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Cited by 377

The DOI matches its Crossref record; 15 of the 15 references it cites were found in a registry or an index.

Topotecan, an active drug in the second-line treatment of epithelial ovarian cancer: results of a large European phase II study.

Creemers, G J, Bolis, G, Gore, M, Scarfone, G, Lacave, A J, Guastalla, J P, Despax, R, Favalli, G, Kreinberg, R, Van Belle, S, Hudson, I, Verweij, J, Ten Bokkel Huinink, W W·1996·Journal of Clinical Oncology

Abstract

PURPOSE: Topotecan is a topoisomerase I inhibitor with preclinical activity against various tumor types. We conducted a large multicenter phase II study with topotecan in ovarian cancer in patients who had failed to respond to one prior cisplatin-based chemotherapeutic regimen. PATIENTS AND METHODS: Topotecan 1.5 mg/m2/d was administered intravenously by 30-minute infusion for 5 days repeated every 3 weeks. As the cisplatin-free interval relates to response in subsequent treatment, patients were stratified in subgroups, ie, cisplatin-refractory, cisplatin-resistant, and cisplatin-sensitive. RESULTS: One-hundred eleven patients entered the study. Nineteen patients were considered to be ineligible; 92 patients were assessable for response. A total of 552 courses were given (median, four per patient; range, one to 17). The major toxicities were leukocytopenia and neutropenia, which were grade 3 to 4 in 54.2% and 69.1% of courses, respectively, but with only 4.3% of these being grade 4 neutropenia plus fever or infectious complications. Prophylactic granulocyte colony-stimulating factor (G-CSF) was given in 20.5% of courses to maintain dose-intensity. Other relatively frequent side effects were alopecia (82%), nausea (36.4%), and vomiting (17.5%). The overall response rate was 16.3%, with one complete response (CR) and 14 partial responses (PRs). In the cisplatin-refractory, cisplatin-resistant, and cisplatin-sensitive strata, the response rates were 5.9%, 17.8%, and 26.7%, respectively. The median duration of time of documented response was 21.7 weeks (range, 4.6 to 41.9). CONCLUSION: Topotecan in a daily-times-five schedule is an effective regimen as second-line treatment in ovarian cancer. Further investigations of topotecan in ovarian cancer, including first-line use and combination with other active agents, are indicated.

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Crossref · 10.1200/jco.1996.14.12.3056

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Metadata

Authors
Creemers, G. J., Bolis, G., Gore, M., Scarfone, G., Lacave, A. J., Guastalla, J. P., Despax, R., Favalli, G., Kreinberg, R., Van Belle, S., Hudson, I., Verweij, J., & Ten Bokkel Huinink, W. W.
Venue
Journal of Clinical Oncology
Published
1996-12
Volume
14
Issue
12
Pages
3056-3061
ISSN
  • 0732-183X (ISSN-L)
  • 1527-7755
OpenAlex
W1831044128
Cited by
377
References
15
FWCI
21.47
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Topotecan, an active drug in the second-line treatment of epithelial ovarian cancer: results of a large European phase II study. https://app.cochat.ai/papers/10.1200/jco.1996.14.12.3056
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Creemers, G. J., Bolis, G., Gore, M., Scarfone, G., Lacave, A. J., Guastalla, J. P., Despax, R., Favalli, G., Kreinberg, R., Van Belle, S., Hudson, I., Verweij, J., & Ten Bokkel Huinink, W. W. (1996). Topotecan, an active drug in the second-line treatment of epithelial ovarian cancer: results of a large European phase II study. Journal of Clinical Oncology. https://doi.org/10.1200/jco.1996.14.12.3056

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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