• 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

[Toxicity of the CYVADIC modification in patients with soft tissue sarcomas or malignant mesotheliomas].

作者信息

Sauer H, Kremer G, Wilmanns W

机构信息

Medizinische Klinik III, Ludwig-Maximilians-Universität, München.

出版信息

Onkologie. 1987 Oct;10(5):294-300. doi: 10.1159/000216426.

DOI:10.1159/000216426
PMID:3317170
Abstract

CYVADIC (cyclophosphamide + vincristine + adriamycin + dacarbazine = DTIC) is frequently used in the treatment of patients with soft tissue sarcomas or malignant mesotheliomas. As a modification of the protocol originally published by Gottlieb, the interval between two cycles was extended to 4 weeks for better bone marrow regeneration and vincristine was given only once instead of twice per cycle. A total of 237 cycles of this modified CYVADIC protocol resulted in tolerable toxicity (except nausea and vomiting) and therapeutic results comparable to the original protocol (6/22 complete remissions and 6/22 partial remissions in sarcomas; 1/5 partial remission in mesotheliomas). Hematotoxicity was cumulative after 6 CYVADIC cycles. In contrast to the original Gottlieb scheme there were no severe infections such as pneumonia or sepsis. Neurotoxicity was weak and reversible; cardiotoxicity was not observed. Compared to the protocol originally suggested by Gottlieb, the modified CYVADIC regimen appears to be as effective but less toxic.

摘要

相似文献

1
[Toxicity of the CYVADIC modification in patients with soft tissue sarcomas or malignant mesotheliomas].
Onkologie. 1987 Oct;10(5):294-300. doi: 10.1159/000216426.
2
Analysis of a series of sixty soft tissue sarcomas in adults treated with a cyclophosphamide-vincristine-adriamycin-dacarbazine (CYVADIC) combination.
Cancer Chemother Pharmacol. 1985;15(1):82-5. doi: 10.1007/BF00257301.
3
Cyvadic in advanced soft tissue sarcoma: a randomized study comparing two schedules. A study of the EORTC Soft Tissue and Bone Sarcoma Group.环磷酰胺在晚期软组织肉瘤中的应用:一项比较两种给药方案的随机研究。欧洲癌症研究与治疗组织软组织和骨肉瘤研究组的一项研究。
Cancer. 1984 May 1;53(9):1825-32. doi: 10.1002/1097-0142(19840501)53:9<1825::aid-cncr2820530904>3.0.co;2-z.
4
Treatment of advanced soft tissue sarcomas with a modified CYVADIC protocol.
Oncology. 1984;41(5):308-13. doi: 10.1159/000225845.
5
Alternatives to CYVADIC-combination therapy of soft tissue sarcomas.
Klin Wochenschr. 1985 Nov 15;63(22):1160-2. doi: 10.1007/BF01740591.
6
Adjuvant CYVADIC chemotherapy for adult soft tissue sarcoma--reduced local recurrence but no improvement in survival: a study of the European Organization for Research and Treatment of Cancer Soft Tissue and Bone Sarcoma Group.成人软组织肉瘤的辅助CYVADIC化疗——降低局部复发率但未改善生存率:欧洲癌症研究与治疗组织软组织和骨肉瘤小组的一项研究
J Clin Oncol. 1994 Jun;12(6):1137-49. doi: 10.1200/JCO.1994.12.6.1137.
7
Cyclophosphamide, vincristine, adriamycin, and DTIC (CYVADIC) combination chemotherapy for the treatment of advanced sarcomas.环磷酰胺、长春新碱、阿霉素和达卡巴嗪(CYVADIC)联合化疗用于治疗晚期肉瘤。
Cancer Treat Rep. 1980 Jan;64(1):93-8.
8
Alternatives to CYVADIC combination therapy of soft tissue sarcomas.
Cancer Chemother Pharmacol. 1986;18 Suppl 2:S20-2. doi: 10.1007/BF00647444.
9
[Palliative chemotherapy of adult soft tissue sarcomas with an association of cyclophosphamide-vincristine-adriamycine-dacarbazine (CYVADIC) (author's transl)].环磷酰胺-长春新碱-阿霉素-达卡巴嗪联合方案(CYVADIC)用于成人软组织肉瘤的姑息化疗(作者译)
Bull Cancer. 1981;68(1):1-5.
10
[Pilot study of an alternative CYVADIC + CBDCA protocol for adult soft tissue sarcoma as adjuvant chemotherapy].[成人软组织肉瘤辅助化疗的替代CYVADIC+卡铂方案的初步研究]
Gan To Kagaku Ryoho. 2002 Sep;29(9):1571-4.

引用本文的文献

1
Chemotherapy in malignant mesothelioma: a review.恶性间皮瘤的化疗:综述
Cancer Chemother Pharmacol. 1991;28(5):319-30. doi: 10.1007/BF00685684.