The clinical benefit of adding radiotherapy to ipilimumab in patients with melanoma brain metastasis: a systematic review and meta-analysis.

IF 4.2 3区 医学 Q2 ONCOLOGY Clinical & Experimental Metastasis Pub Date : 2025-02-10 DOI:10.1007/s10585-025-10333-6
Mohammad Amin Habibi, Pouria Delbari, Farhang Rashidi, Bardia Hajikarimloo, Ali Allahdadi, Saghar Rouzrokh, Mohammad Shahir Eftekhar, Adrina Habibzadeh, Amir Khanmirzaei, Pouya Ebrahimi, Ibrahim Mohammadzadeh, Seyed Ahmad Naseri Alavi
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Abstract

Combining radiotherapy (RT) with Ipilimumab, a CTLA-4 inhibitor, holds promise in treating metastatic brain melanoma (MBM). Despite promising preclinical evidence, clinical studies evaluating their combined efficacy are limited and varied, necessitating a systematic review and meta-analysis to consolidate evidence and identify predictors of response or resistance in this challenging patient population. This study was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). The electronic databases of PubMed, Embase, Scopus, and Web of science were searched on July 9th, 2024, using the relevant key terms without filters. All statistical analysis was performed by STATA v.17. A total of 26 studies with 1059 participants were included. The 1, 2, and 3-year overall survival rates were 0.44 [95% CI: 0.32-0.55], 0.28 [95% CI: 0.17, 0.39], and 0.19 [95% CI: 0.06-0.32], respectively. The pooled 12-month local control and 1-year progression-free survival rate were 0.53 [95% CI: 0.34-0.71] and 0.20 [95%CI: 0.10-0.30]. The pooled overall response rate, partial response rates, and stable disease rate were 0.26 [95% CI: 0.10-0.41], 0.10 [95% CI:0.05-0.15], 0.17 [95%CI:0.10-0.23], and 0.58 [95%CI: 0.45-0.70]. This study demonstrated promising results regarding adding RT to ipilimumab which was associated with significantly higher 1-year OS, 18-month OS, 2-year OS, 3-year OS, overall radiological response rate, and stable disease rate and significantly lower rate of progressive disease rate compared to ipilimumab without RT. However, no significant difference was observed between two groups in 6-month OS, 12-month LC, 1-year PFS, and partial response rate.

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放疗(RT)与CTLA-4抑制剂伊匹单抗(Ipilimumab)的联合治疗有望治疗转移性脑黑色素瘤(MBM)。尽管临床前证据很有希望,但评估其联合疗效的临床研究却很有限,而且各不相同,因此有必要进行系统综述和荟萃分析,以整合证据并确定这一具有挑战性的患者群体的反应或耐药性预测因素。本研究根据《系统综述和荟萃分析首选报告项目》(Preferred Reporting Items for Systematic Reviews and Meta-Analyses,PRISMA)进行。研究人员于 2024 年 7 月 9 日在 PubMed、Embase、Scopus 和 Web of science 等电子数据库中使用相关关键术语进行了检索,未使用过滤器。所有统计分析均使用 STATA v.17 进行。共纳入 26 项研究,1059 名参与者。1年、2年和3年总生存率分别为0.44 [95% CI: 0.32-0.55]、0.28 [95% CI: 0.17, 0.39]和0.19 [95% CI: 0.06-0.32]。汇总的12个月局部控制率和1年无进展生存率分别为0.53[95% CI:0.34-0.71]和0.20[95%CI:0.10-0.30]。汇总总反应率、部分反应率和疾病稳定率分别为 0.26 [95% CI: 0.10-0.41], 0.10 [95% CI:0.05-0.15], 0.17 [95%CI:0.10-0.23], 和 0.58 [95%CI: 0.45-0.70]。与不使用RT的伊匹单抗相比,在伊匹单抗中加入RT可显著提高1年OS、18个月OS、2年OS、3年OS、总体放射学应答率和疾病稳定率,并显著降低疾病进展率。然而,在6个月OS、12个月LC、1年PFS和部分应答率方面,两组间未观察到明显差异。
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来源期刊
CiteScore
7.80
自引率
5.00%
发文量
55
审稿时长
12 months
期刊介绍: The Journal''s scope encompasses all aspects of metastasis research, whether laboratory-based, experimental or clinical and therapeutic. It covers such areas as molecular biology, pharmacology, tumor biology, and clinical cancer treatment (with all its subdivisions of surgery, chemotherapy and radio-therapy as well as pathology and epidemiology) insofar as these disciplines are concerned with the Journal''s core subject of metastasis formation, prevention and treatment.
期刊最新文献
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