治疗 II 期和 T3N0M0 鼻咽癌的同期化放疗与单独放疗:系统回顾与元分析》(Concurrent Chemoradiotherapy versus Radiotherapy Alone in the Treatment of Stage II and T3N0M0 Nasopharyngeal Carcinoma: A Systematic Review and Meta-Analysis.

IF 3.2 3区 医学 Q2 ONCOLOGY
H Zeng, H Wang, S Liu, X Xu
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引用次数: 0

摘要

目的:对于II期和T3N0鼻咽癌(NPC)的同期化学放疗(CCRT)疗效,尤其是在从二维常规放疗(2DCRT)向调强放疗(IMRT)转变的过程中的疗效存在争议:截至2024年4月1日,我们在PubMed、Embase、Cochrane Library和Web of Science等数据库中进行了详尽的文献检索,旨在识别和筛选在治疗II期和T3N0 NPC时比较CCRT与单纯放疗疗效的研究:本次综合分析共纳入了 10 项研究,涵盖 5015 名患者。研究结果表明,除无进展生存期(PFS)外,CCRT并未改善生存结果,包括总生存期(OS)、无远处转移生存期(DMFS)、无局部复发生存期(LRRFS)和无失败生存期(FFS),所有P值均超过0.05。同时,与CCRT相关的≥3级不良事件的发生率显著升高(几率比[OR]=3.77,95%置信区间[CI]=2.75-5.15,P<0.0001)。亚组分析显示,与RT相比,2DCRT联合同期化疗可明显改善OS(危险比[HR] = 0.57,95% CI = 0.46-0.71,P<0.00001)、PFS(HR=0.65,95% CI=0.53-0.78,P<0.00001)、DMFS(HR=0.54,95% CI=0.37-0.79,P=0.002)和LRRFS(HR=0.63,95% CI=0.49-0.82,P=0.0005)。相比之下,IMRT与同期化疗的组合未能改善OS、PFS、DMFS或LRRFS,所有P值均超过0.05:与RT相比,CCRT并不能提高II期和T3N0鼻咽癌患者的生存率,但会引起更多不良反应。2DCRT 联合同期化疗可显著改善 OS、PFS、DMFS 和 LRRFS,而 IMRT 联合同期化疗则无临床益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Concurrent Chemoradiotherapy versus Radiotherapy Alone in the Treatment of Stage II and T3N0M0 Nasopharyngeal Carcinoma: A Systematic Review and Meta-Analysis.

Aims: The efficacy of concurrent chemoradiotherapy (CCRT) for Stage II and T3N0 nasopharyngeal carcinoma (NPC), particularly during the shift from two-dimensional conventional radiotherapy (2DCRT) to intensity-modulated radiotherapy (IMRT) is debated.Therefore this study aims to systematically evaluate and meta-analyze survival benefits of CCRT versus radiotherapy alone for Stage II and T3N0 NPC, stratified by radiotherapy techniques.

Materials and methods: As of April 1, 2024, we conducted an exhaustive literature search across databases such as PubMed, Embase, Cochrane Library, and Web of Science, with the aim of identifying and screening studies that compare the efficacy of CCRT versus radiotherapy alone in the treatment of Stage II and T3N0 NPC.

Results: A total of 10 studies encompassing 5015 patients were included in this comprehensive analysis. The findings indicate that, apart from progression-free survival (PFS), CCRT did not improve survival outcomes, including overall survival (OS), distant metastasis-free survival (DMFS), local recurrence-free survival (LRRFS), and failure-free survival (FFS), with all P values exceeding 0.05. Concurrently, the incidence of grade ≥3 adverse events associated with CCRT was significantly elevated (odds ratio [OR] = 3.77, 95% confidence interval [CI] = 2.75-5.15, P < 0.0001). Subgroup analysis revealed that, compared with RT, the combination of 2DCRT with concurrent chemotherapy significantly improved OS (hazard ratio [HR] = 0.57, 95% CI = 0.46-0.71, P < 0.00001), PFS (HR = 0.65, 95% CI=0.53-0.78, P < 0.00001), DMFS (HR = 0.54, 95% CI = 0.37-0.79, P = 0.002), and LRRFS (HR = 0.63, 95% CI = 0.49-0.82, P = 0.0005). In contrast, the combination of IMRT with concurrent chemotherapy failed to demonstrate improvements in OS, PFS, DMFS, or LRRFS, with all P values exceeding 0.05.

Conclusion: In contrast with RT, CCRT did not enhance survival in stage II and T3N0 NPC patients, yet caused more adverse reactions. 2DCRT combined with concurrent chemotherapy significantly improved OS, PFS, DMFS, and LRRFS, while IMRT with concurrent chemotherapy showed no clinical benefits.

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来源期刊
Clinical oncology
Clinical oncology 医学-肿瘤学
CiteScore
5.20
自引率
8.80%
发文量
332
审稿时长
40 days
期刊介绍: Clinical Oncology is an International cancer journal covering all aspects of the clinical management of cancer patients, reflecting a multidisciplinary approach to therapy. Papers, editorials and reviews are published on all types of malignant disease embracing, pathology, diagnosis and treatment, including radiotherapy, chemotherapy, surgery, combined modality treatment and palliative care. Research and review papers covering epidemiology, radiobiology, radiation physics, tumour biology, and immunology are also published, together with letters to the editor, case reports and book reviews.
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