Department of Radiation Oncology, Dana-Farber Cancer Institute/Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts; Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Department of Data Science, Dana-Farber Cancer Institute, Boston, Massachusetts.
Int J Radiat Oncol Biol Phys. 2022 Nov 15;114(4):747-761. doi: 10.1016/j.ijrobp.2022.06.096. Epub 2022 Jul 15.
Limited data exist to guide optimal patient selection and treatment of bone metastases with curative intent despite the increasing application of stereotactic body radiation therapy (SBRT) for oligometastatic (OM) disease control and reirradiation (Re-RT).
Clinical characteristics for 434 patients consecutively treated with bone SBRT at a single institution from March 2011 to June 2020 were analyzed by OM, spine, and nonspine bone using Cox regression to determine association with local control (LC), progression-free survival (PFS), and overall survival (OS), and the Kaplan-Meier method to estimate PFS and OS.
Most patients had prostate (39%) or breast/lung (21%) cancer and 1 to 3 lesions (96%), with 651 lesions (spine 63%) treated for Re-RT (12%) or OMD (88%), including synchronous (10%), metachronous (28%), repeat (27%), or induced (23%) states as defined by The European Society for Radiotherapy and Oncology and European Organisation for Research and Treatment of Cancer criteria. Biologically effective dose (BED) ≥50 (hazard ratio, 0.68; 95% confidence interval, 0.48-0.96; P < .03) predicted improved LC among OM lesions and planning target volume (PTV) ≥150 cc (hazard ratio, 1.94; 95% confidence interval, 1.02-3.70; P < .04) predicted worse LC for nonspine bone. Prostate histology, performance status (PS) 0 to 1, and metastasis-free interval ≥2 year predicted improved PFS and OS (P < .05). Metachronous, synchronous, or repeat OM had higher PFS and OS (P ≤ .001) than induced OM. With median follow-up 25.7 months, 1- and 2-year PFS was 63% and 47% for OM and 36% and 25% for Re-RT; 1- and 2-year OS was 87% and 73% for OM and 58% and 43% for Re-RT. Acute toxicities included grade 1 to 2 pain flare (9%) and fatigue (14%). Late toxicities included fracture (1%) for OM and myelopathy (2.5%) or nerve pain (1.2%) for Re-RT.
BED ≥50 for OM and PTV <150 cc for nonspine bone lesions was associated with improved LC. Prostate histology, PS 0 to 1, metastasis-free interval ≥2 years, and metachronous, synchronous, or repeat presentations per The European Society for Radiotherapy and Oncology and European Organisation for Research and Treatment of Cancer criteria predicted improved PFS and OS among OM patients treated with bone SBRT.
尽管立体定向体部放射治疗(SBRT)越来越多地用于寡转移(OM)疾病控制和再放射治疗(Re-RT),但仍存在有限的数据来指导有治愈意图的骨转移患者的最佳选择和治疗。
对 2011 年 3 月至 2020 年 6 月期间在一家机构接受骨 SBRT 治疗的 434 例患者的临床特征进行分析,使用 Cox 回归分析 OM、脊柱和非脊柱骨之间的关系,以确定局部控制(LC)、无进展生存期(PFS)和总生存期(OS)的相关性,并使用 Kaplan-Meier 法估计 PFS 和 OS。
大多数患者患有前列腺(39%)或乳腺癌/肺癌(21%),且存在 1-3 个病灶(96%),其中 651 个病灶(脊柱 63%)接受了 Re-RT(12%)或 OMD(88%)的治疗,包括同步(10%)、异时(28%)、重复(27%)或诱导(23%)状态,定义为欧洲放射肿瘤学会和欧洲癌症研究与治疗组织标准。生物有效剂量(BED)≥50(风险比,0.68;95%置信区间,0.48-0.96;P <.03)预测 OM 病变的 LC 改善,计划靶区(PTV)≥150 cc(风险比,1.94;95%置信区间,1.02-3.70;P <.04)预测非脊柱骨的 LC 更差。前列腺组织学、表现状态(PS)0-1 和无转移间隔≥2 年预测 PFS 和 OS 改善(P <.05)。异时、同步或重复 OM 比诱导 OM 有更高的 PFS 和 OS(P ≤.001)。中位随访 25.7 个月,OM 的 1 年和 2 年 PFS 分别为 63%和 47%,Re-RT 分别为 36%和 25%;OM 的 1 年和 2 年 OS 分别为 87%和 73%,Re-RT 分别为 58%和 43%。急性毒性包括 1-2 级疼痛加剧(9%)和疲劳(14%)。晚期毒性包括 OM 的骨折(1%)和 Re-RT 的脊髓病(2.5%)或神经痛(1.2%)。
OM 的 BED≥50 和非脊柱骨病变的 PTV<150 cc 与 LC 改善相关。前列腺组织学、PS 0-1、无转移间隔≥2 年以及欧洲放射肿瘤学会和欧洲癌症研究与治疗组织标准中的异时、同步或重复表现预测 OM 患者接受骨 SBRT 治疗后的 PFS 和 OS 改善。