Gut Microbiome in Patients With Lung and Melanoma Cancer and Intestinal Microbiota in Gynecologic Cancers (CERBERO)
2026年9月8日 更新者:European Institute of Oncology
Leveraging Gut Microbiome and Immune System Dynamics During Immunotherapy to Develop Biomarkers of Response in Patients With Lung and Melanoma Cancer' and 'Intestinal Microbiota Profiling in Gynecologic Cancers to Identify Response-relevant Factors During Immune Checkpoint Blockade'
This study aims to investigate the role of the gut microbiota and its derived factors, including bacterial-associated antigens that mimic tumor-associated antigens, in predicting response to immune checkpoint inhibitor immunotherapies in patients with various types of cancer.
The aim is to explore whether gut microbiota-mediated immunological modulation is specific to the tumor being treated and whether it can be used to enhance antitumor response.
調査の概要
研究の種類
介入
入学 (推定)
360
段階
- 適用できない
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究連絡先
- 名前:Luigi Nezi, PhD
- 電話番号:+39 02 94375171
- メール:luigi.nezi@ieo.it
研究連絡先のバックアップ
- 名前:Giulia Sedda, PhD
- メール:giulia.sedda@ieo.it
研究場所
-
-
MI
-
Milan、MI、イタリア、20141
- Istituto Europeo di Oncologia
-
主任研究者:
- Gianluca Spitaleri, MD
-
コンタクト:
- Luigi Nezi, PhD
- 電話番号:+39 02 94375171
- メール:luigi.nezi@ieo.it
-
コンタクト:
- Giuli Sedda, PhD
- 電話番号:+390294372178
- メール:giulia.sedda@ieo.it
-
主任研究者:
- Monica Casiraghi, MD PhD
-
主任研究者:
- Giuseppe Caruso, MD PhD
-
主任研究者:
- Carolina Cimminiello, MD
-
-
参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
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
いいえ
説明
4.1 INCLUSION CRITERIA:
- Histologically or cytologically confirmed disease (see 3.1)
- (i) patients with local advanced or metastatic NSCLC candidate to first-line ICB monotherapy or chemo-ICB combination OR (ii) patients with cutaneous melanoma candidate to first-line or adjuvant ICB (iii) patients with primary advanced or first recurrence endometrial or cervical cancer candidate to chemo-ICB combination
- Signed Written Informed Consent
- Males and Females, ages ≥18 years of age
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
- Have evaluable disease based on i-RECIST 1.1
- Patients must be willing and able to comply with scheduled visits, treatment schedule, laboratory tests and all protocol procedures.
- Be willing to provide tissue from a newly obtained core or excisional biopsy of a tumor lesion, whenever possible.
- Known mutation/molecular status as determined by local institutional standard (NSCLC: available comprehensive molecular analysis, melanoma: PD-L1 TPS score, BRAF V600, EC: p53, POLE, MMR status, CC: PD-L1 CPS score. Both wild type and mutation positive are eligible. Regarding gynecologic cancers, EC patients will be eligible for the study regardless of the MMR status (MMRd or MMRp), while only CC patients with a PD-L1 combined positive score (CPS) ≥1 will be eligible.
- Patients who have been previously treated in the adjuvant setting for melanoma will be eligible for treatment after a 28-day washout period.
- Patients must be medically fit enough to undergo surgery as determined by the treating medical and surgical oncology team.
- Demonstrate adequate organ function as defined below: Hematologic Absolute neutrophil count (ANC) >/= 1.5 X 10^9/L; Hemoglobin >/= 9.5 g/dL Platelets >/= 100 X 10^9/L PT/INR and PTT </= 1.5 X ULN. Hepatic Total bilirubin </= 1.5 X ULN (isolated bilirubin >1.5 X ULN is acceptable if bilirubin is fractionated and direct bilirubin <35%) AST and ALT Albumin </= 2.5 X ULN 1 >/=2.5 g/dL Renal Creatinine OR Calculated creatinine clearance OR 24-hour urine creatinine clearance </=1.5 X ULN 2 >/= 50 mL/min >/= 50 mL/min.
- The individual methods of contraception and duration should be determined in consultation with the investigator.
- Women must not be breastfeeding.
