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完全切除的 Masaoka/Masaoka-Koga II/III 期胸腺瘤术后放疗可提高总生存率:4746 例患者的更新荟萃分析。

Postoperative Radiotherapy for Completely Resected Masaoka/Masaoka-Koga Stage II/III Thymoma Improves Overall Survival: An Updated Meta-Analysis of 4746 Patients.

机构信息

Radiation Oncology Center, Ofuna Chuo Hospital, Kamakura, Japan.

Department of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.

出版信息

J Thorac Oncol. 2021 Apr;16(4):677-685. doi: 10.1016/j.jtho.2020.12.023. Epub 2021 Jan 27.

Abstract

INTRODUCTION

Our systematic review and meta-analysis aimed to evaluate the effect of postoperative radiotherapy (PORT) on completely resected Masaoka/Masaoka-Koga (M/MK) stage II/III thymomas.

METHODS

We systematically searched four online databases and included studies that compared surgery alone versus surgery plus a PORT for completely resected M/MK stage II/III thymoma. The multivariate-adjusted hazard ratios (HRs) of overall survival (OS) and disease-free survival were evaluated as the primary and secondary end points, respectively. We performed a subgroup analysis for OS with respect to M/MK stage II, III, and inseparable II/III cases. A generic inverse variance meta-analysis using a random model was conducted.

RESULTS

Five studies including 4746 patients (among them, 2408 patients received PORT) met our selection criteria. A meta-analysis of these five studies revealed that PORT was associated with a significantly better OS (HR = 0.68, 95% confidence interval [CI]: 0.57-0.83, p < 0.001, I = 0%, p for heterogeneity = 0.97). Subgroup analyses for M/MK stage II disease (HR = 0.63, 95% CI: 0.44-0.91, p = 0.01, I = 0%, p for heterogeneity = 0.80) and M/MK stage III disease (HR = 0.72, 95% CI: 0.55-0.95, p = 0.02, I = 0%, p for heterogeneity = 0.84) revealed similar results. PORT was not associated with an improved disease-free survival (HR = 0.96, 95% CI: 0.70-1.33, p = 0.83, I = 0%, p for heterogeneity = 0.72).

CONCLUSIONS

Currently available evidence from observational studies suggests PORT for patients with completely resected M/MK stage II/III thymoma. A randomized trial is warranted.

摘要

简介

我们的系统评价和荟萃分析旨在评估完全切除的 Masaoka/Masaoka-Koga(M/MK)分期 II/III 胸腺瘤患者术后放疗(PORT)的效果。

方法

我们系统地检索了四个在线数据库,并纳入了比较单纯手术与手术加 PORT 治疗完全切除的 M/MK 分期 II/III 胸腺瘤的研究。多变量调整后的总生存率(OS)和无病生存率的风险比(HRs)分别作为主要和次要终点进行评估。我们对 OS 进行了 M/MK 分期 II、III 和不可分割的 II/III 病例的亚组分析。使用随机模型进行了通用逆方差荟萃分析。

结果

有 5 项研究共纳入 4746 例患者(其中 2408 例接受 PORT)符合我们的选择标准。对这 5 项研究的荟萃分析表明,PORT 与显著更好的 OS 相关(HR=0.68,95%置信区间[CI]:0.57-0.83,p<0.001,I=0%,p 异质性=0.97)。M/MK 分期 II 疾病(HR=0.63,95%CI:0.44-0.91,p=0.01,I=0%,p 异质性=0.80)和 M/MK 分期 III 疾病(HR=0.72,95%CI:0.55-0.95,p=0.02,I=0%,p 异质性=0.84)的亚组分析得出了类似的结果。PORT 与无病生存率的改善无关(HR=0.96,95%CI:0.70-1.33,p=0.83,I=0%,p 异质性=0.72)。

结论

目前观察性研究的证据表明,PORT 适用于完全切除的 M/MK 分期 II/III 胸腺瘤患者。需要进行随机试验。

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