NEO-ZOTAC

BOOG 2010-01

General Information

BOOG number

BOOG 2010-01

Nickname

NEO-ZOTAC

Status

Date: 06/09/2018

Inclusion closed

05/04/2012

Full title

A phase III randomized trial with NEOadjuvant chemotherapy (TAC) with or without ZOledronic acid for patients with HER2-negative large resectable or locally advanced breast cancer

Indication

Subindication

HER2-, any HR

Target sample size

250

Actual accrual

250
Date: 05/04/2012

Estimated study completion date

31/12/2012

Contact

Sponsor

BOOG Study Center

Principal Investigator(s)

J.R. Kroep, J.W.R. Nortier, G.J. Liefers

Study manager

A. Charehbili, A.E. van Leeuwen-Stok

Central datamanagement and randomization

Leiden University Medical Center Datacenter Surgery K6-R P.O. Box 9600, 2300 RC Leiden Phone +31 71 526 3500 Fax +31 71 526 6744 ClinicalResearchCenter@lumc.nl E-mail datacenter@lumc.nl

Local datamanagement

IKNL

Funding

Funding by KWF

Other

De database is gesloten op 6-9-2018. Follow-up is beperkt tot 5 jaar.

Design

Randomization: Arm A: 6x TAC with Zoledronic acid Arm B: 6x TAC without Zoledronic acid

Objectives

Primary objective: To determine the value of adding zoledronic acid to neoadjuvant chemotherapy with TAC in patients with large resectable or locally advanced HER2-negative breast cancer. Secondary objectives: To evaluate the clinical response, correlated to the pathological responses of both treatment arms. To evaluate the disease free survival and overall survival. To evaluate the safety and tolerability of adding zoledronic acid to neoadjuvant chemotherapy. To evaluate heterogeneity of the ER/PR and HER2 measurement of the core biopsy and the operation specimen.

Endpoints

Primary endpoint:

  • Pathologic complete response (pCR) rate to neoadjuvant chemotherapy with or without zoledronic acid at surgery.

Secondary endpoints:

  • Clinical response (partial and complete according to RECIST v1.1, evaluated with MRI) of neoadjuvant therapy correlated to pathological response.
  • Disease free survival and overall survival after 3 and 5 years follow up, correlated to pCR.
  • Tolerability (grade 3 / 4 CTC toxicities) of both regimens.
  • Pathology: ER/PR and HER2 heterogeneity in core biopsy vs. Operation specimen.

Eligibility Criteria

Inclusion: Women presenting with large resectable or locally advanced breast cancer (T2,T3,T4, every N, M0) Measurable disease (breast and/or ymph nodes) Histological proven HER2-negative breast cancer in the core biopsy material. Age ≥18 years WHO 0-2 Adequate bone marrow function (within 14 days prior to registration): WBC ≥3.0 x 10E9/l, neutrophils ≥1.5 x 10E9/l, platelets ≥100 x 10E9/l Adequate liver function (within 4 weeks prior to start treatment): bilirubin ≤1.5 x upper limit of normal (UNL) range, ALAT and/or ASAT ≤2.5 x UNL, Alkaline Phosphatase ≤5 x UNL Adequate renal function: the calculated creatinine clearance should be ≥50 ml/min Exclusion: Evidence of distant metastases (M1) History of breast cancer Prior breast surgery other than biopsy Prior chemotherapy or radiation therapy Previous malignancy within 5 years, with exception of a history of a previous basal cell carcinoma of the skin or pre-invasive carcinoma of the cervix. Prior bisphosphonate usage. Peripheral neuropathy > grade 2, whatever the cause Serious other diseases as recent myocardial infarction, clinical signs of cardiac failure or clinically significant arrhythmias. Current active dental problems including dental abscess or infection of the jawbone (maxilla or mandible), or a current or prior diagnosis of osteonecrosis of the jaw requiring maxillofacial surgery.Known hypersensitivity reaction to any of the components of the treatment Pregnancy or lactating

Regulatory Information

CCMO approval

Yes
Date: 05/01/2010
Nr: NL30600.058.09

EC approval

Yes
Date: 08/03/2010
Nr:P09.250

EC

Leiden Universitair Medisch Centrum
Amendments:
Yes
Date Last Amendment: 06/04/2011

EudraCT number

2009-016932-11

Trial Register

NCT01099436

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