Department of Radiation Oncology, University of California, San Francisco.
Department of Radiology and Biomedical Imaging, University of California, San Francisco.
JAMA Oncol. 2021 Jul 1;7(7):1033-1040. doi: 10.1001/jamaoncol.2021.1262.
Owing to the proximity to critical neurologic structures, treatment options for brainstem metastases (BSM) are limited, and BSM growth can cause acute morbidity or death. Stereotactic radiosurgery (SRS) is the only local therapy for BSM, but efficacy and safety of this approach are incompletely understood because patients with BSM are excluded from most clinical trials.
To perform a systematic review and comparative meta-analysis of SRS studies for BSM in the context of prospective trials of SRS or molecular therapy for nonbrainstem brain metastases (BM).
A comprehensive search of Pubmed/MEDLINE and Embase was performed on December 6, 2019.
English-language studies of SRS for BSM with at least 10 patients and reporting 1 or more outcomes of interest were included. Duplicate studies or studies with overlapping data sets were excluded. Studies were independently evaluated by 2 reviewers, and discrepancies were resolved by consensus. A total of 32 retrospective studies published between 1999 and 2019 were included in the analysis.
Preferred Reporting Items for Systematic Reviews and Meta-analysis (PRISMA) guidelines were followed to identify studies. Study quality was assessed using Methodological Index for Non-Randomized Studies criteria. Fixed and random-effects meta-analyses and meta-regressions were performed for the outcomes of interest.
Primary study outcomes included 1-year and 2-year local control and overall survival, objective response rate, symptom response rate, neurological death rate, and rate of grade 3 to 5 toxic effects as described in Common Terminology Criteria for Adverse Events, version 4.0.
The 32 retrospective studies included in the analysis comprised 1446 patients with 1590 BSM that were treated with SRS (median [range] dose, 16 [11-39] Gy; median [range] fractions, 1 [1-13]). Local control at 1 year was 86% (95% CI, 83%-88%; I2 = 38%) in 1410 patients across 31 studies, objective response rate was 59% (95% CI, 47%-71%; I2 = 88%) in 642 patients across 17 studies, and symptom improvement was 55% (95% CI, 47%-63%; I2 = 41%) in 323 patients across 13 studies. Deaths from BSM progression after SRS were rare (19 of 703 [2.7%] deaths across 19 studies), and the neurologic death rate in patients with BSM (24%; 95% CI, 19%-31%; I2 = 62%) was equivalent to the neurologic death rate in patients with BM who were treated on prospective trials. The rate of treatment-related grade 3 to 5 toxic effects was 2.4% (95% CI, 1.5%-3.7%; I2 = 33%) in 1421 patients across 31 studies. These results compared favorably to trials of targeted or immunotherapy for BM, which had a wide objective response rate range from 17% to 56%.
Results of this systematic review and meta-analysis show that SRS for BSM was associated with effectiveness and safety and was comparable to SRS for nonbrainstem BM, suggesting that patients with BSM should be eligible for clinical trials of SRS. In this analysis, patients treated with SRS for BSM rarely died from BSM progression and often experienced symptomatic improvement. Given the apparent safety and efficacy of SRS for BSM in the context of acute morbidity or death from BSM growth, consideration of SRS at the time of enrollment on emerging trials of targeted therapy for BM should be considered.
由于靠近关键的神经结构,脑干转移瘤(BSM)的治疗选择有限,而 BSM 的生长可能导致急性发病或死亡。立体定向放射外科(SRS)是治疗 BSM 的唯一局部疗法,但由于患者被排除在大多数临床试验之外,因此对这种方法的疗效和安全性了解不完全。
对 SRS 治疗 BSM 的前瞻性试验或分子治疗非脑转移瘤(BM)的 SRS 研究进行系统评价和比较荟萃分析。
于 2019 年 12 月 6 日在 Pubmed/MEDLINE 和 Embase 上进行了全面检索。
纳入了至少有 10 例患者且报告了 1 个或多个感兴趣结局的 SRS 治疗 BSM 的英文研究。重复研究或数据重叠的研究被排除在外。研究由 2 位独立评估者进行评估,如果存在分歧,则通过共识解决。共有 32 项发表于 1999 年至 2019 年的回顾性研究被纳入分析。
遵循系统评价和荟萃分析的首选报告项目(PRISMA)指南来识别研究。使用非随机研究方法学指数(Methodological Index for Non-Randomized Studies criteria)评估研究质量。对感兴趣的结局进行固定和随机效应荟萃分析和荟萃回归分析。
主要研究结局包括 1 年和 2 年的局部控制和总生存率、客观缓解率、症状缓解率、神经死亡率以及根据常见不良事件术语标准 4.0 描述的 3 级至 5 级毒性反应发生率。
纳入分析的 32 项回顾性研究共包括 1446 例 1590 个 BSM,采用 SRS 治疗(中位[范围]剂量,16[11-39]Gy;中位[范围]分割次数,1[1-13])。在 31 项研究的 1410 例患者中,1 年局部控制率为 86%(95%CI,83%-88%;I2=38%),在 17 项研究的 642 例患者中,客观缓解率为 59%(95%CI,47%-71%;I2=88%),在 13 项研究的 323 例患者中,症状改善率为 55%(95%CI,47%-63%;I2=41%)。SRS 后 BSM 进展导致的死亡很少见(19 例死亡,占 703 例死亡患者的 2.7%,19 项研究),BSM 患者的神经死亡率为 24%(95%CI,19%-31%;I2=62%),与接受前瞻性试验治疗的 BM 患者的神经死亡率相当。与靶向或免疫治疗 BM 的试验相比,治疗相关的 3 级至 5 级毒性反应发生率为 2.4%(95%CI,1.5%-3.7%;I2=33%),这在 31 项研究的 1421 例患者中。这些结果与针对 BM 的靶向或免疫治疗的试验结果相比较为有利,后者的客观缓解率范围为 17%至 56%。
本系统评价和荟萃分析的结果表明,SRS 治疗 BSM 有效且安全,与 SRS 治疗非脑转移瘤相当,提示 BSM 患者应有资格参加 SRS 的临床试验。在本分析中,接受 SRS 治疗的 BSM 患者很少因 BSM 进展而死亡,并且经常出现症状改善。鉴于 SRS 治疗 BSM 在 BSM 生长导致急性发病或死亡的情况下的明显安全性和有效性,在新兴的针对 BM 的靶向治疗试验中,应考虑在招募时进行 SRS。