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PubMed · 17005597

Staging soft tissue sarcoma: evolution and change.

Dhanasekaran Kotilingam·Dina Chelouche Lev·Alexander J F Lazar·Raphael E Pollock
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Abstract

Soft tissue sarcoma (STS) is an extremely heterogeneous group of rare tumors that share a putative mesenchymal cell origin. STS can occur in any soft tissue in the body, yet all share a common feature of primarily disseminating hematogenously, particularly to the lungs. Staging for STS is particularly useful in prognosis, design of effective multimodality treatment programs, and comparing treatment outcomes from different centers and different eras. The current iteration of AJCC STS staging includes Tumor, Grade, Node, and Metastasis with "a" indicating superficial and "b" indicating deep designations. Further opportunities to improve this process exist, particularly as molecular considerations become more apparent, and future evolution into an even more useful STS staging system can be anticipated.

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Biomarkers, TumorDisease-Free SurvivalHumansLymphatic MetastasisNeoplasm StagingPredictive Value of TestsPrognosisRisk FactorsSarcomaSurvival RateJournal ArticleReview

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Dhanasekaran Kotilingam, Dina Chelouche Lev, Alexander J F Lazar, Raphael E Pollock. Staging soft tissue sarcoma: evolution and change.. https://doi.org/10.3322/canjclin.56.5.282

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