Detect V / CHEVENDO (Chemo vs. Endo)

NCT ID: NCT02344472

Last Updated: 2024-06-04

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE3
• Total Enrollment: 271 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-09-30
• Study Completion Date: 2025-01-31

Brief Summary

Chemo- versus endocrine therapy in combination with dual HER2-targeted therapy of Herceptin® (trastuzumab) and Perjeta® (pertuzumab) plus Kisqali® (ribociclib) in patients with HER2 positive and hormone-receptor positive metastatic breast cancer.

Detailed Description

Especially for diseases that are not curable such as metastatic breast cancer (MBC), the maintenance of quality of life is one of the main aims of treatments. Adverse events are well-known side effects of any cytostatic treatment and impact the patients' quality of life. Therefore, new treatment options are developed that should stop or at least slow down metastatic spread of cancer without causing negative side effects in terms of high-grade adverse events. For patients with hormone-receptor positive and HER2 positive MBC the combination of HER2-targeted therapy with endocrine therapy has already been proven to be an effective and in many cases valuable alternative to the combination of HER2-targeted therapy with chemotherapy. The high relevance of HER2-neu-targeted/endocrine treatment combinations derives from the fact that potential chemotherapy-related toxicity can be avoided, which in turn positively affects quality of life. Clinical trials suggest an additional benefit when a CDK4/6 inhibitor is added to the combination of endocrine therapy and anti HER2 treatment. DETECT V is a randomized phase III study comparing the safety and efficacy of trastuzumab plus pertuzumab and the CDK 4/6 inhibitor ribociclib in combination with either endocrine therapy or chemotherapy.

Conditions

Metastatic Breast Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Chemotherapy with docetaxel

dual HER2-targeted therapy with Herceptin® (trastuzumab) and Perjeta® (pertuzumab) plus docetaxel. Up to three weeks after completion of chemotherapy, patients will be treated with maintenance endocrine therapy plus dual HER2-targeted therapy and Kisqali® (Ribociclib).

Group Type: EXPERIMENTAL

pertuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Trastuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Docetaxel

Intervention Type: DRUG

Chemotherapy

Chemotherapy with paclitaxel

dual HER2-targeted therapy with Herceptin® (trastuzumab) and Perjeta® (pertuzumab) plus paclitaxel.Up to three weeks after completion of chemotherapy, patients will be treated with maintenance endocrine therapy plus dual HER2-targeted therapy and Kisqali® (Ribociclib).

Group Type: EXPERIMENTAL

pertuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Trastuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Paclitaxel

Intervention Type: DRUG

Chemotherapy

Chemotherapy with vinorelbine

dual HER2-targeted therapy with Herceptin® (trastuzumab) and Perjeta® (pertuzumab) plus vinorelbine. Up to three weeks after completion of chemotherapy, patients will be treated with maintenance endocrine therapy plus dual HER2-targeted therapy and Kisqali® (Ribociclib).

Group Type: EXPERIMENTAL

pertuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Trastuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Vinorelbine

Intervention Type: DRUG

Chemotherapy

Chemotherapy with capecitabine

dual HER2-targeted therapy with Herceptin® (trastuzumab) and Perjeta® (pertuzumab) plus capecitabine. Up to three weeks after completion of chemotherapy, patients will be treated with maintenance endocrine therapy plus dual HER2-targeted therapy and Kisqali® (Ribociclib).

Group Type: EXPERIMENTAL

pertuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Trastuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Capecitabine

Intervention Type: DRUG

Chemotherapy

endocrine therapy with exemestane

dual HER2-targeted therapy with Herceptin® (trastuzumab), Perjeta® (pertuzumab) and Kisqali® (Ribociclib) plus exemestane.

Group Type: EXPERIMENTAL

pertuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Trastuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Exemestane

Intervention Type: DRUG

endocrine therapy

Ribociclib

Intervention Type: DRUG

CDK 4/6 inhibitor

endocrine therapy with fulvestrant

dual HER2-targeted therapy with Herceptin® (trastuzumab), Perjeta® (pertuzumab) and Kisqali® (Ribociclib) plus fulvestrant.

Group Type: EXPERIMENTAL

pertuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Trastuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Fulvestrant

Intervention Type: DRUG

endocrine therapy

Ribociclib

Intervention Type: DRUG

CDK 4/6 inhibitor

endocrine therapy with anastrozole

dual HER2-targeted therapy with Herceptin® (trastuzumab), Perjeta® (pertuzumab) and Kisqali® (Ribociclib) plus anastrozole.

