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贝伐单抗停用后复发性结肠癌穿孔用于卵巢癌治疗。 (此译文表述稍显生硬,建议优化为:贝伐单抗停用后卵巢癌患者出现复发性结肠穿孔 )

Recurrent colon perforation after discontinuation of bevacizumab for ovarian cancer.

作者信息

Nonaka Michiko, Sato Seiya, Osaku Daiken, Sawada Mayumi, Kudoh Akiko, Chikumi Jun, Sato Shinya, Oishi Tetsuro, Harada Tasuku

机构信息

Department of Obstetrics and Gynecology, Tottori University School of Medicine, 36-1 Nishicho, Yonago-City, Tottori 683-8504, Japan.

Department of Obstetrics and Gynecology, Iwate Medical University School of Medicine, 19-1 Uchimaru, Morioka-City, Iwate 020-8505, Japan.

出版信息

Gynecol Oncol Rep. 2018 Aug 24;26:21-23. doi: 10.1016/j.gore.2018.08.005. eCollection 2018 Nov.

DOI:10.1016/j.gore.2018.08.005
PMID:30175211
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6116855/
Abstract

Bevacizumab (Bev) is an antiangiogenic drug used to treat various malignances, including ovarian cancer (OC). Bev is generally well-tolerated; however, it has a characteristic toxicity profile. In particular, gastrointestinal perforation (GIP) is a rare but serious side effect that can be lethal. A 55-year-old woman with recurrent OC had an episode of GIP during third-line chemotherapy comprising Bev and topotecan (TPT). Bev was discontinued while TPT was continued as monotherapy. Three months after discontinuation of Bev, the patient presented with left lower abdominal pain and was diagnosed with a second GIP. She had emergent surgery. One year later, she is still alive and healthy, and is continuing TPT. This is the first report of recurrent GIP after discontinuation of Bev. Our case suggests that physicians should be aware of GIP even after the discontinuation of Bev.

摘要

贝伐单抗(Bev)是一种用于治疗包括卵巢癌(OC)在内的多种恶性肿瘤的抗血管生成药物。Bev通常耐受性良好;然而,它具有独特的毒性特征。特别是,胃肠道穿孔(GIP)是一种罕见但严重的副作用,可能致命。一名55岁复发性OC女性在接受包含Bev和拓扑替康(TPT)的三线化疗期间发生了一次GIP。停用Bev,而TPT继续作为单一疗法使用。停用Bev三个月后,患者出现左下腹疼痛,被诊断为第二次GIP。她接受了急诊手术。一年后,她仍然健在且健康,并继续接受TPT治疗。这是停用Bev后复发性GIP的首例报告。我们的病例表明,即使在停用Bev后,医生也应意识到GIP的存在。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe55/6116855/c4761d772fc1/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe55/6116855/bb665c40f507/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe55/6116855/c4761d772fc1/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe55/6116855/bb665c40f507/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe55/6116855/c4761d772fc1/gr2.jpg

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本文引用的文献

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The role of bevacizumab in solid tumours: A literature based meta-analysis of randomised trials.贝伐单抗在实体瘤中的作用:基于文献的随机试验荟萃分析。
Eur J Cancer. 2017 Apr;75:245-258. doi: 10.1016/j.ejca.2017.01.026. Epub 2017 Feb 24.
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Bevacizumab combined with chemotherapy for ovarian cancer: an updated systematic review and meta-analysis of randomized controlled trials.贝伐单抗联合化疗治疗卵巢癌:随机对照试验的最新系统评价和荟萃分析
Oncotarget. 2017 Feb 7;8(6):10703-10713. doi: 10.18632/oncotarget.12926.
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Bevacizumab toxicity in heavily pretreated recurrent epithelial ovarian, fallopian tube, and primary peritoneal cancers.
贝伐单抗在多次接受治疗的复发性上皮性卵巢癌、输卵管癌和原发性腹膜癌中的毒性作用。
J Gynecol Oncol. 2016 Sep;27(5):e47. doi: 10.3802/jgo.2016.27.e47. Epub 2016 May 10.
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Profile of bevacizumab in the treatment of platinum-resistant ovarian cancer: current perspectives.贝伐单抗治疗铂耐药卵巢癌的概况:当前观点
Int J Womens Health. 2016 Mar 15;8:59-75. doi: 10.2147/IJWH.S78101. eCollection 2016.
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The pharmacological bases of the antiangiogenic activity of paclitaxel.紫杉醇抗血管生成活性的药理学基础。
Angiogenesis. 2013 Jul;16(3):481-92. doi: 10.1007/s10456-013-9334-0. Epub 2013 Feb 7.
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Curr Opin Obstet Gynecol. 2012 Feb;24(1):8-13. doi: 10.1097/GCO.0b013e32834daeed.
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Safety of bevacizumab in patients with advanced cancer: a meta-analysis of randomized controlled trials.贝伐珠单抗治疗晚期癌症患者的安全性:一项随机对照试验的荟萃分析。
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