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Updated: Aug 4, 2025

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A Mouse Model of Incompletely Resected Soft Tissue Sarcoma for Testing Neoadjuvant Therapies
Published on: July 28, 2020
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Pathologic Complete Response and Clinical Outcomes in Patients With Localized Soft Tissue Sarcoma Treated With
Dian Wang1, Jonathan Harris2, William G Kraybill3
1Rush University Medical Center, Chicago, Illinois.
JAMA Oncology
|March 30, 2023
Summary
Pathologic complete response (pCR) in soft tissue sarcoma (STS) patients treated with neoadjuvant therapy is linked to better survival outcomes. Achieving pCR indicates a positive prognosis and reduced risk of recurrence in STS.
Area of Science:
- Oncology
- Clinical Trials
- Surgical Oncology
Background:
- Pathologic complete response (pCR) is a potential prognostic indicator in soft tissue sarcoma (STS).
- The prognostic significance of pCR in STS patients undergoing neoadjuvant therapy requires further investigation.
Purpose of the Study:
- To determine the prognostic value of pCR on survival outcomes in localized STS patients.
- To provide a long-term update on survival for patients in RTOG 0630.
Main Methods:
- Ancillary analysis of 143 patients from two nonrandomized Phase 2 trials (RTOG 0630 and RTOG 9514).
- Patients received either neoadjuvant chemoradiotherapy (CT-RT) or preoperative radiotherapy (RT) alone.
- Survival outcomes (OS, DFS) were analyzed using Kaplan-Meier and Cox models.
Main Results:
- pCR was achieved by 27.5% in RTOG 9514 and 19.4% in RTOG 0630.
- Patients with pCR had 100% 5-year overall survival (OS) in RTOG 9514.
- pCR was significantly associated with improved OS (P=.01) and DFS (HR, 4.91; P=.008), and reduced local failure rates.
Conclusions:
- pCR is a significant prognostic factor for improved survival in soft tissue sarcoma patients.
- Achieving pCR is associated with superior overall survival and disease-free survival.
- pCR should be considered in future clinical trial designs and prognostic assessments for STS.
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