Study to Evaluate the Safety and Efficacy of Switching From Zoladex® Monthly or Quarterly, to Eligard® Semiannual. (PRIZE)

Zodiac Produtos Farmaceuticos

Status and phase: Completed; Phase 4

Conditions: Prostate Cancer

Treatments: Drug: Leuprorelin Acetate (Eligard® 45 mg).

Study type: Interventional

Funder types: Industry

Identifiers

NCT05304169

1500100

Details and patient eligibility

About

The purpose of this study is to evaluate the efficacy, quality of life and safety of switching from monthly (3.6 mg) or quarterly (10.8 mg) goserelin acetate (Zoladex®) to semiannual leuprorelin acetate 45 mg (Eligard® 45 mg) in prostate cancer patients with adequate hormonal castration level (plasma testosterone levels ≤50 ng/dL).

Full description

When systemic treatment is indicated, androgen deprivation therapy is the standard treatment for patients with prostate cancer. This condition occurs when the patient is diagnosed with metastatic disease or disseminated disease based on PSA values.The exchange of androgen hormone deprivation therapies in patients with metastatic prostate cancer may be required in different situations in clinical practice, such as: lack of medication available at the institution or on the market; alteration of the clinical protocol of the health institution due to economic factors and/or aiming to gain adherence to the treatment, often related to the posological convenience and/or logistics necessary for the administration of the medication, among others.

Additionally, although there is evidence on the efficacy and safety of switching hormone treatments in patients with prostate cancer clinical data on this type of management of patients in Brazil are scarce. There are no data on how the management and switching of treatments is approached, nor on the clinical outcomes related to such a switch of therapy (time to progression, treatments used in combination with androgen deprivation therapy, time to onset of disease symptoms, time to start chemotherapy and costs involved).

Enrollment: 48 patients

Sex: Male

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Patient able to understand the process of the informed consent form (ICF);

2. Male aged ≥18 years old;

3. Having a histologically confirmed diagnosis of prostate adenocarcinoma;

4. Having an indication of androgen deprivation treatment:

   1. Being on treatment with monthly or quarterly goserelin acetate depot formulation for at least 3 months and for a maximum of 18 months OR;
   2. Having an indication to start treatment with quarterly goserelin acetate depot formulation.

5. Patient with ECOG (Eastern Cooperative Oncology Group) performance status 0 to 2;

6. Patient with appropriate castration level, defined by a serum testosterone level ≤50 ng/dL (≤1.73 nmol/L) demonstrated before V1.

7. Appropriate hematologic function in the screening period: neutrophil count >1,500/μL, platelets >100,000/μL, hemoglobin >10 g/dL;

8. Appropriate liver function in the screening period of the study: total serum bilirubin ≤1.5 x upper normal limit, AST (aspartate aminotransferase) or ALT (alanine aminotransferase) ≤40 U/L, alkaline phosphatase <130 U/L, gamma-GT (glutamyl transferase) <100 U/L;

9. Appropriate kidney function in the screening period of the study: serum urea within normal limits for the method used at the institution, serum creatinine between 0.6 and 1.3 mg/dL, creatinine clearance calculated by the Cockroft- Gault formula > 40 mL/min;

Exclusion criteria

1. Patients who did not have or do not have an indication for treatment with goserelin acetate;
2. Patients with goserelin treatment for over 18 months;
3. Patients who have received previous chemotherapy;
4. Patient unable to follow the foreseen study visit schedule;
5. Suspected or proven brain metastasis or active leptomeningeal disease;
6. Uncontrolled arterial hypertension defined as systolic pressure ≥160 mmHg or diastolic pressure ≥95 mmHg;
7. Long-term use of estrogen therapy or peripheral blockade;
8. Another concomitant neoplasm;
9. Any medical condition which, at the investigator's discretion, offers risk to the patient's participation in the study;
10. Having participated in another clinical study within less than 12 months.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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48 participants in 1 patient group

Leuprorelin Acetate (Eligard® 45 mg)

Experimental group

Description:

Patients received two subcutaneous injections of Eligard® 45 mg (leuprorelin acetate), with the first injection given at baseline (Visit 1) and the second after 168 ± 3 days at Visit 4.

Treatment:

Drug: Leuprorelin Acetate (Eligard® 45 mg).