Bevacizumab and Tocotrienol in Recurrent Ovarian Cancer

Phase 2

Completed

• Conditions: Ovarian Cancer Recurrent
• Interventions: Drug: Bevacizumab; Dietary Supplement: Tocotrienol

• Registration Number: NCT04175470
• Lead Sponsor: Vejle Hospital

Brief Summary

A recent study at the Department of Oncology, Vejle Hospital (NCT02399592), investigated bevacizumab and tocotrienol in ovarian cancer patients and concurrently monitored the level of methylated HOXA9 circulating tumor DNA (HOXA9 meth-ctDNA) in the blood.

The rate of disease control was 70% with better results than other studies using bevacizumab alone. The toxicity was very low and attributed to bevacizumab only.

When the study results were worked up they showed that patients with a significant increase of HOXA9 meth-ctDNA after the first cycle of treatment did not benefit from the treatment whereas those with stable or decreasing HOXA9 meth-ctDNA did.

Therefore, in the current study patients with a high increase of HOXA9 meth-ctDNA after the first treatment cycle will discontinue treatment, as it is then considered ineffective. The remaining patients may achieve prolonged survival as predicted by their level of HOXA9 meth-ctDNA.

Detailed Description

Not available

Study Timeline

• Study Start: 2019-10-29
• Study First Submitted: 2019-11-14
• Study First Submitted QC: 2019-11-20
• Study First Posted: 2019-11-25
• Primary Completion: 2024-07-30
• Study Completion: 2024-12-31
• Status Verified: 2025-01
• Last Update Submitted: 2025-01-02
• Last Update Posted: 2025-01-03

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 20

Inclusion Criteria

• Histologically confirmed epithelial ovarian cancer, primary fallopian or primary peritoneal cancer.

• Platinum resistant epithelial ovarian cancer treated with at least two different previous chemotherapeutic regimens

• Progression on previous treatment. Previous treatment with bevacizumab is allowed.

• Measurable disease by the RECIST 1.1 criteria or evaluable by the GCIG CA-125 criteria.

• Age ≥ 18 years.

• Performance status 0-2.

• Adequate bone marrow function, liver function, and renal function (within 7 days prior to inclusion):

  • WBC ≥ 3.0 x 10^9/l or neutrophils (ANC) ≥ 1.5 x 10^9/l
  • Platelet count ≥ 100 x 10^9/l
  • Hemoglobin ≥ 6 mmol/l
  • Serum bilirubin < 2.0 x ULN
  • Serum transaminase ≤ 2.5 x ULN
  • Serum creatinine ≤ 1.5 ULN

• Urine dipstick for protein < 2+. If the dipstick shows protein ≥ 2+, 24 hour urine testing must be performed and show protein contents < 1 g.

• Written informed consent

Exclusion Criteria

• Other malignant disease within 3 years prior to inclusion in the study, except curatively treated basal cell or squamous cell carcinoma of the skin.

• Other experimental therapy or participation in another clinical trial within 28 days prior to treatment initiation.

• Intestinal infiltration or infiltration in major blood vessels at the discretion of the treating physician.

• Underlying medical disease not adequately treated (diabetes, cardiac disease).

• Uncontrolled hypertension (BP > 150/100 despite antihypertensive treatment).

• Surgery including open biopsy, within 4 weeks prior to first dose of bevacizumab.

• Cerebral vascular attack, transient ischemic attack or subarachnoid hemorrhage within 6 months before start of treatment.

• Clinical significant cardiovascular disease, including:

  • Myocardial infarction or unstable angina within 6 months before start of treatment
  • New York Heart Association (NYHA) class ≥ 2
  • Poorly controlled cardiac arrhythmia despite medication
  • Peripheral vascular disease grade ≥ 3

• Allergy to active substance or any of the auxiliary agents

• Bleeding tumor

• Pregnant or breast-feeding patients. For fertile women a negative pregnancy test at screening is mandatory.

• Fertile patients not willing to use effective methods of contraception during treatment and for 6 months after the end of treatment.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SEQUENTIAL

Arm && Interventions

Group	Intervention	Description
Arm B: Continue treatment until progression	Bevacizumab	-
Arm A: Discontinue treatment after first treatment cycle	Bevacizumab	-
Arm A: Discontinue treatment after first treatment cycle	Tocotrienol	-
Arm B: Continue treatment until progression	Tocotrienol	-

Primary Outcome Measures

Name	Time	Method
Progression free survival	6 months after enrollment of the last patient

Secondary Outcome Measures

Name	Time	Method
Overall survival	12 months after enrollment of the last patient
Response rate as measured by RECIST 1.1 or CA-125	6 months after enrollment of the last patient
Safety as measured by CTC version 5.0	Every 9 weeks until progression, up to 3 years	CTC = National Cancer Institute's Common Toxicity Criteria (NCI-CTC)

Trial Locations

Locations (1)

Department of Oncology, Vejle Hospital; 🇩🇰 Vejle, Denmark