The primary objective of the current proposal is to develop new criteria which will identify patients in need of adjuvant therapy and differentiate these patients from those in whom surgical therapy alone is curative. Many oncologists rely on primary tumor depth and clinically detectable disease in their determination of applicable therapy. The management of melanoma can be improved if techniques to detect micrometastases are developed to augment those in current practice. During the last grant period we developed innovative lymphatic mapping and selective lymphadenectomy techniques (Project III). These techniques have allowed us to detect occult melanoma cells by intraoperative frozen sections in regional lymph nodes of clinical Stage I melanoma patients. This technique accurately identifies patients with early stage melanoma who have nodal metastases and are likely to benefit from radial lymphadenectomy. Furthermore, it avoids unnecessary lymph node dissection in those patients whose tumors failed to metastasize. This new approach will be extended to the multicenter cooperative study in the current year. On the other hand, a substantial number of Stage I melanoma patients with occult-node metastases do not benefit from lymphadenectomy since they die from their disseminated metastases. Furthermore, 20% of all patients without occult metastases detected by H&E staining and/or immunostaining recur within 5 years despite resection of their nodes. It is obvious that these patients have subclinical systemic metastases at the time of initial surgical treatment. Therefore, we propose to investigate methods to identify Stage I patients who may require adjuvant therapy. Various histological, immunological, and molecular/biochemical methods will be evaluated.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
2P01CA029605-12
Application #
3093346
Study Section
Special Emphasis Panel (SRC (1D))
Project Start
1981-04-01
Project End
1998-05-31
Budget Start
1993-09-28
Budget End
1994-05-31
Support Year
12
Fiscal Year
1993
Total Cost
Indirect Cost
Name
John Wayne Cancer Institute
Department
Type
DUNS #
556074458
City
Santa Monica
State
CA
Country
United States
Zip Code
90404
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Lessard, Laurent; Liu, Michelle; Marzese, Diego M et al. (2015) The CASC15 Long Intergenic Noncoding RNA Locus Is Involved in Melanoma Progression and Phenotype Switching. J Invest Dermatol 135:2464-2474
Deutsch, Gary B; Kirchoff, Daniel D; Faries, Mark B (2015) Metastasectomy for stage IV melanoma. Surg Oncol Clin N Am 24:279-98
Marzese, Diego M; Hoon, Dave Sb (2015) Emerging technologies for studying DNA methylation for the molecular diagnosis of cancer. Expert Rev Mol Diagn 15:647-64

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