This proposal describes proposed studies for the continuation of the Soft Tissue Sarcoma (STS) Program Project, CA47179. We have continued the overall original objectives of designing and implementing a comprehensive and integrated multi-disciplinary program approach to the biology, pathogenesis and natural history of Soft Tissue Sarcoma (STS) Program Project, CA47179. We have continued the overall original objectives of designing and implementing a comprehensive and integrated multi-disciplinary program approach to the biology, pathogenesis and natural history of soft tissue sarcoma with the goal to translate this information into improve treatment of STS. Thus, our research program on the molecular genetic and biological characteristics of STS is geared to the development of novel therapeutic strategies and agents. A major unique resource of our program is the patient population: over the past 15 years, 3796 adult patients with STS have been admitted to MSKC. We continue and plan to expand the maintenance of the prospective clinical database on this population. In this revised renewal application, based on our accomplishments we have designed 4 projects to expand and explore new directions in the biology of STS and its application to the clinic. In Project, Clinical Studies, we have refined our efforts our efforts using regional lung perfusion to deliver potentially therapeutic agents to patients with metastatic lung disease as well as to continue an integrated preclinical/clinical immunotherapy program aimed at the effective delivery of tumor vaccines. In Project, based on previous studies, we continue the study of functional and immunophenotypic analysis of p53 and Rb pathways. In Project, studies continue our biochemical and molecular characterization of drug resistance with initial efforts of its translation into the design of clinical trials. In Project, a new initiative, we plan a project on defining the molecular genetics on synovial sarcoma and its impact on prognosis and gene expression. These 4 projects are supported by 3 Cores: Administrative/Clinical, pathology and Biostatistics.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA047179-11
Application #
6362552
Study Section
Subcommittee G - Education (NCI)
Program Officer
Krosnick, Steven H
Project Start
1989-01-09
Project End
2005-02-28
Budget Start
2001-03-01
Budget End
2002-02-28
Support Year
11
Fiscal Year
2001
Total Cost
$1,662,853
Indirect Cost
Name
Sloan-Kettering Institute for Cancer Research
Department
Type
DUNS #
064931884
City
New York
State
NY
Country
United States
Zip Code
10065
Xie, Yuanyuan; Cao, Zhen; Wong, Elissa Wp et al. (2018) COP1/DET1/ETS axis regulates ERK transcriptome and sensitivity to MAPK inhibitors. J Clin Invest 128:1442-1457
Weinreb, Ilan; Bishop, Justin A; Chiosea, Simion I et al. (2018) Recurrent RET Gene Rearrangements in Intraductal Carcinomas of Salivary Gland. Am J Surg Pathol 42:442-452
Kao, Yu-Chien; Sung, Yun-Shao; Zhang, Lei et al. (2017) Expanding the molecular signature of ossifying fibromyxoid tumors with two novel gene fusions: CREBBP-BCORL1 and KDM2A-WWTR1. Genes Chromosomes Cancer 56:42-50
Seifert, Adrian M; Zeng, Shan; Zhang, Jennifer Q et al. (2017) PD-1/PD-L1 Blockade Enhances T-cell Activity and Antitumor Efficacy of Imatinib in Gastrointestinal Stromal Tumors. Clin Cancer Res 23:454-465
Argani, Pedram; Zhang, Lei; Reuter, Victor E et al. (2017) RBM10-TFE3 Renal Cell Carcinoma: A Potential Diagnostic Pitfall Due to Cryptic Intrachromosomal Xp11.2 Inversion Resulting in False-negative TFE3 FISH. Am J Surg Pathol 41:655-662
Huang, Shih-Chiang; Zhang, Lei; Sung, Yun-Shao et al. (2016) Recurrent CIC Gene Abnormalities in Angiosarcomas: A Molecular Study of 120 Cases With Concurrent Investigation of PLCG1, KDR, MYC, and FLT4 Gene Alterations. Am J Surg Pathol 40:645-55
Alaggio, Rita; Zhang, Lei; Sung, Yun-Shao et al. (2016) A Molecular Study of Pediatric Spindle and Sclerosing Rhabdomyosarcoma: Identification of Novel and Recurrent VGLL2-related Fusions in Infantile Cases. Am J Surg Pathol 40:224-35
Argani, Pedram; Zhong, Minghao; Reuter, Victor E et al. (2016) TFE3-Fusion Variant Analysis Defines Specific Clinicopathologic Associations Among Xp11 Translocation Cancers. Am J Surg Pathol 40:723-37
Tan, Marcus C B; Brennan, Murray F; Kuk, Deborah et al. (2016) Histology-based Classification Predicts Pattern of Recurrence and Improves Risk Stratification in Primary Retroperitoneal Sarcoma. Ann Surg 263:593-600
Specht, Katja; Zhang, Lei; Sung, Yun-Shao et al. (2016) Novel BCOR-MAML3 and ZC3H7B-BCOR Gene Fusions in Undifferentiated Small Blue Round Cell Sarcomas. Am J Surg Pathol 40:433-42

Showing the most recent 10 out of 336 publications