TOPARP: A Phase II Trial of Olaparib in Patients With Advanced Castration Resistant Prostate Cancer

Adenocarcinoma of the Prostate Clinical Trial

— TOPARP  

Official title:

A Phase II Trial of Olaparib in Patients With Advanced Castration Resistant Prostate Cancer (TOPARP)

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT01682772
• Other study ID #: ICR-CTSU/2011/10030
• Secondary ID: 2011-000601-49CR
• Status: Active, not recruiting
• Phase: Phase 2
• Start date: July 2012
• Est. completion date: February 2020

Study information

• Verified date: August 2019
• Source: Institute of Cancer Research, United Kingdom
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is an open-label, single arm, two part adaptive design phase II trial of Olaparib in patients with advanced castration resistant prostate cancer.

The trial aims to evaluate the the anti-tumour activity of Olaparib in metastatic castration resistant prostate cancer, identify molecular signatures of tumour cells in responding and non-responding patients, and to identify predictive biomarkers of Olaparib response.

Description:

Patients with advanced castration resistant prostate cancer will receive single agent Olaparib at a dose of 400mg twice daily, continuously on a 28 day cycle. Olaparib will be administered until objective disease progression or unacceptable toxicity or patient withdrawal for whatever reason

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 148
• Est. completion date: February 2020
• Est. primary completion date: March 2019
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Subject capable of understanding & complying with protocol requirements & signed the informed consent form

2. Minimum age 18 years

3. Histologically confirmed adenocarcinoma of the prostate with tumour tissue available for molecular analyses

4. At least one but no more than two previous taxane-based chemotherapy regimens. If docetaxel chemotherapy is used more than once, this will be considered as one regime. Patients may have had prior exposure to cabazitaxel treatment

5. At least 28 days since the completion of prior therapy, including major surgery, chemotherapy & other investigational agents. Clinically relevant sequelae should have resolved to grade 1 or less prior to recommencing treatment. For hormonal treatment & radiotherapy refer to the protocol guidelines

6. Documented prostate cancer progression as described in the protocol.

7. Surgically or medically castrated, with testosterone levels of < 50 ng/dL (< 2.0 nM). If the patient is being treated with LHRH agonists this must have been initiated at least 4 weeks prior to Cycle 1 Day 1 & must be continued throughout the study.

8. Eastern Cooperative Oncology Group Performance Status of 0, 1, 2

9. Life expectancy > 12 weeks

10. Able to swallow a whole tablet

11. Patient & the patient's partner of childbearing potential, must agree to use medically accepted methods of contraception during the course of the study & for 3 months after the last dose of study drug

12. Agreeable to have all the biomarker studies including the paired fresh tumour biopsies.

13. CTC count of 5 cells/7.5mls blood or more at screening. Note: For Part B, CTC count >5 cells/7.5mls blood is not mandatory if patient has measurable disease by modified RECIST and a lesion >2cm and PSA greater than or equal to 2ng/ml at screening.

14. Adequate bone marrow, hepatic & renal function as defined in the protocol

15. For Part B only, patients must have genomic defects associated with olaparib sensitivity identified by NGS by the central lab.

Exclusion Criteria:

1. Surgery, or local prostatic intervention (excluding a prostatic biopsy) less than 28 days of Cycle 1 Day 1

2. Less than 28 days from any active anticancer therapy or investigational agents. For hormonal treatment & radiotherapy refer to the guidelines outlined in the inclusion criteria

3. Prior treatment with a PARP inhibitor, platinum, cyclophosphamide or mitoxantrone chemotherapy

4. Uncontrolled intercurrent illness including, but not limited to, active infection, symptomatic congestive heart failure (New York Heart Association Class III or IV heart disease), unstable angina pectoris, cardiac arrhythmia, uncontrolled hypertension or psychiatric illness/social situations that would limit compliance with study requirements

5. Any acute toxicities due to prior chemotherapy & / or radiotherapy that have not resolved to a NCI-CTCAE v4.02 grade 0 or 1 with the exception of chemotherapy induced alopecia & grade 2 peripheral neuropathy

6. Malignancy within the previous 2-years with a > 30% probability of recurrence within 12 months with the exception of non-melanoma skin cancer, in-situ or superficial bladder cancer

7. Patients with myelodysplastic syndrome/acute myeloid leukaemia

8. Patients with known symptomatic brain metastasis are not suitable for enrollment. Patients with asymptomatic, stable, treated brain metastases are eligible for study entry

