Pharmacokinetic Study of Pembrolizumab and Its Impact on Immunity and the Tumor Microenvironment, Which May Explain the Efficacy of Post-immunotherapy Chemotherapy. (CPI)
調査の概要
状態
研究の種類
入学 (推定)
段階
- フェーズ 4
連絡先と場所
研究連絡先
- 名前:Marine SIRVENT
- 電話番号:+33 4 92 03 17 78
- メール:DRCI-Promotion@nice.unicancer.fr
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:
- Patients over 18 years of age
- Patients diagnosed with :
- Non-small cell lung cancer (NSCLC), including adenocarcinoma and squamous cell carcinoma.
Head and neck squamous cell carcinoma, p16-negative for oropharyngeal tumors.
- Recurrent and/or metastatic tumor not amenable to curative locoregional treatment.
Disease progression under Pembrolizumab immunotherapy, administered at the standard dose of 200 mg every 3 weeks, as first-line treatment for metastatic disease, regardless of the number of cycles received, either as monotherapy or in combination with chemotherapy, as defined below:
• For pulmonary adenocarcinomas: i. First-line treatment with Pembrolizumab in combination with a platinum agent (Carboplatin or Cisplatin) and Pemetrexed
ii. Maintenance therapy with Pembrolizumab, with or without Pemetrexed.
• For pulmonary squamous cell carcinomas: i. First-line treatment with Pembrolizumab in combination with a platinum agent (Carboplatin) and Paclitaxel
+/- ii. Maintenance therapy with Pembrolizumab alone.
• For head and neck squamous cell carcinomas : i. First-line treatment with Pembrolizumab in combination with a platinum agent (Carboplatin or Cisplatin) ± 5-Fluorouracil (5-FU) or Paclitaxel
+/- ii. Maintenance therapy with Pembrolizumab alone.
Eligibility for salvage chemotherapy within standard care:
• For pulmonary adenocarcinomas: weekly Paclitaxel, with or without Bevacizumab.
- For pulmonary squamous cell carcinomas: Gemcitabine monotherapy.
- For head and neck squamous cell carcinomas: weekly Paclitaxel and/or Cetuximab. Standard salvage chemotherapy may be initiated between Day 18 and Day 35 following the last Pembrolizumab injection, at standard doses.
- Measurable disease according to RECIST 1.1 criteria.
- Performance status (PS) 0 to 2.
- Baseline laboratory results meeting the usual criteria permitting initiation of salvage chemotherapy.
- Patients who has voluntarily agreed to participate in the study (including additional blood sampling) and has signed the informed consent form.
For the subpopulation with accessible tissue biopsy:
- Patient agrees to undergo biopsy,
- INR < 1.5, Platelets > 50000/μL.
- Patients covered by a social security health insurance scheme.
Exclusion Criteria:
- History of cancer, except for cancers in complete remission for more than 3 years, fully resected cutaneous basal cell carcinomas, or treated carcinoma in situ or cervical intraepithelial neoplasia (in situ cervical epithelioma),
- Patients participating in another clinical trial for which an exclusion period is specified,
- Minor patients,
For the subpopulation with accessible tissue biopsy, patients receiving:
• Clopidogrel (hydrogen sulfate) or Prasugrel (hydrochloride) or Ticlopidine (hydrochloride) without the possibility of discontinuation for 5 days,
• Low-molecular-weight heparin (LMWH) without the possibility of dose suspension prior to the procedure,
• Or Fondaparinux without the possibility of discontinuation,
• Or Abciximab without the possibility of discontinuation for 24 hours and aPTT < 50s and ACT < 150s,
• Or Eptifibatide or Tirofiban hydrochloride monohydrate or Argatroban without the possibility of discontinuation 4 hours before the procedure,
- Or Bivalirudin without the possibility of discontinuation 2-3 hours before the procedure if CrCL > 50 mL/min, or 3-5 hours if CrCL < 50 mL/min,
- Or Dabigatran etexilate without the possibility of discontinuation 2-3 days before the procedure if CrCL > 50 mL/min, or 3-5 days if CrCL < 50 mL/min.
Vulnerable persons as defined in Articles L1121-5 to L1121-8 :
• Pregnant women, women in labour, and breastfeeding mothers,
- Persons deprived of liberty by judicial or administrative decision, and persons hospitalized without consent under Articles L3212-1 and L3213-1 who do not fall under the provisions of Article L1121-8,
- Persons admitted to a health or social care institution for purposes other than research,
- Adults under legal protection measures or unable to express their 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:Residual Pembrolizumab Exposure Assessment
|
Patients will be followed according to standard clinical care.
Biological samples collected include: (1) pharmacokinetic and extracellular vesicle analyses: 10 mL blood samples in EDTA tubes at 21±3, 35±3, 49±3, and 63±3 days after the last pembrolizumab administration (P1-P4); (2) pharmacogenetic analysis: one baseline 5 mL EDTA blood sample; (3) cytokine and immune cell analyses: at P1 and P4, collection of 2×4 mL lithium heparin tubes, 1×10 mL EDTA tube, and 1×5 mL dry tube.
Depending on feasibility of the procedure, and at the discretion of the investigator, two biopsies will be performed in 20 consenting patients:
Due to logistical constraints, these biopsies will be proposed to patients followed at CAL. They will be performed primarily in the interventional radiology department of CAL. |
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 |
|---|---|---|
|
Objective response rate (ORR) at 3 months after initiation of salvage chemotherapy (RECIST v1.1)
時間枠:3 months after initiation of salvage chemotherapy
|
Objective response rate (ORR) includes the proportion of patients achieving complete response (CR) or partial response (PR) according to RECIST version 1.1 criteria. Tumor response will be assessed using routine imaging performed during standard clinical follow-up care. ORR will be analyzed in relation to residual pembrolizumab (anti-PD-1) serum concentration measured 21 days after the last administration of pembrolizumab (P1), immediately prior to initiation of salvage chemotherapy. |
3 months after initiation of salvage chemotherapy
|
協力者と研究者
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
- 2023/60
- 2026-526866-26-00 (Ctis)
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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