The Effect of Metformin in Patients With Newly Diagnosed mHSPC

Sponsor
Sun Yat-sen University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04925063
Collaborator
(none)
266
1
2
74.5
3.6

Study Details

Study Description

Brief Summary

The purpose of this study is to assess the effect of the addition of metformin to abiraterone on survival in patients with newly diagnosed metastatic hormone-sensitive prostate cancer. The half the patients will receive metformin in combination with androgen deprivation therapy (ADT) and abiraterone, and the other half will receive ADT and abiraterone only.

Condition or Disease Intervention/Treatment Phase
Phase 2

Detailed Description

Metastatic hormone-sensitive prostate cancer (mHSPC) can be treated with androgen-deprivation therapy (ADT) alone, ADT plus abiraterone, ADT plus enzalutamide, ADT plus apalutamide, ADT plus docetaxel. However, most patients eventually progress to castration-resistant prostate cancer (CRPC) and die of the disease. Therefore, there is still a need to improve the therapeutic effect for mHSPC.

Many studies have shown that metabolic syndrome and its components are associated with increased development and progression of aggressive prostate cancer. Metformin, a common well-tolerated oral biguanide prescribed for type II diabetes, could be used to decrease the risk of prostate cancer development and improve the efficacy of treatment. Some studies reported that metformin could enhance the effectiveness of ADT, and improve recurrence-free survival, overall survival and cancer-specific survival. A prospective randomized study reported that metformin potentially lengthen time to CRPC in advanced prostate cancer patients when combined with ADT especially in those with high risk localized prostate cancer, clinically node positive and in those with low tumor volume metastatic hormone-sensitive patients.

After extensive research, there is no published results from prospective randomized trials evaluating the effect of metformin in combination with ADT and abiraterone among patients with newly diagnosed mHSPC.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
266 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Prospective, Randomized Trial Comparing Metformin Plus Androgen Deprivation Therapy (ADT) and Abiraterone With ADT Plus Abiraterone in Newly Diagnosed Metastatic Hormone-Sensitive Prostate Cancer
Anticipated Study Start Date :
Jun 16, 2021
Anticipated Primary Completion Date :
Apr 30, 2027
Anticipated Study Completion Date :
Aug 31, 2027

Arms and Interventions

Arm Intervention/Treatment
Experimental: Metformin+ADT+abiraterone

Drug: Metformin The starting daily dose of metformin is 500mg once daily, to be increased to 2000mg once daily if tolerated until disease progression Drug: Abiraterone Abiraterone 1000mg once daily until disease progression

Drug: Metformin
The starting daily dose of metformin is 500mg once daily, and add a dose of 500mg per week until the target dose of 2000mg once daily if tolerated. Metformin will be continued until disease progression.
Other Names:
  • Metformin Hydrochloride Sustained Release Tablets
  • No Intervention: ADT+abiraterone

    Drug: Abiraterone Abiraterone 1000mg once daily until disease progression

    Outcome Measures

    Primary Outcome Measures

    1. Castration-resistant prostate cancer free survival [5 years]

      Duration from randomization to time till development of CRPC (Castration-resistant prostate cancer). CRPC is defined by disease progression despite castration level of testosterone and may present as either a biochemical progression and/or radiological progression.

    Secondary Outcome Measures

    1. Overall Survival [5 years]

      Overall survival is defined from randomization until death due to any reason.

    2. Radiographic progression-free survival [5 years]

      Radiographic progression-free survival is defined from randomization until radiographic progression.

    3. Safety [5 years]

      Adverse events will be assessed according to NCI-CTC AE 5.0.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Histologically confirmed and newly diagnosed metastatic hormone-sensitive adenocarcinoma of the prostate without small cell carcinoma or small cell components.

    • Metastatic adenocarcinoma of the prostate proved by imaging (CT/MRI and/or bone scan).

    • Patient must give written informed consent before registration and prior to any trial related investigations.

    • Age ≥18 years.

