Efficacy and Safety of Darolutamide Combined With Docetaxel and ADT as Neoadjuvant Therapy for Locally Advanced Prostate Cancer.
Efficacy and Safety of Darolutamide Combined With Docetaxel and ADT as Neoadjuvant Therapy for Locally Advanced Prostate Cancer: A Multicenter, Prospective, Randomized Controlled Study
The goal of this study is to evaluate the efficacy and safety of darolutamide combined with docetaxel and ADT compared to docetaxel combined with ADT in treating locally advanced prostate cancer patients scheduled for radical prostatectomy. The participant population includes adult males with locally advanced prostate cancer (cT3b-cT4, N0, M0 or any cT, N1, M0). The main questions it aims to answer are:
Does the combination of darolutamide, docetaxel, and ADT improve treatment outcomes compared to docetaxel combined with ADT? What are the safety profiles and adverse effects associated with each treatment group? Researchers will compare the control group (docetaxel combined with ADT) to the experimental group (darolutamide combined with docetaxel and ADT) to see if the experimental treatment is more effective.
Participants will:
Receive either docetaxel combined with ADT or darolutamide combined with docetaxel and ADT for 4 cycles (16 weeks) as neoadjuvant treatment.
Undergo radical prostatectomy after completing the neoadjuvant treatment. Be followed up for 36 months post-surgery to assess treatment efficacy and safety.
研究概览
研究类型
注册 (估计的)
阶段
- 阶段2
联系人和位置
学习联系方式
- 姓名:Xiaoguang Shao
- 电话号码:+(86)021-1234567
- 邮箱:shaoxgg@163.com
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Male, age >= 18 years and <= 75 years at the time of signing the informed consent form;
- Confirmed as prostate cancer by histological or cytological examination, and planned for radical prostatectomy;
- Clinical stage conforms to the definition of locally advanced prostate cancer: cT3b-cT4, N0, M0 or any cT, N1, M0 (based on PSMA-PET/CT examination);
- Eastern Cooperative Oncology Group (ECOG) performance status score is 0-1;
- Expected lifespan >= 10 years;
- Important laboratory indicators meet the following requirements: a. Hemoglobin >= 90 g/L b. Serum total bilirubin <= 1.5 times the upper limit of normal value, transaminase (AST/ALT) <= 2.5 times the upper limit of normal value c. Serum albumin >= 30 g/L d. Serum creatinine <= 1.5 times the upper limit of normal value e. Absolute neutrophil count >= 1.5 x 10^9/L, platelet count >= 100 x 10^9/L;
- No difficulty in swallowing (can take the medicine in whole), chronic diarrhea, intestinal obstruction or other factors affecting drug administration and absorption;
- No use of opioid analgesics (including codeine, oxycodone, etc.) to relieve cancer pain;
- If the spouse is a fertile female, the subject consents to take effective contraceptive measures during the treatment period and for 4 months after the surgery;
- The subject voluntarily participates in this trial, signs the informed consent form, and is willing to comply with the requirements of the research protocol throughout the study period.
Exclusion Criteria:
- Pathological diagnosis of neuroendocrine prostate cancer, including small cell carcinoma;
- Prior local or systemic treatment for prostate cancer, including but not limited to radiotherapy, chemotherapy, or endocrine therapy;
- Confirmed bone metastasis, hepatic metastasis, brain metastasis, or other visceral metastases on imaging;
- Known hypersensitivity to the study drugs (active ingredients or excipients) or drugs of the same class;
- Contraindications to prednisone acetate or docetaxel, such as active infection, allergy, or other conditions;
- Chronic disease requiring prednisone acetate at doses exceeding those specified in the protocol (5 mg orally twice daily, starting 14 days before docetaxel chemotherapy and stopping 3 weeks after the last chemotherapy cycle);
- Poorly controlled hypertension despite medication (systolic blood pressure >=160 mmHg or diastolic blood pressure >=95 mmHg);
- Active or symptomatic viral hepatitis or other chronic liver disease; known human immunodeficiency virus (HIV) infection;
- History of pituitary or adrenal dysfunction;
- Active autoimmune disease requiring hormonal therapy;
- Major cardiovascular or cerebrovascular disease within 6 months prior to the start of study treatment, including: severe/unstable angina, myocardial infarction, congestive heart failure [New York Heart Association (NYHA) class III or above], cerebrovascular accident, or arrhythmia requiring pharmacological treatment;
- History of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation;
- Grade ≥2 peripheral sensory or motor neuropathy;
- Other malignancies occurring within the past 2 years or currently concurrent malignancies;
- Major surgery requiring general anesthesia within 28 days before the first dose;
- Treatment with strong CYP3A4 inhibitors (e.g., itraconazole, clarithromycin, ketoconazole) or strong CYP3A4 inducers (e.g., carbamazepine, phenytoin, phenobarbital, St. John's wort) that cannot be discontinued, and have not been stopped for at least 7 days before randomization;
- History of epilepsy;
- Alcohol or drug abuse or dependence;
- Participation in another therapeutic clinical study within 1 month before the start of study treatment;
- Any other condition that the investigator considers unsuitable for participation in this study;
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Darolutamide + docetaxel + ADT
Adopting the triple neoadjuvant treatment regimen of Darolutamide + docetaxel + ADT
|
Darolutamide: oral administration, 600 mg per dose, twice daily, taken with food.
