Characterisation of T Lymphocytes, NK Cells and Macrophages in Melanoma Patients (IMMUMELA)
Characterisation of T Lymphocytes, NK Cells and Macrophages in Melanoma Patients: Impact on Immunity Versus Immunosuppression
調査の概要
詳細な説明
The study is divided in 4 parts:
Part 1: study of cellular infiltrate (lymphocytes) performed on large primary melanoma and cutaneous metastasis ( fresh samples) Part 2: NK cells study on metastatic regional lymph nodes ( fresh samples) and blood samples Part 3: a retrospective study of macrophages in sentinel lymph nodes and in corresponding primary melanomas Part 4: study of the cellular modulation by the chemotherapy (DTIC or cisplatin or inhibitor of B-raf) which(who) will be made on two cutaneous metastases by patient (one taken before the treatment(processing) and one taken during the evaluation after 2 or 3 cycles of treatment(processing))
研究の種類
入学 (実際)
連絡先と場所
研究場所
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Ile de France
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Paris、Ile de France、フランス、75014
- Cochin Hospital
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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
サンプリング方法
調査対象母集団
説明
Inclusion Criteria:
- Patients with confirmed melanoma-patients informed of the aims of the study , the modalities
- Patients who signed the consent form ou a non opposition form signed by the patient or by a relative
According to study part:
Part 1: patients with a melanoma larger than 10mm or with cutaneous metastasis Part 2: stage IV melanoma patients who shall undergo a regional lymph node dissection Part 3: retrospective study of patients who underwent a sentinel node procedure Part 4: Patients achieves of inoperable melanomas the stage(stadium) III or IV that must receive in treatment (processing) a chemotherapy (by the dacarbazine or by the cisplatin or by the inhibitor of B-raf) and carrier of at least two cutaneous metastases
Exclusion Criteria:
- Refusal to take part in the study (patient or relative)
- Contraindications known to the xylocaine (groups 1,2, and 4)
- No affiliated to the social security system (groups 1, 2, and 4)
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
コホートと介入
グループ/コホート |
介入・治療 |
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MELANOMA 10mm
patients with a melanoma larger than 10mm or with cutaneous metastasis
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to collect some human cell samples in melanoma
他の名前:
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STAGE III MELANOMA
stage III melanoma patients who shall undergo a regional lymph node dissection
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to collect some human cell samples in melanoma
他の名前:
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SENTINEL NODE PROCEDURE
retrospective study of patients who underwent a sentinel node procedure
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to collect some human cell samples in melanoma
他の名前:
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STAGE IV MELANOMA
stage IV patients achieves of inoperable melanomas the stage(stadium) III or IV that must receive in treatment(processing) a chemotherapy (by the dacarbazine or by the cisplatin or by the inhibitor of B-raf) and carrier of at least two cutaneous metastases
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to collect some human cell samples in melanoma
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 |
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Impact of cellular infiltrate - Group 1
時間枠:2 years
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Impact of cellular infiltrate on disease free survival at 2 years
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2 years
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Impact of NK cell infiltrate - Group 2 and 3
時間枠:2 and 3 years
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Impact of NK cell infiltrate in metastatic lymph node on disease free survival and overall survival at 2 and 3 years
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2 and 3 years
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Modifications of cellular infiltrate - Group 4
時間枠:2 months
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Modifications of cellular infiltrate after chemotherapy (after 2 months)
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2 months
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協力者と研究者
捜査官
- 主任研究者:Marie Françoise Avril, MD, PhD、Assistance Publique - Hôpitaux de Paris
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
研究の完了 (実際)
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 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
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。
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