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本文引用的文献

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Replication of TPMT and ABCC3 genetic variants highly associated with cisplatin-induced hearing loss in children.TPMT 和 ABCC3 基因变异体的复制与儿童顺铂诱导性听力损失高度相关。
Clin Pharmacol Ther. 2013 Aug;94(2):243-51. doi: 10.1038/clpt.2013.80. Epub 2013 Apr 10.
2
Antivirals for idiopathic sudden sensorineural hearing loss.用于特发性突发性感音神经性听力损失的抗病毒药物。
Cochrane Database Syst Rev. 2012 Aug 15;2012(8):CD006987. doi: 10.1002/14651858.CD006987.pub2.
3
Platinum-induced ototoxicity in children: a consensus review on mechanisms, predisposition, and protection, including a new International Society of Pediatric Oncology Boston ototoxicity scale.铂类诱导的儿童耳毒性:机制、易感性和保护的共识综述,包括新的国际儿科肿瘤学会波士顿耳毒性量表。
J Clin Oncol. 2012 Jul 1;30(19):2408-17. doi: 10.1200/JCO.2011.39.1110. Epub 2012 Apr 30.
4
Phase II trial of intraperitoneal cisplatin combined with intravenous paclitaxel in patients with ovarian, primary peritoneal and fallopian tube cancer.卵巢癌、原发性腹膜癌和输卵管癌患者腹腔内顺铂联合静脉紫杉醇的 II 期临床试验。
Gynecol Oncol. 2011 Sep;122(3):527-31. doi: 10.1016/j.ygyno.2011.05.022. Epub 2011 Jun 12.
5
Megalin genetic polymorphisms and individual sensitivity to the ototoxic effect of cisplatin.巨蛋白基因多态性与个体对顺铂耳毒性作用的敏感性
Pharmacogenomics J. 2008 Feb;8(1):23-8. doi: 10.1038/sj.tpj.6500455. Epub 2007 Apr 24.
6
Ototoxicity after intraperitoneal chemotherapy: a case report.腹腔化疗后的耳毒性:一例报告
Int J Gynecol Cancer. 2007 Sep-Oct;17(5):1133-5. doi: 10.1111/j.1525-1438.2007.00940.x. Epub 2007 Apr 13.
7
Intraperitoneal cisplatin and paclitaxel in ovarian cancer.顺铂和紫杉醇腹腔内给药治疗卵巢癌
N Engl J Med. 2006 Jan 5;354(1):34-43. doi: 10.1056/NEJMoa052985.
8
Phase III trial of standard-dose intravenous cisplatin plus paclitaxel versus moderately high-dose carboplatin followed by intravenous paclitaxel and intraperitoneal cisplatin in small-volume stage III ovarian carcinoma: an intergroup study of the Gynecologic Oncology Group, Southwestern Oncology Group, and Eastern Cooperative Oncology Group.标准剂量静脉注射顺铂联合紫杉醇与中高剂量卡铂序贯静脉注射紫杉醇及腹腔内注射顺铂治疗小体积Ⅲ期卵巢癌的Ⅲ期试验:妇科肿瘤学组、西南肿瘤学组和东部肿瘤协作组的一项组间研究
J Clin Oncol. 2001 Feb 15;19(4):1001-7. doi: 10.1200/JCO.2001.19.4.1001.
9
Glutathione S-transferase genetic polymorphisms and individual sensitivity to the ototoxic effect of cisplatin.谷胱甘肽S-转移酶基因多态性与个体对顺铂耳毒性作用的敏感性
Anticancer Drugs. 2000 Sep;11(8):639-43. doi: 10.1097/00001813-200009000-00007.
10
The etiology of idiopathic sudden sensorineural hearing loss. Experimental herpes simplex virus infection of the inner ear.特发性突发性感音神经性听力损失的病因。内耳的实验性单纯疱疹病毒感染。
Am J Otol. 1998 Jul;19(4):447-52.

在晚期卵巢癌治疗中,腹腔内注射顺铂一个疗程后出现严重感音神经性听力损失。

Profound sensorineural hearing loss after one cycle of intraperitoneal cisplatin in treatment of advanced ovarian cancer.

作者信息

McDonald Megan E, Mattson Jordan, Hill Emily

机构信息

Division of Gynecologic Oncology, The University of Iowa Hospitals and Clinics, Iowa City, IA, United States.

Department of Obstetrics and Gynecology, The University of Iowa Hospitals and Clinics, Iowa City, IA, United States.

出版信息

Gynecol Oncol Rep. 2017 Mar 21;20:103-104. doi: 10.1016/j.gore.2017.03.011. eCollection 2017 May.

DOI:10.1016/j.gore.2017.03.011
PMID:28393095
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5377914/
Abstract

Few advances in the treatment of advanced epithelial ovarian cancer have improved patient overall survival. However, the incorporation of intraperitoneal administration of platinum based chemotherapy to standard treatment was one such advancement. It is understood that the intraperitoneal regimen is associated with increased toxicity when compared to intravenous administration alone; however, information regarding the specific risk of ototoxicity is lacking in the literature. We report a case of almost complete sensorineural hearing loss after one cycle of intraperitoneal cisplatin. Three days after receiving an intravenous 24 h paclitaxel at 135 mg/m and subsequent intraperitoneal infusion of cisplatin at 75 mg/m, the patient presented with profound bilateral sensorineural hearing loss. The patient experienced no recovery of hearing despite an aggressive systemic steroid taper and change in chemotherapy regimen to alternative agents. She is currently under consideration for cochlear device implantation. Generally, cisplatin related ototoxicity during treatment of epithelial ovarian cancer is gradual, limited to high-frequency ranges and dose-related; however, the toxicity with only one standard dose can be profound and irreversible. This risk should be addressed when counseling patients prior to initiation of treatment.

摘要

晚期上皮性卵巢癌治疗方面的进展很少能改善患者的总体生存率。然而,将基于铂的化疗腹腔内给药纳入标准治疗是其中一项进展。据了解,与单纯静脉给药相比,腹腔内给药方案的毒性增加;然而,文献中缺乏关于耳毒性具体风险的信息。我们报告一例腹腔内顺铂治疗一个周期后几乎完全性感音神经性听力丧失的病例。在接受135mg/m²静脉输注24小时紫杉醇及随后75mg/m²腹腔内输注顺铂三天后,患者出现双侧严重感音神经性听力丧失。尽管积极进行全身性类固醇减量并将化疗方案改为替代药物,但患者听力未恢复。她目前正在考虑植入人工耳蜗装置。一般来说,上皮性卵巢癌治疗期间顺铂相关耳毒性是渐进性的,局限于高频范围且与剂量相关;然而,仅一个标准剂量的毒性也可能严重且不可逆。在治疗开始前为患者提供咨询时应提及这种风险。