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脑转移瘤的新辅助立体定向放射治疗:文献系统评价与荟萃分析及正在进行的临床试验

Neoadjuvant Stereotactic Radiotherapy for Brain Metastases: Systematic Review and Meta-Analysis of the Literature and Ongoing Clinical Trials.

作者信息

Palmisciano Paolo, Ferini Gianluca, Khan Ramlah, Bin-Alamer Othman, Umana Giuseppe E, Yu Kenny, Cohen-Gadol Aaron A, El Ahmadieh Tarek Y, Haider Ali S

机构信息

Department of Neurosurgery, University of Cincinnati College of Medicine, Cincinnati, OH 45220, USA.

Department of Radiation Oncology, REM Radioterapia srl, 95029 Viagrande, Italy.

出版信息

Cancers (Basel). 2022 Sep 4;14(17):4328. doi: 10.3390/cancers14174328.

Abstract

BACKGROUND

Brain metastases (BMs) carry a high morbidity and mortality burden. Neoadjuvant stereotactic radiotherapy (NaSRT) has shown promising results. We systematically reviewed the literature on NaSRT for BMs.

METHODS

PubMed, EMBASE, Scopus, Web-of-Science, Cochrane, and ClinicalTrial.gov were searched following the PRISMA guidelines to include studies and ongoing trials reporting NaSRT for BMs. Indications, protocols, and outcomes were analyzed using indirect random-effect meta-analyses.

RESULTS

We included 7 studies comprising 460 patients with 483 BMs, and 13 ongoing trials. Most BMs originated from non-small lung cell carcinoma (41.4%), breast cancer (18.7%) and melanoma (43.6%). Most patients had single-BM (69.8%) located supratentorial (77.8%). Patients were eligible if they had histologically-proven primary tumors and ≤4 synchronous BMs candidate for non-urgent surgery and radiation. Patients with primary tumors clinically responsive to radiotherapy, prior brain radiation, and leptomeningeal metastases were deemed non-eligible. Median planning target volume was 9.9 cm (range, 2.9-57.1), and NaSRT was delivered in 1-fraction (90.9%), 5-fraction (4.8%), or 3-fraction (4.3%), with a median biological effective dose of 39.6 Gy10 (range, 35.7-60). Most patients received piecemeal (76.3%) and gross-total (94%) resection after a median of 1-day (range, 1-10) post-NaSRT. Median follow-up was 19.2-months (range, 1-41.3). Actuarial post-treatment rates were 4% (95%CI: 2-6%) for symptomatic radiation necrosis, 15% (95%CI: 12-18%) and 47% (95%CI: 42-52%) for local and distant recurrences, 6% (95%CI: 3-8%) for leptomeningeal metastases, 81% (95%CI: 75-87%) and 59% (95%CI: 54-63%) for 1-year local tumor control and overall survival.

CONCLUSION

NaSRT is effective and safe for BMs. Ongoing trials will provide high-level evidence on long-term post-treatment outcomes, further compared to adjuvant stereotactic radiotherapy.

摘要

背景

脑转移瘤(BMs)具有较高的发病率和死亡率负担。新辅助立体定向放射治疗(NaSRT)已显示出有前景的结果。我们系统回顾了关于NaSRT治疗BMs的文献。

方法

按照PRISMA指南检索PubMed、EMBASE、Scopus、Web of Science、Cochrane和ClinicalTrial.gov,以纳入报告NaSRT治疗BMs的研究和正在进行的试验。使用间接随机效应荟萃分析来分析适应证、方案和结果。

结果

我们纳入了7项研究,共460例患者有483个脑转移瘤,以及13项正在进行的试验。大多数脑转移瘤起源于非小细胞肺癌(41.4%)、乳腺癌(18.7%)和黑色素瘤(43.6%)。大多数患者有单个脑转移瘤(69.8%),位于幕上(77.8%)。如果患者有组织学证实的原发性肿瘤且≤4个同步脑转移瘤,适合非紧急手术和放疗,则符合入选标准。原发性肿瘤对放疗有临床反应、既往有脑部放疗史和软脑膜转移的患者被视为不符合入选标准。计划靶体积中位数为9.9 cm(范围2.9 - 57.1),NaSRT采用单次分割(90.9%)、5次分割(4.8%)或3次分割(4.3%),生物等效剂量中位数为39.6 Gy10(范围35.7 - 60)。大多数患者在NaSRT后中位数1天(范围1 - 10)接受了分块切除(76.3%)和全切除(94%)。中位随访时间为19.2个月(范围1 - 41.3)。有症状的放射性坏死的治疗后精算发生率为4%(95%CI:2 - 6%),局部和远处复发的发生率分别为15%(95%CI:12 - 18%)和47%(95%CI:42 - 52%),软脑膜转移的发生率为6%(95%CI:3 - 8%),1年局部肿瘤控制率和总生存率分别为81%(95%CI:75 - 87%)和59%(95%CI:54 - 63%)。

结论

NaSRT治疗BMs有效且安全。正在进行的试验将提供关于治疗后长期结果的高级别证据,与辅助立体定向放射治疗相比将有进一步比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ad0/9455064/397fd09c75da/cancers-14-04328-g001.jpg

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