• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Histological changes following high-dose methotrexate and cisplatinum administration and the influence of dosage scheduling.

作者信息

el-Badawi M G, Amer M H, Dahaba N M, Fatani J A, Sabah D M, Mustafa F A

出版信息

Chemotherapy. 1987;33(4):278-86. doi: 10.1159/000238508.

DOI:10.1159/000238508
PMID:3608628
Abstract

Histological changes were studied in experimental animals following the intraperitoneal administration of high-dose cisplatin with or without high-dose methotrexate and citrovorum factor. There were pronounced renal toxicities with high-dose (10 mg/kg) cisplatin, particularly involving distal tubules with glomerular congestion. However, lower toxicities were noted with reduced dosage of cisplatin (5 mg/kg) and especially if given once as a single bolus injection instead of a 5-day regimen. Renal and hepatic toxicities were marked with concomitant methotrexate administration leading to hemorrhagic diathesis and shorter survival. However, toxicities were relatively reduced when cisplatin was given as a single bolus injection instead of a 5-day divided course. Such information may prove helpful in future planning of combination chemotherapy in patients with malignancies using these two agents.

摘要

相似文献

1
Histological changes following high-dose methotrexate and cisplatinum administration and the influence of dosage scheduling.
Chemotherapy. 1987;33(4):278-86. doi: 10.1159/000238508.
2
Possible survival benefit of high-dose-intensity methotrexate, vinblastine, doxorubicin, and cisplatin combination therapy (HD-MVAC) over conventional MVAC in metastatic urothelial carcinoma patients.在转移性尿路上皮癌患者中,高剂量强度甲氨蝶呤、长春碱、阿霉素和顺铂联合疗法(HD-MVAC)相对于传统MVAC可能具有生存获益。
Hinyokika Kiyo. 2007 Sep;53(9):613-8.
3
A dose-seeking trial of edatrexate in combination with vinblastine, adriamycin, cisplatin, and filgrastim (EVAC/G-CSF) in patients with advanced malignancies: promising antineoplastic activity against non-small cell lung carcinomas.一项关于依达曲沙联合长春碱、阿霉素、顺铂和非格司亭(EVAC/G-CSF)用于晚期恶性肿瘤患者的剂量探索性试验:对非小细胞肺癌具有有前景的抗肿瘤活性。
Cancer J Sci Am. 1997 Sep-Oct;3(5):297-302.
4
Renal immunolocalization of kallikrein in cisplatin nephrotoxicity in rats.大鼠顺铂肾毒性中激肽释放酶的肾脏免疫定位
Histochem J. 1993 Oct;25(10):772-7. doi: 10.1007/BF00211772.
5
High-dose 7-hydromethotrexate: acute toxicity and lethality in a rat model.高剂量7-氢甲氨蝶呤:大鼠模型中的急性毒性和致死率
Cancer Chemother Pharmacol. 1996;37(5):415-22. doi: 10.1007/s002800050406.
6
[Morphofunctional correlates of the nephrotoxic action of cis-platin].[顺铂肾毒性作用的形态功能相关性]
Arkh Patol. 1987;49(3):48-54.
7
Standard or accelerated methotrexate, vinblastine, doxorubicin and cisplatin as neoadjuvant chemotherapy for locally advanced urothelial bladder cancer: Does dose intensity matter?标准或加速甲氨蝶呤、长春碱、多柔比星和顺铂作为局部晚期尿路上皮膀胱癌的新辅助化疗:剂量强度重要吗?
Eur J Cancer. 2016 Feb;54:69-74. doi: 10.1016/j.ejca.2015.11.017. Epub 2015 Dec 25.
8
[Pharmacokinetics of cisplatin and methotrexate in a patient suffering from advanced ureteral tumor accompanied by chronic renal failure, undergoing combined hemodialysis and systemic M-VAC chemotherapy].
Gan To Kagaku Ryoho. 2000 Nov;27(13):2079-85.
9
[The importance of dose intensity in preoperative chemotherapy for osteosarcoma--retrospective analysis of a short intensive chemotherapy regimen preoperatively using high-dose methotrexate and cisplatinum].[剂量强度在骨肉瘤术前化疗中的重要性——对术前使用大剂量甲氨蝶呤和顺铂的短期强化化疗方案的回顾性分析]
Gan To Kagaku Ryoho. 1994 Mar;21(4):459-64.
10
Nephrotoxicity of low-dose methotrexate in guinea pigs: an ultrastructural study.低剂量甲氨蝶呤对豚鼠的肾毒性:一项超微结构研究。
Nephron. 1996;73(3):462-6. doi: 10.1159/000189111.

引用本文的文献

1
Histological vis-a-vis biochemical assessment on the toxic level and antineoplastic efficacy of a synthetic drug Pt-ATP on experimental animal models.关于合成药物Pt-ATP对实验动物模型的毒性水平和抗肿瘤疗效的组织学与生化评估
J Exp Clin Cancer Res. 2008 Nov 12;27(1):68. doi: 10.1186/1756-9966-27-68.