首页> 外文期刊>Radiotherapy and oncology: Journal of the European Society for Therapeutic Radiology and Oncology >Central thoracic lesions treated with hypofractionated stereotactic body radiotherapy.
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Central thoracic lesions treated with hypofractionated stereotactic body radiotherapy.

机译:中央胸腔病变采用分级立体定向放射治疗。

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PURPOSE: To investigate the toxicity and outcome after moderately hypofractionated stereotactic body radiotherapy (SBRT) for central thoracic lesions. METHODS: Fifty-three patients undergoing 63 courses of SBRT for central thoracic lesions were retrospectively reviewed. Ninety-eight lesions received 30-63 Gy in 2.5-5.0 Gy fractions using the Novalis ExacTrac patient positioning platform. RESULTS: The 2-year lesion local control was 73%. Larger lesion volume was associated with poorer local control. The 2-year overall survival of patients with Stage I NSCLC, Stages II-III NSCLC and limited metastatic disease was 72%, 12% and 49%, respectively. There were four patient deaths from pulmonary causes, potentially grade 5 toxicities, though three had comorbid pulmonary conditions which may have contributed to the cause of death. One patient died from hemoptysis after undergoing two courses of SBRT to a mediastinal lesion. Most other deaths were attributable to metastatic progression. CONCLUSIONS: Moderately hypofractionated SBRT to central thoracic lesions is effective with respect to local control and toxicity. Further dose escalation can provide an opportunity for better tumor control. Even with less aggressive dose fractionation, pulmonary deaths can occur, though it is difficult to ascertain the extent to which SBRT contributed to the death of patients with comorbid pulmonary conditions.
机译:目的:研究中度分级立体定向放射治疗(SBRT)对中央胸腔病变的毒性和预后。方法:对53例因胸中央部病变行SBRT疗程的患者进行回顾性分析。使用Novalis ExacTrac患者定位平台,以2.5-5.0 Gy的分数接受了38-63 Gy的九十八个病变。结果:2年病灶局部控制率为73%。较大的病变体积与较差的局部控制有关。 I期NSCLC,II-III期NSCLC和有限转移性疾病患者的2年总生存率分别为72%,12%和49%。尽管有3例合并肺部疾病,可能是导致死亡的原因,但有4例因肺部原因导致的死亡,可能是5级毒性。一名患者接受了两个疗程的SBRT纵隔病变治疗后,死于咯血。其他大多数死亡可归因于转移性进展。结论:中度低度SBRT对胸中央病变的局部控制和毒性方面是有效的。进一步的剂量增加可以提供更好控制肿瘤的机会。即使很难确定剂量分数,也可能发生肺部死亡,尽管很难确定SBRT对合并症合并肺部疾病患者死亡的程度。

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