ASSESSING METASTASIS/RELAPSE IN SENTINEL LYMPH NODE DISSECTION MELANOMA PATIENTS
ASSESSING METASTASIS/RELAPSE IN SENTINEL LYMPH NODE DISSECTION MELANOMA PATIENTS
批准号:
6563795
负责人:
Dave S B Hoon
金额:
$7.89万
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-02-14 至 2002-11-30
关键词:
SDS polyacrylamide gel electrophoresis biomarker biopsy blood chemistry cancer registry /resource clinical research cryopreservation diagnosis design /evaluation genetic markers high performance liquid chromatography human subject human therapy evaluation human tissue lymph nodes lymphadenectomy melanoma metastasis neoplasm /cancer classification /staging neoplasm /cancer diagnosis neoplasm /cancer relapse /recurrence neoplasm /cancer surgery neoplastic process polymerase chain reaction prognosis southern blotting
中文摘要
该计划项目的重点是评估
高危 AJCC II 期患者的前哨淋巴结清扫术 (SLND)
参加了多中心试验(MSLT)。准确识别和
前哨淋巴结分析可以改善疾病分期并指导
进一步治疗。然而,需要更好的方法来检测
早期患者的转移性疾病和复发预测。的
接受 SLND 的患者的黑色素瘤病灶、前哨淋巴结和血液
是评估新分子方法学的宝贵资源。
该项目将重点开发新的分子方法来改善
检测血液和前哨淋巴结中的转移性疾病。
为 RT-PCR 和自动 Souther 印迹分析开发的黑色素瘤标记物
将用于评估血液和前哨淋巴结。我们将评估
这些分子标记在检测中的临床应用
使用来自以下组织的血液样本进行亚临床疾病和复发预测
SLND 患者。我们还将使用黑色素瘤标记物 RT-PCR 来检测
前哨淋巴结冷冻和存档石蜡选择中的转移
节点。主要目标是改善微转移的检测
前哨淋巴结疾病。主要目标是改善
前哨淋巴结微转移病灶和复发病灶的检测
血液中的亚临床疾病以确定其潜力
临床病理学在疾病分期和预后中的应用。一个方法有
被开发用于评估血清中的肿瘤特异性 DNA 标记。这些
标记物将使用前瞻性评估作为肿瘤进展指标
和档案血清。目标是识别患有高
发展侵袭性疾病的可能性。 MSLT 档案和
前瞻性样本及其临床随访提供了独特的
验证和确定这些新分子的临床效用的资源
接近。
英文摘要
The Program Project's focus os on the assessment of the efficacy of
sentinel lymph node dissection (SLND) in high-risk AJCC Stage II patients
enrolled in the multi-center trial (MSLT). Accurate identification and
analysis of the sentinel node can improve disease staging and guide
further treatment. However, better methods are needed for the detection of
metastatic disease and prediction of relapse in early-stage patients. The
melanoma lesion, sentinel lymph node and blood of patients undergoing SLND
are valuable resource for assessing new molecular methodologies.
The project will focus on developing new molecular approaches to improve
detection of metastatic disease in blood and sentinel lymph nodes.
Melanoma markers developed for RT-PCR and automated Souther blot analysis
will be used to evaluate blood and sentinel lymph nodes. We will assess
the clinical utility of these molecular markers for detection of
subclinical disease and prediction of relapse using blood specimens from
SLND patients. We will also use melanoma marker RT-PCR to detect
metastasis in frozen and archival paraffin selection of sentinel lymph
nodes. The main objective will be to improve detection of micrometastic
disease in sentinel lymph nodes. The main objective will be to improve
detection of micrometastatic disease in sentinel lymph nodes and recurrent
subclinical disease in blood to determine their potential
clinicopathological utility in disease staging and prognosis. A method has
been developed to asses tumor- specific DNA markers in serum. These
markers will be assessed as tumor progression indicators using prospective
and archival serum. The objective will be to identify patients with high
potential for developing aggressive disease. The MSLT archival and
prospective specimens along with their clinical follow up provide a unique
resource to validate and determine clinical utility of these new molecular
approaches.
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