Literature DB >> 8893874

Chemotherapy for advanced bladder cancer.

B J Roth1.   

Abstract

For the past 10 years, chemotherapy for advanced urothelial carcinoma has centered on cisplatin-based combination regimens such as methotrexate, vinblastine, doxorubicin and cisplatin (MVAC). Although such regimens have provided modest improvements in response rates, time to progression and survival, this has been achieved with moderate to severe toxicity. The median survival of patients with advanced disease remains at 12 to 13 months, and attempts to increase the dose intensity of existing regimens have been unsuccessful. Increasingly, attention has turned to the identification of new active agents, and a number have been recently identified, including paclitaxel, gemcitabine, ifosfamide, trimetrexate, piritrexim, and gallium nitrate. These agents will form the basis of new combination regimens that will attempt to improve on the advances in response and survival achieved with combination chemotherapy during the past decade.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8893874

Source DB:  PubMed          Journal:  Semin Oncol        ISSN: 0093-7754            Impact factor:   4.929


  4 in total

Review 1.  From methotrexate to pemetrexed and beyond. A review of the pharmacodynamic and clinical properties of antifolates.

Authors:  Jackie Walling
Journal:  Invest New Drugs       Date:  2006-01       Impact factor: 3.651

2.  Characterization of a novel transplantable orthotopic rat bladder transitional cell tumour model.

Authors:  Z Xiao; T J McCallum; K M Brown; G G Miller; S B Halls; I Parney; R B Moore
Journal:  Br J Cancer       Date:  1999-10       Impact factor: 7.640

3.  Docetaxel (Taxotere): an active agent in metastatic urothelial cancer; results of a phase II study in non-chemotherapy-pretreated patients.

Authors:  R de Wit; W H Kruit; G Stoter; M de Boer; J Kerger; J Verweij
Journal:  Br J Cancer       Date:  1998-11       Impact factor: 7.640

4.  Cisplatin-incorporating polymeric micelles (NC-6004) can reduce nephrotoxicity and neurotoxicity of cisplatin in rats.

Authors:  H Uchino; Y Matsumura; T Negishi; F Koizumi; T Hayashi; T Honda; N Nishiyama; K Kataoka; S Naito; T Kakizoe
Journal:  Br J Cancer       Date:  2005-09-19       Impact factor: 7.640

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.