A Trial of 177Lu-PSMA617 Theranostic Versus Cabazitaxel in Progressive Metastatic Castration Resistant Prostate Cancer

Metastatic Cancer Clinical Trial

— TheraP  

Official title:

TheraP: A Randomised Phase 2 Trial of 177Lu-PSMA617 Theranostic Versus Cabazitaxel in Progressive Metastatic Castration Resistant Prostate Cancer (ANZUP Protocol 1603)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03392428
• Other study ID #: ANZUP 1603
• Status: Completed
• Phase: Phase 2
• Start date: January 29, 2018
• Est. completion date: December 31, 2021

Study information

• Verified date: June 2022
• 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 open label, randomised, stratified, 2-arm, multicentre, phase 2 trial aims to determine the activity and safety of Lu-PSMA vs cabazitaxel in men with progressive metastatic castration resistant prostate cancer

Description:

Despite recent advances in the treatment of prostate cancer, metastatic disease remains incurable. Prostate specific membrane antigen (PSMA) is present in high quantities on the cell surface of prostate cancers, and is also further increased in metastatic hormone refractory carcinomas. PSMA is an attractive target for both imaging and treatment of prostate cancer. PSMA bound to the radioactive substance Gallium68 (GaPSMA) is rapidly being adopted for imaging prostate cancer using positron emission tomography (PET) scanning. Radionuclide therapy is an approach for the treatment of cancer that uses tumour targeting agents to deliver high doses of radiation to sites of tumours. The PSMA molecule used for PET imaging can also be labelled with Lutetium177 (Lu177), a radioactive substance. The aim of this study is to determine the activity and safety of LuPSMA radionuclide therapy. Patients with metastatic prostate cancer who have progressed despite hormonal therapy and chemotherapy, will be randomised to receive either LuPSMA radionuclide therapy (up to a maximum of 6 cycles of therapy) or cabazitaxel chemotherapy (up to a maximum of 10 cycles of therapy). 200 participants will be recruited from sites across Australia. The study will determine the effects on PSA response rate (primary endpoint), pain response, progression free survival, quality of life, and frequency and severity of adverse events. Correlative outcomes include associations between PET imaging and clinical outcomes, and biomarkers and clinical outcomes.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 201
• Est. completion date: December 31, 2021
• Est. primary completion date: December 31, 2019
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Male aged 18 or older with metastatic adenocarcinoma of the prostate defined by:

• Documented histopathology of prostate adenocarcinoma OR
• Metastatic disease typical of prostate cancer (i.e. involving bone or pelvic lymph nodes or para-aortic lymph nodes)

2. Castration-resistant prostate cancer (defined as disease progressing despite castration by orchiectomy or ongoing Luteinizing Hormone-Releasing Hormone (LHRH) analog

3. Progressive disease with rising PSA on 3 consecutive measurements, and PSA = 20 ng/mL

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

5. Prior treatment with docetaxel

6. Significant PSMA avidity on 68Ga-PSMA PET/CT, defined as a minimum uptake of SUVmax 20 at a site of disease, and SUVmax > 10 at sites of measurable disease =10mm (unless subject to factors explaining a lower uptake, e.g. respiratory motion, reconstruction artefact)

7. ECOG Performance status 0 to 2

8. Assessed by a medical oncologist as suitable for chemotherapy with cabazitaxel

9. Adequate renal function:

• Cr Cl = 40mL/min (Cockcroft-Gault formula)

10. Adequate bone marrow function:

• Platelets = 100 x10 billion /L
• Hb = 90g/L (no red blood cell transfusion in last 4 weeks)
• Neutrophils > 1.5 x10 billion/L

11. Adequate liver function:

• Bilirubin < 1.5 x upper limit of normal (ULN) (or if bilirubin is between 1.5-2x ULN, must have a normal conjugated bilirubin)
• AST or ALT = 2.0 x ULN (or = 5.0 x ULN in the presence of liver metastases)

12. Estimated life expectancy > 12 weeks

13. Study treatment both planned and able to start within 21 days of randomisation

14. Willing and able to comply with all study requirements, including all treatments (cabazitaxel or Lu-PSMA); and, the timing and nature of all required assessments

15. Signed, written informed consent

Exclusion Criteria:

1. Prostate cancer with significant sarcomatoid or spindle cell or neuroendocrine small cell components

2. Site(s) of disease that are FDG positive with minimal PSMA expression defined as FDG intensity > 68Ga-PSMA activity OR 68Ga-PSMA SUVmax < 10

3. Sjogren's syndrome

4. Prior treatment with cabazitaxel or Lu-PSMA

5. Contraindications to the use of corticosteroid treatment

6. Active malignancy other than prostate cancer

7. Concurrent illness, including severe infection that may jeopardise the ability of the participant to undergo the procedures outlined in this protocol with reasonable safety

8. Presence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule, including alcohol dependence or drug abuse

9. Patients who are sexually active and not willing/able to use medically acceptable forms of barrier contraception

Related Conditions & MeSH terms

• Cancer of the Prostate
• Metastatic Cancer
• Prostatic Neoplasms

Intervention

Other:
• 177Lu-PSMA617
Patients randomised to the 177Lu-PSMA617 arm will receive 6-8.5GBq of 177Lu-PSMA617 by intravenous injection once every 6 weeks until progressive disease, prohibitive toxicity or a maximum of 6 cycles. The first dose will be administered at 8.5GBq, reducing by 0.5GBq with every cycle given (i.e. to 6.0GBq on the sixth cycle, if reached). In some patients who have an exceptional response, treatment will be paused but can be re-commenced up to the maximum of 6 cycles upon progression.

