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Surgery and Vaccine Therapy in Treating Patients With Early Cervical Cancer
This study is ongoing, but not recruiting participants.
Study NCT00002916   Information provided by National Cancer Institute (NCI)
First Received: November 1, 1999   Last Updated: February 6, 2009   History of Changes

November 1, 1999
February 6, 2009
November 1996
 
  • Immunological response to HPV [ Designated as safety issue: No ]
  • Toxicity and safety of TA-HPV [ Designated as safety issue: Yes ]
  • Immunological response to HPV
  • Toxicity and safety of TA-HPV
Complete list of historical versions of study NCT00002916 on ClinicalTrials.gov Archive Site
  • Proliferative capacity of T-cells to the E6 and E7 proteins [ Designated as safety issue: No ]
  • Influence of vaccination with TA-HPV on the disease free interval or patterns of recurrence [ Designated as safety issue: No ]
  • Proliferative capacity of T-cells to the E6 and E7 proteins
  • Influence of vaccination with TA-HPV on the disease free interval or patterns of recurrence
 
Surgery and Vaccine Therapy in Treating Patients With Early Cervical Cancer
A Phase II Trial in Patients With Early Cervical Cancer to Study The Safety and The Immunological Effects of Vaccination With TA-HPV, A Live Recombinant Vaccinia Virus Expressing The Human Papilloma Virus 16 and 18 E6 and E7 Proteins

RATIONALE: Vaccines made from human papillomavirus may make the body build an immune response to and kill cervical cancer cells. Combining vaccine therapy with surgery may be a more effective treatment for cervical cancer.

PURPOSE: This phase II trial is studying how well giving vaccine therapy together with surgery works in treating patients with early cervical cancer.

OBJECTIVES:

  • Evaluate the systemic immunological response to the human papilloma virus vaccine (TA-HPV) expressing the proteins 16, 18, E6 and E7 examining the cytolytic T cell and the antibody responses in cervical cancer patients.
  • Investigate further the safety and toxic effects of TA-HPV in these patients.
  • Assess the proliferative capacity of T cells to the E6 and E7 proteins.
  • Observe any influence of vaccination with TA-HPV on the disease free interval or patterns of recurrence in these patients.

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

Patients receive 2 vaccinations of the human papilloma virus with proteins 16, 18, E6 and E7 at least 4 weeks apart, with the first vaccination at least 2 weeks before surgery and the second 8 weeks after the first one, unless unacceptable toxicity occurs. Patients who require radiotherapy following surgery receive their second vaccination 4-8 weeks after the first vaccination.

Twenty-eight patients are entered initially; if at least 2 patients show an immunologic response, 16 additional patients are entered.

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

PROJECTED ACCRUAL: 44 patients will be entered over 1 year.

Phase II
Interventional
Treatment
Cervical Cancer
  • Biological: human papillomavirus 16 E7 peptide
  • Biological: synthetic human papillomavirus 16 E6 peptide
  • Procedure: adjuvant therapy
  • Procedure: surgical procedure
  • Radiation: radiation therapy
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Active, not recruiting
44
 
 

DISEASE CHARACTERISTICS:

  • Histologically proven untreated stage Ib or IIa cervical carcinoma, squamous or adenocarcinoma suitable for surgical excision

    • No CNS metastases
  • Circulating CD4+ lymphocyte count at least 400
  • Proven absence of hepatitis B and C antibodies
  • Previous exposure to vaccinia from smallpox vaccination, as well as no previous exposure, is allowed
  • Reaction to 2 or more antigens on Pasteur Merieux CMI test required
  • Ability to collaborate planned follow-up required

PATIENT CHARACTERISTICS:

Age:

  • 19 and over

Performance status:

  • WHO/ECOG no greater than 2

Life expectancy:

  • At least 3 months

Hematopoietic:

  • WBC greater than 3,000 (3,000 x 10 to the ninth/L)
  • Platelet count greater than 120,000 (120 x 10 to the ninth/L)
  • No bleeding disorder

Hepatic:

  • Bilirubin less than 1.5 times normal
  • AST and ALT less than 1.5 times normal
  • Prothrombin or partial thromboplastin time no greater than 2 times normal

Renal:

  • Creatinine less than 1.3 mg/dL (120 micromoles/L)

Other:

  • No ongoing infection
  • No HIV antibody
  • No serious medical or psychiatric illness
  • No second malignancy within 5 years except for curatively treated basal cell skin cancer which required surgery, hormone therapy, immunotherapy or chemotherapy
  • Not pregnant or nursing
  • Adequate contraception required
  • Patient or her household contacts must not have any of the following:

    • Chronic steroid therapy
    • Renal or other allograft
    • Known immunodeficiency
    • Eczema
    • Children under 5 years old

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • Not specified

Chemotherapy:

  • Not specified

Endocrine therapy:

  • Not specified

Radiotherapy:

  • Not specified

Surgery:

  • Not specified
Female
19 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Austria,   France,   Germany,   Netherlands,   Norway,   Sweden,   United Kingdom
 
NCT00002916
 
CDR0000065295, EORTC-13961
European Organization for Research and Treatment of Cancer
 
Study Chair: Elaine M. Rankin, MD Ninewells Hospital
National Cancer Institute (NCI)
January 2006

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP