跳至主要内容
临床试验/NCT04759781
NCT04759781进行中(未招募)不适用

A Prospective Registry Study of a Primary Melanoma Gene-signature to Predict Sentinel Node (SN) Status and Determine Its Prognostic Value for More Accurate Staging of SN-negative Melanoma Patients.

SkylineDx9 个研究点 分布在 1 个国家目标入组 1,820 人开始时间: 2021年8月25日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
1,820
试验地点
9
主要终点
Positive Predictive Value (PPV)

研究概览

简要总结

MERLIN_001 is a prospective registry study of a primary melanoma gene-signature to predict sentinel node (SN) status and to determine its prognostic value for more accurate staging of SN-negative melanoma patients.

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

  • Newly diagnosed patients with invasive malignant melanoma of the skin (AJCC 8th edition staging guidelines) elected to undergo sentinel lymph node biopsy per the treating physician's recommendation.
  • Male or female, age ≥18 years.

排除标准

  • Full primary melanoma pathology report unavailable.
  • Documented clinically apparent nodal metastases at diagnosis.
  • Distant metastatic disease (M1a,b,c,d) clinically present at primary diagnosis
  • Any prior or concurrent primary invasive melanoma mapping to the same draining lymph node basin(s).
  • Documented history of another (prior or concurrent) primary invasive melanoma of T1b or greater at any site within the last 5 years.
  • Previous surgery in or radiation therapy to the draining lymph node basin(s) of the current primary melanoma.
  • Ocular, vulvar, perianal or mucosal melanomas or melanocytic tumors of uncertain malignant potential (MELTUMP) or atypical Spitz tumors.

结局指标

主要结局

Positive Predictive Value (PPV)

时间窗: 2 years after inclusion

The predictive capability of the Merlin Assay to identify newly diagnosed primary cutaneous melanoma patients who have a low risk of presenting with a positive sentinel lymph node.

Negative Predictive Value (NPV)

时间窗: 2 years after inclusion

The predictive capability of the Merlin Assay to identify newly diagnosed primary cutaneous melanoma patients who have a low risk of presenting with a positive sentinel lymph node.

Sensitivity and Specificity.

时间窗: 2 years after inclusion

The predictive capability of the Merlin Assay to identify newly diagnosed primary cutaneous melanoma patients who have a low risk of presenting with a positive sentinel lymph node.

次要结局

  • 3-5 year Recurrence-Free Survival (RFS)(3-5 years after patient inclusion)
  • 3-5 year Distant Metastasis-Free Survival (DMFS)(3-5 years after patient inclusion)
  • 3-5 year Overall Survival (OS)(3-5 years after patient inclusion)

研究者

发起方
SkylineDx
申办方类型
Industry
责任方
Sponsor

研究点 (9)

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