Department of Radiotherapy, Beacon Hospital, Dublin, Ireland.
University College Dublin School of Medicine, Dublin, Ireland.
Clin Oncol (R Coll Radiol). 2021 Oct;33(10):627-637. doi: 10.1016/j.clon.2021.05.005. Epub 2021 Jun 4.
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.
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.
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.
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.
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。
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。
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%。
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。