西妥昔单抗与铂基放化疗治疗HNSCC的疗效和安全性:来自10项随机对照试验的荟萃分析证据

IF 2.5 3区 医学 Q2 ONCOLOGY
Tarun Kumar, Nishu Kesh, Atindra Kumar Pandey, Ankita Chakrawal, Bhavana Singh, Manjusha Pal, Monika Rajput, Ruhi Dixit, Esha Pai, Manoj Pandey
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引用次数: 0

摘要

背景:铂基放化疗(CTRT)是头颈部鳞状细胞癌(HNSCC)的标准治疗方法。虽然以西妥昔单抗为基础的放疗(CxRT)已被提出作为一种替代方案,但其疗效仍存在争议。多个荟萃分析比较了CxRT和CTRT治疗HNSCC的效果,尽管他们将随机对照试验(rct)与低证据研究相结合,从而降低了结果的有效性。本研究首次采用随机对照试验数据进行荟萃分析,为临床决策提供了最高水平的证据。方法:系统检索MEDLINE、Embase、Cochrane和SCOPUS,纳入10项rct (n = 2557例患者)。主要结局包括总生存期(OS)、无病生存期(DFS)和全因死亡率;次要结局为≥3级毒性。采用随机效应模型汇总风险比(hr)和优势比(ORs)。结果:与CTRT相比,CxRT的复发风险增加50% (HR 1.50, 95% CI 1.07-2.10),全因死亡率增加27% (OR 1.27, 95% CI 1.05-1.55)。OS无显著差异(HR 1.33, 95% CI 0.79-2.22)。毒性特征各不相同:CxRT有较高的粘膜炎(OR 1.17, 95% CI 1.04-1.32)和皮疹(OR 3.46, 95% CI 1.28-9.36),而CTRT有较高的贫血(OR 0.15, 95% CI 0.05-0.52)和恶心/呕吐(OR 0.31, 95% CI 0.19-0.53)。结论:在HNSCC中,CxRT不如CTRT,疾病控制和生存结果较差。试验中缺乏生物标志物(EGFR/RAS)分层可能导致患者选择不理想。虽然对于不适合顺铂治疗的患者,CxRT可能是一种选择,但基于铂的治疗似乎是标准。未来的研究应该通过生物标志物驱动的选择来优化西妥昔单抗的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy and safety of cetuximab-based versus platinum-based chemoradiation in HNSCC: evidence from a meta-analysis of 10 randomized controlled trials.

Background: Platinum-based chemoradiotherapy (CTRT) is the standard treatment for head and neck squamous cell carcinoma (HNSCC). While cetuximab-based radiotherapy (CxRT) has been proposed as an alternative, its efficacy remains controversial. Multiple meta-analyses have compared CxRT with CTRT for HNSCC though they combined randomized controlled trials (RCTs) with lower-evidence studies, compromising result validity. This study presents the first meta-analysis using exclusively RCT data, providing the highest level of evidence for clinical decision-making.

Methods: We systematically searched MEDLINE, Embase, Cochrane, and SCOPUS, identifying 10 RCTs (n = 2,557 patients). Primary outcomes included overall survival (OS), disease-free survival (DFS), and all-cause mortality; secondary outcomes were Grade ≥ 3 toxicities. Hazard ratios (HRs) and odds ratios (ORs) were pooled using random effect models.

Results: CxRT was associated with a 50% higher recurrence risk (HR 1.50, 95% CI 1.07-2.10) and 27% increased all-cause mortality (OR 1.27, 95% CI 1.05-1.55) compared to CTRT. OS did not differ significantly (HR 1.33, 95% CI 0.79-2.22). Toxicity profiles varied: CxRT had higher mucositis (OR 1.17, 95% CI 1.04-1.32) and skin rash (OR 3.46, 95% CI 1.28-9.36), while CTRT showed more anemia (OR 0.15, 95% CI 0.05-0.52) and nausea/vomiting (OR 0.31, 95% CI 0.19-0.53).

Conclusion: CxRT is inferior to CTRT in HNSCC, with poorer disease control and survival outcomes. The lack of biomarker (EGFR/RAS) stratification in trials may have contributed to suboptimal patient selection. While CxRT may be an option for cisplatin-ineligible patients, platinum-based therapy appears to be the standard. Future research should optimize cetuximab's role through biomarker-driven selection.

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来源期刊
CiteScore
6.20
自引率
2.90%
发文量
240
审稿时长
1 months
期刊介绍: Clinical and Translational Oncology is an international journal devoted to fostering interaction between experimental and clinical oncology. It covers all aspects of research on cancer, from the more basic discoveries dealing with both cell and molecular biology of tumour cells, to the most advanced clinical assays of conventional and new drugs. In addition, the journal has a strong commitment to facilitating the transfer of knowledge from the basic laboratory to the clinical practice, with the publication of educational series devoted to closing the gap between molecular and clinical oncologists. Molecular biology of tumours, identification of new targets for cancer therapy, and new technologies for research and treatment of cancer are the major themes covered by the educational series. Full research articles on a broad spectrum of subjects, including the molecular and cellular bases of disease, aetiology, pathophysiology, pathology, epidemiology, clinical features, and the diagnosis, prognosis and treatment of cancer, will be considered for publication.
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