4.7 Article

Neoadjuvant hypofractionated radiotherapy and chemotherapy for extremity soft tissue sarcomas: Safety, feasibility, and early oncologic outcomes of a phase 2 trial

期刊

RADIOTHERAPY AND ONCOLOGY
卷 159, 期 -, 页码 161-167

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.radonc.2021.03.033

关键词

Extremity soft tissue sarcoma; Combined modality treatment; Hypofractionated radiotherapy; Wound complications; Pathologic response; Neoadjuvant chemotherapy and radiotherapy

向作者/读者索取更多资源

This study evaluated neoadjuvant chemotherapy and hypofractionated radiotherapy in extremity soft tissue sarcomas, showing that the treatment regimen is safe and feasible, with high rates of limb preservation and local control, supporting further investigation in a multi-institutional setting with promising early outcomes.
Background and purpose: Optimal treatment of extremity soft tissue sarcomas (ESTS) is controversial. The aim of this study was to evaluate neoadjuvant chemotherapy (ChT) plus concomitant hypofractionated RT (hypo-RT) in local and distant disease relapse. Here we report safety, feasibility and early outcomes. Materials and methods: This was a prospective, single arm study with a goal accrual of 70 patients. Between 2015 and 2018, 18 patients with histologically confirmed nonmetastatic ESTS were assigned to receive doxorubicin and ifosfamide for three neoadjuvant cycles, concomitant with hypo-RT (25 Gy in 5 fractions) followed by surgery. The primary endpoint was disease-free survival (DFS). Secondary outcomes were pathologic response, wound complications (WC), and morbidity rates. Results: Median follow-up was 29 months. At last follow-up, 13/18 patients were alive without evidence of local or systemic disease (DFS 72%), 1 had died due to metastatic disease, and 3 were alive with distant metastasis. One patient presented with local relapse within the irradiated field. Mean DFS time was 48.6 months (95% CI: 37.3-59.9). Six patients (33%) had no residual viable tumor detected in pathologic specimens (3 of these myxoid liposarcomas). There was a significant difference in WC among patients with acute RT skin toxicity. Six patients (33%) developed major WC. No grade 3 or 4 ChT adverse events were reported. Conclusion: Despite the limited sample size, these early outcomes demonstrate that this treatment regimen is feasible and well tolerated with high rates of limb preservation, local control, and pathologic complete response, supporting further investigation in a multi-institutional setting. Trial Registration: ClinicalTrials.gov NCT02812654; https://clinicaltrials.gov/ct2/show/NCT02812654. (c) 2021 Elsevier B.V. All rights reserved. Radiotherapy and Oncology 159 (2021) 161-167

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据