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临床试验/NCT05321862
NCT05321862撤回2 期

Exploratory Study Evaluating the Relevance of [68Ga]Ga-PentixaFor for Initial Staging and Detection of Minimal Residual Disease in Multiple Myeloma Patients Eligible for Autologous Stem Cell Transplantation Less Than 66 Years Included in the Prospective IFM 2020-02.

Nantes University Hospital1 个研究点 分布在 1 个国家开始时间: 2023年3月14日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
撤回
试验地点
1
主要终点
Sensitivity

研究概览

简要总结

The aim of our study is to confirm the relevance of PET using [68Ga]Ga-PentixaFor ligand, in comparison with FDG, for initial staging and detection of minimal residual disease in multiple myeloma patients eligible for autologous stem cell transplantation less than 66 years.

The prognostic value of positive CXCR4 expression will also be assessed and [68Ga]Ga-PentixaFor/FDG discordances explored.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Inclusion criteria are identical to inclusion criteria in MIDAS study (EudraCT Number: 2020-005216-21, ClinicalTrials.gov Identifier: NCT04934475) .

排除标准

  • Non inclusion criteria are identical to non inclusion criteria in MIDAS study (EudraCT Number: 2020-005216-21, ClinicalTrials.gov Identifier: NCT04934475) added with:
  • eGFR < 50 ml/min by MDRD or CKDEPI.
  • Previous or concurrent second malignancy except for adequately treated basal cell carcinoma of the skin, curatively treated in situ carcinoma of the cervix, curatively treated solid cancer, with no evidence of disease for at least 2 years.
  • Patient with uncontrolled insulin-dependent or non-insulin-dependent diabetes mellitus.

研究组 & 干预措施

[68Ga]Ga-PentixaFor

Experimental

干预措施: [68Ga]Ga-PentixaFor (Drug)

结局指标

主要结局

Sensitivity

时间窗: 6 months

To determine the sensitivity of \[68Ga\]Ga-PentixaFor-PET to detect Multiple Myeloma lesions \[Bone marrow (BM) lesions and/or extra-medullary disease (EMD)\] at the time of initial diagnosis in high risk MM patients included in the MIDAS study.

次要结局

  • Specificity, positive predictive value (PPV) and negative predictive value (NPV) of [68Ga]Ga-PentixaFor-PET.(1 month)
  • Prognostic impact of FDG-PET and of [68Ga]Ga-PentixaFor-PET depending on the uptake detected by each imaging technique.(1 month)
  • Discrepancies rate between FDG-PET and [68Ga]Ga-PentixaFor-PET and factors associated with.(1 month and 6 months)
  • Correlation between FDG-PET and [68Ga]Ga-PentixaFor-PET uptakes evaluated by SUV.(1 month)
  • Correlation between FDG-PET and [68Ga]Ga-PentixaFor-PET uptakes evaluated by the RNAseq data evaluated on the myelogram.(1 month)
  • Prognostic impact of FDG-PET and [68Ga]Ga-PentixaFor-PET depending on the positivity, number and intensity of uptake detected by each imaging technique.(6 months)
  • Link between FDG-PET, [68Ga]Ga-PentixaFor-PET results and minimal residual disease evaluated by NGS.(6 months)
  • Tolerance of [68Ga]Ga-PentixaFor-PET.(1 month and 6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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