EVOLUTION: 177Lu-PSMA Therapy Versus 177Lu-PSMA in Combination With Ipilimumab and Nivolumab for Men With mCRPC

Prostate Cancer Clinical Trial

— ANZUP2001  

Official title:

Phase II Study of Radionuclide 177Lu-PSMA Therapy Versus 177Lu-PSMA in Combination With Ipilimumab and Nivolumab for Men With MetastaticCastration Resistant Prostate Cancer (mCRPC)

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05150236
• Other study ID #: ANZUP 2001
• Status: Active, not recruiting
• Phase: Phase 2
• Start date: April 29, 2022
• Est. completion date: December 2024

Study information

• Verified date: December 2023
• Source: Australian and New Zealand Urogenital and Prostate Cancer Trials Group
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This phase II study will investigate the activity and safety of radionuclide 177Lu-PSMA therapy versus 177Lu-PSMA in combination with Ipilimumab and Nivolumab in patients with metastatic castrate resistant prostate cancer (mCRPC).

Description:

This is an open label, randomised, stratified, multicentre phase 2 clinical trial recruiting 110 participants over 18 months and followed for 12 months. Participants will be randomised to 177Lu-PSMA in combination with Ipilimumab and Nivolumab and 177Lu-PSMA alone in a 2:1 ratio (using minimisation with a random component) stratified by prior exposure to docetaxel.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 93
• Est. completion date: December 2024
• Est. primary completion date: August 31, 2024
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Aged 18 years or older, with histologically confirmed adenocarcinoma of the prostate.

2. Castration-resistant metastatic prostate cancer (defined as disease progressing despite castration by orchidectomy or ongoing luteinising hormone-releasing hormone agonist or antagonist).

3. Patients must have progressed on prior novel AR targeted agents for treatment of prostate cancer. Progressive disease defined by at least one of the following:

• PSA progression, minimum of two rising PSA values from a baseline measurement with an interval of = 1 week between each measurement. The PSA value at screening should be = 5ng/ml

• Soft tissue or visceral disease progression as per RECIST 1.1

• Bone progression: = 2 new lesions on bone scan as per PCWG3

4. Target or non-target lesions according to RECIST 1.1 and PCWG3

5. Significant PSMA avidity on PET/CT using 68GaPSMA, defined as SUVmax =15 at a site of disease, and SUVmax = 10 at other sites of disease =10mm (where there is no impact from partial voluming.

6. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.

7. Adequate bone marrow, hepatic and renal function documented within 28 days of registration, defined as:

• Haemoglobin =90 g/L independent of transfusions (no red blood cell transfusion in last 4 weeks)

• Absolute neutrophil count =1.5x109/L

• Platelets =100 x109/L

• Total bilirubin =1.5 x upper limit of normal (ULN) except for patients with known Gilbert's syndrome

• Aspartate transaminase (AST/SGOT) and alanine transaminase (ALT/SGPT) =2.5 × ULN or =5 × ULN for participants with liver metastases

• Serum creatinine =1.5 x ULN or a calculated creatinine clearance > 50mL/min (Cockcroft-Gault equation)

8. Patients must have a life expectancy = 24 weeks.

9. Willing and able to comply with all study requirements, including treatment, timing and/or nature of required assessments

10. Signed, written informed consent.

Exclusion Criteria:

1. Prostate cancer with known significant sarcomatoid, spindle cell or neuroendocrine cell components, or metastasis of other cancers to the prostate.

2. 18F-FDG-PET/CT SUVmax =10 at a site of measurable disease with no concurrent PSMA expression > 10mm

3. Prior treatment with anti-PD1, anti-PD-L1/L2, anti-CTLA-4 antibody, or any other antibody or drug specifically targeting T cell co-stimulation or checkpoint pathways.

4. Patients must not have had more than one line of chemotherapy. If a patient has had docetaxel chemotherapy for hormone sensitive or castrate resistant setting, this will be considered one line.

