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超中心肺部肿瘤患者接受调强放疗立体定向消融体放射治疗的同质剂量处方的晚期毒性和长期局部控制。

Late Toxicity and Long-Term Local Control in Patients With Ultra-Central Lung Tumours Treated by Intensity-Modulated Radiotherapy-Based Stereotactic Ablative Body Radiotherapy With Homogenous Dose Prescription.

机构信息

Department of Radiotherapy, Beacon Hospital, Dublin, Ireland.

University College Dublin School of Medicine, Dublin, Ireland.

出版信息

Clin Oncol (R Coll Radiol). 2021 Oct;33(10):627-637. doi: 10.1016/j.clon.2021.05.005. Epub 2021 Jun 4.

Abstract

AIMS

To report late toxicity and long-term outcomes of intensity-modulated radiotherapy (IMRT)-based stereotactic ablative body radiotherapy (SABR) in patients with ultra-central lung tumours.

MATERIALS AND METHODS

This is a single-institution retrospective analysis of patients treated with SABR for ultra-central tumours between May 2008 and April 2016. Ultra-central location was defined as tumour (GTV) abutting or involving trachea, main or lobar bronchi. Respiratory motion management and static-field dynamic-IMRT were used, with dose prescribed homogeneously (maximum <120%). Descriptive analysis, Kaplan-Meier method, log-rank test and Cox regression were used to assess outcomes.

RESULTS

Sixty-five per cent of patients had inoperable primary non-small cell lung cancer and 35% had lung oligometastases. The median age was 72 (range 34-85) years. The median gross tumour volume and planning target volume (PTV) were 19.6 (range 1.7-203.3) cm and 57.4 (range 7.7-426.6) cm, respectively. The most commonly used dose fractionation was 60 Gy in eight fractions (n = 51, 87.8%). Median BED for D98%PTV and D2%PTV were 102.6 Gy and 115.06 Gy, respectively. With a median follow-up of 26.5 (range 3.2-100.5) months, fatal haemoptysis occurred in five patients (8.7%), of which two were directly attributable to SABR. A statistically significant difference was identified between median BED for 4 cm of airway, for patients who developed haemoptysis versus those who did not (147.4 versus 47.2 Gy, P = 0.005). At the last known follow-up, 50 patients (87.7%) were without local recurrence. Freedom from local progression at 2 and 4 years was 92 and 79.8%, respectively. The median overall survival was 34.3 (95% confidence interval 6.1-61.6) months. Overall survival at 2 and 4 years was 55.1 and 41.2%, respectively.

CONCLUSION

In patients with high-risk ultra-central lung tumours, IMRT-based SABR with homogenous dose prescription achieves high local control, similar to that reported for peripheral tumours. Although fatal haemoptysis occurred in 8.7% of patients, a direct causality with SABR was evident in only 3%. Larger studies are warranted to ascertain factors associated with outcomes, especially toxicity, and identify patients who would probably benefit from this treatment.

摘要

目的

报告基于强度调制放疗(IMRT)的立体定向消融放疗(SABR)治疗超中心肺部肿瘤患者的晚期毒性和长期结果。

材料和方法

这是一项对 2008 年 5 月至 2016 年 4 月期间接受 SABR 治疗超中心肿瘤的患者进行的单机构回顾性分析。超中心位置定义为肿瘤(GTV)紧邻或累及气管、主支气管或叶支气管。采用呼吸运动管理和静态场动态 IMRT,均匀给予剂量(最大<120%)。采用描述性分析、Kaplan-Meier 法、对数秩检验和 Cox 回归评估结果。

结果

65%的患者为不可手术的原发性非小细胞肺癌,35%为肺部寡转移瘤。中位年龄为 72 岁(范围 34-85 岁)。肿瘤总体积和计划靶区(PTV)的中位数分别为 19.6cm(范围 1.7-203.3cm)和 57.4cm(范围 7.7-426.6cm)。最常用的剂量分割方案是 60Gy/8 次(n=51,87.8%)。98%PTV 和 2%PTV 的中位生物等效剂量(BED)分别为 102.6Gy 和 115.06Gy。中位随访时间为 26.5 个月(范围 3.2-100.5 个月),5 例患者(8.7%)发生致命性咯血,其中 2 例直接归因于 SABR。在发生咯血的患者和未发生咯血的患者中,中位气道 4cm 处的 BED 有统计学显著差异(147.4Gy 比 47.2Gy,P=0.005)。在最后一次已知随访时,50 例患者(87.7%)无局部复发。2 年和 4 年无局部进展率分别为 92%和 79.8%。中位总生存期为 34.3 个月(95%置信区间为 6.1-61.6 个月)。2 年和 4 年的总生存率分别为 55.1%和 41.2%。

结论

对于高危超中心肺部肿瘤患者,采用均匀剂量处方的基于 IMRT 的 SABR 可实现高局部控制率,与周围肿瘤报道的结果相似。尽管有 8.7%的患者发生致命性咯血,但只有 3%的患者明确与 SABR 有直接因果关系。需要进行更大规模的研究来确定与结果相关的因素,特别是毒性,并确定可能从这种治疗中获益的患者。

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