Pharmacokinetically guided phase I trial of topotecan and etoposide phosphate in recurrent ovarian cancer
2005

Trial of Topotecan and Etoposide in Ovarian Cancer

Sample size: 21 publication Evidence: moderate

Author Information

Author(s): Levitt N C, Propper D J, Madhusudan S, Braybrooke J P, Echeta C, te Poele R, Davies S L, Flanagan E, Hickson I D, Joel S, Ganesan T S

Primary Institution: Cancer Research UK Cancer Centre, Churchill Hospital, Oxford

Hypothesis

The sequential combination of topotecan and etoposide phosphate will demonstrate good activity in recurrent ovarian cancer.

Conclusion

The combination of topotecan followed by etoposide phosphate showed good activity and higher toxicity than expected in patients with recurrent ovarian cancer.

Supporting Evidence

  • 28% of evaluable patients showed a response to the treatment.
  • 48% of patients were classified as platinum-resistant.
  • 71% of patients had received prior paclitaxel treatment.
  • Main toxicities included grade 4 neutropenia and thrombocytopenia.

Takeaway

Doctors tested a new way to treat ovarian cancer using two drugs, topotecan and etoposide, and found it worked better than expected, but it also made patients very sick.

Methodology

This was a phase I trial where patients received topotecan followed by etoposide phosphate, with dose adjustments based on plasma drug levels.

Limitations

The study had a small sample size and was limited to patients with recurrent ovarian cancer.

Participant Demographics

Patients had recurrent ovarian cancer, with a performance status of 0-2, and had previously received platinum-containing chemotherapy.

Digital Object Identifier (DOI)

10.1038/sj.bjc.6602657

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication