Literature DB >> 10225304

Chemotherapy of advanced and recurrent cervical carcinoma.

H N Nguyen1, S R Nordqvist.   

Abstract

Chemotherapy is used primarily to treat advanced or recurrent cervical cancer. There are three major applications: primary therapy, as a radiation sensitizer, and neoadjuvant therapy. Primary chemotherapy is employed in advanced and disseminated cervical carcinoma (Stage VB). The four best single drugs with moderate activity against cervical cancer are: cisplatin, ifosfamide, dibromodulcitol (mitolactol), and Adriamycin (doxorubicin). Cisplatin and ifosfamide appear to be the best combination therapy: they provide an objective response rate of 33%. However, because the overall survival was not significantly improved with combination therapy, single-agent therapy with one of the above active drugs is acceptable. For stages IIB, III and IVA, the primary therapy is still radiation. Concomitant chemotherapy with hydroxyurea or a combination of cisplatin and 5-fluorouracil (5-FU) have been shown to enhance radiation response in several randomized trials. Hydroxyurea is the preferred radiation sensitizer because it offers less toxicity, ease of administration, and equivalent results. Chemotherapy in neoadjuvant setting produces promising results. Various cisplatin combinations of mitomycin C, 5-FU, vincristine, and bleomycin have been employed to shrink locally advanced cervical cancer and permit safe, radical excision. Early results with these combinations in small trials are encouraging but further studies are needed to fully evaluate their potential.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10225304     DOI: 10.1002/(sici)1098-2388(199904/05)16:3<247::aid-ssu10>3.0.co;2-4

Source DB:  PubMed          Journal:  Semin Surg Oncol        ISSN: 1098-2388


  3 in total

Review 1.  Recurrent cervical cancer.

Authors:  Mario M Leitao; Dennis S Chi
Journal:  Curr Treat Options Oncol       Date:  2002-04

2.  Knockdown of PLC-gamma-2 and calmodulin 1 genes sensitizes human cervical adenocarcinoma cells to doxorubicin and paclitaxel.

Authors:  Anthony Stanislaus; Athirah Bakhtiar; Diyana Salleh; Snigdha Tiash; Tahereh Fatemian; Sharif Hossain; Toshihiro Akaike; Ezharul Hoque Chowdhury
Journal:  Cancer Cell Int       Date:  2012-06-18       Impact factor: 5.722

3.  Targeting phosphodiesterase 3B enhances cisplatin sensitivity in human cancer cells.

Authors:  Katsuhiro Uzawa; Atsushi Kasamatsu; Takao Baba; Katsuya Usukura; Yasuhiro Saito; Kentaro Sakuma; Manabu Iyoda; Yosuke Sakamoto; Katsunori Ogawara; Masashi Shiiba; Hideki Tanzawa
Journal:  Cancer Med       Date:  2013-02-03       Impact factor: 4.452

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.