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局部晚期头颈部鳞状细胞癌铂类药物不耐受患者的治疗选择:系统评价。

Treatment options for cisplatin-ineligible patients with locally advanced head and neck squamous cell carcinoma: a systematic review.

机构信息

Department of Medicine, Catholic University of Pelotas, Pelotas, Brazil.

Department of Internal Medicine, Federal University of Pelotas Teaching Hospital (EBSERH), Pelotas, Brazil.

出版信息

J Cancer Res Clin Oncol. 2024 Aug 2;150(8):379. doi: 10.1007/s00432-024-05887-z.

DOI:10.1007/s00432-024-05887-z
PMID:39093329
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11297068/
Abstract

PURPOSE

There is no agreed-upon standard option for patients with locally advanced head and neck squamous cell carcinoma (LA HNSCC) unfit for cisplatin-based regimens. Therefore, we performed a systematic review to explore alternative options for this population.

METHODS

We searched PubMed, Cochrane, and Embase databases for observational studies and clinical trials (CTs) assessing treatment options for LA HNSCC cisplatin-ineligible patients. This study was registered in PROSPERO under the number CRD42023483156.

RESULTS

This systematic review included 24 studies (18 observational studies and 6 CTs), comprising 4450 LA HNSCC cisplatin-ineligible patients. Most patients were treated with cetuximab-radiotherapy [RT] (50.3%), followed by carboplatin-RT (31.7%). In seven studies reporting median overall survival (OS) in patients treated with cetuximab-RT, it ranged from 12.8 to 46 months. The median OS was superior to 40 months in two studies assessing carboplatin-RT, and superior to 15 months in two studies assessing RT alone. For other regimens such as nimotuzumab-RT, docetaxel-RT, and carboplatin-RT plus paclitaxel the median OS was 21, 25.5, and 28 months, respectively.

CONCLUSIONS

Our systematic review supports the use of a variety of therapy combinations for LA HNSCC cisplatin-ineligible patients. We highlight the urgent need for clinical studies assessing treatment approaches in this population.

摘要

目的

对于不适合顺铂方案的局部晚期头颈部鳞状细胞癌(LA HNSCC)患者,目前尚无公认的标准治疗选择。因此,我们进行了一项系统评价,以探讨该人群的替代治疗选择。

方法

我们检索了 PubMed、Cochrane 和 Embase 数据库,以评估不适合接受顺铂治疗的 LA HNSCC 患者的治疗选择的观察性研究和临床试验(CT)。本研究在 PROSPERO 注册,编号为 CRD42023483156。

结果

本系统评价纳入了 24 项研究(18 项观察性研究和 6 项 CT),共纳入 4450 例不适合接受顺铂治疗的 LA HNSCC 患者。大多数患者接受西妥昔单抗联合放疗(50.3%),其次是卡铂联合放疗(31.7%)。在 7 项报告接受西妥昔单抗联合放疗的患者中位总生存期(OS)的研究中,OS 范围为 12.8 至 46 个月。两项评估卡铂联合放疗的研究中,中位 OS 超过 40 个月,两项评估单纯放疗的研究中,中位 OS 超过 15 个月。对于其他方案,如尼妥珠单抗联合放疗、多西他赛联合放疗和卡铂联合紫杉醇联合放疗,中位 OS 分别为 21、25.5 和 28 个月。

结论

本系统评价支持为不适合顺铂治疗的 LA HNSCC 患者使用多种治疗联合方案。我们强调迫切需要开展评估该人群治疗方法的临床研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eef5/11793760/c742e38fd130/432_2024_5887_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eef5/11793760/c742e38fd130/432_2024_5887_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eef5/11793760/c742e38fd130/432_2024_5887_Fig1_HTML.jpg

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本文引用的文献

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