Development of a Peripheral Blood Assay to Replace Bone Marrow Biopsy in Myeloproliferative Neoplasms- a Multi-center Observational Study
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 500
- 主要终点
- To development PERIBLOOD-MPN Diagnostic Test
研究概览
简要总结
The PERIBLOOD-MPN study aims to develop and validate a minimally invasive peripheral blood test using single-cell RNA sequencing to accurately diagnose and classify myeloproliferative neoplasms, potentially reducing the need for invasive bone marrow biopsies.
详细描述
PERIBLOOD-MPN is an observational, multi-center study that aims to collect data to develop a novel, minimally invasive diagnostic tool for myeloproliferative neoplasms (MPN) based on peripheral blood (PB) profiling of circulating hematopoietic stem and progenitor cells (cHSPCs) using single-cell RNA sequencing (scRNA-seq). Current diagnostic practice relies on bone marrow (BM) biopsy, a procedure that is invasive, technically demanding, and may be inconclusive in early or prefibrotic disease stages.
Prior work in the field has established a reference atlas of healthy cHSPC subtypes and a computational pipeline capable of identifying disease-specific transcriptional changes by quantifying deviations from this reference. This study will assess whether PB-based genomic profiling can accurately distinguish MPN from non-clonal cytoses, including secondary erythrocytosis or thrombocytosis.
Patients referred for a bone marrow biopsy due to suspected myeloproliferative neoplasm (MPN) will undergo PB collection for genomic profiling. The primary objective is to develop a PB-based test by comparing the new test's diagnoses to conventional BM-based diagnostics. The secondary objectives include evaluating its potential for MPN subtype classification and risk stratification, as well as assessing its ability to reduce the need for BM biopsies.
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
- 否
入选标准
- •Age ≥ 18 years
- •Confirmed MPN diagnosis, based on the WHO criteria (Barbui 2018), which includes:
- •Polycythemia Vera (PV) Criteria:
- •Elevated hemoglobin (>16.5 g/dL for men, >16.0 g/dL for women), hematocrit (>49% for men, >48% for women), or increased red cell mass
- •Bone marrow biopsy showing hypercellularity with trilineage growth (panmyelosis)
- •Presence of JAK2 mutation (V617F or exon 12)
- •Essential Thrombocythemia (ET) Criteria:
- •Platelet count ≥450 ×10⁹/L
- •Bone marrow biopsy showing proliferation mainly of the megakaryocyte lineage
- •Not meeting WHO criteria (Alaggio et al., 2022) for other myeloid neoplasms (such as CML, PV, PMF, MDS).
- •Presence of JAK2, CALR, or MPL mutation Primary Myelofibrosis (PMF) Criteria
- •Megakaryocytic proliferation and atypia, with or without reticulin fibrosis, and increased marrow cellularity (for prefibrotic/early PMF) or significant reticulin/collagen fibrosis (for overt PMF)
- •Not meeting criteria for other myeloid neoplasms
- •Presence of JAK2, CALR, or MPL mutation, or in their absence, another clonal marker
- •Patients who are referred for a bone marrow biopsy due to a suspected diagnosis of MPN
排除标准
- •Patients diagnosed with MPN receiving therapy
- •Patients who have undergone a bone marrow transplant
结局指标
主要结局
To development PERIBLOOD-MPN Diagnostic Test
时间窗: Three months following the PB sample
Development of PERIBLOOD-MPN Diagnostic Test Using PB-Derived CD34+ cHSPCs for Diagnosis of MPN
次要结局
未报告次要终点