Drug:
• Cabazitaxel
Patients randomised to the Cabazitaxel arm will receive 20mg/m2 Cabazitaxel by intravenous infusion once every 3 weeks until progressive disease, prohibitive toxicity or a maximum of 10 cycles. Patients in this arm will also receive prednisolone 10mg orally per day for the duration of their cabazitaxel treatment.

Locations

Country	Name	City	State
Australia	Royal Adelaide Hospital	Adelaide	South Australia
Australia	Royal Brisbane and Womens Hospital	Brisbane	Queensland
Australia	Liverpool Hospital	Liverpool	New South Wales
Australia	Austin Hospital	Melbourne	Victoria
Australia	Peter MacCallum Cancer Centre	Melbourne	Victoria
Australia	Monash Moorabbin Hospital	Moorabbin	Victoria
Australia	Fiona Stanley Hospital	Murdoch	Western Australia
Australia	Sir Charles Gairdner Hospital	Nedlands	Western Australia
Australia	Royal North Shore Hospital	Sydney	New South Wales
Australia	St Vincent's Hospital	Sydney	New South Wales
Australia	Calvary Mater Newcastle Hospital	Waratah	New South Wales

Sponsors (6)

Lead Sponsor	Collaborator
Australian and New Zealand Urogenital and Prostate Cancer Trials Group	Australasian Radiopharmaceutical Trials network (ARTnet), Australian Nuclear Science and Technology Organisation (ANSTO), Endocyte, Movember Foundation, Prostate Cancer Foundation of Australia (PCFA)

Country where clinical trial is conducted

Australia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Tertiary Correlative objectives: Associations between Ga-68 PSMA PET/CT, FDG-PET/CT baseline characteristics, and outcomes	Identification of Ga-68 PSMA PET/CT, FDG-PET/CT markers to predict outcomes.	Through study completion, on average 4 years
Other	Tertiary Correlative objectives: Associations between clinical outcomes and possible prognostic and/or predictive biomarkers (tissue and circulating) including ctDNA	Identification of biomarkers to predict outcomes.	Through study completion, on average 4 years
Primary	Prostate Specific Antigen response rate (PSA RR)	PSA RR defined as the proportion of participants in each group with a PSA reduction of = 50% from baseline.	Through study completion, on average 4 years
Secondary	Pain Response (PPI and Analgesic Score)	Pain response rate, defined as: >=2 point reduction in PPI score from baseline with no increase in analgesic score; and/or; >=50% decrease in analgesic score with no increase in PPI PPI: McGill-Melzack Present Pain Intensity Scale (PPI) Analgesic score: Using Morphine Equivalent Daily Dose (MEDD)	Through study completion, on average 4 years
Secondary	Objective Tumour Response Rate	Objective Tumour Response Rate - defined as the proportion of participants with a confirmed complete response (CR) or partial response (PR) divided by the total number of participants (using RECIST 1.1).	Through study completion, on average 4 years
Secondary	Progression free survival	Progression free survival - the time from randomisation to date of PSA progression (blood samples), pain progression (on PPI) or radiographic progression (PCWG3 for bone and RECIST 1.1 for soft tissue), whichever occurs first	Through study completion, on average 4 years
Secondary	PSA progression free survival	PSA progression free survival, defined as the time from randomisation to PSA progression, assessed using PCWG3 criteria on blood test results.	Through study completion, on average 4 years
Secondary	Pain progression free survival	Pain progression free survival - defined as the time from randomisation to pain progression (>=1 point increase on PPI from nadir and >=25% increase in analgesic score (MEDD) from nadir, OR need for palliative radiotherapy).	Through study completion, on average 4 years
Secondary	Radiographic progression free survival	Radiographic progression free survival - defined as the time from randomisation to radiographic progression (assessed using PCWG3 criteria for bone lesions and RECIST 1.1 for soft tissue lesions).	Through study completion, on average 4 years
Secondary	Health-related quality of life	Health-related quality of life, assessed using a composite of the EORTC core quality of life questionnaire (QLQ C-30) and the Patient Disease and Treatment Assessment Form (PDF).	Through study completion, on average 4 years
Secondary	Overall survival	Overall survival - time from registration to death from any cause or last known follow-up alive.	Through study completion, on average 4 years
Secondary	Frequency and severity of adverse events	Frequency and severity of adverse events (composite), assessed using CTCAE v4.03.	From first study dose to 12 weeks after completing study treatment