Key result
In patients with pelvic and retroperitoneal bone and soft tissue sarcoma, the 3-year overall survival and local control rates were 71.7% and 79.1%, respectively.
Why the study?
The study aimed to retrospectively analyze clinical outcomes and prognostic factors in patients with pelvic and retroperitoneal bone and soft tissue sarcoma.
Cohort (n=187)
Yes
In patients with pelvic and retroperitoneal bone and soft tissue sarcoma in Japan, 3-year overall survival was 71.7%, with osteosarcoma and larger tumor size identified as poor prognostic factors.
Provides survival benchmarks for pelvic/retroperitoneal sarcomas; leaves open optimal strategies and generalizability pending prospective validation.
This study aimed to retrospectively analyze the clinical outcomes of patients with pelvic and retroperitoneal bone and soft tissue sarcoma (BSTS). Overall, 187 patients with BSTS in the pelvis and retroperitoneal region treated at 19 specialized sarcoma centers in Japan were included. The prognostic factors related to overall survival (OS), local control (LC), and progression-free survival (PFS) were evaluated. The 3-year OS and LC rates in the 187 patients were 71.7% and 79.1%, respectively. The 3-year PFS in 166 patients without any distant metastases at the time of primary tumor diagnosis was 48.6%. Osteosarcoma showed significantly worse OS and PFS than other sarcomas of the pelvis and retroperitoneum. In the univariate analyses, larger primary tumor size, soft tissue tumor, distant metastasis at the time of primary tumor diagnosis, P2 location, chemotherapy, and osteosarcoma were poor prognostic factors correlated with OS. Larger primary tumor size, higher age, soft tissue tumor, chemotherapy, and osteosarcoma were poor prognostic factors correlated with PFS in patients without any metastasis at the initial presentation. Larger primary tumor size was the only poor prognostic factor correlation with LC. This study has clarified the epidemiology and prognosis of patients with pelvic and retroperitoneal BSTS in Japan.
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Takemori et al. (2022) conducted a cohort in Pelvic and retroperitoneal bone and soft tissue sarcoma (n=187). Prognostic factors (e.g., tumor size, osteosarcoma) was evaluated on Overall survival (OS), local control (LC), and progression-free survival (PFS). In patients with pelvic and retroperitoneal bone and soft tissue sarcoma, the 3-year overall survival and local control rates were 71.7% and 79.1%, respectively.
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