Cabazitaxel in Combination With 177Lu-PSMA-617 in Metastatic Castration-resistant Prostate Cancer
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 35
- 试验地点
- 2
- 主要终点
- Number of participants with Dose Limiting Toxicities (DLTs)
研究概览
简要总结
This clinical trial will evaluate the safety of Cabazitaxel in combination with 177Lu-PSMA-617 in metastatic castration-resistant prostate cancer.
详细描述
This prospective, single-centre, single-arm, open label, phase I/II trial will assess the safety, efficacy and anti-tumour activity of cabazitaxel in combination with 177Lu-PSMA-617 in patients with metastatic castration-resistant prostate cancer (mCRPC).
This study aims to assess and establish the maximum tolerated dose (MTD), dose-limiting toxicities (DLTs), and recommended phase 2 dose (RP2D) of cabazitaxel in combination with 177Lu-PSMA-617 in patients with mCRPC.
32-44 men with mCRPC who have progressed on prior docetaxel and a second-generation AR antagonist will be enrolled in this trial in two stages: dose escalation and a dose expansion phase over a period of 18 months.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Male
- 接受健康志愿者
- 否
入选标准
- •Male patients aged 18 years or older at the time of informed consent.
- •Patient has provided written informed consent.
- •Histologically confirmed adenocarcinoma of the prostate without neuroendocrine or small cell differentiation.
- •Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 1
- •Patients must have had prior treatment with docetaxel.
- •Patients must have progressed on a second-generation androgen receptor (AR)-targeted agent (e.g., enzalutamide, abiraterone, or apalutamide) in the castrate-resistant setting.
- •Patients must have progressive disease. The Prostate Cancer Clinical Trials Working Group 3 (PCWG3) defines this as any 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
- •Soft tissue or visceral disease progression as per Response Evaluation Criteria in Solid Tumours version 1.1 (RECIST 1.1) criteria
- •Bone progression: ≥ 2 new lesions on bone scan
- •At least three weeks since the completion of surgery prior to registration.
- •Prior surgical orchiectomy or chemical castration maintained on luteinizing hormone-releasing hormone (LHRH) analogue (agonist or antagonist).
- •Serum testosterone levels ≤ 1.75nmol/L within 28 days prior to registration.
- •Imaging evidence of metastatic disease documented with either whole body bone scan (WBBS) or computed tomography (CT) scan performed within 28 days prior to registration.
- •Significant prostate-specific membrane antigen (PSMA) avidity on PSMA PET/CT, defined as a minimum uptake of SUVmax 15 at a site of disease.
- •Patients must have a life expectancy ≥ 12 weeks.
- •Assessed by a medical oncologist as suitable for treatment with cabazitaxel and 177Lu-PSMA-
- •Patients must have adequate bone marrow, hepatic and renal function documented within 28 days prior to registration, defined as:
- •Haemoglobin ≥ 90 g/L independent of transfusions (no red blood cell transfusion in last 28 days prior to registration)
- •Absolute neutrophil count (ANC) ≥ 1.5x10^9/L
- •Platelets ≥ 150 x10^9/L
- •Total bilirubin ≤ 1.5 x upper limit of normal (ULN) except for patients with known Gilbert's syndrome, where this applies for the unconjugated bilirubin component
- •Aspartate transaminase (AST) and alanine transaminase (ALT) ≤ 2.5 x ULN if there is no evidence of liver metastasis or ≤ 5 x ULN in the presence of liver metastases
- •Albumin ≥ 25 g/L
- •Adequate renal function: patients must have a creatinine clearance estimated of ≥ 40 mL/min using the Cockcroft-Gault equation
- •Sexually active patients are willing to use medically acceptable forms of barrier contraception.
- •Willing and able to comply with all study requirements, including all treatments and the timing and nature of all required assessments.
排除标准
- •Superscan on WBBS or diffuse marrow disease on PSMA PET.
