ASSESSING METASTASIS/RELAPSE IN SENTINEL LYMPH NODE DISSECTION MELANOMA PATIENTS
ASSESSING METASTASIS/RELAPSE IN SENTINEL LYMPH NODE DISSECTION MELANOMA PATIENTS
批准号:
6203058
负责人:
Dave S B Hoon
金额:
$79.41万
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-12-01 至 2000-11-30
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
该方案项目的重点是评估
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(MECHANISM)。精准识别和
前哨淋巴结的分析可以改善疾病分期,
进一步治疗。然而,需要更好的方法来检测
转移性疾病和早期患者复发的预测。的
SLND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。
该项目将侧重于开发新的分子方法,以改善
检测血液和前哨淋巴结中的转移性疾病。
开发用于RT-PCR和自动化Souther印迹分析的黑色素瘤标志物
将用于评估血液和前哨淋巴结。我们将评估
这些分子标记物用于检测
亚临床疾病和使用血液样本预测复发
SLND患者。我们还将使用黑色素瘤标志物RT-PCR检测
前哨淋巴结冷冻石蜡标本选择中的转移
结主要目的是提高微转移的检测
前哨淋巴结疾病。主要目标是改善
前哨淋巴结微转移疾病的检测和复发
血液中的亚临床疾病,以确定其潜力
在疾病分期和预后中的临床病理学效用。了一种方法
用来检测血清中的肿瘤特异性DNA标记这些
将使用前瞻性方法评估标记物作为肿瘤进展指标,
和存档血清目的是确定高血压患者,
发展为侵袭性疾病的可能性。马格德堡档案馆和
前瞻性标本沿着其临床随访提供了一个独特的
用于验证和确定这些新分子的临床效用的资源
方法。
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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