跳至主要内容
临床试验/NCT01942603
NCT01942603进行中(未招募)不适用

Minitub: Prospective Registry of Sentinel Node (SN) Positive Melanoma Patients With Minimal SN Tumor Burden Who Undergo Completion Lymph Node Dissection (CLND) or Nodal Observation

European Organisation for Research and Treatment of Cancer - EORTC22 个研究点 分布在 10 个国家目标入组 296 人开始时间: 2009年7月最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
296
试验地点
22
主要终点
Distant Metastasis Free Interval (DMFI)

研究概览

简要总结

The purpose of this registry is to collect data in order to discover whether melanoma patients with minimal SN tumor burden should undergo a complete lymph node dissection (CLND) or not.

Currently, if a patient has a positive (or metastatic) SN, this patient will be offered a CLND, which is a surgical intervention aiming to remove all lymph nodes from the same nodal basin as the SN. However, if the positive (or metastatic) SN is only minimally involved, some centers and/or countries do not offer a CLND routinely. As a matter of fact, the CLND procedure does not increase survival for patients with a minimal SN tumor burden, but can add prognostic information, potentially useful in the subsequent decision-making process. However, this is a surgical operation for the patient, which might be accompanied by significant side effects. Moreover, only approximately 20% of patients with a metastatic SN have further lymph node metastases in the same basin, which means that about 4 patients out of 5 will not benefit from a CLND. Thus, there is an urgent need to identify which SN positive patients could be safely spared from a CLND. It has been demonstrated that breast cancer patients with minimal SN tumor burden can be safely managed with nodal observation only, without performing a CLND. There is evidence that the same situation exists in melanoma as well, but this needs to be validated and this is why we are conducting this registry.

The results of this registry will be crucial to establish an accepted standard of care (CLND or nodal observation) for melanoma patients with minimal SN tumor burden.

研究设计

研究类型
Observational
观察模型
Case Control
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

  • 18 years of age or older
  • Histological evidence of primary cutaneous melanoma
  • Metastases solely confined within the SN:
  • in the sub-capsular space (with no parenchymal infiltration) and with a maximum diameter of the largest metastasis not greater than 0.4 mm or
  • regardless of the site, any sub-micrometastasis with a maximum diameter not greater than 0.1 mm If there is more than 1 metastatic SN, the patient will be still eligible provided that all involved SN have minimal tumor burden, regardless of the amount of positive SNs and the interested basin

排除标准

  • No history of any other malignancy within the past 5 years, except for non-melanoma skin cancer (Basal Cell Carcinomas or Squamous Cell Carcinomas) and in situ cervical cancer
  • Absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial -

结局指标

主要结局

Distant Metastasis Free Interval (DMFI)

时间窗: 5 years after last patient in

次要结局

  • Regional Control Rate (secondary endpoint):(5 years after last patient in)
  • Relapse Free Interval (RFI)(5 years after last patient in)
  • Morbidity: rates of wound infections, lymphedema and neurological damage(5 years after last patient in)
  • Melanoma Specific Survival (MSS)(5 years after last patient in)
  • Overall Survival (OS)(5 years after last patient in)

研究者

申办方类型
Network
责任方
Sponsor

研究点 (22)

Loading locations...

相似试验