Exclusion Criteria:
- Previous chemotherapy (< 28 days washout), radiation therapy, immunotherapy, or biologic therapy
- Any major surgery within the last 3 weeks
- Pregnant or lactating female
- Unwillingness or inability to follow the procedures
- Grade 3 and 4 adverse event conditioning ICB interruption
- Known oncogene-addicted NSCLC, with the exception of KRAS G12C and BRAF V600E mutant NSCLC Any serious or uncontrolled medical disorder
- Prior malignancy active within the previous 2 years except for locally curable cancers that have been apparently cured, such as basal or squamous cell skin cancer, superficial bladder cancer, or carcinoma in situ of the prostate, cervix, or breast with local control measures (surgery, radiation).
- Patients with active, known or suspected autoimmune disease such as Inflammatory Bowel Disease, Lupus, etc. or other conditions requiring systemic corticosteroids or other systemic immunosuppressive medications.
- Patients with a condition requiring systemic treatment with either corticosteroids (> 10 mg daily prednisone equivalents) or other immunosuppressive medications within 14 days of study drug administration.
- Prior treatment with an anti-PD-1, anti-PD-L1 or anti-CTLA-4 antibody.
- Antibiotic or antimycotic medications within 45 days from the beginning of ICB
- Positive test result for hepatitis B or C virus
- Human immunodeficiency virus or known acquired immunodeficiency syndrome
- Concomitant Medications/Vaccinations: medications or vaccinations specifically prohibited in the exclusion criteria are not allowed during the ongoing study. If there is a clinical indication for one of these or other medications or vaccinations specifically prohibited during the study that the investigator considers necessary for a subject's welfare, it will be administered at the discretion of the investigator in keeping with the community standards of medical care. All concomitant medication (within 28 days before the first dose) will be recorded on the case report form (CRF).
- Patients are prohibited from receiving the following therapies during the Screening and Treatment Phase (including retreatment for post-complete response relapse) of this study:
- Immunotherapy not specified in this protocol
- Chemotherapy not specified in this protocol
- other Investigational agents
- Radiation therapy
- Live vaccines within 30 days prior to the first dose of trial treatment and while participating in the trial. Examples of live vaccines include, but are not limited to, the following: measles, mumps, rubella, varicella/zoster, yellow fever, rabies, BCG, and typhoid vaccine.
- Systemic glucocorticoids for any purpose other than to modulate symptoms from an event of clinical interest of suspected immunologic aetiology. The use of physiologic doses of corticosteroids may be approved after consultation with the Sponsor.
- Patients who, in the assessment by the investigator, require the use of any of the aforementioned treatments for clinical management should be removed from the study. Patients may receive other medications that the investigator deems to be medically necessary. The Exclusion Criteria describes other medications which are prohibited in this study.
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
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:Biological Sample collection
Biological Sample
|
Clinical and radiological assessment will be performed at the enrollment and every 3 +/- 1 months.
Clinical information and biological samples will be collected also at 2 years from surgery or start of therapy.
We plan collection of a maximum of 13 faecal and blood samples per patient (1 baseline + a maximum of 11 during treatment ± 1 disease progression, ± 10%).
In addition, we expect to collect fresh stools and tissue biopsies from at least 3-5 patients per group every year, which will be dedicated to our translational studies.
|
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 |
|---|---|---|
|
Primary Endopoint
時間枠:1 year
|
Correlation between Bacterial Antigens Mimicking-Tumor associated antigens (BAM-Ts) and clinical response to Immune Checkpoint Blockade (ICB).
|
1 year
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Secondary Endpoints
時間枠:2 year
|
A. Correlation between circulating immunological factors during ICB and clinical response: Relapse-Free Survival (RFS) or Progression Free Survival (PFS), Overall Response Rate (ORR), Overall Survival (OS);
|
2 year
|
その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Exploratory Endpoints
時間枠:5 year
|
Correlation between, HLA allotypes and microbiota in correlation with clinical response RFS or PFS and OS;
|
5 year
|
協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
捜査官
- 主任研究者:Luigi Nezi, PhD、Istituto Europeo di Oncologia
- 主任研究者:Monica Casiraghi, MD PhD、Istituto Europeo di Oncologia
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (推定)
2026年10月1日
一次修了 (推定)
2027年10月1日
研究の完了 (推定)
2031年4月1日
試験登録日
最初に提出
2026年7月24日
QC基準を満たした最初の提出物
2026年9月8日
最初の投稿 (実際)
2026年9月11日
学習記録の更新
投稿された最後の更新 (実際)
2026年9月11日
QC基準を満たした最後の更新が送信されました
2026年9月8日
最終確認日
2026年7月1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
- UID 4840
- L2-614 (その他の識別子:Comitato Etico Lombardia 2)
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
はい
IPD プランの説明
We will insert all information into the paper.
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
いいえ
米国FDA規制機器製品の研究
いいえ
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。