Bevacizumab in Combination With Chemotherapy in the Neo-adjuvant Setting for HER2 (-) Breast Cancer

Breast Cancer Clinical Trial

Official title:

Phase II, Open-label Non-randomized Trial to Investigate the Efficacy of Bevacizumab in Combination With Dose Dense Sequential Chemotherapy in the Neo-adjuvant Setting for HER2 Negative Breast Cancer Patients

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01985841
• Other study ID #: CT/10.15
• Status: Terminated
• Phase: Phase 2
• First received: September 13, 2013
• Last updated: October 7, 2015
• Start date: October 2011
• Est. completion date: April 2015

Study information

• Verified date: October 2015
• Source: Hellenic Oncology Research Group
• Contact: n/a
• Is FDA regulated: No
• Health authority: Greece: National Organization of Medicines
• Study type: Interventional

Clinical Trial Summary

Investigators propose to study the efficacy of Bevacizumab plus systemic chemotherapy prior to surgery in order to make a locally advanced tumor operable. Treatment is thus expected to induce a maximum tumor shrinkage within a short period (usually 3-6 months). In addition Bevacizumab (Avastin) is to be administered as early as possible during the disease stages. The primary aim of this study is to evaluate the preliminary antitumor activity in terms of pathological complete responses (pCR) of bevacizumab in combination with chemotherapy.

Description:

The aim of administering systemic therapy prior to surgery is to make a locally advanced tumor operable or to allow conservative surgery in the case of a T2-T3 tumor. Therefore, treatment is expected to induce a maximum tumor shrinkage within a short period. In addition and based on the anti-angiogenic MoA, bevacizumab (Avastin) is to be administered as early as possible during the disease stages. Bevacizumab has already been tested in the neoadjuvant setting with encouraging results. In a first trial patients with inoperable locally advanced breast cancer received docetaxel with or without bevacizumab with five clinical Complete Responses and 24 Partial Responses. In a second trial there was also reported the results of the combination of bevacizumab with doxorubicin and docetaxel for the treatment of inflammatory breast cancer. Then, a set of studies of primary therapy exploring the activity of different regimens have confirmed the role of baseline pathological features of the tumor in predicting the responsiveness to primary therapy. A 22% pathological complete responses (pCR) rate has been achieved in a study combining bevacizumab together with Xeloda and Taxotere suggesting that bevacizumab addition to chemotherapy in the neoadjuvant treatment is feasible showing promising activity while no unexpected toxicities were reported.

Thus, a very high interest exists from our clinicians mostly within our cooperative groups which cover the largest national oncology centers to be involved and run such a study.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 34
• Est. completion date: April 2015
• Est. primary completion date: April 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Female patients with histologic proven, corebiopsied, invasive ductal adenocarcinoma of the breast >2 cm in size and of any N stage (clinical and/or radiological T-stage > T1, including T4d), scheduled to receive preoperative chemotherapy.

• Age 18-70 years

• ECOG performance-status =1

• No prior or current neoplasm except for curatively treated non melanoma skin cancer, in situ carcinoma of the cervix

• No distant disease/secondary carcinoma

• Normal cardiac function

• Results of the following assessments at the time of inclusion must be available:

1. bilateral Mammography (before enrolment)

2. histology

3. grading

4. hormone-receptor-status

5. HER2 status negative (is defined as FISH/CISH negative or IHC0 or IHC1+, or IHC2+ and FISH/CISH negative)

• Laboratory requirements (within 1 week before enrolment):

1. Hematology: Neutrophils = 1.5 x 109/l, Platelets = 100 x 109/l, Hemoglobin>11 g/dl

2. Hepatic function: Total bilirubin < 1 x ULN, SGOT and SGPT < 1.5 x ULN, Alkaline phosphatases < 1.5 x ULN. In case of abnormal values, the liver function tests have to be repeated within 3 days before study treatment.

