This proposal describes the continuation and expansion of our program funded under CA 47179. We maintain our original overall objectives of implementing a comprehensive multi-disciplinary program designed to address issues related to improved treatment of and understanding of the biology of soft tissue sarcomas (STS). A major resource of this program is the patient population: over the past 9 years, 1802 adult patients with STS have been admitted to MSKCC. We maintain a comprehensive prospective database on this population. In this revised proposal, the clinical studies (Project 0004) continue the multimodality approaches (chemotherapy, immunotherapy, and radiation therapy) to the diagnosis and treatment of selected groups of patients with STS. The monoclonal antibody studies represent a major expansion of our focus and are on the strong institutional commitment and program in the development of new biologicals for the treatment of cancer. Our initial studies of radiolabelled antibodies are a first step in the development of an expanded immunotherapy program. Both the chemotherapy and immunological approaches are tightly linked to the laboratory efforts and accomplishments in immunopathology (Project 0005) and drug resistance (Project 0003). The immunopathology project (Project 0005) will continue the immunophenotypic analysis of sarcomas with a focus on the study of (i) differentiation of myogenic tumors (ii) multistage carcinogenesis and tumor progression in sarcomas. Hypotheses generated in Project 0003 will be tested in some of the clinical trials in Project 1. The research projects are supported by 4 cores: Administrative, Clinical, Pathology and Biostatistical. Thus, the disciplines of surgery, medical and radiation oncology, pathology, immunology and biostatistics have been marshalled to study the biology and clinical care of STS.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA047179-05
Application #
3094232
Study Section
Special Emphasis Panel (SRC (M1))
Project Start
1989-01-09
Project End
1995-08-31
Budget Start
1993-09-01
Budget End
1994-08-31
Support Year
5
Fiscal Year
1993
Total Cost
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
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
Huang, Shih-Chiang; Ghossein, Ronald A; Bishop, Justin A et al. (2016) Novel PAX3-NCOA1 Fusions in Biphenotypic Sinonasal Sarcoma With Focal Rhabdomyoblastic Differentiation. Am J Surg Pathol 40:51-9
Dickson, Mark A; Schwartz, Gary K; Keohan, Mary Louise et al. (2016) Progression-Free Survival Among Patients With Well-Differentiated or Dedifferentiated Liposarcoma Treated With CDK4 Inhibitor Palbociclib: A Phase 2 Clinical Trial. JAMA Oncol 2:937-40

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