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How Do the Outcomes of Radiation-Associated Pelvic and Sacral Bone Sarcomas Compare to Primary Osteosarcomas following Surgical Resection?

SIMPLE SUMMARY: Primary osteosarcomas, spindle cell sarcomas, and radiation-associated sarcomas arising in the pelvis and sacrum (RASB) represent challenging disease processes. The oncologic outcomes are similarly poor between these entities; however, the rates of perioperative death and 5-year dise...

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Detalles Bibliográficos
Autores principales: Lazarides, Alexander L., Burke, Zachary D. C., Gundavda, Manit K., Novak, Rostislav, Ghert, Michelle, Wilson, David A., Rose, Peter S., Wong, Philip, Griffin, Anthony M., Ferguson, Peter C., Wunder, Jay S., Houdek, Matthew T., Tsoi, Kim M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9104334/
https://www.ncbi.nlm.nih.gov/pubmed/35565308
http://dx.doi.org/10.3390/cancers14092179
Descripción
Sumario:SIMPLE SUMMARY: Primary osteosarcomas, spindle cell sarcomas, and radiation-associated sarcomas arising in the pelvis and sacrum (RASB) represent challenging disease processes. The oncologic outcomes are similarly poor between these entities; however, the rates of perioperative death and 5-year disease specific survival for patients with RASB appear to be worse overall. While surgery can result in a favorable outcome for a small subset of patients, surgical treatment is fraught with complications. ABSTRACT: Radiation-associated sarcoma of the pelvis and/or sacrum (RASB) is a rare but challenging disease process associated with a poor prognosis. We hypothesized that patients with RASB would have worse surgical and oncologic outcomes than patients diagnosed with primary pelvic or sacral bone sarcomas. This was a retrospective, multi-institution, comparative analysis. We reviewed surgically treated patients from multiple tertiary care centers who were diagnosed with a localized RASB. We also identified a comparison group including all patients diagnosed with a primary localized pelvic or sacral osteosarcoma/spindle cell sarcoma of bone (POPS). There were 35 patients with localized RASB and 73 patients with POPS treated with surgical resection. Patients with RASB were older than those with POPS (57 years vs. 38 years, p < 0.001). Patients with RASB were less likely to receive chemotherapy (71% for RASB vs. 90% for POPS, p = 0.01). Seventeen percent of patients with RASB died in the perioperative period (within 90 days of surgery) as compared to 4% with POPS (p = 0.03). Five-year disease-specific survival (DSS) (31% vs. 54% p = 0.02) was worse for patients with RASB vs. POPS. There was no difference in 5-year local recurrence free survival (LRFS) or metastasis free survival (MFS). RASB and POPS present challenging disease processes with poor oncologic outcomes. Rates of perioperative mortality and 5-year DSS are worse for RASB when compared to POPS.