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Pathologic Complete Response and Outcomes in Localized Soft-Tissue Sarcoma Treated With Neoadjuvant Chemoradiotherapy or Radiotherapy


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In an analysis reported in JAMA Oncology, Wang et al found that pathologic complete response (pCR) was associated with improved outcomes among patients with localized soft-tissue sarcoma receiving neoadjuvant chemoradiotherapy or radiotherapy.

The analysis included data from patients from two RTOG single-arm phase II trials in soft-tissue sarcoma: 79 patients from RTOG 0630, which evaluated preoperative radiotherapy alone and 64 from RTOG 9514, which evaluated preoperative chemoradiotherapy.

Key Findings

A total of 123 patients from both studies were evaluable for pCR: 14 (27.5%) of 51 in trial 9514 and 14 (19.4%) of 72 in trial 0630 had pCR.

Five-year overall survival was 100% for patients with pCR vs 76.5% (95% confidence interval [CI] = 62.3%–90.8%) and 56.4% (95% CI = 43.3%–69.5%) for patients with less than pCR in trials 9514 and 0630, respectively. Five-year disease-free survival for patients with pCR vs less than pCR was 88.9% vs 62.7% in trial 9514 and 90.9% vs 40.0% in trial 0630. Local failure rates at 5 years were 0% in patients with pCR vs 11.7% and 9.1% in trials 9514 and 0630, respectively.

On multivariate analysis in patients from both trials , pCR vs less than pCR was associated with improved overall survival (hazard ratio [HR] not estimable due to absence of events in pCR group, P = .01), improved disease-free survival (HR for less than pCR vs pCR = 4.91, 95% CI = 1.51–15.93, P = .008), improved distant disease-free survival (HR = 4.33, 95% CI = 1.32–14.14, P = .02), and reduced risk of distant metastasis (HR = 4.09, 95% CI = 1.25–13.36, P =.02).

On multivariate analysis, histologic types other than leiomyosarcoma, liposarcoma, and myxofibrosarcoma were associated with worse overall survival (HR = 2.24, 95% CI = 1.12–4.45, P = .02).

The investigators concluded: “This ancillary analysis of [two] nonrandomized clinical trials found that pCR was associated with improved survival in patients with [soft-tissue sarcoma] and should be considered as a prognostic factor of clinical outcomes for future studies.”

Dian Wang, MD, PhD, of Rush University Medical Center, is the corresponding author for the JAMA Oncology article.

Disclosure: The study was supported by grants from the National Cancer Institute. For full disclosures of the study authors, visit jamanetwork.com.

The content in this post has not been reviewed by the American Society of Clinical Oncology, Inc. (ASCO®) and does not necessarily reflect the ideas and opinions of ASCO®.
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