Tumor Vaccine and Interferon Gamma in Treating Patients With Refractory Epithelial Ovarian Cancer

Intraperitoneal (IP) Autologous Therapeutic Tumor Vaccine AUT-OV-ALVAC-h.B7.1 Plus IP rIFN-gamma for Patients With Ovarian Cancer. A Pilot Study

Status

Completed

Phases

Phase 1

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00004032

Enrollment

Registered

2003-08-25

Start date

1997-10-31

Completion date

Unknown

Last updated

2013-01-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Recurrent Ovarian Epithelial Cancer

Brief summary

Phase I trial to study the effectiveness of a tumor cell vaccine and interferon gamma in patients with refractory epithelial ovarian cancer. Vaccines made from a person's cancer cells may make the body build an immune response to and kill their tumor cells. Combining vaccine therapy with interferon gamma may be a more effective treatment for epithelial ovarian cancer

Detailed description

OBJECTIVES: I. Determine whether intraperitoneal (IP) injections of epithelial ovarian carcinoma cells infected with ALVAC-hB7.1 and IP interferon gamma have acceptable toxicity and produce any clinical responses in patients with refractory ovarian epithelial cancer. OUTLINE: This is a dose-escalation study of ALVAC-hB7.1 infected tumor cells. Patients receive ALVAC-hB7.1 infected tumor cells intraperitoneally (IP) on days 4, 11, and 18. Patients also receive interferon gamma IP on days 8, 10, 15, and 17. In the absence of disease progression, up to 6 courses of therapy may be given. If insufficient tumor cells are available to continue treatment with tumor cell derived vaccine, interferon gamma may be given alone. Cohorts of 3 to 6 patients receive escalating doses of ALVAC-hB7.1 infected tumor cells until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose at which no more than 2 of 6 patients experience dose-limiting toxicity. Patients are followed every 6 months until disease progression. PROJECTED ACCRUAL: A total of 12 patients will be accrued for this study.

Interventions

BIOLOGICALALVAC-hB7.1

Given IP

BIOLOGICALrecombinant interferon gamma

Given IP

OTHERlaboratory biomarker analysis

Correlative studies

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

FEMALE

Healthy volunteers

Inclusion criteria

* Diagnosis of ovarian epithelial carcinoma * Previously treated with an adequate course of platinum based chemotherapy * Evidence of intraabdominal disease * No significant adhesions * Performance status - Zubrod 0-2 * Lymphocyte count at least 500/mm\^3 * Bilirubin no greater than 1.5 mg/dL * SGOT less than 2.5 times upper limit of normal * Creatinine no greater than 1.5 mg/dL * No major disorder of the cardiovascular system * No major disorder of the pulmonary system * Not pregnant or nursing * Fertile patients must use effective contraception * Successful placement of peritoneal catheter * No overt autoimmune disease * No concurrent chronic steroid therapy * No prior radiotherapy * Prior surgery allowed * Recovered from prior therapy

Design outcomes

Primary

Measure	Time frame
Autologous tumor cell cytotoxicity lymphocyte (CTL)	Up to 7 years
Cytokine production (IFN gamma, IL-10, IL-2) by RT-PCR	Up to 7 years
Toxicity as assessed by NCI Common Terminology Criteria (CTC)	3 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026