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放射性诱导软组织肉瘤患者的临床和功能预后。

The clinical and functional outcome for patients with radiation-induced soft tissue sarcoma.

机构信息

Mount Sinai Hospital, Toronto, Ontario, Canada.

出版信息

Cancer. 2012 May 15;118(10):2682-92. doi: 10.1002/cncr.26543. Epub 2011 Oct 11.

Abstract

BACKGROUND

Radiation-induced soft tissue sarcomas (RI-STS) are rare, and it is believed that they are associated with a poor prognosis.The authors of this report compared the clinical and functional outcomes of adults who had extremity RI-STS with the outcomes of adults with sporadic STS.

METHODS

Forty-four patients who were diagnosed with RI-STS from 1989 to 2009 were identified from 4 prospectively collected databases. Patient demographics, surgical and adjuvant treatment parameters, and oncologic and functional outcomes were evaluated.

RESULTS

The median latent period from irradiation of the primary condition to RI-STS diagnosis was 16 years. The median radiotherapy dose used for the index condition was 45 gray. The median age at RI-STS diagnosis was 56 years. The most common primary diagnoses were breast cancer (36.4%) and lymphoma (34.1%). The most common RI-STS histologies were malignant fibrous histiocytoma (36.4%) and angiosarcoma (18.2%). Forty-two patients underwent surgery, 13 patients received adjuvant radiotherapy, and 8 patients received adjuvant chemotherapy. Systemic metastases occurred in 50% of treated patients (n = 21), and 26% (n = 11) developed local recurrence, the risk of which was lower among patients who received reirradiation (P = .043). The 5-year disease-free interval (DFI) and overall survival (OS) rates for patients with RI-STS who presented without metastasis were 36% and 44%, respectively. Patients who had International Union Against Cancer TNM stage III RI-STS had a significantly worse DFI compared with patients who had stage III sporadic STS (multivariate analysis, P = .051). Eighteen patients with RI-STS underwent functional assessment after surgery, and their results were comparable to those of patients with sporadic STS.

CONCLUSIONS

Despite aggressive surgical treatment, patients who have RI-STS remain at greater risk of both local and systemic recurrence compared with patients who have sporadic STS, but they can anticipate similar functional outcomes. Reirradiation can be relatively safe and effective if used properly.

摘要

背景

放射性诱导的软组织肉瘤(RI-STS)较为罕见,据信与预后不良有关。本研究报告的作者比较了患有四肢 RI-STS 的成年人与患有散发性 STS 的成年人的临床和功能结局。

方法

从 4 个前瞻性收集的数据库中确定了 1989 年至 2009 年期间诊断为 RI-STS 的 44 名患者。评估了患者的人口统计学、手术和辅助治疗参数以及肿瘤学和功能结局。

结果

从原发疾病放疗到 RI-STS 诊断的潜伏期中位数为 16 年。用于原发疾病的中位放射剂量为 45 戈瑞。RI-STS 诊断时的中位年龄为 56 岁。最常见的原发性诊断是乳腺癌(36.4%)和淋巴瘤(34.1%)。最常见的 RI-STS 组织学类型是恶性纤维组织细胞瘤(36.4%)和血管肉瘤(18.2%)。42 名患者接受了手术,13 名患者接受了辅助放疗,8 名患者接受了辅助化疗。治疗患者中有 50%(n=21)发生全身转移,26%(n=11)发生局部复发,接受再放疗的患者风险较低(P=0.043)。无转移的 RI-STS 患者的 5 年无病间隔(DFI)和总生存率(OS)分别为 36%和 44%。国际抗癌联盟 TNM 分期 III 期 RI-STS 患者的 DFI 明显差于 III 期散发性 STS 患者(多变量分析,P=0.051)。18 名 RI-STS 患者在手术后进行了功能评估,其结果与散发性 STS 患者的结果相当。

结论

尽管进行了积极的手术治疗,但 RI-STS 患者的局部和全身复发风险仍高于散发性 STS 患者,但他们可以预期类似的功能结局。如果使用得当,再放疗可能相对安全有效。

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