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西妥昔单抗治疗头颈部鳞状细胞癌:系统评价数据。

Cetuximab therapy for head and neck squamous cell carcinoma: a systematic review of the data.

机构信息

Department of Otolaryngology–Head and Neck Surgery, Medical University of South Carolina, Charleston, South Carolina 29425, USA.

出版信息

Otolaryngol Head Neck Surg. 2011 May;144(5):676-84. doi: 10.1177/0194599811399559.

Abstract

OBJECTIVE

To review the current state of the data on the use of cetuximab in head and neck squamous cell carcinoma (HNSCC).

DATA SOURCES

The National Center for Biotechnology Information's PubMed and the Cochrane collection.

REVIEW METHODS

Search terms included cetuximab and head and neck cancer. These results were reviewed, and a second search was performed using limits: meta-analysis, randomized controlled trial, and clinical trial.

RESULTS

The literature search yielded 412 articles. Fifteen were identified for analysis. For patients with recurrent/metastatic disease who received combination chemotherapy in phase I/II trials, the overall response (OR) was 18.7% (95% confidence interval [CI], 10.4%-27.0%). Phase III trial data for combination chemotherapy in recurrent/metastatic disease showed OR to be 17.0% (95% CI, 12.6%-21.4%) for platinum-based regimens and 34.2% (28.6%-39.7%) for platinum-based regimens with cetuximab. For this same group, the estimated aggregate hazard ratio comparing platinum-based therapy plus cetuximab to platinum therapy alone was 1.10 (95% CI, 0.78- 1.54), indicating no significant improvement in overall survival in the aggregate analysis. Combination chemoradiation with cetuximab in both phase I/II trials and the single phase III trial shows enhanced responsiveness, but the data are difficult to interpret because it is not used with standard-of-care regimens for advanced-stage disease.

CONCLUSION

Early evidence has shown cetuximab to be effective in the treatment of HNSCC, and it should be used to enhance, but not replace, current treatment paradigms until further phase III data are available.

摘要

目的

综述西妥昔单抗在头颈部鳞状细胞癌(HNSCC)中的应用数据现状。

资料来源

美国国立生物技术信息中心的 PubMed 和 Cochrane 数据库。

检索方法

检索词包括西妥昔单抗和头颈部癌症。对这些结果进行了审查,并使用限制条件(荟萃分析、随机对照试验和临床试验)进行了第二次搜索。

结果

文献检索产生了 412 篇文章。确定了 15 篇进行分析。对于接受 I/II 期试验联合化疗的复发性/转移性疾病患者,总缓解率(OR)为 18.7%(95%置信区间 [CI],10.4%-27.0%)。复发性/转移性疾病联合化疗的 III 期试验数据显示,铂类方案的 OR 为 17.0%(95%CI,12.6%-21.4%),而含西妥昔单抗的铂类方案为 34.2%(28.6%-39.7%)。对于同一组患者,铂类联合西妥昔单抗治疗与单纯铂类治疗的总危险比估计值为 1.10(95%CI,0.78-1.54),表明在总体分析中总生存期无显著改善。I/II 期试验和单 III 期试验中的西妥昔单抗联合放化疗显示出更高的反应率,但由于未与晚期疾病的标准治疗方案联合使用,数据难以解释。

结论

早期证据表明西妥昔单抗对头颈部鳞状细胞癌有效,应将其用于增强而非替代当前的治疗模式,直至获得进一步的 III 期数据。

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