- Recruiting
- Observational
- Drug
- Uppsala University
- 18 Years -
Study Purpose
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.
Intervention
Drug : ADT + NHT + Docetaxel
Drug : ADT + NHT
Eligibility Requirements
Patients eligible for inclusion in this study must meet all of the following criteria:
Patients should have initiated triple or double therapy no longer than 3 months from the start of ADT,
Patients must have mHSPC at the time of enrolment, and high metastatic burden.
Patients must be ≥ 18 years old at the time of enrolment. Note: NHT could be abiraterone acetate, apalutamide, darolutamide or enzalutamide.
Minimum age: 18
Participants meeting any of the of the following criteria are not eligible for inclusion:
Patients who do not understand written and/or oral instructions in Swedish.
Recruiting status
Recruiting
Estimated enrollment
1400
Study start date
Oct 20, 2024
Study end date
Dec 31, 2031
Last updated
Mar 23, 2025
Primary purpose
N/A
Design
Observational
Intervention
Drug
Study phase
N/A
Allocation
N/A
Sponsor:
Uppsala University
Collaborator:
Uppsala University Hospital
University Hospital, Umeå
Sahlgrenska University Hospital
Saint Göran Hospital
Swedish Cancer Society
Uddevalla Hospital
Östersund Hospital
Ryhov County Hospital
Mälarsjukhuset Hospital, Eskilstuna
Västmanlands Hospital, Västerås, Sweden
Gävle Hospital
Investigator:
Sophie Langenskiöld, SRLECT & PhD
Publications
N/A
Websites
N/A
NCT06446401
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