5. Prior treatment with 177Lu-PSMA.

6. Patients with active, known, or suspected autoimmune disease. Sjogren's syndrome is considered an autoimmune disease. Exceptions: Patients with vitiligo, type I diabetes mellitus, residual hypothyroidism due to an autoimmune condition only requiring hormone replacement, or conditions not expected to recur in the absence of an external trigger, may be eligible.

7. Patients with a condition requiring systemic treatment with either corticosteroids (>10mg daily prednisone equivalents) or other immunosuppressive medications within 14 days of registration. Inhaled or topical steroids, and adrenal replacement doses = 10 mg daily prednisone equivalents are permitted in the absence of active autoimmune disease.

8. Participants must have recovered from all AE due to previous therapies to =Grade 1 or baseline. Participants with = Grade 2 neuropathy may be eligible.

9. Active malignancies within the previous 2-years with >30% probability of recurrence within 1 year. Melanoma in situ, basal cell or squamous cell carcinomas of skin, are permitted.

10. Significant infection, including chronic active hepatitis B, hepatitis C, or HIV. Testing for these is not mandatory unless clinically indicated.

11. Radiation or surgery within 2 weeks of randomisation.

12. Previous history of interstitial lung disease or non-infectious pneumonitis.

13. Administration of a live vaccine within 30 days prior to the first dose of study drug.

14. Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.

15. Inadequate contraception. Men must have been surgically sterilised or use a (double if required) barrier method of contraception.

Related Conditions & MeSH terms

• Genital Neoplasms, Male
• Neoplasms
• Neoplasms by Site
• Prostate Cancer
• Prostatic Disease
• Prostatic Diseases
• Prostatic Neoplasms
• Urogenital Neoplasms

Intervention

Drug:
• 177Lu-PSMA-617
Patients will be given 7.5GBq of Lu-PSMA every 6 weeks up to 6 cycles unless there is unacceptable toxicity, commencing following result of 68Ga-PSMA PET within 28 days of registration.
• Ipilimumab
Patients will be given 3mg/kg of Ipilimumab every 6 weeks up to 4 doses unless there is unacceptable toxicity, concurrently with Lu-PSMA and Nivolumab.
• Nivolumab
Patients will be given 1mg/kg of Nivolumab every 3 weeks up to 8 doses, concurrently with Lu-PSMA and Ipilimumab unless there is unacceptable toxicity. Followed by 480mg nivolumab monotherapy commencing at week 32. Nivolumab monotherapy will be given to patients every 4 weeks up to 18 doses, or until disease progression or unacceptable toxicity.

Locations

Country	Name	City	State
Australia	Royal Adelaide Hospital	Adelaide	South Australia
Australia	St Vincents Hospital	Darlinghurst	New South Wales
Australia	Austin Health	Heidelberg	Victoria
Australia	Royal Brisbane and Womens hospital	Herston	Queensland
Australia	Alfred Hospital	Melbourne	Victoria
Australia	Peter MacCallum Cancer Centre	Melbourne	Victoria
Australia	Sir Charles Gairdner	Nedlands	Western Australia
Australia	Calvary Mater Newcastle	Newcastle	New South Wales

Sponsors (5)

Lead Sponsor	Collaborator
Australian and New Zealand Urogenital and Prostate Cancer Trials Group	Advanced Accelerator Applications, Bristol-Myers Squibb, Prostate Cancer Foundation of Australia, University of Sydney