3. Renal function: Creatinine < 1 x ULN

4. Urinalysis: Urine dipstick of proteinuria < 2+. Patients discovered to have = 2+ proteinuria on dipstick urinalysis at baseline should undergo a 24-hour urine collection and must demonstrate <1 g of protein / 24 hours.

• Signed and dated Informed Consent before the start of specific protocol procedures

• If of childbearing potential, negative pregnancy test

Exclusion Criteria:

• Cytological only confirmation of diagnosis

• Lobular or other non-ductal types of breast cancer

• Pregnant, or lactating patients; patients of childbearing potential must implement adequate contraceptive measures during study participation

• Pre-existing motor or sensory neurotoxicity of a severity > grade 2 by NCI-CTC AE

• Preoperative local treatment for breast cancer (i.e. incomplete surgery, radiotherapy)

• Prior or concurrent systemic antitumor therapy

• Evidence of wound healing complications, bone fracture, ulcer or the presence of clinically significant peripheral vascular disease

• Clinically significant cardiac disease e.g. congestive heart failure.

• Other serious illness or medical condition-uncontrolled hypertension or high risk uncontrolled arrythmias -history of significant neurologic or psychiatric disorders including psychotic disorders, dementia or seizures that would prohibit the understanding and giving of informed consent-active uncontrolled infection-unstable peptic ulcer, unstable diabetes mellitus or other contraindication for the use of corticosteroids

• Known hypersensitivity reaction to the compounds or incorporated substances.

• Evidence of bleeding diathesis or coagulopathy

• The use of full-dose oral or parenteral anticoagulants is permitted as long as the INR, or appropriate monitoring test is within therapeutic limits and the patient has been on a stable dose of anticoagulants for at least two weeks at the time of randomization. Patients not receiving anti coagulant medication must have an INR = 1.5 an aPTT = 1.5 x ULN within 7 days of randomization.

• Ongoing treatment with aspirin (> 325mg / day) or other medications known to predispose to gastrointestinal ulceration.

• Major surgery (including open biopsy), significant traumatic injury within 28 days prior to enrolment.

• Minor surgery, including insertion of an indwelling catheter, within 24 hours prior to the first bevacizumab infusion

• Treatment with an investigational drug within 30 days prior to study entry.

• Legally incapacitated and/or other circumstances which make it undesirable for the subject to understand the nature, meaning and consequences of the clinical study

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Drug:
• Bevacizumb
Avastin
• 5-Fluorouracil
5-FU
• Epirubicin
Farmorubicin
• Cyclophosphamide
Endoxan
• Docetaxel
Taxotere

Locations

Country	Name	City	State
Greece	"IASO" General Hospital of Athens	Athens
Greece	Air Forces Military Hospital of Athens	Athens
Greece	University Hospital of Crete, Dep of Medical Oncology Heraklion, Greece	Heraklion
Greece	"Metaxa's" Anticancer Hospital of Piraeus, 1st Dep of Medical Oncology	Piraeus
Greece	"Euromedica" Hospital of Thessaloniki	Thessaloniki
Greece	"Theagenion" Anticancer Hospital of Thessaloniki, 2nd Dep of Medical Oncology	Thessaloniki

Sponsors (1)

Lead Sponsor	Collaborator
Hellenic Oncology Research Group

Country where clinical trial is conducted

Greece, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Patients with Complete Response	Patients will be assessed for tumor response on week 8 and on week 16. Patients with tumor reduction will proceed on surgery. Histology report will confirm the complete or partial responses to chemotherapy.	On week 8 and 16	No
Secondary	Overall Survival	Patients overall survival will be calculated from the date of the first chemotherapy cycle until the date of death from any cause	3 years	No
Secondary	Progression Free Survival	Patients will be assessed every 8 weeks, from date of randomization until the end of treatment and then every 3 months until the date of first documented disease progression or date of death from any cause, whichever came first, up to 260 weeks (65 months).	5 years	No