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本文引用的文献

1
Oral complications of targeted cancer therapies: a narrative literature review.靶向癌症治疗的口腔并发症:一篇叙述性文献综述。
Oral Oncol. 2011 Jun;47(6):441-8. doi: 10.1016/j.oraloncology.2011.03.028. Epub 2011 Apr 22.
2
Sorafenib in patients with metastatic renal cell carcinoma refractory to either sunitinib or bevacizumab.索拉非尼治疗对舒尼替尼或贝伐珠单抗耐药的转移性肾细胞癌患者。
Cancer. 2010 Dec 1;116(23):5383-90. doi: 10.1002/cncr.25327. Epub 2010 Aug 30.
3
A proposed EGFR inhibitor dermatologic adverse event-specific grading scale from the MASCC skin toxicity study group.MASCC 皮肤毒性研究组提出的一种针对 EGFR 抑制剂皮肤不良反应的特定分级量表。
Support Care Cancer. 2010 Apr;18(4):509-22. doi: 10.1007/s00520-009-0744-x. Epub 2010 Feb 10.
4
Phase II study of axitinib in sorafenib-refractory metastatic renal cell carcinoma.阿昔替尼用于索拉非尼难治性转移性肾细胞癌的II期研究。
J Clin Oncol. 2009 Sep 20;27(27):4462-8. doi: 10.1200/JCO.2008.21.7034. Epub 2009 Aug 3.
5
Overall survival and updated results for sunitinib compared with interferon alfa in patients with metastatic renal cell carcinoma.舒尼替尼与干扰素α治疗转移性肾细胞癌患者的总生存期及更新结果比较
J Clin Oncol. 2009 Aug 1;27(22):3584-90. doi: 10.1200/JCO.2008.20.1293. Epub 2009 Jun 1.
6
Phase II trial of sorafenib in metastatic thyroid cancer.索拉非尼用于转移性甲状腺癌的II期试验。
J Clin Oncol. 2009 Apr 1;27(10):1675-84. doi: 10.1200/JCO.2008.18.2717. Epub 2009 Mar 2.
7
Combination of bisphosphonates and antiangiogenic factors induces osteonecrosis of the jaw more frequently than bisphosphonates alone.双膦酸盐与抗血管生成因子联合使用比单独使用双膦酸盐更频繁地诱发颌骨坏死。
Oncology. 2009;76(3):209-11. doi: 10.1159/000201931. Epub 2009 Feb 12.
8
Randomized phase II trial of first-line treatment with sorafenib versus interferon Alfa-2a in patients with metastatic renal cell carcinoma.索拉非尼与干扰素α-2a一线治疗转移性肾细胞癌患者的随机II期试验。
J Clin Oncol. 2009 Mar 10;27(8):1280-9. doi: 10.1200/JCO.2008.19.3342. Epub 2009 Jan 26.
9
Phase I trial and pharmacokinetic study of bevacizumab in pediatric patients with refractory solid tumors: a Children's Oncology Group Study.贝伐单抗在难治性实体瘤儿科患者中的I期试验及药代动力学研究:一项儿童肿瘤学组研究
J Clin Oncol. 2008 Jan 20;26(3):399-405. doi: 10.1200/JCO.2007.11.9230.
10
Review: side effects of approved molecular targeted therapies in solid cancers.综述:已获批的实体癌分子靶向治疗的副作用
Oncologist. 2007 Dec;12(12):1443-55. doi: 10.1634/theoncologist.12-12-1443.

用于治疗癌症的分子靶向药物:口腔并发症与病理生理学

Molecularly targeted drugs for the treatment of cancer: oral complications and pathophysiology.

作者信息

Dietrich Em, Antoniades K

机构信息

Department of Oral and Maxillofacial Surgery, General Hospital "G. Papanikolaou", Thessaloniki, Greece.

出版信息

Hippokratia. 2012 Jul;16(3):196-9.

PMID:23935282
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3738722/
Abstract

BACKGROUND

Targeted cancer therapy is a new approach for the treatment of cancer. It involves a specific molecular target, mainly a receptor that serves as a target for monoclonal antibodies or tyrosine kinase inhibitors. Side-effects of these new regimens are described to be mild, compared to those of classical chemotherapy. There is a lack in the documentation and understanding of oral complications related to molecularly targeted drugs.

METHODS

In this review, we tried to make a systematic review of the databases Pubmed and Scopus, using "targeted cancer therapy" and "oral", or "mucositis", or "stomatitis", or "bleeding", or "hemorrhage" as search terms. Specific drug name searches were not conducted. The search yielded 97 results. Only articles related to EGFR and VEGFR inhibition were selected. Finally 13 articles met the criteria. RESULTS are discussed and possible pathogenetic mechanisms for the complications of targeted cancer therapy regimens are presented.

RESULTS

It appears that the most serious side-effect is mucositis/stomatitis that may affect the whole gastrointestinal tract. It rarely results in treatment discontinuation. Reduced saliva secretion, xerostomia and dysphagia can be severe with some regimens and interfere with food uptake. Osteonecrosis, wound healing impairment, spontaneous gingival bleeding and dysgeusia were also reported.

CONCLUSIONS

Considering these data it is obvious that symptoms related to cancer treatment should be considered in the context of the holistic management of patients. Oral complications should not be ignored but recorded during physical examination, because they may significantly impair daily activities and patients' quality of life.

摘要

背景

靶向癌症治疗是一种治疗癌症的新方法。它涉及一个特定的分子靶点,主要是一种作为单克隆抗体或酪氨酸激酶抑制剂靶点的受体。与传统化疗相比,这些新治疗方案的副作用被描述为较轻。目前缺乏关于分子靶向药物相关口腔并发症的文献记录和了解。

方法

在本综述中,我们试图对数据库PubMed和Scopus进行系统综述,使用“靶向癌症治疗”和“口腔”,或“粘膜炎”,或“口腔炎”,或“出血”作为检索词。未进行特定药物名称检索。检索结果有97条。仅选择与表皮生长因子受体(EGFR)和血管内皮生长因子受体(VEGFR)抑制相关的文章。最终有13篇文章符合标准。对结果进行了讨论,并提出了靶向癌症治疗方案并发症可能的发病机制。

结果

似乎最严重的副作用是可能影响整个胃肠道的粘膜炎/口腔炎。它很少导致治疗中断。某些治疗方案可能会导致严重的唾液分泌减少、口干和吞咽困难,并干扰食物摄取。还报告了骨坏死、伤口愈合受损、自发性牙龈出血和味觉障碍。

结论

考虑到这些数据,显然在患者的整体管理背景下应考虑与癌症治疗相关的症状。口腔并发症不应被忽视,而应在体格检查时记录下来,因为它们可能会严重损害日常活动和患者的生活质量。