Gene Therapy in Treating Women With Refractory or Relapsed Ovarian Epithelial Cancer, Fallopian Tube Cancer, or Peritoneal Cancer

Ovarian Cancer Clinical Trial

Official title:

A Phase II Trial of In Vivo Gene Therapy With the Herpes Simplex Thymidine Kinase for the Treatment of Ovarian Cancer

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT00005025
• Other study ID #: CDR0000067546
• Secondary ID: HGTRI-0105NCI-V0
• Status: Active, not recruiting
• Phase: Phase 2
• First received: April 6, 2000
• Last updated: November 5, 2013
• Start date: June 2000

Study information

• Verified date: March 2003
• Source: National Cancer Institute (NCI)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Gene therapy may make the body build an immune response to kill tumor cells.

PURPOSE: Phase II trial to study the effectiveness of gene therapy in treating women who have refractory or relapsed ovarian epithelial cancer, fallopian tube cancer, or peritoneal cancer.

Description:

OBJECTIVES:

• Determine the efficacy and safety of in vivo gene therapy with herpes simplex thymidine kinase (HSVtk) vector producer cells (VPC) followed by ganciclovir in women with refractory or relapsed ovarian epithelial adenocarcinoma, fallopian tube cancer, or peritoneal cancer.

• Determine any development of systemic immunity to this regimen or tumor in these patients.

• Determine the toxic effects of intraperitoneal HSVtk VPC in these patients.

OUTLINE: All patients receive an intraperitoneal catheter prior to infusion.

Patients receive herpes simplex thymidine kinase (HSVtk) vector producer cells (VPC) IP over 15-60 minutes on day 0, followed by ganciclovir IV 2 times daily on days 28-41. Treatment repeats for up to 3 courses in patients with stable or responsive disease.

Patients are followed every 3 months for 1 year.

PROJECTED ACCRUAL: A total of 14-20 patients will be accrued for this study within 18-24 months.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 0
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

DISEASE CHARACTERISTICS:

• Histologically confirmed, refractory or relapsed, ovarian epithelial adenocarcinoma, fallopian tube cancer, or extraovarian peritoneal cancer for which no curative therapy exists

• Must have tissue available from tumor biopsy to grow tumor cells ex vivo

• Must have failed standard therapy with both a platinum agent (cisplatin or carboplatin) and paclitaxel

• Site of disease must be less than 5 cm in greatest diameter

• Evaluable disease by CT scan, physical exam, or laparoscopy

• No significant peritoneal fibrosis either from disease or prior surgery

• Surgical lysis of adhesions allowed

PATIENT CHARACTERISTICS:

Age:

• 18 and over

Performance status:

• ECOG 0-2

Life expectancy:

• Not specified

Hematopoietic:

• WBC greater than 2,000/mm3

• Absolute neutrophil count at least 1,000/mm3

• Platelet count at least 50,000/mm3

• Hemoglobin at least 8.5 g/dL (without transfusion)

Hepatic:

• Bilirubin no greater than 2.0 mg/dL

• SGOT or SGPT no greater than 4 times upper limit of normal (ULN)

• Alkaline phosphatase no greater than 4 times ULN

• Hepatitis B surface antigen test required prior to study if transaminases greater than 2.0 times ULN

• No hepatitis B surface antigen

• Amylase normal

• PT and PTT normal

Renal:

• Creatinine no greater than 2.0 mg/dL OR

• Creatinine clearance at least 50 mL/min

Cardiovascular:

• No cardiac dysfunction by history and exam

• No ischemic heart disease that may be considered anesthetic or operative risk

Pulmonary:

• No lung disease that may be considered anesthetic or operative risk

Other:

• HIV negative

• Not pregnant or nursing

• No acute viral, bacterial, or fungal infection requiring medication within 14 days prior to study

• No patient with greater than 2 L of ascites at the time of intraperitoneal infusion

• No underlying condition that would preclude compliance

• No allergies to study reagent

PRIOR CONCURRENT THERAPY:

Biologic therapy:

• Not specified

Chemotherapy:

• See Disease Characteristics

• No concurrent chemotherapy

Endocrine therapy:

• Not specified

Radiotherapy:

• Not specified

Surgery:

• See Disease Characteristics

Other:

• No concurrent high dose vitamin regimens

Study Design

Primary Purpose: Treatment

Related Conditions & MeSH terms

• Fallopian Tube Cancer
• Fallopian Tube Neoplasms
• Ovarian Cancer
• Ovarian Neoplasms
• Peritoneal Neoplasms
• Primary Peritoneal Cavity Cancer

Intervention

Biological:
• herpes simplex thymidine kinase

Drug:
• ganciclovir

Locations

Country	Name	City	State
United States	Human Gene Therapy Research Institute	Des Moines	Iowa

Sponsors (1)

Lead Sponsor	Collaborator
John Stoddard Cancer Center at Iowa Methodist Medical Center

Country where clinical trial is conducted

United States,