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抗肿瘤药物的神经毒性

Neurotoxicity of antineoplastic agents.

作者信息

Hussain M, Wozniak A J, Edelstein M B

机构信息

Department of Medicine, Wayne State University School of Medicine, Detroit, MI 48201.

出版信息

Crit Rev Oncol Hematol. 1993 Feb;14(1):61-75. doi: 10.1016/1040-8428(93)90006-p.

DOI:10.1016/1040-8428(93)90006-p
PMID:8373541
Abstract

PURPOSE

to review the neurotoxicity associated with antineoplastic agents.

METHODS

four hundred articles, abstracts and book chapters were selected for review. One hundred and ninety (articles, book chapters and abstracts) were identified as representative of the important aspects of neurotoxicity to be presented in this review.

RESULTS

in general the dose, schedule and route of administration significantly determine the incidence and outcome of antineoplastic agents neurotoxicity. An updated and detailed review of neurotoxicity is provided with special attention to vinca alkaloids, cisplatin and biologic response modifiers. The neurotoxic side effects of some of the new approaches in cancer therapy and some of the investigational agents are discussed. Guidelines for the prevention and management of this toxicity are presented. In addition, suggestions are made in regard to the preclinical and clinical screening of new agents for neurotoxicity.

CONCLUSION

quality of life issues have become a focal point in many clinical trials. Neurotoxicity associated with antineoplastic therapy clearly has an impact on the short and long term quality of the life of cancer patients. A better understanding of this toxicity requires developing reliable and predictive models to screen new agents prior to their introduction into clinical trials; a more detailed and uniform grading system; and the prospective evaluation of neurotoxicity in clinical trials of new antineoplastic agents.

摘要

目的

综述与抗肿瘤药物相关的神经毒性。

方法

选取400篇文章、摘要和书籍章节进行综述。其中190篇(文章、书籍章节和摘要)被确定为本次综述中神经毒性重要方面的代表。

结果

总体而言,剂量、给药方案和给药途径显著决定了抗肿瘤药物神经毒性的发生率和结果。本文对神经毒性进行了更新且详细的综述,特别关注长春花生物碱、顺铂和生物反应调节剂。讨论了癌症治疗中一些新方法及某些研究性药物的神经毒性副作用。提出了预防和管理这种毒性的指南。此外,还就新药神经毒性的临床前和临床筛查提出了建议。

结论

生活质量问题已成为许多临床试验的焦点。与抗肿瘤治疗相关的神经毒性显然会对癌症患者的短期和长期生活质量产生影响。要更好地理解这种毒性,需要开发可靠且具有预测性的模型,以便在新药进入临床试验前对其进行筛查;需要更详细和统一的分级系统;以及在新抗肿瘤药物的临床试验中对神经毒性进行前瞻性评估。

相似文献

1
Neurotoxicity of antineoplastic agents.抗肿瘤药物的神经毒性
Crit Rev Oncol Hematol. 1993 Feb;14(1):61-75. doi: 10.1016/1040-8428(93)90006-p.
2
Neurotoxicity in cancer chemotherapy: vinca alkaloids.癌症化疗中的神经毒性:长春花生物碱
Crit Care Nurse. 1997 Aug;17(4):71-9.
3
Chemotherapy-Induced Peripheral Neuropathy in Long-term Survivors of Childhood Cancer: Clinical, Neurophysiological, Functional, and Patient-Reported Outcomes.儿童癌症长期幸存者的化疗诱导性周围神经病:临床、神经生理学、功能和患者报告结局。
JAMA Neurol. 2018 Aug 1;75(8):980-988. doi: 10.1001/jamaneurol.2018.0963.
4
[Neurotoxicity and dermatologic toxicity of cancer chemotherapy].癌症化疗的神经毒性和皮肤毒性
Gan To Kagaku Ryoho. 2006 Jan;33(1):29-33.
5
Cisplatin neurotoxicity: the relationship between dosage, time, and platinum concentration in neurologic tissues, and morphologic evidence of toxicity.顺铂神经毒性:剂量、时间与神经组织中铂浓度之间的关系以及毒性的形态学证据。
J Clin Oncol. 1992 May;10(5):795-803. doi: 10.1200/JCO.1992.10.5.795.
6
Neurotoxicity secondary to antineoplastic drugs.抗肿瘤药物继发的神经毒性。
Cancer Treat Rev. 1994 Apr;20(2):191-214. doi: 10.1016/0305-7372(94)90027-2.
7
Animal models for the comparative assessment of neurotoxicity following repeated administration of vinca alkaloids.用于比较评估长春花生物碱重复给药后神经毒性的动物模型。
Cancer Treat Rep. 1979 Jan;63(1):35-41.
8
Neurotoxicity of antineoplastic drugs.抗肿瘤药物的神经毒性
Semin Oncol. 1982 Mar;9(1):103-30.
9
Mechanisms underlying chemotherapy-induced neurotoxicity and the potential for neuroprotective strategies.化疗诱导的神经毒性的潜在机制及神经保护策略的可能性。
Curr Med Chem. 2008;15(29):3081-94. doi: 10.2174/092986708786848569.
10
Chemotherapy-induced neurotoxicity: assessment and interventions for patients at risk.化疗引起的神经毒性:对高危患者的评估与干预
Am J Nurs. 2002 Apr;102 Suppl 4:16-9; quiz 49-52.

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Cancer Chemother Pharmacol. 2019 Sep;84(3):471-485. doi: 10.1007/s00280-019-03884-5. Epub 2019 Jun 18.
2
A tubulin binding peptide targets glioma cells disrupting their microtubules, blocking migration, and inducing apoptosis.一个微管结合肽靶向神经胶质瘤细胞,破坏其微管,阻止迁移,并诱导细胞凋亡。
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Dose-finding and pharmacokinetic study of orally administered indibulin (D-24851) to patients with advanced solid tumors.
口服吲达帕胺(D-24851)治疗晚期实体瘤患者的剂量探索和药代动力学研究。
Invest New Drugs. 2010 Apr;28(2):163-70. doi: 10.1007/s10637-009-9244-6. Epub 2009 Apr 30.
4
Phase I dose-finding and pharmacokinetic trial of orally administered indibulin (D-24851) to patients with solid tumors.口服吲哚布立林(D-24851)用于实体瘤患者的I期剂量探索和药代动力学试验。
Invest New Drugs. 2007 Jun;25(3):227-35. doi: 10.1007/s10637-006-9027-2. Epub 2006 Dec 5.
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Delayed, transient encephalopathy after marrow transplantation: case reports and MRI findings in four patients.骨髓移植后迟发性短暂性脑病:4例患者的病例报告及MRI表现
J Neurooncol. 1996 Mar;27(3):241-50. doi: 10.1007/BF00165481.