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Making progress in a rare disease: emerging therapeutics in soft tissue sarcomas.

Publication ,  Journal Article
Choe, J; Riedel, R
Published in: F1000Res
2018

Sarcomas are rare tumors derived from mesenchymal connective tissues in the body. Because there are well over 50 histologic sarcoma subtypes, including malignant and non-malignant pathologies, clinical courses and therapeutic management are widely divergent. In general, therapeutic options across all soft tissue sarcomas are limited in number and are often generalized across multiple sarcoma histologies. The recent emergence of molecularly targeted therapies and immune-based agents presents a future of refined systemic treatment practices that are rationally tailored to the tumor by histologic subtype and biologic mechanisms.

Duke Scholars

Published In

F1000Res

DOI

EISSN

2046-1402

Publication Date

2018

Volume

7

Location

England

Related Subject Headings

  • Sarcoma
  • Rare Diseases
  • Molecular Targeted Therapy
  • Immunotherapy
  • Humans
  • 1112 Oncology and Carcinogenesis
  • 1103 Clinical Sciences
  • 0601 Biochemistry and Cell Biology
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Choe, J., & Riedel, R. (2018). Making progress in a rare disease: emerging therapeutics in soft tissue sarcomas. F1000Res, 7. https://doi.org/10.12688/f1000research.15868.1
Choe, Jennifer, and Richard Riedel. “Making progress in a rare disease: emerging therapeutics in soft tissue sarcomas.F1000Res 7 (2018). https://doi.org/10.12688/f1000research.15868.1.
Choe, Jennifer, and Richard Riedel. “Making progress in a rare disease: emerging therapeutics in soft tissue sarcomas.F1000Res, vol. 7, 2018. Pubmed, doi:10.12688/f1000research.15868.1.

Published In

F1000Res

DOI

EISSN

2046-1402

Publication Date

2018

Volume

7

Location

England

Related Subject Headings

  • Sarcoma
  • Rare Diseases
  • Molecular Targeted Therapy
  • Immunotherapy
  • Humans
  • 1112 Oncology and Carcinogenesis
  • 1103 Clinical Sciences
  • 0601 Biochemistry and Cell Biology