Modulation of the Expression of Papillomavirus (HPV) Oncoproteins to Major the Radiosensitivity: Trial Combining an Antiviral Agent VISTIDE and Radiochemotherapy in Cervical Cancers (HPV-RX)
Primary Purpose
Cervical Cancer
Status
Completed
Phase
Phase 1
Locations
France
Study Type
Interventional
Intervention
External radiotherapy + curietherapy
Vistide
Carboplatin
Sponsored by
About this trial
This is an interventional treatment trial for Cervical Cancer
Eligibility Criteria
Inclusion Criteria:
- Patients with cervix cancer : Squamous cell carcinoma or adenocarcinoma of stage IB2> 4 cm, II, III or IVA (International Federation of Gynecology Obstetrics, regardless of pelvic lymph node status (optional surgical exploration) without paraaortic metastasis.
- Detection of the virus genome of HPV positive on the primary tumor.
- General state ECOG performance status 0-1.
- 18 </ = age </ = 70 years.
- PN> 2000 / mm3
- hemoglobin> 9 g/l after transfusion if necessary .
- platelets > 100 000 / mm3
- Serum creatinine <1.5 upper limit of normal.
- Liver function tests (SGOT, SGPT, alkaline phosphatase and bilirubin) <1.5 upper limit of normal.
- Life expectancy> 3 months.
- Systematic Beta HCG Dosage for premenopausal women.
- Informed consent signed after informing the patient.
- Proteinuria <2g / L (200mg / dL) and creatinine clearance of> / = 55 ml / min.
Exclusion Criteria:
- Other histological types of cervix tumor than those mentioned in the inclusion criteria.
- Search of viral sequences on the negative HPV tumor diagnosis.
- History of cancer other than basal cell carcinoma.
- Pre-treatment with radiotherapy or chemotherapy.
- Ongoing pregnancy.
- History or active psychiatric illness.
- Nephropathy whatever the grade.
- Infection scalable.
- Active infection or other serious underlying pathology may prevent the patient receiving the treatment (in particular hepatic or cardiac).
- Inclusion in another clinical trial protocol with an experimental molecule (during the study or within one month before inclusion).
- Inability to submit to medical monitoring study for geographical, social or psychological.
Sites / Locations
- Gustave Roussy Cancer Campus Grand Paris
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Radiotherapy + Vistide + Chemoterapy
Arm Description
Outcomes
Primary Outcome Measures
Dose limiting toxicity
Secondary Outcome Measures
Efficacy Using RECIST criteria
Using RECIST criteria
Full Information
NCT ID
NCT02515877
First Posted
August 3, 2015
Last Updated
June 8, 2016
Sponsor
Gustave Roussy, Cancer Campus, Grand Paris
Collaborators
National Cancer Institute, France
1. Study Identification
Unique Protocol Identification Number
NCT02515877
Brief Title
Modulation of the Expression of Papillomavirus (HPV) Oncoproteins to Major the Radiosensitivity: Trial Combining an Antiviral Agent VISTIDE and Radiochemotherapy in Cervical Cancers
Acronym
HPV-RX
Official Title
Modulation of the Expression of Papillomavirus (HPV) Oncoproteins to Major the Radiosensitivity: Phase I Trial Combining an Antiviral Agent VISTIDE and Radiochemotherapy in Cervical Cancers
Study Type
Interventional
2. Study Status
Record Verification Date
June 2016
Overall Recruitment Status
Completed
Study Start Date
January 2008 (undefined)
Primary Completion Date
April 2013 (Actual)
Study Completion Date
April 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Gustave Roussy, Cancer Campus, Grand Paris
Collaborators
National Cancer Institute, France
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The treatment of cervical tumors depends on the stage of the disease. In advanced forms (nodal and / or local extension to the vagina and / or parameters) , radiotherapy associated with curietherapy , plays a major role. Until recently this association was the standard treatment for advanced stage uterine cancer. With this combination, rates of local failures (evolutionary prosecution and local recurrences) were 20 to 50% in stages IIb and 50-75 % for stage III. More than 50% for patients with a cervical cancer locally advanced (FIGO stages II / IV) . The standard treatment, external radiotherapy followed by curietherapy allows expect survival rates at 5 years for approximately 