    • Serum potassium ≥3.5mmol/ L.

    • ECOG performance status 0-2

    • Ongoing androgen deprivation therapy with drugs or bilateral orchiectomy, and continuous abiraterone plus prednisone.

    • Patient agrees not to father a child during participation in the trial and during 3 months thereafter.

    • Patient agrees not to participate other interventional trials.

    • Patients are able to swallow study drug as whole tablet.

    Exclusion Criteria:
    • Diagnosed diabetes or fasting blood-glucose ≥ 6.1mmol/L, or glycosylated hemoglobin ≥ 5.6%.

    • Previous malignancy within 2 years prior to randomization, with the exception of localized non-melanoma skin cancer and Ta bladder cancer.

    • Prior treatment for prostate cancer with drugs, radiotherapy and surgery, with the exception below:

    • ADT within 3 months before randomization, and no evidence of progression.

    • Palliative radiotherapy or surgery for metastases due to symptoms, at least 4 weeks before randomization.

    • Major surgery within 4 weeks prior to randomization.

    • Treatments with 5a-reductase inhibitors, estrogen, cyproterone acetate, and androgen within 4 weeks prior to randomization.

    • Known or suspected Central nervous system CNS metastases or active leptomeningeal disease.

    • Equivalent dosage of >5mg/day prednisone of glucocorticoids for the treatment of prostate cancer within 4 weeks prior to randomization, or treatment with glucocorticoids for other reasons.

    • Prior treatment for prostate cancer with flutamide, bicalutamide, ketoconazole, abiraterone, enzalutamide, apalutamide, docetaxel chemotherapy, or other interventional drugs for prostate cancer.

    • Neutrophils < 1.5 x 109/L, platelets < 75 x 109/L, hemoglobin < 100 g/L.

    • ALT and AST ≥ 2.5 x ULN, bilirubin ≥ 1.5 x ULN.

    • eGFR<45 ml/min/1.73m2.

    • Allergic to metformin or any ingredients of this tablet.

    • Acute or chronic metabolic acidosis, including diabetic ketoacidosis.

    • Albumin< 30 g/L.

    • Clinically significant cardiovascular disease including:

    • Myocardial infarction within 6 months prior to randomization.

    • Uncontrolled angina within 3 months prior to registration.

    • Congestive heart failure NYHA class III or IV.

    • History of clinically significant ventricular arrhythmias (e.g. ventricular tachycardia, ventricular fibrillation, torsades de pointes).

    • History of Mobitz II second or third degree heart block without a permanent pacemaker in place.

    • Systolic pressure< 86 mmHg.

    • Bradycardia, heart rate<45/min.

    • Uncontrolled hypertension as indicated by systolic blood pressure > 170 mmHg OR diastolic blood pressure > 105 mmHg.

    • ADT with or without anti-androgens more than 3 months prior to randomization.

    • Prior treatment with metformin after diagnosis of prostate cancer.

    • Allergic to metformin or any drugs used in this trial.

    • Serious underlying medical condition (at the judgment of the investigator) which could impair the ability of the patient to participate in the trial (e.g. uncontrolled or acute severe infection, uncontrolled diabetes).

    • Active or symptomatic viral hepatitis or chronic liver disease.

    • History of pituitary or adrenal dysfunction.

    • Gastrointestinal disorder affecting absorption.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Sun Yat-Sen University Cancer Center Guangzhou Guangdong China 510060

    Sponsors and Collaborators

    • Sun Yat-sen University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Yonghong Li, Prinicipal Investigator, Sun Yat-sen University
    ClinicalTrials.gov Identifier:
    NCT04925063
    Other Study ID Numbers:
    • 2021-FXY-078
    First Posted:
    Jun 14, 2021
    Last Update Posted:
    Jun 14, 2021
    Last Verified:
    Jun 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Keywords provided by Yonghong Li, Prinicipal Investigator, Sun Yat-sen University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 14, 2021