Survival and Prognosis of Chondrosarcoma Subtypes: SEER Database Analysis.

Publication/Presentation Date

2-1-2020

Abstract

Chondrosarcomas are rare tumors and, historically, investigation of these tumors has been limited to small series and single-institution studies. There have been no studies that evaluated the identification or comparison of differences in prognostic factors between the five known non-conventional chondrosarcoma subtypes (myxoid, juxtacortical, clear-cell, mesenchymal, and dedifferentiated). The purpose of this paper was to determine the demographic, clinical, incidence, and tumor characteristics of all five known non-conventional chondrosarcoma subtypes, determine the 1-, 5-year, and median survival differences between these subtypes, and to determine the demographic and clinical variables that are significant prognostic indicators for each chondrosarcoma subtypes. We retrospectively reviewed the SEER database for all patients with non-conventional chondrosarcoma. χ

Volume

38

Issue

2

First Page

311

Last Page

319

ISSN

1554-527X

Disciplines

Medicine and Health Sciences

PubMedID

31498474

Department(s)

Hematology-Medical Oncology Division

Document Type

Article

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