9. Patients with symptomatic or impending cord compression unless appropriately treated beforehand & clinically stable & asymptomatic

10. Patients who have experienced a seizure or seizures within 6 months of study treatment or who are currently being treated with cytochrome P450 enzyme inducing anti-epileptic drugs for seizures

11. Patients receiving any of the following classes of inhibitors of CYP3A4 (see protocol for guidelines & wash out periods)

12. Patients with gastrointestinal disorders likely to interfere with absorption of the study medication

13. Initiating bisphosphonate therapy or adjusting bisphosphonate dose/regimen within 30 days prior to Cycle 1 Day 1. Patients on a stable bisphosphonate regimen are eligible & may continue

14. Presence of a condition or situation, which, may put the patient at significant risk, confound the study results, or interfere significantly with participation in the study

Related Conditions & MeSH terms

• Adenocarcinoma
• Adenocarcinoma of the Prostate
• Prostatic Neoplasms

Intervention

Drug:
• Olaparib
Until objective disease progression, unacceptable toxicity or patient withdrawal for whatever reason

Locations

Country	Name	City	State
United Kingdom	University College Hospital London	London
United Kingdom	Royal Marsden NHS Foundation Trust	Sutton	Surrey

Sponsors (2)

Lead Sponsor	Collaborator
Institute of Cancer Research, United Kingdom	Royal Marsden NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Response rate to Olaparib	Response will be defined on the basis of the following outcomes, if any of these occur patients will be considered to have responded: Objective response by modified RECIST; PSA decline of =50% according to the Prostate Cancer Working Group 2; Conversion of circulating tumour cell count from =5 cells/7.5ml blood at baseline to <5 cells/7.5ml blood confirmed by at least two readings 4 weeks apart	Response will be evaluated 6 months post trial entry
Secondary	Radiographic progression free survival	rPFS will be defined by either RECIST progression and/or progression on bone scan. It will be measured from the date of trial entry to the first occurence of radiographic progression or death from any cause	Radiographic progression free survival will be evaluated 6 months post trial entry
Secondary	Progression free survival	PFS will be measured from date of trial entry until radiographic progression, unequivocal clinical progression or death	Progression free survival will be evaluated 6 months post trial entry
Secondary	Time to PSA Progression	For patients who have achieved =50% decrease from the cycle 1 day 1 (baseline), the PSA progression date is defined as the date that a =25% increase and an absolute increase of =2ng.mL above the nadir is documented. This must be confirmed by a second consecutive value. For patients without a PSA decrease of this magnitude or no decrease at all, PSA progression date is defined as the date that a = 25% increase and an absolute increase of = 2 ng/mL above the baseline is documented. This must also be confirmed by a second consecutive value.	Time to PSA progression will be evaluated 6 months post trial entry
Secondary	CTC count conversion rate	Proportion of patients with conversion of CTC count from =5/7.5ml blood at baseline to <5/7.5ml blood nadir	CTC count conversion rate will be evaluated 6 months post trial entry
Secondary	Duration of PSA response	Duration of PSA response is calculated from the time the PSA value first declines by at least 50% of the cycle 1 day 1 (baseline) value (must be confirmed by a second value) until the time there is an increase of 25% of PSA nadir, provided the absolute increase is at least 2 ng/mL. The increase must be confirmed by a second consecutive measurement.	Duration of PSA response will be evaluated 6 months post trial entry
Secondary	Number of participants with grade 3 or 4 adverse events as a measure of safety and tolerability.	The proportion of patients with grade 3/4 adverse events will be described along with other descriptive measures of safety and tolerability and evaluated by the IDMC	Will be evaluated 1) when the first 5 and 10 participants have completed the 1st cycle of treatment and, 2) at 6 months post trial entry.
Secondary	Time to radiographic progression	Time to radiographic progression (progression defined by either RECIST progression and /or progression on bone scan) will be measured from the date of trial entry to the first occurrence of radiographic progression. Death from prostate cancer or any other cause without prior radiographic evidence of progression will not count as an event.	Will be evaluated 6 months post trial entry
Secondary	Overall survival	OS will be measured from the date of trial entry to the date of death (whatever the cause). Survival time of living patients will be censored on the last date a patient is known to be alive or lost to follow-up	Will be evaluated 6 months post trial entry
Secondary	PSA objective response	PSA response and PSA progression are defined according to the consensus guidelines of the Prostate Cancer Clinical Trials Working Group 2.	Will be evaluated 6 months post trial entry