Doxorubicin Hydrochloride Liposome and Carboplatin in Treating Patients With Recurrent, Stage III, or Stage IV Primary Endometrial Cancer

Endometrial Cancer Clinical Trial

Official title:

A Multi-center Phase II Study of Doxil®/Carboplatin in Patients With Advanced or Recurrent Endometrial Carcinoma

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00470067
• Other study ID #: CDR0000543389
• Secondary ID: RPCI-I-68005
• Status: Terminated
• Phase: Phase 2
• First received: May 3, 2007
• Last updated: August 8, 2014
• Start date: February 2007
• Est. completion date: December 2009

Study information

• Verified date: August 2014
• Source: Roswell Park Cancer Institute
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Drugs used in chemotherapy, such as doxorubicin hydrochloride liposome and carboplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells.

PURPOSE: This phase II trial is studying how well giving doxorubicin hydrochloride liposome together with carboplatin works in treating patients with recurrent, stage III, or stage IV primary endometrial cancer.

Description:

OBJECTIVES:

Primary

• Estimate the response rate in patients with recurrent or stage III or IV primary endometrial carcinoma treated with doxorubicin hydrochloride liposome and carboplatin.

Secondary

• Determine progression-free survival of patients treated with this regimen.

• Determine overall survival of patients treated with this regimen.

• Determine the toxicity of this regimen in these patients.

OUTLINE: This is a multicenter study.

Patients receive doxorubicin hydrochloride liposome IV over 1 hour on day 1 and carboplatin IV over 30 minutes on day 1. Treatment repeats every 28 days for up to 8 courses in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed at 6 months and then every 3 months thereafter.

PROJECTED ACCRUAL: A total of 37 patients will be accrued for this study.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 9
• Est. completion date: December 2009
• Est. primary completion date: May 2008
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

DISEASE CHARACTERISTICS:

• Histologically confirmed primary endometrial carcinoma meeting 1 of the following criteria:

• Stage III or IV disease according to FIGO staging criteria

• Recurrent disease that is considered incurable

• Measurable disease

• A lesion within a previously irradiated field is acceptable as measurable disease only if there has been clear progression since completion of radiotherapy

PATIENT CHARACTERISTICS:

• GOG performance status 0-2

• Absolute neutrophil count = 1,500/mm^3

• Platelet count = 100,000/mm^3

• Hemoglobin = 9 g/dL

• Creatinine < 2.5 mg/dL OR creatinine clearance = 60 mL/min

• ALT and AST = 1.5 times upper limit of normal (ULN) (3 times ULN in the presence of liver metastases)

• Alkaline phosphatase = 1.5 times ULN (3 times ULN in the presence of liver metastases)

• Total bilirubin = 1.5 times ULN (3 times ULN in the presence of liver metastases)

• Not pregnant or nursing

• Left ventricular ejection fraction (LVEF) = 50% by MUGA scan or ECHO

• No history of severe hypersensitivity reaction to doxorubicin hydrochloride liposome

• No other invasive malignancy (i.e., breast cancer) within the past 5 years except nonmelanoma skin cancer

• No cardiac disease, including any of the following:

• Myocardial infarction within the past 6 months

• NYHA class II-IV heart failure

• Uncontrolled angina

• Severe uncontrolled ventricular arrhythmias

• Clinically significant pericardial disease

• Acute ischemic or active conduction system abnormalities by ECHO

PRIOR CONCURRENT THERAPY:

• No prior chemotherapy

• No prior cancer therapy that would contraindicate study treatment

• No concurrent investigational agents

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Endometrial Cancer

Intervention

Drug:
• carboplatin
IV
• pegylated liposomal doxorubicin hydrochloride
IV

Locations

Country	Name	City	State
United States	Roswell Park Cancer Institute	Buffalo	New York

Sponsors (1)

Lead Sponsor	Collaborator
Roswell Park Cancer Institute

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Response (Complete and Partial)	Response Rate	Every 28 days	No