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本文引用的文献

1
Evaluation of combined bevacizumab and intraperitoneal carboplatin or paclitaxel therapy in a mouse model of ovarian cancer.评估贝伐珠单抗联合腹腔内卡铂或紫杉醇治疗卵巢癌小鼠模型的疗效。
Cancer Chemother Pharmacol. 2011 Oct;68(4):951-8. doi: 10.1007/s00280-011-1566-3. Epub 2011 Feb 9.
2
Effects of bevacizumab in mouse model of endometrial cancer: Defining the molecular basis for resistance.贝伐珠单抗在子宫内膜癌小鼠模型中的作用:耐药分子机制的研究。
Oncol Rep. 2011 Mar;25(3):855-62. doi: 10.3892/or.2011.1147. Epub 2011 Jan 14.
3
Intraperitoneal VEGF inhibition using bevacizumab: a potential approach for the symptomatic treatment of malignant ascites?贝伐珠单抗腹腔内抑制:一种治疗恶性腹水症状的潜在方法?
Oncologist. 2009 Dec;14(12):1242-51. doi: 10.1634/theoncologist.2009-0109. Epub 2009 Dec 11.
4
Use of an anti-vascular endothelial growth factor antibody in a pharmacokinetic strategy to increase the efficacy of intraperitoneal chemotherapy.在药代动力学策略中使用抗血管内皮生长因子抗体以提高腹腔化疗疗效。
J Pharmacol Exp Ther. 2009 May;329(2):580-91. doi: 10.1124/jpet.108.149443. Epub 2009 Feb 20.
5
Maintenance treatment with bevacizumab prolongs survival in an in vivo ovarian cancer model.在体内卵巢癌模型中,使用贝伐单抗进行维持治疗可延长生存期。
Clin Cancer Res. 2008 Dec 1;14(23):7781-9. doi: 10.1158/1078-0432.CCR-08-0243.
6
Intraperitoneal bevacizumab for the palliation of malignant ascites in refractory ovarian cancer.腹腔内注射贝伐单抗用于缓解难治性卵巢癌的恶性腹水
Gynecol Oncol. 2008 Dec;111(3):530-2. doi: 10.1016/j.ygyno.2008.04.028. Epub 2008 Jun 18.
7
Bevacizumab and rapamycin inhibit tumor growth in peritoneal model of human ovarian cancer.贝伐单抗和雷帕霉素抑制人卵巢癌腹膜模型中的肿瘤生长。
Mol Cancer Ther. 2007 Nov;6(11):2959-66. doi: 10.1158/1535-7163.MCT-07-0237.
8
Phase II study of bevacizumab in patients with platinum-resistant ovarian cancer or peritoneal serous cancer.贝伐单抗用于铂耐药卵巢癌或腹膜浆液性癌患者的II期研究。
J Clin Oncol. 2007 Nov 20;25(33):5180-6. doi: 10.1200/JCO.2007.12.0782.
9
Phase II trial of bevacizumab in persistent or recurrent epithelial ovarian cancer or primary peritoneal cancer: a Gynecologic Oncology Group Study.贝伐单抗用于持续性或复发性上皮性卵巢癌或原发性腹膜癌的II期试验:一项妇科肿瘤学组研究
J Clin Oncol. 2007 Nov 20;25(33):5165-71. doi: 10.1200/JCO.2007.11.5345.
10
Avoiding bevacizumab related gastrointestinal toxicity for recurrent ovarian cancer by careful patient screening.通过仔细的患者筛查避免贝伐单抗相关的复发性卵巢癌胃肠道毒性。
Gynecol Oncol. 2007 Oct;107(1):118-23. doi: 10.1016/j.ygyno.2007.06.004. Epub 2007 Jul 23.

在铂类预处理的卵巢癌体内模型中,全身给予贝伐单抗可延长生存期。

Systemic administration of bevacizumab prolongs survival in an in vivo model of platinum pre-treated ovarian cancer.

作者信息

Rein Daniel T, Volkmer Anne Kathrin, Volkmer Jens, Beyer Ines M, Janni Wolfgang, Fleisch Markus C, Welter Anne Kathrin, Bauerschlag Dirk, Schöndorf Thomas, Breidenbach Martina

机构信息

Department of Obstetrics and Gynaecology, University of Düsseldorf Medical Centre, D-40225 Düsseldorf, Germany.

出版信息

Oncol Lett. 2012 Mar;3(3):530-534. doi: 10.3892/ol.2012.553. Epub 2012 Jan 3.

DOI:10.3892/ol.2012.553
PMID:22740945
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3362354/
Abstract

Ovarian cancer patients often suffer from malignant ascites and pleural effusion. Apart from worsening the outcome, this condition frequently impairs the quality of life in patients who are already distressed by ovarian cancer. This study investigated whether single intraperitoneal administration of the anti-VEGF antibody bevacizumab is capable of reducing the ascites-related body surface and prolonging survival. The study was performed in an orthotopic murine model of peritoneal disseminated platin-resistant ovarian cancer. Mice were treated with bevacizumab and/or paclitaxel or buffer (control). Reduction of body surface and increased survival rates were assessed as therapeutic success. Survival of mice in all treatment groups was significantly enhanced when compared to the non-treatment control group. The combination of paclitaxel plus bevacizumab significantly improved body surface as well as overall survival in comparison to a treatment with only one of the drugs. Treatment of malignant effusion with a single dose of bevacizumab as an intraperitoneal application, with or without cytostatic co-medication, may be a powerful alternative to systemic treatment.

摘要

卵巢癌患者常伴有恶性腹水和胸腔积液。除了使病情恶化外,这种情况还经常损害已因卵巢癌而痛苦的患者的生活质量。本研究调查了腹腔单次注射抗血管内皮生长因子(VEGF)抗体贝伐单抗是否能够减少与腹水相关的体表面积并延长生存期。该研究在铂耐药性卵巢癌腹膜播散的原位小鼠模型中进行。小鼠接受贝伐单抗和/或紫杉醇或缓冲液(对照)治疗。将体表面积的减少和生存率的提高评估为治疗成功。与未治疗的对照组相比,所有治疗组小鼠的生存期均显著延长。与仅使用一种药物治疗相比,紫杉醇加贝伐单抗的联合治疗显著改善了体表面积和总生存期。单剂量贝伐单抗腹腔内应用治疗恶性积液,无论是否联合使用细胞抑制剂,都可能是全身治疗的有力替代方案。