• 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

丝裂霉素:其在乳腺癌治疗中不断演变的作用。

Mitomycin: its evolving role in the treatment of breast cancer.

作者信息

Hortobagyi G N

机构信息

University of Texas M.D. Anderson Cancer Center, Department of Medical Oncology, Houston 77030.

出版信息

Oncology. 1993 Apr;50 Suppl 1:1-8.

PMID:8483556
Abstract

Investigators have compiled extensive experience with mitomycin in the treatment of patients with breast cancer. Given as a single agent in intermittent schedules, mitomycin has induced responses of 26-38% in previously untreated patients and of 15-25% in those exposed to multiple prior chemotherapy regimens. Duration of response has been short. Toxicity, primarily myelosuppression, is largely dose-dependent. The dose-dependent efficacy of mitomycin has not yet been addressed. Preclinical studies suggest that optimal single-agent results are obtained when mitomycin is given in intermittent, high-dose schedules. Combination chemotherapy with mitomycin has proven more effective than single-agent therapy. Mitomycin given in combination with doxorubicin produces higher response rates than have been obtained with mitomycin alone. The 3M combination (mitomycin/mitoxantrone/methotrexate) appears effective and well tolerated at the doses described. Future research should focus on the development of polychemotherapeutic regimens that can be delivered in sequential or alternating schedules. Such regimens may yield quicker responses, and thus improve survival, in patients with breast cancer.

摘要

研究人员在丝裂霉素治疗乳腺癌患者方面积累了丰富经验。丝裂霉素作为单一药物采用间歇给药方案时,在既往未接受过治疗的患者中诱导的缓解率为26% - 38%,在接受过多种先前化疗方案的患者中为15% - 25%。缓解持续时间较短。毒性主要为骨髓抑制,在很大程度上取决于剂量。丝裂霉素的剂量依赖性疗效尚未得到研究。临床前研究表明,当丝裂霉素采用间歇、高剂量给药方案时可获得最佳单药治疗效果。丝裂霉素联合化疗已被证明比单药治疗更有效。丝裂霉素与阿霉素联合使用产生的缓解率高于单独使用丝裂霉素时。3M联合方案(丝裂霉素/米托蒽醌/甲氨蝶呤)在所描述的剂量下似乎有效且耐受性良好。未来的研究应集中在开发可采用序贯或交替给药方案的多药化疗方案。此类方案可能使乳腺癌患者获得更快的缓解,从而提高生存率。

