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OpenTrials
Completed

NCT Number: NCT00003065

Topotecan and Paclitaxel in Treating Patients With Recurrent or Metastatic Cancer of the Cervix

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells.

PURPOSE: Phase II trial to study the effectiveness of topotecan and paclitaxel in treating patients who have recurrent or metastatic cancer of the cervix.

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Key information

Age range

18 year–60 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

Herbert Irving Comprehensive Cancer Center at Columbia University

New York, 10032, United States

About this study

OBJECTIVES:

  • Determine the response, time to progression, disease free survival, and overall survival of patients with recurrent and/or metastatic cancer of the cervix treated with a combination of topotecan and paclitaxel.
  • Determine the feasibility and toxicity of this regimen in these patients.

OUTLINE: Patients receive paclitaxel IV over 3 hours on day 1 and topotecan IV over 30 minutes on days 1-5. Filgrastim (G-CSF) is administered on days 6-14. Treatment repeats every 21 days for a minimum of 2 courses in the absence of disease progression or unacceptable toxicity.

Patients are followed every 3 weeks.

PROJECTED ACCRUAL: A total of 25 patients will be accrued for this study within 2 years.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

DISEASE CHARACTERISTICS:

  • Histologically confirmed recurrent, persistent or metastatic cervical carcinoma (squamous or adenocarcinoma), with no potentially curative standard treatment
  • Measurable disease or evaluable disease

PATIENT CHARACTERISTICS:

Age:

  • 18 to physiological 60

Performance status:

  • ECOG 0-2

Life expectancy:

  • Greater than 2 months

Hematopoietic:

  • WBC greater than 3000/mm3
  • Platelet count greater than 100,000/mm3

Hepatic:

  • Bilirubin less than 1.5 times normal
  • SGOT/SGPT less than 1.5 times normal

Renal:

  • BUN less than 1.5 times normal
  • Creatinine less than 1.5 times normal
  • Creatinine clearance greater than 50 mL/min

Other:

  • Ineligible for other high priority national or institutional study
  • Not pregnant or nursing
  • HIV negative
  • No prior malignancy except nonmelanoma skin cancer
  • No serious medical or psychiatric illness preventing treatment or informed consent

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • Not specified

Chemotherapy:

  • Greater than 4 weeks since prior chemotherapy
  • No greater than 2 prior chemotherapy regimens
  • No prior taxane or camptothecin

Endocrine therapy:

  • No concurrent hormonal therapy except that required for nondisease related conditions (e.g., insulin for diabetes)

Radiotherapy:

  • Greater than 4 weeks since prior radiation therapy
  • No concurrent radiation therapy

Surgery:

  • Greater than 4 weeks since prior surgery

Treatment and study plan

filgrastim

Biological

paclitaxel

Drug

Topotecan Hydrochloride

Drug

Sponsors and collaborators

Lead sponsor

Herbert Irving Comprehensive Cancer Center

Other

Registry information

Official study title

Phase II Investigation of Topotecan and Taxol in Patients With Recurrent/Metastatic Cancer of the Cervix

Important dates

Study start
1997
Study completion
2004
First posted
Jan 27, 2003
Registry last updated
Jan 6, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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