Feasibility Study of Short Term Fondaparinux (Arixtra) in Chemotherapy-Pretreated Ovarian Carcinoma Patients at High Risk of Progression

Sponsor

NYU Langone Health (Other)

Overall Status

Withdrawn

CT.gov ID

NCT00659399

Collaborator

GlaxoSmithKline (Industry)

Enrollment

Location

Duration (Months)

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this study is to assess feasibility and safety of using once daily Fondaparinux Sodium (ARIXTRA®) in patients with ovarian cancer who are in 'clinical remission' (no clinical evidence of disease) after chemotherapy but at high risk of ovarian cancer recurrence.

Condition or Disease	Intervention/Treatment	Phase
Ovarian Carcinoma	Drug: Fondaparinux	Phase 1

Detailed Description

Rationale:

A large body of work supports the association of abnormal coagulation (blood clot formation) and malignancy. A coagulation enzyme thrombin is able to 1) enhance cancer cell adhesion to platelets and endothelial cells 2) stimulate tumor cell growth, 3) increase metastasis and 4) stimulate tumor angiogenesis.

Thrombin inhibition has anti-metastatic and anti-tumor activity in mouse models. Recent meta-analysis of 4 major randomized clinical trials that have evaluated the effect of anticoagulants on overall survival in cancer patients comparing low molecular weight heparin (LMWH) to placebo demonstrates a 13% risk reduction in mortality at 1 year and 10% risk reduction at 2 years, which is statistically significant and independent of the potential confounding effect of anticoagulation in the prevention of venous thromboembolic disease.

Fondaparinux sodium (ARIXTRA® ) is a highly effective newer anticoagulant that is a fully synthetic pentasaccharide. Arixtra binds to antithrombin III and subsequently inhibits Factor Xa and hence thrombin generation. Arixtra has an excellent safety profile in clinical trials of over 10,000 patients. When compared to LMWHs, ARIXTRA® has a potential pharmacokinetic advantage based on its longer half-life of 16-17 hours.

Hypothesis:

The hypothesis to be tested is whether the completion of 8 weeks of ARIXTRA® in patients with ovarian cancer who are in 'clinical remission' (no clinical evidence of disease) after chemotherapy but at high risk of ovarian cancer recurrence is feasible and safe and if the inhibition of thrombin generation by ARIXTRA® in ovarian cancer will result in decrease ovarian cancer recurrence.

A concise description of the methodology:

The trial will be a prospective open-label cohort feasibility study of giving 2 months of ARIXTRA® in patients at high risk of recurrence of ovarian cancer. The planned accrual is 15 patients. Patients will be treated with a fixed dose of ARIXTRA® 2.5 mg by subcutaneous injection once daily. Treatment will continue for 2 months or until disease recurrence or grade 3 adverse events or patient refusal.

In addition, all patients will be followed for survival and recurrence.

Study Design

Study Type:

Interventional

Actual Enrollment :

0 participants

Allocation:

Non-Randomized

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

07-742 Phase I/ Feasibility Study of Short Term Fondaparinux (Arixtra) in Chemotherapy-Pretreated Ovarian Carcinoma Patients at High Risk of Progression

Study Start Date :

Jan 1, 2008

Anticipated Primary Completion Date :

Sep 1, 2010

Anticipated Study Completion Date :

Nov 1, 2010

Outcome Measures

Primary Outcome Measures

Estimate the proportion of patients who complete an eight week course of once daily administration of fondaparinux (Arixtra). [15 months]

Secondary Outcome Measures

Time to Recurrence [24 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 75 Years

Sexes Eligible for Study:

Female

Accepts Healthy Volunteers:

Inclusion Criteria:

Patients 18 years of age and ≤75 years of age
Biopsy-proven ovarian, tubal or primary peritoneal epithelial adenocarcinomas;
Performance status 0,1 (ECOG) ( table 2)
Patients at high risk of clinical relapse: first remission stage III/IV who were suboptimally debulked (residual disease >1 cm)
Patients of any stage who have recurred and are in second chemotherapy induced remission. Clinical remission defined as:
absence of symptoms that may be related to disease
imaging without abnormalities greater then or equal to 1 cm suspicious for disease (no ascites)
CA 125 obtained x 1 and <35 units/ml.
Adequate end organ function, defined as the following:
Total bilirubin < 1.5 x ULN
SGOT and SGPT < 2.5 x UNL
Creatinine < 1.5 x ULN
ANC > 1.5 x 109/L
Platelets > 100 x 109/L
Weight ≥ 50 kg

Exclusion Criteria:

Patients with performance status ECOG =2,3,4
Patients who are on warfarin or prior therapeutic anticoagulation
Patient has another primary malignancy that has required active intervention within 5 years, with the exception of basal cell skin cancer or a cervical carcinoma in situ.
Patient has a severe and/or uncontrolled medical disease (i.e., uncontrolled diabetes, chronic renal disease, or active uncontrolled infection).
Patient who had a major surgery within 2 weeks prior to study entry
Patients with the following lab abnormalities:
WBC <3000
absolute neutrophil count < 1,500
hemoglobin <10 g/dL
platelet < 100,000
creatinine clearance <30 cc/min
serum ALT, AST, or total bilirubin >1.5X the upper limit of normal
Patients with known bleeding disorder