Neo Adjuvant Chemotherapy in Triple Negative Breast Cancer (neo-TN)

Netherlands Cancer Institute (NKI)

Status and phase: Active, not recruiting; Phase 3; Phase 2

Conditions: Breast Cancer

Treatments: Drug: Doxorubicin, cyclophosphamide; Drug: Carboplatin and Paclitaxel; Drug: Doxorubicin, cyclophosphamide, carboplatin, thiotepa, cyclophosphamide

Study type: Interventional

Funder types: Other

Identifiers

NCT01057069

M09TNM

2009-015238-31 (EudraCT Number)

Details and patient eligibility

About

This study aims to compare the response of triple-negative breast cancer with deficient homologous recombination to intensified alkylating chemotherapy versus standard chemotherapy with dose dense AC and/or Docetaxel-Capecitabine.

Full description

Homologous Recombination (HR) is a DNA repair mechanism that can repair double-strand DNA breaks. It is the only reliable repair mechanism that can repair the consequences of DNA adducts caused by bifunctional alkylating agents (such as cyclophosphamide, thiotepa or carboplatin). Alternative DNA repair mechanisms exist, but these unavoidably induce DNA mutations, deletions and chromosome aberrations, giving give rise to genetic instability. HRD may be a consequence of inactivation of the BRCA-1 or BRCA-2 genes (as in hereditary breast cancer), but it may also be caused by defects in the Fanconi anemia pathway or by amplification of the EMSY gene. HRD is present in breast cancer cells but not in healthy cells of BRCA-1 or BRCA-2 mutation carriers, and also in about half of the sporadic triple-negative breast cancers.

This phase II/III controlled multicenter trial will investigate the ability of individualized chemotherapy to improve the objective response rate of 'triple-negative' breast cancer (estrogen receptor and progesterone receptor-negative, no HER2 amplification) to preoperative (neoadjuvant) chemotherapy. It will answer the question whether intensified alkylating chemotherapy improves the response rate of tumors with a Homologous Recombination Defect (HRD) and it will gather data required for the design of a phase III study documenting the efficacy of response monitoring by contrast-enhanced MRI in TN breast cancer without HRD.

Enrollment: 310 patients

Sex: All

Ages: 18 to 59 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Proven infiltrating breast cancer with either a primary tumor over 2 cm in size (MRI or ultrasound examination) and/or cytologically proven spread to the axillary lymph nodes.
• Patients with 'locally advanced breast cancer' are consequently eligible, including those with ipsilateral supraclavicular lymph node metastases.
• The tumor must be HER2/neu-negative (either score 0 or 1 at immunohistochemistry or negative at in situ hybridization [CISH or FISH] in case of score 2 or 3 at immunohistochemistry).
• The tumor must be Estrogen receptor (ER) -negative (< 10% nuclear staining at IHC) and Progesterone receptor (PR) -negative (< 10% nuclear staining at IHC). However, the rare tumors that are ER-negative and PR-positive will be eligible, if this pattern of hormone receptor expression can be verified in the NKI-AVL reference pathology lab.
• Age 18 to 59 years; patients older than 59 years may be included when considered 'biologically 59 years or younger' (as judged by the investigator).
• Performance status: WHO 0 or I.
• Adequate bone marrow function (W.B.C. count > 3.0 x 109/l, platelets > 100 x 109/l).
• Adequate hepatic function (ALAT, ASAT and bilirubin < 2 x upper limit of normal, or minor abnormalities of these tests judged to be of no consequence by the study coordinator).
• Adequate renal function (creatinine clearance > 60 ml/min).
• Informed consent

Exclusion criteria

• Previous radiation therapy or chemotherapy.
• Other malignancy except carcinoma in situ, unless the other malignancy was treated 5 or more years ago with curative intent without the use of chemotherapy or radiation therapy.
• Pregnancy or breast feeding.
• Evidence of distant metastases. Staging examinations must have included a chest roentgenogram, an ultrasound examination of the liver and an isotope bone scan. Abnormal uptake on the isotope bone scan can only be accepted if bone metastases were excluded by MRI

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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310 participants in 5 patient groups

HRD; 1x ddAC, 2x tCTC

Experimental group

Description:

HRD positive tumors; irrespective of response; - a fourth course of AC followed by Peripheral Blood Progenitor Cell (PBPC) harvest and tandem intermediate-dose alkylating therapy (miniCTC, carboplatin 800 mg/m2, thiotepa 250 mg/m2, and cyclophosphamide 3000 mg/m2) with PBPC-reinfusion.

Treatment:

Drug: Doxorubicin, cyclophosphamide, carboplatin, thiotepa, cyclophosphamide

HRD; 3x CP

Active Comparator group

Description:

HRD tumors; any response to 3x ddAC; 3 courses of CP

Treatment:

Drug: Carboplatin and Paclitaxel

non-HRD;3x CP

Active Comparator group

Description:

non-HRD tumors; unfavourable response to 3x ddAC; 3 courses of Carboplatin and Paclitaxel

Treatment:

Drug: Carboplatin and Paclitaxel

non-HRD; response; 3x ddAC

Active Comparator group

Description:

non-HRD tumors; favourable response to 3x ddAC; 3 more courses of ddAC

Treatment:

Drug: Doxorubicin, cyclophosphamide

non-HRD; response; 3x CP

Active Comparator group

Description:

non-HRD tumors; favourable response to 3x ddAC; 3 courses of Carboplatin and Paclitaxel

Treatment:

Drug: Carboplatin and Paclitaxel