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临床试验/NCT05786105
NCT05786105已完成不适用

Optical Genome Mapping in Characterization of Multiple Myeloma

Institut de cancérologie Strasbourg Europe1 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2023年4月21日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
8
试验地点
1
主要终点
Validate the use of Optical Genome Mapping in Multiple Myeloma characterization

研究概览

简要总结

The current cytogenetic characterization of Multiple Myeloma (including chromosome and gene abnormalities identification in abnormal plasma cells) encounters some limitations. Indeed current techniques only enable to analyze a limited numbers of predefined abnormalities. New tools that will allow for characterization of abnormalities involved in multiple myeloma development are thus required. The interest of Optical Genome Mapping has already been demonstrated in other hematological diseases. The present study aims at validating Optical Genome Mapping in genetic abnormalities identification for patients with Multiple Myeloma (MM).

详细描述

For this study, supplementary samples will be collected during bone marrow biopsy performed at MM diagnosis. These will be used for CD138+ Plasma Cell Isolation and sent to GENTYANE (GEnoTYpage and sequencing in AuvergNE) platform in Clermont-Ferrand for Optical Genome Mapping.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Age ≥ 18 years
  • Non previously treated Multiple Myeloma (criteria from the International Myeloma Working Group)
  • Presence of CRAB criteria (Calcium Renal Anemia Bone : Calcemia > 2.75 mmol/l or > 0.25 mmol/l higher than the Upper Limit of Normal ; serum creatinine > 173 μmol/l or creatinine clearance < 40ml per minute attributed to myeloma ; anemia with hemoglobin value < 10g/dl or more than 2g/dl below the Lower Limit of Normal, bone lesions with osteolytic lesions or osteoporotic vertebral collapses attributed to myeloma)

排除标准

  • Opposition of the patient
  • Failure of myelogram
  • Previous treatment of multiple myeloma (except with corticosteroids)
  • Failure of FISH
  • Minor or patients placed under guardianship or supervision
  • Patients deprived of liberty
  • Patients placed under judicial protection
  • Patients that are not able to express their consent
  • Pregnant and breastfeeding women

结局指标

主要结局

Validate the use of Optical Genome Mapping in Multiple Myeloma characterization

时间窗: At MM diagnosis

Concordance scores for abnormalities detected with Optical Genome Mapping and Fluorescence In Situ Hybridization (FISH)

次要结局

  • Evaluate Optical Genome Mapping for identification of genetic abnormalities that are not detected with FISH in Multiple Myeloma(At MM diagnosis)

研究者

发起方
Institut de cancérologie Strasbourg Europe
申办方类型
Other
责任方
Sponsor

研究点 (1)

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