Bevacizumab Plus Paclitaxel Optimization Study With Interventional Aintenance Endocrine Therapy in Breast Cancer

Metastatic Breast Cancer Clinical Trial

— BOOSTER  

Official title:

Bevacizumab Plus Paclitaxel Optimization Study With Interventional Maintenance Endocrine Therapy in Advanced or Metastatic ER-positive HER2-negative Breast Cancer -BOOSTER Trial, a Multicenter Randomized Phase II Study-

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01989780
• Other study ID #: JBCRG-M04
• Secondary ID: UMIN000012179
• Status: Completed
• Phase: Phase 2
• Start date: January 2014
• Est. completion date: June 2019

Study information

• Verified date: July 2019
• Source: Japan Breast Cancer Research Group
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To compare continuing bevacizumab + paclitaxel or switching to bevacizumab + endocrine maintenance therapy followed by bevacizumab + paclitaxel, after 1st line induction therapy with bevacizumab + paclitaxel in ER+HER2- advanced or metastatic breast cancer.

Description:

This multicenter, randomized Phase II study of patients with advanced or metastatic estrogen receptor-positive human epidermal receptor type 2-negative breast cancer aims to compare two treatment strategies following induction therapy with 4-6 cycles of the combined use of weekly paclitaxel (wPTX) and bevacizumab (BV). In arm A, wPTX+BV is continued, while in arm B, wPTX is switched to maintenance endocrine therapy (hormone+BV) until disease progression, followed by wPTX+BV re-induction. The primary endpoint is time to failure of strategy, which is the time from randomization to a qualifying event (addition of a new agent not in the primary regimen, progressive disease during or after planned therapy, or death).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 160
• Est. completion date: June 2019
• Est. primary completion date: June 2018
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 20 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Histologically confirmed adenocarcinoma of the breast

2. Female aged 20-75 years old at getting informed consent

3. HER2 negative disease (IHC 0/1+ or 2+ with FISH negative)

4. Documented estrogen receptor (ER) positive (>=1% by IHC)

5. Inoperative locally advanced or metastatic breast cancer at enrolment

6. Performance status (ECOG): 0-1 at enrolment

7. Life expectancy of at least 3 months from enrolment

8. No prior systemic therapy for recurrent breast cancer (excluding hormone therapy)

9. No prior neo and/or adjuvant chemotherapy with taxane or adjuvant setting with a disease-free interval from completion of the taxane treatment to metastatic diagnosis of >= 12 months

10. Patients with measurable lesion regarding with Response Evaluation Criteria in Solid Tumors(RECIST) criteria or who have evaluable lesion

11. Patients with only bone lesion will be acceptable if the osteolytic lesion has a measurable soft tissue component by MRI or CT

12. No influence on protocol treatment is considered in case prior therapy or examination.

13. Adequate following organ function within 2 weeks before starting treatment. The latest examination results should be adopted and blood transfusion or treatment of hematopoietic factor drugs is not allowed 2 weeks before examination.

• Absolute neutrophil count >= 1500 /mm3 or white blood cell(WBC) count >= 3000 /mm3

• Platelets >=10 x 10000 /mm3

• Hb >= 9 g/dL

• Total bilirubin <= 1.5 mg/dL

• aspartate aminotransferase(AST) and alanine aminotransferase(ALT) <= 100 international unit(IU)/L

• Serum creatinine <= 1.5 mg/dL

• Urine dipstick for proteinuria <= 1+

14. Written informed consent signed by patients before completing any treatment related procedure

Exclusion Criteria:

1. Prior therapy with bevacizumab

2. Active infection requiring intrvenous antibiotics at enrollment or infection with active HBV and/or HCV.

3. Pregnancy, lactetion or in case of potentialy pregnancy women Not mind contraception in trial period.

4. Known hypersensitivity to bevacizumab or paclitaxel

5. History of hemoptysis (>= 2.5mL of bright red blood per episord).

6. Use of disulfiram,cyanamide, carmofur or procarbazine Hydrochloride

7. Patients with CNS metastases (except for not symptomatic)

8. Persistent Grade >= 2 sensory neuropathy at enrollment

9. Grade 3 >= hypertension (>= 2 use of antihypertensive drug)

10. Evidence with arterial thromboembolism (Cerebral infarction, Myocardial infarction) or history within 1 year prior to enrollment.

11. Evidence withvenous thromboembolism (deep vein thrombosis, pulmonary embolism) or history within 1 year prior to enrollment.

12. History of GI perforation and/or serious abdominal fistula within 1 year prior to enrollment

13. Cases that the investigator judged as inappropriate as the subject of this clinical study

Related Conditions & MeSH terms

• Breast Neoplasms
• Metastatic Breast Cancer

Intervention

Drug:
• Paclitaxel

• Bevacizumab

• Letrozole

• Anastrozole

• Exemestane

• Fulvestrant

• Goserelin

• leuprorelin

Locations

Country	Name	City	State
Japan	Japan Breast Cancer Research Group	Chuo-ku, Nihonbashi, Koami-cho	Tokyo

Sponsors (2)

Lead Sponsor	Collaborator
Japan Breast Cancer Research Group	Chugai Pharmaceutical

Country where clinical trial is conducted

Japan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Time to failure of strategy (TFS)		2.5 years
Secondary	2y Overall Survival rate		3.5 years
Secondary	Overall Survival		3.5years
Secondary	Progression Free Survival(PFS)		2.5years
Secondary	QOL		2.5years
Secondary	Biomarker(IMPACT assay Chips, whole blood, tumor tissue, Serum)	vascular endothelial growth factor(VEGF)-A, VEGFR-2, VEGF-C, platelet derived growth factor(PDGF)-C, Soluble fms-like tyrosine kinase-1, VEGFR-3, Interleukin(IL)-8, Basic Fibroblast Growth Factor(FGFb), placental growth factor(PLGF), E-Selectin, intercellular adhesion molecule(ICAM)-1, neuropilin of Tumor tissue, single nucleotide polymorphism(SNP):VEGFR-1 and VEGF of whole blood DNA, angiotensin(ANG) and Apelin of serum.	2.5years
Secondary	Safety(Collection of adverse events)		2.5years