- •Site(s) of measurable disease that are FDG-positive with low PSMA expression (SUVmax <10).
- •Prior treatment with cabazitaxel or 177Lu-PSMA-
- •Contraindications to the use of corticosteroid treatment.
- •Other malignancies within the previous 2-years other than basal cell or squamous cell carcinomas of skin or other cancers that are unlikely to recur within 24 months.
- •Presence of untreated brain metastases or leptomeningeal metastases.
- •Patients with symptomatic or impending cord compression unless appropriately treated beforehand and clinically stable for ≥ four weeks.
- •Concurrent illness, including severe infection that may jeopardise the ability of the patient to undergo the procedures outlined in this protocol with reasonable safety.
- •Persistent toxicities (CTCAE v5.0 >/= Grade 2) caused by previous cancer therapy, excluding alopecia.
- •Known HIV or hepatitis B or C infection.
- •Radiotherapy or systemic anti-cancer therapies administered within 14 days prior to registration, excluding androgen deprivation therapy (ADT).
研究组 & 干预措施
Treatment Arm
In this single-arm study, patients will receive 7.4 GBq of 177Lu-PSMA-617 on Day 1 of every 6 week Cycle. Cabazitaxel will be administered concurrently on Day 2 and Day 23 of each Cycle (every 3 weeks). The dose of cabazitaxel will vary in dose-escalation. Up to 6 Cycles will be given.
干预措施: Cabazitaxel (Drug)
Treatment Arm
In this single-arm study, patients will receive 7.4 GBq of 177Lu-PSMA-617 on Day 1 of every 6 week Cycle. Cabazitaxel will be administered concurrently on Day 2 and Day 23 of each Cycle (every 3 weeks). The dose of cabazitaxel will vary in dose-escalation. Up to 6 Cycles will be given.
干预措施: 177Lu-PSMA-617 (Drug)
结局指标
主要结局
Number of participants with Dose Limiting Toxicities (DLTs)
时间窗: Dose escalation phase is expected to be completed 9 months from the time the first patient is recruited.
A DLT is defined as a toxicity that prevents further administration of the trial treatment at that dose level. Each cohort of 3 patients be assessed for DLTs in the first 6 weeks (cycle 1) of treatment and a dose for the next cohort will be determined.
Maximum Tolerated dose (MTD)
时间窗: Dose escalation phase is expected to be completed 9 months from the time the first patient is recruited.
The MTD is defined as the highest dose level at which the incidence of DLT was less than 2/6.
Recommended Phase 2 Dose (RP2D)
时间窗: Up to 30 months from the time the first patient is recruited.
After the MTD is established, additional patients will be treated at the MTD. Safety and efficacy data from the study will be used to define the RP2D.
次要结局
- Objective response rate (ORR) by Response Evaluation Criteria in Solid Tumours version 1.1 (RECIST1.1) in patients with measurable disease(Through study completion, up until 24 months after the last patient commences treatment)
- PSA progression free survival (PSA-PFS)(Through study completion, up until 24 months after the last patient commences treatment)
- Overall survival (OS)(Through study completion, up until 24 months after the last patient commences treatment)
- Describe pain within 12 months of treatment commencement(Through completion of 12 months after treatment commencement of last patient)
- Describe health-related quality of life (QoL) within 12 months of treatment commencement(Through completion of 12 months after treatment commencement of last patient)
- Rate of treatment discontinuation due to toxicity(Through study completion, up until 24 months after the last patient commences treatment)
- Adverse Events (AEs) and Serious Adverse Events (SAEs) measured using National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) v5.0(Through study completion, up until 24 months after the last patient commences treatment)
- 50% Prostate-Specific Antigen Response Rate (PSA-RR)(Through study completion, up until 24 months after the last patient commences treatment)
- Radiographic Progression-Free Survival (rPFS)(Through study completion, up until 24 months after the last patient commences treatment)