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.
調査の概要
研究の種類
入学 (推定)
段階
- フェーズ2
連絡先と場所
研究連絡先
- 名前:Xiaoguang Shao
- 電話番号:+(86)021-1234567
- メール:shaoxgg@163.com
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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;
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的: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.
|
|
アクティブコンパレータ: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.
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
時間枠 |
|---|---|
|
3-year biochemical progression-free survival (bPFS)
時間枠:Every 3 months (±14 days) up to 36 months after surgery
|
Every 3 months (±14 days) up to 36 months after surgery
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
3-year biochemical progression-free survival (bPFS)
時間枠: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
時間枠:On Surgery day
|
On Surgery day
|
|
|
Incidence of Treatment-Related Adverse Events
時間枠: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
時間枠: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)
時間枠:2-4 weeks after completion of neoadjuvant therapy
|
2-4 weeks after completion of neoadjuvant therapy
|
|
|
3-year Radiographic Progression-Free Survival (rPFS)
時間枠: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
時間枠: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
時間枠: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.
|
Baseline (V0), post-neoadjuvant/pre-surgery (V5), and at 6, 12, 24, 36 months post-surgery (±14 days)
|
|
Perioperative Complications
時間枠:From surgery date through 90 days post-surgery
|
From surgery date through 90 days post-surgery
|
|
|
Positive Surgical Margin Rate after Radical Prostatectomy
時間枠:On surgery day
|
On surgery day
|
|
|
Time to Castration-Resistant Prostate Cancer (CRPC) at 3 Years
時間枠: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
時間枠:On surgery day
|
On surgery day
|
|
|
3-year Overall Survival (OS)
時間枠:Every 3 months (+/-1 month) post-surgery until 36 months post-surgery
|
Every 3 months (+/-1 month) post-surgery until 36 months post-surgery
|
協力者と研究者
スポンサー
協力者
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- 23233
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