Group Type: EXPERIMENTAL

pertuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Trastuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Anastrozole

Intervention Type: DRUG

endocrine therapy

Ribociclib

Intervention Type: DRUG

CDK 4/6 inhibitor

endocrine therapy with letrozole

dual HER2-targeted therapy with Herceptin® (trastuzumab), Perjeta® (pertuzumab) and Kisqali® (Ribociclib) plus letrozole.

Group Type: EXPERIMENTAL

pertuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Trastuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Letrozole

Intervention Type: DRUG

endocrine therapy

Ribociclib

Intervention Type: DRUG

CDK 4/6 inhibitor

Chemotherapy with nab-Paclitaxel

dual HER2-targeted therapy with Herceptin® (trastuzumab) and Perjeta® (pertuzumab) plus nab-Paclitaxel. Up to three weeks after completion of chemotherapy, patients will be treated with maintenance endocrine therapy plus dual HER2-targeted therapy and Kisqali® (Ribociclib).

Group Type: EXPERIMENTAL

pertuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Trastuzumab

Intervention Type: DRUG

HER2 targeted Therapy

nab-Paclitaxel

Intervention Type: DRUG

chemotherapy

Chemotherapy with eribulin

dual HER2-targeted therapy with Herceptin® (trastuzumab), Perjeta® (pertuzumab) and Kisqali® (Ribociclib) plus eribulin. Up to three weeks after completion of chemotherapy, patients will be treated with maintenance endocrine therapy plus dual HER2-targeted therapy and Kisqali® (Ribociclib).

Group Type: EXPERIMENTAL

pertuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Trastuzumab

Intervention Type: DRUG

HER2 targeted Therapy

eribulin

Intervention Type: DRUG

chemotherapy

endocrine therapy with leuprorelin

dual HER2-targeted therapy with Herceptin® (trastuzumab), Perjeta® (pertuzumab) and Kisqali® (Ribociclib) plus leuprorelin.

Group Type: EXPERIMENTAL

pertuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Trastuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Ribociclib

Intervention Type: DRUG

CDK 4/6 inhibitor

leuprorelin

Intervention Type: DRUG

endocrine therapy

endocrine therapy with goserelin

dual HER2-targeted therapy with Herceptin® (trastuzumab), Perjeta® (pertuzumab) and Kisqali® (Ribociclib) plus goserelin.

Group Type: EXPERIMENTAL

pertuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Trastuzumab

Intervention Type: DRUG

HER2 targeted Therapy

Ribociclib

Intervention Type: DRUG

CDK 4/6 inhibitor

goserelin

Intervention Type: DRUG

endocrine therapy

Interventions

pertuzumab

HER2 targeted Therapy

Intervention Type: DRUG

Trastuzumab

HER2 targeted Therapy

Intervention Type: DRUG

Capecitabine

Chemotherapy

Intervention Type: DRUG

Paclitaxel

Chemotherapy

Intervention Type: DRUG

Vinorelbine

Chemotherapy

Intervention Type: DRUG

Docetaxel

Chemotherapy

Intervention Type: DRUG

Exemestane

endocrine therapy

Intervention Type: DRUG

Letrozole

endocrine therapy

Intervention Type: DRUG

Anastrozole

endocrine therapy

Intervention Type: DRUG

Fulvestrant

endocrine therapy

Intervention Type: DRUG

Ribociclib

CDK 4/6 inhibitor

Intervention Type: DRUG

nab-Paclitaxel

chemotherapy

Intervention Type: DRUG

eribulin

chemotherapy

Intervention Type: DRUG

leuprorelin

endocrine therapy

Intervention Type: DRUG

goserelin

endocrine therapy

Intervention Type: DRUG

Other Intervention Names

Perjeta®; Herceptin®; Kisqali®

Eligibility Criteria

Inclusion Criteria

• Signed, written informed consent in study participation
• The primary tumor and/or biopsies from metastatic sites or locoregional recurrences have been confirmed as HER2-positive (FISH-positive or IHC 3+) and hormone receptor positive breast cancer by histopathology according to local testing
• Metastatic breast cancer or locally advanced BC, which cannot be treated by surgery or radiotherapy only
• Pre- and postmenopausal women are allowed
• No more than two prior chemotherapies for metastatic disease
• No more than two prior anti-HER2 therapies for metastatic disease
• Pertuzumab retreatment is allowed if prior pertuzumab treatment was finished 12 months before
• At least one measurable lesion assessable using standard techniques by Response Evaluation Criteria In Solid Tumors Version 1.1 (RECIST v1.1)
• Tumor evaluation according to RECIST version 1.1 has been performed within 4 weeks before randomization based on local assessment
• Age ≥ 18 years
• Standard 12-lead ECG values assessed by the local laboratory:

