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局限性软组织肉瘤新辅助放化疗:2 期临床试验的安全性、可行性和早期肿瘤学结果。

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

机构信息

Department of Radiation Oncology, A C Camargo Cancer Center, São Paulo, Brazil.

Department of Clinical Oncology, A C Camargo Cancer Center, São Paulo, Brazil.

出版信息

Radiother Oncol. 2021 Jun;159:161-167. doi: 10.1016/j.radonc.2021.03.033. Epub 2021 Mar 31.

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.

摘要

背景与目的

肢体软组织肉瘤(ESTS)的最佳治疗方法仍存在争议。本研究旨在评估新辅助化疗(ChT)联合同期低分割放疗(hypo-RT)对局部和远处疾病复发的效果。本研究报告其安全性、可行性和早期结果。

材料与方法

这是一项前瞻性、单臂研究,目标入组患者 70 例。2015 年至 2018 年,18 例组织学证实的非转移性 ESTS 患者接受多柔比星和异环磷酰胺新辅助化疗 3 个周期,同时接受 hypo-RT(25Gy/5 次)治疗,随后进行手术。主要终点为无疾病生存(DFS)。次要终点为病理缓解、伤口并发症(WC)和发病率。

结果

中位随访时间为 29 个月。末次随访时,18 例患者中 13 例(72%)无局部或全身疾病存活,1 例死于远处转移,3 例远处转移存活。1 例患者在放疗野内出现局部复发。DFS 时间的平均值为 48.6 个月(95%CI:37.3-59.9)。6 例(33%)患者的病理标本中未检测到残留的存活肿瘤(其中 3 例为黏液样脂肪肉瘤)。有急性放疗皮肤毒性的患者 WC 有显著差异。6 例(33%)患者发生严重 WC。未报告 3 或 4 级 ChT 不良事件。

结论

尽管样本量有限,但这些早期结果表明,该治疗方案可行且耐受良好,保肢率、局部控制率和病理完全缓解率均较高,支持在多中心环境中进一步研究。

试验注册

ClinicalTrials.gov NCT02812654;https://clinicaltrials.gov/ct2/show/NCT02812654。

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