進行性去勢抵抗性前立腺がん(CRPC)を治療するために、黄体形成ホルモン放出ホルモン(LHRH)アゴニストからLHRHアンタゴニストに切り替えた場合の有効性研究
LHRHアゴニスト療法にもかかわらず前立腺特異抗原(PSA)が上昇している去勢抵抗性前立腺がんの男性を対象としたデガレリクスの第II相単群研究。
Men with castrate resistant prostate cancer who are switched from a luteinizing hormone-releasing hormone (LHRH) antagonists from a LHRH agonist will experience a fall in prostate-specific antigen (PSA).
調査の概要
詳細な説明
To determine the proportion of patients with castrate resistant Prostate Cancer who have a PSA decline of ≥50% from baseline PSA when switched from an LHRH agonist to an LHRH antagonist.
研究の種類
段階
- フェーズ2
連絡先と場所
研究場所
-
-
British Columbia
-
Vancouver、British Columbia、カナダ、V5Z4E6
- British Columbia Cancer Agency
-
-
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:
- histologically confirmed adenocarcinoma of the prostate
- currently receiving LHRH agonist
- Anti-androgen oral therapy is permitted but will be discontinued upon enrollment
- PSA > 2 ng/ml
- rising PSA despite LHRH agonist
- patients may or may not have clinical evidence off metastases. If metastases are present, they must be asymptomatic and in bone or lymph node only
- Prior chemotherapy allowed
- ECOG performance status 0-1
Exclusion Criteria:
- Patients with a history of other active malignancies, except: adequately treated non-melanoma skin cancer, superficial bladder cancer, or other solid tumours curatively treated with no evidence of disease for ≥ 3 years.
- Other serious illness, psychiatric or medical condition that would not permit the patient to be managed according to the protocol including: i)Significant cardiovascular condition including but not limited to: uncontrolled hypertension, unstable angina, significant congestive heart failure or myocardial infarction, deep venous thrombosis, pulmonary embolus or cerebrovascular attack within the last 6 months. ii) History of significant neurological disorder that would impair the ability to obtain consent
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 |
|---|---|
|
実験的:Degarelix
Degarelix 240mg subcutaneously loading dose, then 80mg sc every month until disease progression. |
Standard dosing and schedule for administration of degarelix will be used. 240mg s.c. loading dose, 80mg s.c. monthly maintenance dose.
他の名前:
|
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 |
|---|---|---|
|
50% fall in PSA
時間枠:8 weekly
|
Proportion of patients with castrate resistant prostate cancer (CRPC) who have a PSA decline of ≥50% from baseline when switched from an LHRH agonist to an LHRH antagonist |
8 weekly
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Luteinizing hormone (LH)
時間枠:8 weekly
|
Circulating androgen and pituitary hormones will be measured during the course of the study (8 weekly). |
8 weekly
|
|
Follicle stimulating hormone (FSH)
時間枠:8 weekly
|
Circulating androgen and pituitary hormones will be measured during the course of the study (8 weekly). |
8 weekly
|
|
Testosterone (TT)
時間枠:8 weekly
|
Circulating androgen and pituitary hormones will be measured during the course of the study (8 weekly). |
8 weekly
|
|
dehydroepiandrosterone (DHEA)
時間枠:8 weekly
|
Circulating androgen and pituitary hormones will be measured during the course of the study (8 weekly). |
8 weekly
|
|
dehydroepiandrosterone-sulfate (DHEA-S)
時間枠:8 weekly
|
Circulating androgen and pituitary hormones will be measured during the course of the study (8 weekly). |
8 weekly
|
|
androstenedione (AED)
時間枠:8 weekly
|
Circulating androgen and pituitary hormones will be measured during the course of the study (8 weekly). |
8 weekly
|
|
dihydrotestosterone (DHT)
時間枠:8 weekly
|
Circulating androgen and pituitary hormones will be measured during the course of the study (8 weekly). |
8 weekly
|
協力者と研究者
捜査官
- 主任研究者:Kim N Chi, MD、British Columbia Cancer Agency, Univeristy of British Columbia
出版物と役立つリンク
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 (推定)
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
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。