Pamiparib in mCRPC With HRD or BRCA1/2 Mutation
A Single Arm, Open-label, Phase II Study to Assess the Efficacy of Pamiparib in Metastatic Castration-Resistant Prostate Cancer Patients With Homologous Recombination Deficiency (HRD) or BRCA1/2 Mutation
調査の概要
詳細な説明
研究の種類
入学 (予想される)
段階
- フェーズ2
連絡先と場所
研究連絡先
- 名前:Fangjian Zhou, M.D.
- 電話番号:020-87343656
- メール:zhoufj@sysucc.org.cn
研究場所
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Guangdong
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Guangzhou、Guangdong、中国、510060
- 募集
- Sun Yat-sen University Cancer Center
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コンタクト:
- Fangjian Zhou, M.D.
- 電話番号:020-87343656
- メール:zhoufj@sysucc.org.cn
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-
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- ≥18 years old, male
- Have a histologically or cytologically confirmed adenocarcinoma or poorly differentiated carcinoma without neuroendocrine differentiation of the prostate. Mixed histology is accepted, except for small cell carcinoma.
- Have a deleterious mutation in BRCA1/2 , or HRD score ≥ 9.
- Eastern Cooperative Oncology Group (ECOG) performance status ≤1
- BPI<4
- Metastatic Castration-resistant Prostate Cancer (mCRPC): Presence of measurable target lesion according to RECIST criteria v1.1
- Male subject has been surgically or medically sterilized and has serum testosterone level ≤1.73nmol/L.
- Unsterilized male subject uses an acceptable method of contraception (defined as a barrier method with spermicide) to prevent pregnancy during the duration of the study and for 6 months after the last dose of Pamiparib.
- Experienced disease progression after having received at least 1 prior next-generation androgen receptor-targeted therapies, for metastatic castration-resistant disease.
- Capable of swallowing the whole capsule.
Subjects must have normal organ and bone marrow function at baseline, as defined below:
Hemoglobin ≥ 9.0 g/dL at least 28 days after transfusion . Absolute neutrophil count ≥ 1.5 × 10^9/L. Platelet count ≥ 100 × 10^9/L. Total bilirubin ≤ 1.5 × the upper limit of normal (ULN) specified. Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase/alanine aminotransferase (ALT) serum glutamic pyruvic transaminase) ≤ 3 × the specified ULN, unless liver metastases are present, in which case it must be ≤ 5 × ULN.
- Agree to sign informed consent form
- Agree not to participate in other interventional trials during this trial.
Exclusion Criteria:
Subjects should not enter the study if any of the following exclusion criteria are fulfilled:
- Acute toxicity (CTCAE > grade 2) due to prior cancer therapy.
- Received chemotherapy, endocrine therapy, biotherapy, radionuclide therapy, immunotherapy, experimental drugs, proprietary anticancer drugs or Chinese herbal medicines within 5 (if known) half-lives or 14 days(if unknown) prior to the first day of taking Pamiparib; For bisphosphonates or approved bone targeting therapy, Pamiparib must be administered at a steady dose for ≥28 days prior to the first day of taking Pamiparib.
- Received radiation therapy within 21 days.
- Prior treatment with any PARP inhibitor. Prior chemotherapy with mitoxantrone or platinum-based chemotherapy or cyclophosphamide. Prior treatment with sipuleucel-T or immune check point inhibitors are allowed.
- Subjects with major surgery within 2 weeks before starting study treatment. Subjects expected to receive major surgery during the trial.
- Active second malignancy, with the exception of curatively treated non-melanoma skin cancer, carcinoma in situ, or superficial bladder cancer
- Symptomatic and/or untreated central nervous system metastases
- Immunocompromised subjects, such as those with positive human immunodeficiency virus (HIV) serology.
- Subjects with known active hepatitis (e.g. hepatitis B or C).
- The subject has a serious cardiovascular disease. ( For example, but not limited to: uncontrolled arrhythmia, myocardial infarction)
- Concomitant use of strong CYP3A inducers or moderate CYP3A inducers . If half-lives is known, a 5 half-lives washout period is required before the start of Pamiparib therapy and a 2-week washout period is required when the half-lives is unknown.
- History of intolerance to Pamiparib capsule excipients
- Excluded by investigators
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:なし
- 介入モデル:単一グループの割り当て
- 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 |
|---|---|
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実験的:Pamiparib
Tablets 20mg per os : 40 mg / bid every day in continuous.
Patients will be treated with Pamiparib.
Cycles are defined in 28-day periods.
Disease response will be assessed every 8 weeks (RECIST 1.1).
Safety will be assessed continuously.
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40 mg bid per os , 28 day cycle, number of cycles: until progression or unacceptable toxicity develops.
他の名前:
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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 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
放射線学的無増悪生存期間 (rPFS)
時間枠:3年
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放射線学的無増悪生存期間は、初回投与時から放射線学的疾患の進行または何らかの原因による死亡のいずれか早い方まで評価されます。
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3年
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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臨床利益率
時間枠:3年
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RECIST によると、完全奏効 (CR)、部分奏効 (PR)、または疾患安定 (SD) のいずれかが少なくとも 16 週間続く
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3年
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客観的応答率 (ORR)
時間枠:入学から一次修了まで(最長約3年間)
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完全寛解(CR)と部分寛解(PR)の患者の割合
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入学から一次修了まで(最長約3年間)
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反応期間 (DOR)
時間枠:入学から一次修了まで(最長約3年間)
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CR または PR としての腫瘍の最初の評価の開始から、PD (進行性疾患) または何らかの原因による死亡の最初の評価までの時間。
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入学から一次修了まで(最長約3年間)
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Time to Response (TTR)
時間枠:From enrollment to primary completion of study (up to approximately 3 years)
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Time from initiation of treatment to first assessment of tumor as CR or PR.
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From enrollment to primary completion of study (up to approximately 3 years)
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前立腺特異抗原 (PSA) 反応率
時間枠:入学から一次修了まで(最長約3年間)
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PSAがベースラインから50%減少した患者の割合
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入学から一次修了まで(最長約3年間)
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Time to PSA Progression
時間枠:From enrollment to primary completion of study (up to approximately 3 years)
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Time from initiation of treatment to two consecutive 50% PSA increases from baseline level
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From enrollment to primary completion of study (up to approximately 3 years)
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全体的な生存 (OS)
時間枠:入学から一次修了まで(最長約3年間)
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治療開始から何らかの原因による死亡までの時間
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入学から一次修了まで(最長約3年間)
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Adverse events
時間枠:3 years
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Adverse events are graded according to the CTCAE V4.03
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3 years
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その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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rPFS stratified by baseline HRD score (HRD score threshold is defined as 9)
時間枠:3 years
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The rPFS is defined as the duration from Pamiparib initiation to radiologic disease progression or death from any cause, whichever comes first.
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3 years
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OS stratified by baseline HRD score (HRD score threshold is defined as 9)
時間枠:3 years
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The OS is defined as the duration from Pamiparib initiation to any death.
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3 years
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協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (予想される)
一次修了 (予想される)
研究の完了 (予想される)
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
その他の研究ID番号
- 2021-FXY-385
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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