MedPath

Trastuzumab in Treating Patients With Stage III, Stage IV, or Recurrent Endometrial Cancer

Phase 2
Completed
Conditions
Endometrial Adenocarcinoma
Stage III Uterine Corpus Cancer AJCC v7
ERBB2 Gene Amplification
Stage IV Uterine Corpus Cancer AJCC v7
Recurrent Uterine Corpus Carcinoma
Interventions
Other: Laboratory Biomarker Analysis
Biological: Trastuzumab
Registration Number
NCT00006089
Lead Sponsor
National Cancer Institute (NCI)
Brief Summary

Monoclonal antibodies such as trastuzumab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Phase II trial to study the effectiveness of trastuzumab in treating patients who have stage III, stage IV, or recurrent endometrial cancer.

Detailed Description

PRIMARY OOBJECTIVES:

I. Determine the antitumor activity of trastuzumab (Herceptin), in terms of response, in patients with advanced, recurrent, or persistent endometrial adenocarcinoma that demonstrates HER2/neu gene amplification by fluorescent in situ hybridization.

II. Determine the toxicity of this regimen in these patients.

SECONDARY OBJECTIVES:

I. Determine the progression-free and overall survival of patients treated with this regimen.

II. Determine the effects of prognostic factors (i.e., initial performance status and histological grade) in patients treated with this regimen.

OUTLINE: This is an open-label, multicenter study.

Patients receive trastuzumab (Herceptin) IV over 30-90 minutes on days 1, 8, 15, and 22. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

Patients are followed every 3 months for 2 years and then every 6 months for 3 years.

PROJECTED ACCRUAL: A total of 25-42 patients will be accrued for this study within 12 years.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
34
Inclusion Criteria
  • Histologically confirmed endometrial adenocarcinoma

    • Advanced, recurrent, or persistent disease
    • Refractory to curative therapy
  • HER2/neu gene amplification by fluorescent in situ hybridization

  • Measurable disease

    • Previously irradiated field as sole site of measurable disease allowed if evidence of progression since completion of radiotherapy
  • Performance status - GOG 0-2

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

  • Platelet count ? 100,000/mm^3

  • Bilirubin ? 1.5 times upper limit of normal (ULN)

  • Creatinine ? 1.5 times ULN

  • LVEF ? 45% by echocardiogram or MUGA

  • History of coronary artery disease and/or congestive heart failure allowed if medical management of condition has been stable within the past 6 months

  • No active or unstable cardiac disease

  • No active angina

  • No myocardial infarction within the past 6 months

  • No requirement for supplemental oxygen at rest or with ambulation

  • Not pregnant or nursing

  • Negative pregnancy test

  • Fertile patients must use effective contraception

  • No active infection requiring antibiotics

  • No uncontrolled infection

  • No other invasive malignancy within the past 5 years except nonmelanoma skin cancer

  • No other unstable medical condition that would preclude study participation

  • At least 3 weeks since prior biologic and immunologic agents directed at the malignant tumor

  • No prior anti-HER2 monoclonal antibody preparation

  • No other concurrent immunotherapy

  • Recovered from prior chemotherapy

  • Multiple prior chemotherapy regimens allowed

  • No more than 320 mg/m^2 total dose of prior doxorubicin allowed (including doxorubicin HCl liposome or other liposomally encapsulated doxorubicin preparations)

  • No concurrent chemotherapy

  • At least 1 week since prior hormonal therapy directed at the malignant tumor

  • No concurrent hormonal therapy

    • Continuation of hormone replacement therapy allowed
  • See Disease Characteristics

  • At least 3 weeks since prior radiotherapy for the malignant tumor and recovered

  • No concurrent radiotherapy

  • Recovered from prior recent surgery

  • At least 3 weeks since any prior therapy directed at the malignant tumor

  • No prior cancer treatment that would contraindicate study therapy

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Treatment (trastuzumab)Laboratory Biomarker AnalysisPatients receive trastuzumab (Herceptin) IV over 30-90 minutes on days 1, 8, 15, and 22. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
Treatment (trastuzumab)TrastuzumabPatients receive trastuzumab (Herceptin) IV over 30-90 minutes on days 1, 8, 15, and 22. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
Primary Outcome Measures
NameTimeMethod
Frequency and severity of observed adverse effects assessed using Common Terminology Criteria (CTC) version 2.0Up to 5 years
Frequency and duration of objective responseUp to 5 years
Secondary Outcome Measures
NameTimeMethod
Duration of progression-free survivalFrom study entry until disease progression, death or date or last contact, assessed up to 5 years

Will be evaluated with non-parametric statistics (such as the log-rank test) through comparisons with the historical controls.

Prognostic factors (i.e., initial performance status and histological grade)Not Provided

Comparisons will be made through a Cox model, which allows for adjustments with the prognostic variables.

Duration of overall survivalFrom study entry to death or date or last contact, assessed up to 5 years

Will be evaluated with non-parametric statistics (such as the log-rank test) through comparisons with the historical controls.

Trial Locations

Locations (1)

Gynecologic Oncology Group

🇺🇸

Philadelphia, Pennsylvania, United States

© Copyright 2025. All Rights Reserved by MedPath