Actively Recruiting
The Case of "Triple" Versus "Double" Therapy for Patients With High Volume Metastatic Hormone Sensitive Prostate Cancer
Led by Uppsala University · Updated on 2025-03-04
1400
Participants Needed
2
Research Sites
375 weeks
Total Duration
On this page
Sponsors
U
Uppsala University
Lead Sponsor
U
Uppsala University Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
Lead4Care is an observational, open-label, multicenter study evaluating the effectiveness, tolerance, and cost-effectiveness of triple against double therapy in matched groups of mHSPC patients with high tumor burden. In addition to androgen deprivation therapy (ADT), the triple constitutes of docetaxel and novel hormonal therapy (NHT), and the double of NHT therapy in addition to ADT. Their effectiveness is compared in terms of mortality and morbidity, which is captured by HRQoL, pain, fatigue. Potential side effects are captured by neuropathy, diarrhea, constipation, anxiety, sickness, and dyssomnia. The cost-effectiveness is evaluated within a Markov model from a societal perspective in which the main disease stages are mHSPC, mCRPC and death. In connection with a regular visit in hospital care, prostate cancer patients who in addition to ADT will initiate double or triple therapy are offered participation in the study. If the patient consent on-line, the patient will receive 13 online surveys over a 60-month period. The surveys are sent with an interval of two months for the first six months, quarterly thereafter until two years, and thereafter yearly. Once all participants have been recruited, the baseline data shared by healthcare personnel and patients will be enriched with registry data. This baseline and registry data involves information about the patients' historical and current health- and socioeconomic status. Thereby, Lead4Care will be able to identify comparable groups of patients on triple and double treatments by using advanced matching methods. In order to assure an objective analysis, Lead4Care will not allow any data extraction until Lead4Care has predefined and published all details regarding the comparison. The existing protocol is then complemented with a more detailed description of the comparison groups, the hierarchy of outcomes, and the analysis methods for these outcomes. For these treatments, the main objectives are to: * Compare mortality and morbidity on triple and double therapy, and their relative side-effects. * Capture patient preferences for these different treatment outcomes over time. * Evaluate cost-effectiveness of triple versus double therapy from a societal perspective.
CONDITIONS
Official Title
The Case of "Triple" Versus "Double" Therapy for Patients With High Volume Metastatic Hormone Sensitive Prostate Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients who have started triple or double therapy no longer than 3 months from the start of androgen deprivation therapy
- Patients must have metastatic hormone-sensitive prostate cancer with high metastatic burden at enrollment
- Patients must be 18 years or older at the time of enrollment
- Novel hormonal therapy may include abiraterone acetate, apalutamide, darolutamide, or enzalutamide
You will not qualify if you...
- Patients who do not understand written or spoken instructions in Swedish
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Uppsala University Hospital
Uppsala, Region Uppsala, Sweden, 751 85
Not Yet Recruiting
2
Uppsala University
Uppsala, Uppsala County, Sweden, 753 10
Actively Recruiting
Research Team
S
Sophie Langenskiöld, SRLECT & PhD
CONTACT
V
Vincent Nordgren, PhD-student
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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