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寡转移结直肠癌的立体定向放疗:102 例患者和 150 个病灶的结果。

Stereotactic radiation therapy in oligometastatic colorectal cancer: outcome of 102 patients and 150 lesions.

机构信息

Division of Radiotherapy, IEO European Institute of Oncology, IRCCS, Via Ripamonti 435, 20141, Milan, Italy.

Division of Oncology, University Hospital Centre "Mother Theresa", Rruga e Dibrës 372, 1000, Tirana, Albania.

出版信息

Clin Exp Metastasis. 2019 Aug;36(4):331-342. doi: 10.1007/s10585-019-09976-z. Epub 2019 Jun 4.

Abstract

To evaluate the local control (LC), progression free survival (PFS), out-field PFS, overall survival (OS), toxicity and failure predictors of SRT in a series of various sites oligometastatic CRC patients. Patients with oligometastatic CRC disease were analyzed retrospectively. The SRT prescribed dose was dependent on the lesion volume and its location. 102 consecutive oligometastatic CRC patients (150 lesions) were included. They underwent SRT between 2012 and 2015. Median prescription dose was 45 Gy (median dose/fraction was 15 Gy/3 fractions biological equivalent dose (BED) 112.5 Gy). Median follow-up was 11.4 months. No patients experienced G3 and G4 toxicity. No progression was found in 82% (radiological response at 3 months) and 85% (best radiological response) out of 150 evaluable lesions. At 1 and 2 years: LC was 70% and 55%; OS was 90% and 90%; PFS was 37% and 27%; out-field PFS was 37% and 23% respectively. Progressive disease was correlated with BED (better LC when BED was ≥ 75 Gy (p < 0.0001)). In multivariate analysis, LC was higher in lesions with a Plpnning target volume (PTV) volume < 42 cm and BED ≥ 75 Gy. Patients with Karnofsky performance status < 90 showed higher out-field progression. SRT is an effective treatment for patients with oligometastases from CRC. Its low treatment-associated morbidity and acceptable LC make of SRT an option not only in selected cases. Further studies should be focused to clarify which patient subgroup will benefit most from this treatment modality and to define the optimal dose to improve LC while maintaining low toxicity profile.

摘要

评估一系列不同部位寡转移结直肠癌患者 SRT 的局部控制 (LC)、无进展生存期 (PFS)、野外 PFS、总生存期 (OS)、毒性和失败预测因子。对寡转移结直肠癌患者进行回顾性分析。SRT 规定的剂量取决于病变体积及其位置。102 例连续的寡转移结直肠癌患者(150 个病灶)纳入研究。他们在 2012 年至 2015 年间接受了 SRT。中位处方剂量为 45Gy(中位剂量/分次为 15Gy/3 分次生物等效剂量 (BED)112.5Gy)。中位随访时间为 11.4 个月。没有患者出现 G3 和 G4 毒性。在 150 个可评估病灶中,82%(3 个月时的影像学反应)和 85%(最佳影像学反应)的病灶没有进展。1 年和 2 年时的 LC 分别为 70%和 55%;OS 分别为 90%和 90%;PFS 分别为 37%和 27%;野外 PFS 分别为 37%和 23%。进展性疾病与 BED 相关(BED≥75Gy 时 LC 更好(p<0.0001))。多变量分析显示,PTV 体积<42cm 和 BED≥75Gy 的病灶 LC 更高。Karnofsky 表现状态<90 的患者野外进展更高。SRT 是治疗结直肠癌寡转移的有效方法。其治疗相关发病率低且 LC 可接受,这使得 SRT 不仅是一种选择。应进一步研究以阐明哪些患者亚组将从这种治疗方式中获益最大,并确定改善 LC 同时保持低毒性特征的最佳剂量。

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