Overview

Study of Clinical and Biological Prognostic Factors in Patients With Ovarian Cancer Receiving Carboplatin +Paclitaxel With Bevacizumab

Status:
Active, not recruiting
Trial end date:
2022-11-01
Target enrollment:
0
Participant gender:
Female
Summary
The addition of bevacizumab to first-line chemotherapy has been shown to improve progression free survival for patients with ovarian cancer. The purpose of this study is to explore the potential role of clinical and biologic factors in identifying those patients who benefit most from this combined therapy in terms of progression free and overall survival.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
National Cancer Institute, Naples
Collaborator:
Mario Negri Institute for Pharmacological Research
Treatments:
Albumin-Bound Paclitaxel
Bevacizumab
Carboplatin
Paclitaxel
Criteria
Inclusion Criteria:

- Female patients ≥18 years of age.

- Patients with histologically confirmed epithelial ovarian carcinoma, fallopian tube
carcinoma or primary peritoneal carcinoma, including mixed Mullerian Tumours Or
Recurrent early stage epithelial ovarian or fallopian tube carcinoma treated with
surgery alone.

- FIGO stage IIIB & C or IV

- ECOG Performance Status of 0-2.

- Life expectancy of at least 12 weeks.

- Signed informed consent obtained prior to initiation of any study-specific procedures
and treatment as confirmation of the patient's awareness and willingness to comply
with the study requirements.

- Availability of tumour samples for molecular analyses

Exclusion Criteria:

Cancer related

- Ovarian tumours with low malignant potential (i.e. borderline tumours)

- Previous systemic anti-cancer therapy for advanced ovarian cancer.

- History or evidence of brain metastases or spinal cord compression.

- History or evidence of synchronous primary endometrial carcinoma, unless all of the
following criteria related to the endometrial carcinoma are met:

- stage ≤Ia

- no more than superficial myometrial invasion

- no lymphovascular invasion

- not poorly differentiated (grade 3 or papillary serous or clear cell carcinoma).

- Other malignancy within the last 5 years, except for adequately treated carcinoma in
situ of the cervix or squamous carcinoma of the skin, or adequately controlled limited
basal cell skin cancer.

Other-treatment related

- Any prior radiotherapy to the pelvis or abdomen.

- Surgery (including open biopsy) within 4 weeks prior to the first bevacizumab dose or
planned (In this case the patient can be enrolled but the administration of
bevacizumab should be omitted at first cycle).

- Current or recent (within 10 days prior to the first study drug dose) use of full-dose
oral or parenteral anticoagulant or thrombolytic agent for therapeutic purposes
(except for central venous access patency, in which case international normalized
ratio [INR] must be maintained below 1.5). Post operative prophylaxis with low
molecular weight heparin sc is allowed.

- Current or recent (within 30 days of first study dosing) treatment with another
investigational drug.

Laboratory related

- Inadequate bone marrow function: ANC: <1.5 x 109/l, or platelet count <100 x 109/l or
Haemoglobin <9 g/dl. Patients may be transfused to maintain haemoglobin values ≥9
g/dl.

- Inadequate coagulation parameters:

- activated partial thromboplastin time (APTT) >1.5 xULN or

- INR >1.5

- Inadequate liver function, defined as:

- serum (total) bilirubin >1.5 x the upper limit of normal (ULN) for the
institution

- AST/SGOT or ALT/SGPT >2.5 x ULN.

- Inadequate renal function, defined as serum creatinine >2.0 mg/dl or >177 micromol/l

- Proteinuria >1g in a 24-hour urine collection (to be performed only among patients who
showed a ≥3+ at urine dipstick).

Patient related

- Pregnant or lactating patients.

- History or evidence of thrombotic or hemorrhagic disorders; including cerebrovascular
accident (CVA) / stroke or transient ischemic attack (TIA) or sub-arachnoid
haemorrhage within ≤6 months prior to the first study treatment).

- Uncontrolled hypertension (sustained systolic >150 mm Hg and/or diastolic >100 mm Hg
despite antihypertensive therapy) or clinically significant (i.e. active)
cardiovascular disease, including:

- myocardial infarction or unstable angina within ≤6 months prior to the first
study treatment

- New York Heart Association (NYHA) grade II or greater congestive heart failure
(CHF)

- serious cardiac arrhythmia requiring medication (with the exception of atrial
fibrillation or paroxysmal supraventricular tachycardia)

- peripheral vascular disease ≥grade 3 (i.e. symptomatic and interfering with
activities of daily living requiring repair or revision).

- History of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess
within 6 months prior to the first study treatment.

- Non-healing wound, ulcer or bone fracture. Patients with granulating incisions healing
by secondary intention with no evidence of fascial dehiscence or infection are
eligible but require three weekly wound examinations.

- Evidence of any other medical conditions (such as psychiatric illness, peptic ulcer,
etc.), physical examination or laboratory findings that may interfere with the planned
treatment, affect patient compliance or place the patient at high risk from
treatment-related complications.