Eberhard-Karls-University Tuebingen, Department of Radiation Oncology, Tuebingen, Germany.
RKH-Kliniken Ludwigsburg, Department of Radiation Oncology and Radiotherapy, Ludwigsburg, Germany.
Radiol Oncol. 2022 Dec 13;56(4):515-524. doi: 10.2478/raon-2022-0053. eCollection 2022 Dec 1.
Stereotactic body radiotherapy (SBRT) concepts for dose escalation are increasingly used for bone metastases in patients with oligometastatic or oligoprogressive disease. For metastases that are not suitable for SBRT-regimens, a treatment with 30/40 Gy with simultaneous integrated boost (SIB) in 10 fractions represents a possible regimen. The aim of this study was to investigate the feasibility of this concept and the acute and subacute toxicities.
Clinical records for dose-escalated radiotherapy of all consecutive patients treated with this regimen were evaluated retrospectively (24 patients with 28 target volumes for oncologic outcomes and 25 patients with 29 target volumes for treatment feasibility and dose parameters analysis). Analysis of radiotherapy plans included size of target volumes and dosimetric parameter for target volumes and organs at risk (OAR). Acute and subacute toxicities were evaluated according to Common Terminology Criteria for Adverse Events (CTCAE) V4.0.
The most common localization was the spine (71.4%). The most common histology was prostate cancer (45.8%). Oligometastatic or oligoprogressive disease was the indication for dose-escalated radiotherapy in 19/24 patients (79.2%). Treatment was feasible with all patients completing radiotherapy. Acute toxicity grade 1 was documented in 36.0% of the patients. During follow up, one patient underwent surgery due to bone instability. The 1-year local control and patient-related progression-free survival (PFS) were 90.0 ± 6.7% and 33.3 ± 11.6%, respectively.
Dose-escalated hypofractionated radiotherapy with simultaneous integrated boost for bone metastases resulted in good local control with limited acute toxicities. Only one patient required surgical intervention. The regimen represents an alternative to SBRT in selected patients.
立体定向体部放疗(SBRT)剂量递增概念越来越多地用于寡转移或寡进展性疾病患者的骨转移。对于不适合 SBRT 方案的转移灶,10 次分割、30/40 Gy 同步整合 boost(SIB)治疗可能是一种方案。本研究旨在探讨该方案的可行性以及急性和亚急性毒性。
回顾性评估了采用该方案治疗的所有连续患者的剂量递增放疗的临床记录(24 例患者 28 个靶区用于肿瘤学结果评估,25 例患者 29 个靶区用于治疗可行性和剂量参数分析)。放疗计划分析包括靶区和危及器官(OAR)的靶区大小和剂量学参数。根据不良事件通用术语标准(CTCAE)V4.0 评估急性和亚急性毒性。
最常见的部位是脊柱(71.4%)。最常见的组织学类型是前列腺癌(45.8%)。19/24 例(79.2%)患者因寡转移或寡进展性疾病接受剂量递增放疗。所有患者均能完成放疗,治疗具有可行性。36.0%的患者出现 1 级急性毒性。在随访期间,1 例患者因骨不稳定而行手术治疗。1 年局部控制率和患者相关无进展生存率(PFS)分别为 90.0±6.7%和 33.3±11.6%。
对于骨转移,采用同步整合 boost 的大分割调强放疗剂量递增可获得良好的局部控制效果,急性毒性有限。仅 1 例患者需要手术干预。该方案是选择性患者 SBRT 的替代方案。