, gene-level events, survival analysis
Associated figures:
8 supplementary figures, 2 supplementary tables
Statistical analyses:
Spearman correlation, Kruskal-Wallis test, Mann-Whitney U test, Kaplan-Meier survival estimates, log-rank test
Year:
[Insert year]
Region / city:
[Insert region/city]
Subject:
Medical treatment request
Document type:
Authorization request letter
Institution:
[Insert institution name]
Author:
[Physician’s name]
Target audience:
Medical/Pharmacy Director
Effective period:
[Insert effective period]
Approval date:
[Insert approval date]
Date of modifications:
[Insert modification date]
Diagnosis:
[Insert diagnosis]
Treatment:
ERLEADA® (apalutamide)
Clinical trial:
TITAN trial
Clinical guidelines reference:
NCCN Guidelines®, AUA/SUO Guidelines
Patient history:
[Insert patient history]
Risk of disease progression:
[Insert risk]
Adverse reactions:
Rash, hot flush, hypertension, arthralgia, pruritus
Publication reference:
Journal of Clinical Oncology
Study data source:
Precision Point Specialty (PPS) Analytics, Komodo Research Database
Study design:
Retrospective, longitudinal, head-to-head analysis
Outcome:
Overall survival at 24 months
Document type:
Supplementary tables from a scientific research study
Research field:
Oncology; Cancer genomics
Disease focus:
Prostate cancer
Study design:
Retrospective cohort analysis
Cohorts included:
JHMI; Mayo; TJU; Durham; Kaiser; BWH; TCGA
Tissue type:
Radical prostatectomy specimens and biopsy samples
Total sample sizes:
Cohorts ranging from 100 to 355 patients
Clinical variables:
Age at diagnosis; PSA at diagnosis; Gleason Grade Group; ADT treatment status; metastatic outcome or recurrence; follow-up duration
Statistical measures:
Adjusted p-values after FDR multiple test correction; hazard ratios; confidence intervals; p-values
Genetic markers analyzed:
DNA repair signatures; immune cell signatures; mismatch repair genes; neuroendocrine markers; multiple individual genes (e.g., PMS2, MLH1, ESR1, SOX2)
Outcome measures:
Metastatic progression or recurrence
Statistical models:
Batch-stratified competing risks regression
Key variables in regression:
AR-A expression level; Gleason grade ≥8; surgical margins; PSA level; age at radical prostatectomy; ADT treatment type; extracapsular extension; seminal vesicle invasion; lymph node invasion
Follow-up period:
Median follow-up ranging from 28 to 108 months across cohorts
Year:
2023
Region / City:
USA
Subject:
Cancer Research, Prostate Cancer, Dietary Supplements
Document Type:
Research Article
Author:
Anait S. Levenson
Target Audience:
Researchers, Oncologists, Medical Professionals
Period of Action:
Not specified
Date of Approval:
Not specified
Date of Changes:
Not specified
Year:
2023
Region / city:
UK
Theme:
Oncology, Lung Cancer, Treatment Guidelines
Document type:
Clinical guidelines
Organization / institution:
NICE
Author:
NICE
Target audience:
Healthcare professionals
Period of validity:
Not specified
Approval date:
Not specified
Date of changes:
Not specified
Contextual description:
Detailed clinical guidelines outlining the recommended systemic treatments for advanced non-small-cell lung cancer based on disease progression and previous therapies.
Year:
2023
Region / City:
United States
Subject:
Cancer Care Delivery, Oncology Research
Document Type:
Submission Worksheet
Organization / Institution:
National Cancer Institute (NCI)
Author:
NCI Protocol Information Office
Target Audience:
Researchers, Investigators, Study Coordinators
Period of Validity:
Ongoing
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2023
Region / City:
United Kingdom
Theme:
Colorectal Cancer Referral Guidelines
Document Type:
Medical Guidelines
Organization:
National Health Service (NHS)
Author:
National Institute for Health and Care Excellence (NICE), British Society of Gastroenterology (BSG), Association of Coloproctology of Great Britain and Ireland (ACPGBI)
Target Audience:
Healthcare professionals in primary and secondary care
Effective Period:
From August 2023
Date of Approval:
August 2023
Date of Amendments:
None mentioned
Year:
2025
Region / City:
North West NHS GMS region
Topic:
ctDNA testing for NSCLC and breast cancer
Document Type:
Notification
Organization:
NHS England
Author:
Genomics Unit
Target Audience:
NHS Trusts
Period of Action:
2025/26 financial year
Approval Date:
7 November 2025
Date of Changes:
N/A
Context:
Notification regarding the continuation and expansion of ctDNA testing for lung and breast cancer in the North West NHS region for the 2025/26 financial year.
Service:
Lung Cancer Whole Pathway
Document type:
Commissioning guidance
Health system:
NHS England
Period:
2024/25
Date of review:
April 2026
Scope:
Direct and specialised commissioning
Clinical focus:
Lung cancer
Geographical context:
United Kingdom
Policy context:
NHS Long Term Plan
Related pathway:
National Optimal Lung Cancer Pathway
Commissioning themes:
Early diagnosis, reducing variation, living with cancer
Evidence base:
NICE guidance and national standards