30-45 %. For ten years, numerous studies have evaluated the addition of concurrent chemotherapy to radiotherapy in cancer of the cervix. More than 19 randomized trials have been published. A meta-analysis of these trials was undertaken to assess the role of radiochemotherapy in cancers of the cervix. The first meta-analysis published by the Cochrane Collaborative Group, taking into account 4580 patient, shows an improvement in survival, both in terms of progression free survival and overall survival for patients treated with radio chemotherapy respectively 16% and 12 % (p < 0.0001). The rate of metastasis is also decreased (p < 0.0001). Survival rates were significantly better when platinum salt was used ( p < 0.0001 ) . However, no clinical benefit of chemoradiotherapy has been demonstrated for tumors stages [1, 2] locally advanced, possibly due to small number of patients. The investigators have previously shown that antiviral agents used in preclinical models, Cidofovir® causes the selective radiosensitization of cells infected by the papillomavirus (HPV). This trial proposes to study a new concept to increase radiochemotherapy efficiency: the modulation of the expression of viral oncoproteins HPV virus by an antiviral agent.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cervical Cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Radiotherapy + Vistide + Chemoterapy
Arm Type
Experimental
Intervention Type
Radiation
Intervention Name(s)
External radiotherapy + curietherapy
Intervention Description
External radiotherapy: 45 Gy in 5 weeks Curietherapy: 15Gy
Intervention Type
Drug
Intervention Name(s)
Vistide
Intervention Description
VISTIDE® (mg/kg) Level 1: 1mg/kg Level 2: 2,5 mg/kg Level 3: 5 mg/kg Level 4: 6,5 mg/kg
Intervention Type
Drug
Intervention Name(s)
Carboplatin
Intervention Description
AUC= 2,5 (Calvert formula)
Primary Outcome Measure Information:
Title
Dose limiting toxicity
Time Frame
Assessed every week after inclusion up to 10 weeks
Secondary Outcome Measure Information:
Title
Efficacy Using RECIST criteria
Description
Using RECIST criteria
Time Frame
Assessed 14 weeks after inclusion
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with cervix cancer : Squamous cell carcinoma or adenocarcinoma of stage IB2> 4 cm, II, III or IVA (International Federation of Gynecology Obstetrics, regardless of pelvic lymph node status (optional surgical exploration) without paraaortic metastasis.
Detection of the virus genome of HPV positive on the primary tumor.
General state ECOG performance status 0-1.
18 </ = age </ = 70 years.
PN> 2000 / mm3
hemoglobin> 9 g/l after transfusion if necessary .
platelets > 100 000 / mm3
Serum creatinine <1.5 upper limit of normal.
Liver function tests (SGOT, SGPT, alkaline phosphatase and bilirubin) <1.5 upper limit of normal.
Life expectancy> 3 months.
Systematic Beta HCG Dosage for premenopausal women.
Informed consent signed after informing the patient.
Proteinuria <2g / L (200mg / dL) and creatinine clearance of> / = 55 ml / min.
Exclusion Criteria:
Other histological types of cervix tumor than those mentioned in the inclusion criteria.
Search of viral sequences on the negative HPV tumor diagnosis.
History of cancer other than basal cell carcinoma.
Pre-treatment with radiotherapy or chemotherapy.
Ongoing pregnancy.
History or active psychiatric illness.
Nephropathy whatever the grade.
Infection scalable.
Active infection or other serious underlying pathology may prevent the patient receiving the treatment (in particular hepatic or cardiac).
Inclusion in another clinical trial protocol with an experimental molecule (during the study or within one month before inclusion).
Inability to submit to medical monitoring study for geographical, social or psychological.
Facility Information:
Facility Name
Gustave Roussy Cancer Campus Grand Paris
City
Villejuif
State/Province
Val de Marne
ZIP/Postal Code
94805
Country
France
12. IPD Sharing Statement
Learn more about this trial
Modulation of the Expression of Papillomavirus (HPV) Oncoproteins to Major the Radiosensitivity: Trial Combining an Antiviral Agent VISTIDE and Radiochemotherapy in Cervical Cancers
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