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立体定向体部放疗治疗寡转移软组织肉瘤。

Stereotactic body radiotherapy for oligometastatic soft tissue sarcoma.

机构信息

Department of Radiation Oncology, Erasmus MC Cancer Institute, PO Box 2040, 3000 CA, Rotterdam, The Netherlands.

Department of Surgical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

出版信息

Radiol Med. 2018 Nov;123(11):871-878. doi: 10.1007/s11547-018-0912-5. Epub 2018 Jun 19.

Abstract

BACKGROUND

Stereotactic body radiotherapy (SBRT) is emerging as a novel treatment option in metastatic soft tissue sarcoma (STS). The aim of our study was to evaluate the effectiveness of exclusive SBRT on disease control and survival in oligometastatic (≤ 3 synchronous lesions) STS.

MATERIALS AND METHODS

In total, 16 consecutive patients, accounting for 26 metastases (including 21 lung and 5 lymph node or soft tissue metastases), were treated at our institution with SBRT. Patient- and treatment-related characteristics were collected. Local control (LC), overall survival (OS), distant metastases-free survival (DMFS), and time to initiation of chemotherapy or best supportive care (corrected disease-free survival, cDFS) were assessed.

RESULTS

Four-year OS was 54% and median OS was 69 months [95% confidence interval (CI) 20-118 months]. LC of 26 lesions at 4 years was 78%. Median DMFS and cDFS were 17 (95% CI 5-30 months) and 28 months (95% CI 5-52 months), respectively. Disease-free interval < 24 months from primary tumor treatment to first metastasis was the only predictor of reduced LC, cDFS, and OS (p = 0.022, 0.023, and 0.028, respectively). No acute or chronic grade ≥ 3 toxicity was observed. Median follow-up was 36 months (IQR 18-71 months).

CONCLUSIONS

In patients with oligometastatic STS, SBRT yields satisfying local control with minimal toxicity. Median OS was 69 months. Repeated SBRT may be considered to extend disease-free and systemic therapy-free interval. Increased time from primary tumor to first metastasis identifies patients with potentially greater benefit from SBRT.

摘要

背景

立体定向体部放疗(SBRT)作为一种新的治疗选择,正在转移性软组织肉瘤(STS)中出现。我们的研究目的是评估单纯 SBRT 对寡转移(≤3 个同步病变)STS 的疾病控制和生存的疗效。

材料和方法

共 16 例患者(26 个转移灶,包括 21 个肺转移灶和 5 个淋巴结或软组织转移灶)在我们机构接受 SBRT 治疗。收集患者和治疗相关特征。评估局部控制(LC)、总生存(OS)、无远处转移生存(DMFS)和开始化疗或最佳支持治疗的时间(校正无疾病生存,cDFS)。

结果

4 年 OS 为 54%,中位 OS 为 69 个月(95%CI 20-118 个月)。26 个病灶的 4 年 LC 为 78%。DMFS 和 cDFS 的中位值分别为 17 个月(95%CI 5-30 个月)和 28 个月(95%CI 5-52 个月)。从原发肿瘤治疗到首次转移的无疾病间期<24 个月是 LC、cDFS 和 OS 降低的唯一预测因素(p=0.022、0.023 和 0.028)。未观察到急性或慢性≥3 级毒性。中位随访时间为 36 个月(IQR 18-71 个月)。

结论

在寡转移 STS 患者中,SBRT 具有令人满意的局部控制效果,且毒性最小。中位 OS 为 69 个月。重复 SBRT 可能延长无疾病和无系统治疗间隔。原发肿瘤至首次转移的时间增加可识别出更有可能从 SBRT 中获益的患者。

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