Docetaxel: intravenous injection, 75 mg/m², once every 3 weeks, for a total of 4 doses/cycles.
(Oral prednisone acetate should be started 14 days before docetaxel chemotherapy at 5 mg twice daily and discontinued 3 weeks after the last chemotherapy cycle.)
ADT: leuprorelin, goserelin, or triptorelin, selected by the investigator according to the patient's condition, administered by subcutaneous or intramuscular injection, using a once-monthly formulation uniformly.
|
|
有源比较器:Docetaxel + ADT
Adopting the dual neoadjuvant treatment regimen of docetaxel + ADT
|
Docetaxel: intravenous injection, 75 mg/m², once every 3 weeks, for a total of 4 doses/cycles.
(Oral prednisone acetate should be started 14 days before docetaxel chemotherapy at 5 mg twice daily and discontinued 3 weeks after the last chemotherapy cycle.)
ADT: leuprorelin, goserelin, or triptorelin, selected by the investigator according to the patient's condition, administered by subcutaneous or intramuscular injection, using a once-monthly formulation uniformly.
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研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
3-year biochemical progression-free survival (bPFS)
大体时间:Every 3 months (±14 days) up to 36 months after surgery
|
Every 3 months (±14 days) up to 36 months after surgery
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
3-year biochemical progression-free survival (bPFS)
大体时间:Every 3 months (±14 days) up to 36 months after surgery
|
Every 3 months (±14 days) up to 36 months after surgery
|
|
|
Pathological Downstaging Rate after Radical Prostatectomy
大体时间:On Surgery day
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On Surgery day
|
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Incidence of Treatment-Related Adverse Events
大体时间:From screening visit to 30 days after the last neoadjuvant dose or start of new anticancer therapy
|
From screening visit to 30 days after the last neoadjuvant dose or start of new anticancer therapy
|
|
|
Time to Castration-Resistant Prostate Cancer (CRPC) at 3 Years
大体时间:every 3 months PSA tests and every 6 months imaging assessments up to 36 months after surgery
|
every 3 months PSA tests and every 6 months imaging assessments up to 36 months after surgery
|
|
|
Objective Response Rate (ORR)
大体时间:2-4 weeks after completion of neoadjuvant therapy
|
2-4 weeks after completion of neoadjuvant therapy
|
|
|
3-year Radiographic Progression-Free Survival (rPFS)
大体时间:Every 6 months (±1 month) post-surgery until 36 months post-surgery (months 6, 12, 18, 24, 30, 36)
|
Every 6 months (±1 month) post-surgery until 36 months post-surgery (months 6, 12, 18, 24, 30, 36)
|
|
|
Undetectable PSA Rate post-Radical Prostatectomy
大体时间:6 weeks post-surgery (±7 days)
|
6 weeks post-surgery (±7 days)
|
|
|
Subject Quality of Life as assessed by FACT-P( Functional Assessment of Cancer Therapy - Prostate) scale
大体时间:Baseline (V0), post-neoadjuvant/pre-surgery (V5), and at 6, 12, 24, 36 months post-surgery (±14 days)
|
The FACT-P(Functional Assessment of Cancer Therapy - Prostate) scale will be used to assess the quality of life of subjects.
The total score is calculated from the general functional and prostate cancer-specific subscale scores, with a total score range of 0 to 156, where higher scores indicate better functional status.
Changes in the total score and individual domain scores will be analyzed.
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Baseline (V0), post-neoadjuvant/pre-surgery (V5), and at 6, 12, 24, 36 months post-surgery (±14 days)
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Perioperative Complications
大体时间:From surgery date through 90 days post-surgery
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From surgery date through 90 days post-surgery
|
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Positive Surgical Margin Rate after Radical Prostatectomy
大体时间:On surgery day
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On surgery day
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Time to Castration-Resistant Prostate Cancer (CRPC) at 3 Years
大体时间:PSA tests every 3 months and imaging assessments every 6 months up to 36 months post-surgery
|
PSA tests every 3 months and imaging assessments every 6 months up to 36 months post-surgery
|
|
|
Pathological Complete Response (pCR) or Minimal Residual Disease (MRD) Rate
大体时间:On surgery day
|
On surgery day
|
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3-year Overall Survival (OS)
大体时间:Every 3 months (+/-1 month) post-surgery until 36 months post-surgery
|
Every 3 months (+/-1 month) post-surgery until 36 months post-surgery
|
合作者和调查者
合作者
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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