• QTcF interval at screening < 450 msec (using Fridericia's correction)
• Resting heart rate 50-90 bpm
• Left ventricular cardiac ejection fraction (LVEF) ≥ 50% at baseline (as measured by echocardiogram)
• ECOG Score ≤ 2
• Adequate organ function within 14 days before randomization, evidenced by the following laboratory results below:

• absolute neutrophil count ≥ 1500 cells/µL,
• platelet count ≥ 100000 cells/µL,
• hemoglobin ≥ 9 g/dL,
• ALT (SGPT) ≤ 2.0 × ULN (≤ 3.0 × ULN in case of liver metastases)
• AST (SGOT) ≤ 2.0 × ULN (≤ 3.0 × ULN in case of liver metastases)
• bilirubin ≤ 1.5 × ULN (with the exception of Gilbert's syndrome)
• creatinine ≤ 2.0 mg/dl or 177µmol/L INR ≤ 1,5
• Patients must have the following laboratory values within normal limits or corrected to within normal limits with supplemets before the first dose of study medication:

• Sodium
• Potassium
• Total calcium
• In case of patients of child bearing potential:

Negative serum pregnancy test at baseline (within 7 days prior to randomization) and agreement to remain abstinent (if it is in line with the preferred and usual lifestyle) or use single or combined non-hormonal contraceptive methods that result in a failure rate of < 1% per year during the treatment period and for at least 7 months after the last dose of study treatment

Exclusion Criteria

Patients will be excluded from the study for any of the following reasons:

• History of hypersensitivity reactions attributed to trastuzumab, pertuzumab, ribociclib or to other components of drug formulation
• Mandatory need for cytostatic treatment at time of study entry based on clinical judgment and national/international treatment guidelines
• Known CNS metastases
• Any concurrent severe, uncontrolled systemic disease, social or psychiatric condition that might interfere with the planned treatment and with the patient's adherence to the protocol
• Progression on prior Pertuzumab therapy
• Treatment with Pertuzumab within the last 12 months
• Prior treatment with any mTOR- or CDK4/6-inhibitor
• Treatment with any other investigational agents during trial
• Known hypersensitivity to lecithin (soya) or peanuts
• Life expectancy < 6 months
• Patients with pre-existing grade ≥2 peripheral neuropathy are excluded from taxane-based chemotherapy
• History of serious cardiac disease, including but not confined to:

• history of documented heart failure or systolic dysfunction (LVEF < 50%)
• high-risk uncontrolled arrhythmias i.e., atrial tachycardia with a heart rate ≥100/min at rest, significant ventricular arrhythmia (ventricular tachycardia) or higher-grade AV-block (second degree AV-block Type 2 [Mobitz 2] or third degree AV-block)
• angina pectoris requiring anti-anginal medication
• clinically significant valvular heart disease
• evidence of transmural infarction on ECG
• poorly controlled hypertension (e.g., systolic >180 mm Hg or diastolic >100 mm Hg)
• any other cardiac condition, which in the opinion of the treating physician would make this protocol unreasonably hazardous for the patient
• Dyspnea at rest or other diseases that require continuous oxygen therapy
• Patients with poorly controlled diabetes or with evidence of clinically significant diabetic vascular complications
• Patients with known infection with HIV, hepatitis B virus, or hepatitis C virus
• Male patients
• Pregnant, lactating or women of childbearing potential without a negative pregnancy test (serum) within 7 days prior to randomization, irrespective of the method of contraception used
• Medical or psychological conditions that would not permit the subject to complete the study or sign informed consent
• Participation in another clinical study within the 30 days before registration
• Legal incapacity or limited legal capacity

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Roche Pharma AG

INDUSTRY

Sponsor Role: collaborator

Novartis Pharmaceuticals

INDUSTRY

Sponsor Role: collaborator

Eisai GmbH

INDUSTRY

Sponsor Role: collaborator

Celgene Corporation

INDUSTRY

Sponsor Role: collaborator

Prof. Wolfgang Janni

OTHER

Sponsor Role: lead

Responsible Party

Prof. Wolfgang Janni

Director Department of Obstetrics and Gynecology

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Jens Huober, MD PhD

Role: PRINCIPAL_INVESTIGATOR

Studienzentrale Dpt. Gyn/OB University Ulm

Locations

University Hospital Ulm Gynecology/Obstetrics

Ulm, , Germany

Countries

Germany

Related Links

http://www.detect-studien.de

The DETECT study concept

Other Identifiers

2014-002249-22

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

D-V

Identifier Type: -

Identifier Source: org_study_id