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

医学 软组织肉瘤 放射治疗 肿瘤科 化疗 新辅助治疗 放射科 内科学 软组织 外科
作者
Maria Leticia Gobo Silva,Celso Abdon Lopes de Mello,Samuel Aguiar Junior,Felipe D'Almeida Costa,Paulo Roberto Stevanato Filho,Tiago Santoro Bezerra,Suely Akiko Nakagawa,Antonio Geraldo Nascimento,Isabela Werneck da Cunha,Ranyell Spencer Sobreira Batista,Ulisses Ribaldo Nicolau Daher,Maria Nirvana Formiga,Janaina Naiara Germano,Bruna Elisa Catin Kupper,Antonio Cassio Assis Pellizzon,Ademar Lopes
出处
期刊:Radiotherapy and Oncology [Elsevier BV]
卷期号:159: 161-167
标识
DOI:10.1016/j.radonc.2021.03.033
摘要

Abstract 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 .
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