search
Back to results

Maintenance Treatment for Ovarian Carcinoma in Remission by an Antiangiogenic Treatment Strategy

Primary Purpose

Ovarian Carcinoma

Status
Terminated
Phase
Phase 2
Locations
Israel
Study Type
Interventional
Intervention
Cytophosphan, Celecoxib, Methotrexate
Sponsored by
HaEmek Medical Center, Israel
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ovarian Carcinoma focused on measuring Ovary, Carcinoma, Maintenance, Metronomic, Chemotherapy, Time to Progression, overall survival

Eligibility Criteria

20 Years - 80 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Histologic proof of papillary-serous ovarian cancer or 1ary peritoneal carcinomatosis.
  2. Histological grade III.
  3. Original disease in stage III.
  4. ECOG performance status: 0-2.
  5. Age: 20-80 years.
  6. Previous chemotherapy with paclitaxel and carboplatin (only).
  7. Previous cyto-reductive surgery.
  8. Clinical Complete Response (both physically and by imaging).
  9. CA 125 should be either normalized (in at least 50 patients) or while still in decreasing values at monthly measurements.
  10. CBC at normal values or with any toxicity at a grade limited to I by NCIC-CTC.
  11. Liver and renal functions < 1.5 upper normal limits (UNL) by SMA.
  12. The patient's signature on the informed consent.

Exclusion Criteria:

  1. Mucinous type ovarian carcinoma.
  2. Histological Grade I-II.
  3. Current continuous treatment by steroids or by NSAIDs, or by anti-coagulants for "non protocol" reasons.
  4. Previous history of active peptic ulcer.
  5. Current participation in any other treatment study.

Sites / Locations

  • HaEmek Medical Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Metronomic Chemoterapy

Arm Description

Maintenance Treatment for Ovary Carcinoma by Metronomic Chemotherapy

Outcomes

Primary Outcome Measures

Time to Progression
Median time to progression of the cohort will be compared with equivalent measure in the literature.

Secondary Outcome Measures

Full Information

First Posted
August 1, 2010
Last Updated
June 21, 2015
Sponsor
HaEmek Medical Center, Israel
search

1. Study Identification

Unique Protocol Identification Number
NCT01175772
Brief Title
Maintenance Treatment for Ovarian Carcinoma in Remission by an Antiangiogenic Treatment Strategy
Official Title
Maintenance Treatment for Ovarian Carcinoma in Remission by an Antiangiogenic Treatment Strategy With Metronomic/Oral Chemotherapy (Cytophosphan Combined With Low-dose Methotrexate)and COX-2 Inhibition (Celecoxib)
Study Type
Interventional

2. Study Status

Record Verification Date
June 2015
Overall Recruitment Status
Terminated
Why Stopped
Due to change in the national policy of medications
Study Start Date
August 2010 (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
HaEmek Medical Center, Israel

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Preclinical studies showed that metronomic chemotherapy can induce tumor regression secondary to apoptosis of the tumor blood vessels. This effect was increased by combining metronomic chemotherapy with anti-angiogenic drugs. Metronomic chemotherapy has already proved clinical effects too, especially on patients with breast or prostate carcinoma. This study is aimed to test the efficacy of an experimental metronomic chemotherapy regimen in a cohort of patients with ovarian cancer. Patients will receive the proposed regimen as maintenance treatment following response induction by the conventional maximal tolerated dose (MTD) regimen of Carboplatin and Paclitaxel. Our regimen will include Cytophosphan combined with two agents which are expected to act as indirect angiogenic inhibitors: (a) celecoxib, as a selective COX-2 inhibitor and (b) low-dose Methotrexate, as successfully practiced for suppressing the inflammatory manifestations of rheumatoid arthritis. All components of our regimen will be administered orally and continuously for one year based on the hypothesis that its anti-angiogenic properties will be able to suppress the recovery of residual disease, thus extending the time to progression (TTP), and possibly the overall survival as well.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ovarian Carcinoma
Keywords
Ovary, Carcinoma, Maintenance, Metronomic, Chemotherapy, Time to Progression, overall survival

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
6 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Metronomic Chemoterapy
Arm Type
Experimental
Arm Description
Maintenance Treatment for Ovary Carcinoma by Metronomic Chemotherapy
Intervention Type
Drug
Intervention Name(s)
Cytophosphan, Celecoxib, Methotrexate
Intervention Description
Metronomic Chemotherapy as maintenance treatment for patients with Ovarian Cancer Cytophosphan tab 50 mg -1x1 per day, continuous Celecoxib tab 200 mg - 1x2 per day, continuous Methotrexate tab 2.5 mg - 1x2 per day, 2 days weekly
Primary Outcome Measure Information:
Title
Time to Progression
Description
Median time to progression of the cohort will be compared with equivalent measure in the literature.
Time Frame
18 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologic proof of papillary-serous ovarian cancer or 1ary peritoneal carcinomatosis. Histological grade III. Original disease in stage III. ECOG performance status: 0-2. Age: 20-80 years. Previous chemotherapy with paclitaxel and carboplatin (only). Previous cyto-reductive surgery. Clinical Complete Response (both physically and by imaging). CA 125 should be either normalized (in at least 50 patients) or while still in decreasing values at monthly measurements. CBC at normal values or with any toxicity at a grade limited to I by NCIC-CTC. Liver and renal functions < 1.5 upper normal limits (UNL) by SMA. The patient's signature on the informed consent. Exclusion Criteria: Mucinous type ovarian carcinoma. Histological Grade I-II. Current continuous treatment by steroids or by NSAIDs, or by anti-coagulants for "non protocol" reasons. Previous history of active peptic ulcer. Current participation in any other treatment study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David Loven, M.D.
Organizational Affiliation
HaEmek Medical Center, Oncology Unit
Official's Role
Study Director
Facility Information:
Facility Name
HaEmek Medical Center
City
Afula
ZIP/Postal Code
18101
Country
Israel

12. IPD Sharing Statement

Learn more about this trial

Maintenance Treatment for Ovarian Carcinoma in Remission by an Antiangiogenic Treatment Strategy

We'll reach out to this number within 24 hrs