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A rapid and systematic review of the clinical effectiveness and cost-effectiveness of topotecan for ovarian cancer
Author(s) -
Carol Forbes,
Liz Shirran,
AnneMarie Bagnall,
Steven Duffy,
Gerben ter Riet
Publication year - 2001
Publication title -
health technology assessment
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.426
H-Index - 126
eISSN - 2046-4924
pISSN - 1366-5278
DOI - 10.3310/hta5280
Subject(s) - medicine , topotecan , cost effectiveness , health technology , ovarian cancer , health economics , intensive care medicine , cancer , gynecology , health care , risk analysis (engineering) , public health , nursing , chemotherapy , economic growth , economics
Ovarian cancer is the most common gynaecological cancer with an annual incidence of 21.6 per 100,000 in England and Wales. Due to the often asymptomatic nature of the early stages of the disease, most cases are not detected until the advanced stages. Consequently, the prognosis after diagnosis is poor and the 5-year survival rate in the UK is only about 30%. Current recommendations suggest that first-line chemotherapy for ovarian cancer should involve paclitaxel and platinum (Pt)-based therapy (cisplatin/ carboplatin), however, most patients develop resistant or refractory disease and require second-line therapy. Patients may respond to re-challenge with Pt-agents if the treatment-free interval is > 6 months, but an alternative is often required. Topotecan is one of six drugs currently licensed in the UK for second-line therapy, and recent reviews suggest that it has modest efficacy in the treatment of advanced disease and performs favourably against paclitaxel. However, these reviews are based on a limited number of reports mainly consisting of non-randomised Phase I and II studies.

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