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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.

研究概览

研究类型

介入性

注册 (估计的)

360

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

学习地点

    • MI
      • Milan、MI、意大利、20141
        • Istituto Europeo di Oncologia
        • 首席研究员:
          • Gianluca Spitaleri, MD
        • 接触:
        • 接触:
        • 首席研究员:
          • Monica Casiraghi, MD PhD
        • 首席研究员:
          • Giuseppe Caruso, MD PhD
        • 首席研究员:
          • Carolina Cimminiello, MD

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

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.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的: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.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Primary Endopoint
大体时间:1 year
Correlation between Bacterial Antigens Mimicking-Tumor associated antigens (BAM-Ts) and clinical response to Immune Checkpoint Blockade (ICB).
1 year

次要结果测量

结果测量
措施说明
大体时间
Secondary Endpoints
大体时间: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

其他结果措施

结果测量
措施说明
大体时间
Exploratory Endpoints
大体时间:5 year
Correlation between, HLA allotypes and microbiota in correlation with clinical response RFS or PFS and OS;
5 year

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Luigi Nezi, PhD、Istituto Europeo di Oncologia
  • 首席研究员:Monica Casiraghi, MD PhD、Istituto Europeo di Oncologia

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年10月1日

初级完成 (估计的)

2027年10月1日

研究完成 (估计的)

2031年4月1日

研究注册日期

首次提交

2026年7月24日

首先提交符合 QC 标准的

2026年9月8日

首次发布 (实际的)

2026年9月11日

研究记录更新

最后更新发布 (实际的)

2026年9月11日

上次提交的符合 QC 标准的更新

2026年9月8日

最后验证

2026年7月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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