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

Prostate Cancer Clinical Trial

— PRIZE  

Official title:

PRospective, Multicenter Study to Evaluate Safety and Efficacy of Switching Treatments of Prostate Cancer Patients, Initially on Use of Monthly or Quarterly Goserelin Acetate (Zoladex®), to Semiannually Leuprorelin Acetate (Eligard®)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05304169
• Other study ID #: 1500100
• Status: Completed
• Phase: Phase 4
• Start date: November 14, 2017
• Est. completion date: June 15, 2020

Study information

• Verified date: March 2022
• Source: Zodiac Produtos Farmaceuticos S.A.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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).

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).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 48
• Est. completion date: June 15, 2020
• Est. primary completion date: June 15, 2018
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

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.

Related Conditions & MeSH terms

• Prostate Cancer
• Prostatic Neoplasms

Intervention

Drug:
• Leuprorelin Acetate (Eligard® 45 mg).
Semiannually Leuprorelin Acetate (Eligard® 45 mg).

Locations

Country	Name	City	State
Brazil	HCB - Hospital do Câncer de Barretos	Barretos	SP
Brazil	Hospital Amaral Carvalho	Jaú	SP
Brazil	CPMEC - Hospital Nossa Senhora da Conceição	Porto Alegre	RS
Brazil	CIP - Centro Integrado de Pesquisa	São José do Rio Preto	SP
Brazil	IAMSPE - Instituto de Assistência Médica ao Servidor Público Estadual de S. Paulo	São Paulo
Brazil	ICESP - Instituto do Câncer do Estado de São Paulo	São Paulo	SP

Sponsors (1)

Lead Sponsor	Collaborator
Zodiac Produtos Farmaceuticos S.A.

Country where clinical trial is conducted

Brazil, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Baseline testosterone levels (=50 ng/dL)	Maintenance of baseline testosterone levels (=50 ng/dL) after switching from goserelin acetate to leuprorelin acetate 45 mg (Eligard® 45 mg, Zodiac).	One year of treatment
Secondary	Efficacy (consecutive PSA > 4 ng/mL)	Disease progression rate from visit 2, defined as 3 consecutive elevations of PSA levels (with PSA > 4 ng/mL) and/or new clinical evidence of disease.	One year of treatment
Secondary	Adverse events frequency (%)	Collection and descriptive analysis of adverse events.	One year of treatment
Secondary	Number of Participants With Abnormal Laboratory Values (Number of participants)	Determination of the number of participants with abnormal laboratory values defined at discretion of the principal investigator according to reference values. Evaluation of hematologic, kidney and liver function.	One year of treatment
Secondary	Number of Participants With Abnormal Vital Signs (Number of participants)	Determination of the number of participants with abnormal vital signs defined at discretion of the principal investigator, according to reference values. Evaluation of vital signs (e.g. electrocardiogram, blood pressure, pulse)	One year of treatment
Secondary	Number of Participants With Abnormal Parameters for Quality of Life according to EORTC QLQ-C30 (Number of Participants)	Determination of the number of participants with abnormal parameters for quality of life at discretion of the principal investigator. Quality of life was evaluated using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30)	One year of treatment
Secondary	Number of Participants With Abnormal Parameters for Quality of Life according to EORTC QLQ-PR25 (Number of participants)	Determination of the number of participants with abnormal parameters for quality of life at discretion of the principal investigator. Quality of life was evaluated using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-PR25)	One year of treatment