Radiation Oncology, IRCCS, Sacro Cuore-Don Calabria Hospital, Negrar-Verona, Italy.
Radiation Oncology, LMU Munich, Munich, Germany.
Strahlenther Onkol. 2019 Aug;195(8):719-724. doi: 10.1007/s00066-018-01419-0. Epub 2019 Jan 28.
It is recognized that stereotactic body radiotherapy (SBRT) for centrally located lung metastases is affected by higher rates of severe toxicity. In the present study, we report the clinical outcomes following a novel intensity-modulated radiotherapy prescription dose, termed simultaneous integrated protection (SIP), for nearby organs at risk (OARs).
The prescribed total doses of SBRT were 70 Gy in 10 fractions and 60 Gy in 8 fractions. For ultra-centrally located lesions, a dose of 60 Gy in 10 fractions was delivered. The main planning instructions were: (1) to remain within the limits of the given dose constraints for an OAR; (2) to make use of the maximum possible dose to the OARs to minimize dose inhomogeneity for the Planning Target Volume (PTV). SBRT-related toxicity was prospectively assessed according to the Common Terminology Criteria for Adverse Events (CTCAE) v4.0. The primary clinical endpoint was the SBRT-related toxicity. Secondary endpoint was local control.
Forty patients affected by a single central malignancy were analyzed. The median follow-up was 20 months (range, 6-58 months). Acute and late clinical pulmonary toxicity ≥grade 2 was recorded in 2 out of 40 patients (5%) and 3 out of 40 patients (7%), respectively. No patient experienced cardiac toxicity. No narrowing or stenosis of any airway or vessel was registered. One-year local control rate was 91%. The median time to local progression was 13 months (range, 6-46 months).
SBRT using a PTV-SIP approach for single central lung metastases achieved low SBRT-related toxicity with acceptable local control.
立体定向体部放疗(SBRT)治疗中央型肺转移瘤与严重毒性反应发生率较高有关。本研究报告了一种新的调强放疗处方剂量(同步综合保护[SIP])用于临近危及器官(OAR)的临床结果。
SBRT 的总剂量为 70Gy/10 次和 60Gy/8 次。对于超中央型病变,给予 60Gy/10 次的剂量。主要的计划指导原则是:(1)OAR 的剂量限制在给定剂量限制范围内;(2)最大限度地利用 OAR 剂量,使计划靶区(PTV)的剂量不均匀性最小化。根据不良事件通用术语标准(CTCAE)v4.0 对 SBRT 相关毒性进行前瞻性评估。主要临床终点是 SBRT 相关毒性。次要终点是局部控制。
分析了 40 例单一中央性恶性肿瘤患者。中位随访时间为 20 个月(范围 6-58 个月)。40 例患者中有 2 例(5%)和 3 例(7%)分别记录到急性和晚期临床肺部毒性≥2 级。无患者发生心脏毒性。未发现任何气道或血管狭窄或狭窄。1 年局部控制率为 91%。局部进展的中位时间为 13 个月(范围 6-46 个月)。
采用 PTV-SIP 方法治疗单发中央型肺转移瘤的 SBRT 可实现低 SBRT 相关毒性和可接受的局部控制。