Country where clinical trial is conducted

Australia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Association between Clinical Outcomes and Possible Prognostic/Predictive Biomarkers (tissue and circulating) including PBMCs, ctDNA and CTCs	Translational research will include identifying tissue and circulating biomarkers that are prognostic and/or predictive of response to treatment, safety and resistance to study treatment.; These include but are not limited to analyses of: PBMC samples may be used for immunophenotyping or characterisation of the immune cell subsets in the periphery; ctDNA, immunological markers, and response data will be used to prospectively investigate the utility of early changes in ctDNA levels; CTCs may be enumerated and analysed for their potential to predict or correlate with toxicity and efficacy of immune checkpoint inhibitors.	Date of randomisation through to study completion, approximately 3 years from start of recruitment.
Primary	PSA progression free survival (PSA-PFS) at 1 year (PCWG3)	PSA progression is defined as a rise in PSA by = 25% AND = 2 ng/mL above the nadir (lowest PSA point). This needs to be confirmed by a repeat PSA performed at least 3 weeks later.	Date of randomisation to the date of first evidence of PSA progression at 53 weeks post randomisation.
Secondary	PSA response rate (PSA-RR)	PSA response rate is defined as the proportion of participants in each group with a PSA reduction of = 50% from baseline.	Date of randomisation through to study completion, approximately 3 years from start of recruitment. Early rises in PSA prior to 12 weeks will be disregarded in determining PSA response.
Secondary	Frequency and severity of adverse events (CTCAE v5.0)	CTCAE v5.0 will be used to measure frequency and severity of AEs during study treatment.	Date of first dose of study treatment until 100 days after cessation of study treatment.
Secondary	Radiological progression free survival (PCWG3/RECIST1.1)	Radiographic PFS is defined as the interval from the date of randomisation to the date of first evidence of radiographic progression, or the date of last known follow-up without progression.	Date of randomisation to the date of first evidence of progression on imaging (PCWG3 criteria for bone lesions and RECIST 1.1 for soft tissue lesions) assessed every 12 weeks through to study completion, approximately 3 years from start of recruitment.
Secondary	PSA progression free survival (PCWG3)	PSA progression free survival is defined as the interval from the date of randomisation to the date of first evidence of PSA progression or the date of last known follow-up without PSA progression.	Date of randomisation through to study completion, approximately 3 years from start of recruitment.
Secondary	Overall survival (OS)	OS is defined as the interval from the date of randomisation to date of death from any cause, or the date of last known follow-up alive.	Through to study completion, approximately 3 years from start of recruitment.
Secondary	Objective response rate (ORR)	ORR is defined as partial or complete response at any stage of the study (from the date of randomisation to date of subsequent anti-cancer treatment). RECIST 1.1 will be used to assess ORR in participants with measurable disease.	Date of randomisation through to study completion, approximately 3 years from start of recruitment.
Secondary	Duration of response	Duration of response is defined as the interval from the date of first response (Complete Response / Partial Response as per RECIST 1.1) to the date of first documented radiological progression as per RECIST 1.1 in participants with measurable disease.	Date of randomisation through to first radiological progression or through to study completion, approximately 3 years from start of recruitment.
Secondary	Time to treatment response	Time to treatment response is defined as the interval from the date of randomisation to the date of first response (Complete Response / Partial Response as per RECIST 1.1) in participants with measurable disease.	Date of randomisation through to study completion, approximately 3 years from start of recruitment.
Secondary	Aspects of Health Related Quality of Life (HRQoL) - 1	The EORTC QLQ-C30 (European Organisation for Research on Treatment of Cancer - Quality of Life Questionnaire for cancer patients) instrument uses 28 questions about overall quality of life with each question answerable using a scale from 1 (not at all) to 4 (very much). Overall scores can be from a minimum of 28 indicating a better quality of life and higher scores with a maximum of 112 indicating lower overall quality of life. The questionnaire also has two summary questions which asks participants to rank 1) overall health and 2) overall quality of life on scale of from 1 (very poor) to 7 (excellent).	Within 7 days prior to randomisation, assessed every 12 weeks, through to study completion, approximately 3 years from start of recruitment.
Secondary	Aspects of Health Related Quality of Life (HRQoL) - 2	Patient DATA Form (Patient Disease and Treatment Assessment Form - 47 items) is a simple, multi-item quality of life instrument based on 11-point numeric rating scales for a range of relevant symptoms and functions. It combines cancer specific items from the UBQ-C, GLQ-8 and LASA cancer-specific quality of life instruments.	Within 7 days prior to randomisation, assessed every 12 weeks, through to study completion, approximately 3 years from start of recruitment.