相似文献

1
Mitomycin: its evolving role in the treatment of breast cancer.丝裂霉素:其在乳腺癌治疗中不断演变的作用。
Oncology. 1993 Apr;50 Suppl 1:1-8.
2
Mitoxantrone, mitomycin-C, methotrexate combination chemotherapy with radiotherapy and/or surgery in stage III (T4B, NO-2, M0) breast cancer.米托蒽醌、丝裂霉素-C、甲氨蝶呤联合化疗并结合放疗和/或手术治疗Ⅲ期(T4B,NO-2,M0)乳腺癌。
J Assoc Physicians India. 1998 Nov;46(11):926-9.
3
A review of mitomycin regimens in advanced breast cancer therapy.
Clin Ther. 1985;7(3):286-307.
4
A feasibility study of multiple cycle therapy with melphalan, thiotepa, and paclitaxel followed by mitoxantrone, thiotepa, and paclitaxel with autologous hematopoietic cell support for metastatic breast cancer.美法仑、噻替派和紫杉醇多周期治疗后序贯米托蒽醌、噻替派和紫杉醇并采用自体造血细胞支持治疗转移性乳腺癌的可行性研究
Clin Cancer Res. 1999 Nov;5(11):3411-8.
5
Paclitaxel with mitoxantrone with or without 5-fluorouracil and high-dose leucovorin in the treatment of metastatic breast cancer.紫杉醇联合米托蒽醌,联合或不联合5-氟尿嘧啶及高剂量亚叶酸钙用于治疗转移性乳腺癌。
Semin Oncol. 1997 Oct;24(5 Suppl 17):S17-61-S17-64.
6
Possible use of combination chemotherapy with mitomycin C and methotrexate for metastatic breast cancer pretreated with anthracycline and taxanes.丝裂霉素C与甲氨蝶呤联合化疗在经蒽环类和紫杉烷类药物预处理的转移性乳腺癌中的可能应用。
Breast Cancer. 2009;16(4):301-6. doi: 10.1007/s12282-009-0093-0. Epub 2009 Feb 10.
7
Salvage therapy for metastatic disease.转移性疾病的挽救治疗。
Semin Oncol. 1990 Aug;17(4 Suppl 7):45-9.
8
A short course of induction chemotherapy followed by two cycles of high-dose chemotherapy with stem cell rescue for chemotherapy naive metastatic breast cancer.对于初治转移性乳腺癌,先进行短疗程诱导化疗,然后进行两个周期的高剂量化疗并联合干细胞救援。
Bone Marrow Transplant. 2001 Feb;27(3):269-78. doi: 10.1038/sj.bmt.1702780.
9
[Chemo-endocrine therapy including mitomycin C and medroxyprogesterone acetate in doxorubicin-refractory advanced breast cancer].
Gan To Kagaku Ryoho. 1996 Mar;23(4):439-45.
10
Mitoxantrone, 5-fluorouracil, and high dose leucovorin (NFL) versus intravenous cyclophosphamide, methotrexate, and 5-fluorouracil (CMF) in first-line chemotherapy for patients with metastatic breast carcinoma: a randomized phase II trial.米托蒽醌、5-氟尿嘧啶和高剂量亚叶酸钙(NFL)与静脉注射环磷酰胺、甲氨蝶呤和5-氟尿嘧啶(CMF)用于转移性乳腺癌患者一线化疗的比较:一项随机II期试验。
Cancer. 1997 Feb 15;79(4):740-8.

引用本文的文献

1
Importance of integrating nanotechnology with pharmacology and physiology for innovative drug delivery and therapy - an illustration with firsthand examples.将纳米技术与药理学和生理学相结合对于创新药物输送和治疗的重要性——以第一手实例说明。
Acta Pharmacol Sin. 2018 May;39(5):825-844. doi: 10.1038/aps.2018.33. Epub 2018 Apr 26.
2
A Model for NAD(P)H:Quinoneoxidoreductase 1 (NQO1) Targeted Individualized Cancer Chemotherapy.一种针对烟酰胺腺嘌呤二核苷酸磷酸(NAD(P)H):醌氧化还原酶1(NQO1)的个体化癌症化疗模型。
Drug Target Insights. 2009;4:1-8. doi: 10.4137/dti.s1146. Epub 2009 Jan 15.
3
The haemotoxicity of mitomycin in a repeat dose study in the female CD-1 mouse.
丝裂霉素在雌性CD-1小鼠重复给药研究中的血液毒性。
Int J Exp Pathol. 2005 Dec;86(6):415-30. doi: 10.1111/j.0959-9673.2005.00452.x.
4
Dietary induction of NQO1 increases the antitumour activity of mitomycin C in human colon tumours in vivo.通过饮食诱导NQO1可增强丝裂霉素C在人结肠肿瘤体内的抗肿瘤活性。
Br J Cancer. 2004 Oct 18;91(8):1624-31. doi: 10.1038/sj.bjc.6602171.
5
Enhanced cytotoxicity of mitomycin C in human tumour cells with inducers of DT-diaphorase.用 DT-黄递酶诱导剂增强丝裂霉素 C 对人肿瘤细胞的细胞毒性。
Br J Cancer. 1999 Jun;80(8):1223-30. doi: 10.1038/sj.bjc.6690489.
6
Induction of DT-diaphorase by 1,2-dithiole-3-thiones in human tumour and normal cells and effect on anti-tumour activity of bioreductive agents.1,2-二硫醇-3-硫酮对人肿瘤细胞和正常细胞中DT-黄递酶的诱导作用及其对生物还原药物抗肿瘤活性的影响。
Br J Cancer. 1998 Apr;77(8):1241-52. doi: 10.1038/bjc.1998.209.