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靶向胃肠道癌症:卡培他滨的作用

Targeting cancers in the gastrointestinal tract: role of capecitabine.

作者信息

Saif Muhammad Wasif

机构信息

Yale Cancer Center, Yale University School of Medicine, New Haven, CT, USA.

出版信息

Onco Targets Ther. 2009 Feb 18;2:29-41. doi: 10.2147/ott.s3469.

DOI:10.2147/ott.s3469
PMID:20616892
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2886333/
Abstract

Capecitabine is currently the only novel, orally home-administered fluorouracil prodrug. It offers patients more freedom from hospital visits and less inconvenience and complications associated with infusion devices. The drug has been extensively studied in large clinical trials in many solid tumors, including breast cancer, colorectal cancer, gastric cancer, and many others. Furthermore, the drug compares favorably with fluorouracil in patients with such cancers, with a safe toxicity profile, consisting mainly of gastrointestinal and dermatologic adverse effects. Whereas gastrointestinal events and hand-foot syndrome occur often with capecitabine, the tolerability profile is comparatively favorable. Prompt recognition of severe adverse effects is the key to successful management of capecitabine. Ongoing and future clinical trials will continue to examine, and likely expand, the role of capecitabine as a single agent and/or in combination with other anticancer agents for the treatment of gastrointestinal as well as other solid tumors, both in the advanced palliative and adjuvant settings. The author summarizes the current data on the role of capecitabine in the management of gastrointestinal cancers.

摘要

卡培他滨是目前唯一一种新型的、可在家口服的氟尿嘧啶前体药物。它使患者减少了去医院就诊的次数,减少了与输液装置相关的不便和并发症。该药物已在包括乳腺癌、结直肠癌、胃癌等多种实体瘤的大型临床试验中得到广泛研究。此外,在患有此类癌症的患者中,该药物与氟尿嘧啶相比具有优势,其毒性特征安全,主要包括胃肠道和皮肤不良反应。虽然卡培他滨常出现胃肠道事件和手足综合征,但其耐受性相对较好。及时识别严重不良反应是成功管理卡培他滨的关键。正在进行和未来的临床试验将继续研究,并可能扩大卡培他滨作为单一药物和/或与其他抗癌药物联合用于治疗晚期姑息和辅助治疗环境中的胃肠道以及其他实体瘤的作用。作者总结了卡培他滨在胃肠道癌症管理中的当前数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/472a/2886333/44c0f7699c44/ott-2-029f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/472a/2886333/1b131b5a8b3f/ott-2-029f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/472a/2886333/cc3b22a3893d/ott-2-029f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/472a/2886333/4fc5776527fb/ott-2-029f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/472a/2886333/6e7ea49f43fa/ott-2-029f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/472a/2886333/44c0f7699c44/ott-2-029f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/472a/2886333/1b131b5a8b3f/ott-2-029f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/472a/2886333/cc3b22a3893d/ott-2-029f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/472a/2886333/4fc5776527fb/ott-2-029f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/472a/2886333/6e7ea49f43fa/ott-2-029f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/472a/2886333/44c0f7699c44/ott-2-029f5.jpg

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本文引用的文献

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Irinotecan plus capecitabine as first-line chemotherapy in advanced colorectal cancer.伊立替康联合卡培他滨用于晚期结直肠癌的一线化疗。
Anticancer Res. 2008 May-Jun;28(3B):1923-6.
2
Severe sequence-specific toxicity when capecitabine is given after Fluorouracil and leucovorin.在氟尿嘧啶和亚叶酸钙之后给予卡培他滨时,会出现严重的序列特异性毒性。
J Clin Oncol. 2008 Jul 10;26(20):3411-7. doi: 10.1200/JCO.2007.15.9426.
3
Oxaliplatin and capecitabine-based chemoradiotherapy for gastric cancer--an extended phase I MARGIT and AIO trial.奥沙利铂联合卡培他滨用于胃癌的放化疗——MARGIT和AIO扩展I期试验
卡培他滨摄入与放疗时间间隔对局部晚期直肠癌术前放化疗局部无复发生存率的影响。
Radiat Oncol J. 2017 Jun;35(2):129-136. doi: 10.3857/roj.2017.00010. Epub 2017 Jun 30.
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New frontiers in the treatment of colorectal cancer: Autophagy and the unfolded protein response as promising targets.结直肠癌治疗的新前沿:自噬和未折叠蛋白反应作为有前景的靶点。
Autophagy. 2017 May 4;13(5):781-819. doi: 10.1080/15548627.2017.1290751. Epub 2017 Feb 23.
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First Case of Foot Drop Associated with Capecitabine in a Patient with Thymidylate Synthase Polymorphism.胸苷酸合成酶基因多态性患者中首例与卡培他滨相关的足下垂病例
Cureus. 2017 Jan 24;9(1):e995. doi: 10.7759/cureus.995.
6
Non-covalent interactions involving halogenated derivatives of capecitabine and thymidylate synthase: a computational approach.涉及卡培他滨卤代衍生物与胸苷酸合成酶的非共价相互作用:一种计算方法。
Springerplus. 2016 Feb 24;5:146. doi: 10.1186/s40064-016-1844-y. eCollection 2016.
Int J Radiat Oncol Biol Phys. 2009 Jan 1;73(1):142-7. doi: 10.1016/j.ijrobp.2008.04.033. Epub 2008 Jun 6.
4
EXTRA--a multicenter phase II study of chemoradiation using a 5 day per week oral regimen of capecitabine and intravenous mitomycin C in anal cancer.EXTRA——一项关于肛管癌的多中心II期研究,采用每周5天口服卡培他滨和静脉注射丝裂霉素C的放化疗方案。
Int J Radiat Oncol Biol Phys. 2008 Sep 1;72(1):119-26. doi: 10.1016/j.ijrobp.2007.12.012. Epub 2008 May 9.
5
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J Clin Oncol. 2008 Apr 20;26(12):2013-9. doi: 10.1200/JCO.2007.14.9930.
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J Clin Oncol. 2008 Apr 20;26(12):2006-12. doi: 10.1200/JCO.2007.14.9898.
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