Key result
Achieving a pathologic complete response (≤5% viable cells) after neoadjuvant radiotherapy in soft tissue sarcoma was associated with improved local recurrence-free and overall survival.
Why the study?
The relationship between pathologic findings after neoadjuvant treatment and oncological outcomes in soft tissue sarcoma remains uncertain due to varying evaluation methods and cut-off values.
Does the EORTC-STBSG response score or pathologic complete response predict survival outcomes in patients with soft tissue sarcoma treated with neoadjuvant radiotherapy?
Cohort (n=44)
No
Does the EORTC-STBSG response score or pathologic complete response predict survival outcomes in patients with soft tissue sarcoma treated with neoadjuvant radiotherapy?
A pathologic complete response (≤5% viable cells) after neoadjuvant radiotherapy predicts improved local recurrence-free and overall survival in soft tissue sarcoma, whereas the EORTC-STBSG score does not.
Answers are grounded in this paper and cite their sources.
EORTC-STBSG score lacks prognostic value post-neoadjuvant RT in STS; leaves open whether ≤5% viable cells predict outcomes in prospective studies.
Background/Objectives: The relationship between pathologic findings in soft tissue sarcoma (STS) after neoadjuvant treatment and oncological outcomes remains uncertain due to varying evaluation methods and cut-off values. This study aims to assess pathologic findings after neoadjuvant radiotherapy in STS using the EORTC-STBSG response score and evaluate its prognostic value. Methods: Clinical and outcome data from 44 patients were reviewed. Resected specimens were re-evaluated to measure viable cells, necrosis, fibrosis, and hyalinization. Local recurrence-free survival (LRFS), distant metastasis-free survival (DMFS), and overall survival (OS) were analyzed using Kaplan–Meier survival analysis. Cox proportional hazards regression was used for univariate and multivariate analyses to correlate outcomes with pathologic response. Results: The median percentages of viable cells, necrosis, and fibrosis/hyalinization were 20%, 11%, and 40%, respectively. A pathologic complete response (pCR), defined as ≤5% viable cells, was achieved in 25% of cases. Local recurrence occurred in 33% of cases, with a significantly higher rate of 64% after R1 resection compared to 22% after R0 resection. Distant metastases were observed in 42% of patients, primarily in the lungs. The 3-year rates for LRFS, DMFS, and OS were 65%, 54%, and 67%, respectively. A correlation between outcomes and tumor size, grade and histological subtype was observed. Classifying pathologic response by the EORTC-STBSG score failed to show an association with outcomes. Patients achieving pCR showed lower risk of LR and improved OS. Conclusions: While the EORTC-STBSG score did not show a prognostic value, resection specimens with ≤5% viable cells were linked to improved LRFS and OS.
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Stergioula et al. (2024) conducted a cohort in Soft tissue sarcoma (n=44). Pathologic complete response (≤5% viable cells) vs. Non-pathologic complete response (>5% viable cells) was evaluated on Local recurrence-free survival (LRFS), distant metastasis-free survival (DMFS), and overall survival (OS). Achieving a pathologic complete response (≤5% viable cells) after neoadjuvant radiotherapy in soft tissue sarcoma was associated with improved local recurrence-free and overall survival.
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