Atezolizumab, Pertuzumab and Trastuzumab With Chemotherapy as Neoadjuvant Treatment of HER2 Positive Early High-risk and Locally Advanced Breast Cancer (APTneo)

Who is this study for? Adult women with HER2+ breast cancer
What treatments are being studied? pertuzumab+Trastuzumab
Status: Active_not_recruiting
Location: See all (65) locations...
Intervention Type: Drug, Procedure
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

n the present study the neoadjuvant approach with the anti-HER2 trastuzumab and pertuzumab combined with carboplatin and paclitaxel will be used to compare the Event-Free Survival (EFS) in regimens with and without atezolizumab. Following the neoadjuvant part of the study, after surgery all patients will continue to receive trastuzumab and pertuzumab to complete one year of anti-HER2 therapy. Similarly, patients allocated to receive atezolizumab will continue atezolizumab to complete one year In addition, several IHC and molecular assays will be performed before and during the period of chemotherapy administration and at surgery with the goal of defining a marker of efficacy to be later validated in a larger adjuvant setting.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Female patients aged 18 years or older with early high-risk ((T1cN1; T2N1; T3N0) or locally advanced and inflammatory breast cancers (stage III A-C according to AJCC) suitable for neoadjuvant treatment

• Histologically confirmed unilateral invasive breast cancer

• HER2 positive disease according to ASCO/CAP guidelines 2013 \[defined as IHC 3+ or ISH positive (by gene copy number or HER2 gene/CEP17 ratio of 2 or greater)\]

• Known estrogen (ER) and progesterone receptor (PgR)

• Availability of a representative paraffin-embedded (FFPE) tumor block taken at diagnostic biopsy for central confirmation of HER2 eligibility, for assessment of ER, PgR, Ki67 and PD-L1 expression and for biomarker evaluation is mandatory. Note: the diagnostic biopsy of the breast lesion may have been taken before the required screening procedures. If diagnostic sentinel node biopsy if performed, an FFPE block must be available. An FFPE tumor block is also mandatory after the first cycle of therapy. Surgery tissue (residual tumor or tumor bed in case of pCR and axillary node material) is also mandatory.

• Consent to the collection of blood samples mandatorily before starting neoadjuvant treatment, after the first cycle of therapy, at the end of neoadjuvant treatment (before surgery), 6 months after surgery and at the end of all treatments.

• ECOG performance status 0 or 1

• For women who are not postmenopausal (≥ 12 months of non-therapy-induced amenorrhea) or surgically sterile (absence of ovaries and/or uterus): agreement to remain abstinent or use single or combined contraceptive methods that result in a failure rate of \< 1% per year during the treatment period and for at least 6 months after the last dose of study drugs. Abstinence is only acceptable if it is in line with the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or postovulation methods) and withdrawal are not acceptable methods of contraception. Examples of contraceptive methods with a failure rate of \< 1% per year include tubal ligation, male sterilization, hormonal implants, established, proper use of combined oral or injected hormonal contraceptives, and certain intrauterine devices. Alternatively, two methods (e.g., two barrier methods such as a condom and a cervical cap) may be combined to achieve a failure rate of \< 1% per year. Barrier methods must always be supplemented with the use of a spermicide

• Written informed consent to participate in the trial (approved by the Institutional Review Board \[IRB\]/ Independent Ethics Committee \[IEC\]) obtained prior to any study specific screening procedures

⁃ Willing and able to comply with the protocol

Locations
Other Locations
Austria
Klinikum Klagenfurt am Wörthersee Abteilung für Innede Medizin und Hämatologie und internistische Onkologie
Klagenfurt
Krankenhaus der Barmherzigen Schwestern
Linz
Universitätsklinikum St. Pölten Klinische Abteilung für Innere Medizin
Sankt Pölten
Klinische Abteilung für Allgemeine Gynäkologie und Gynäkologische Onkologie - Universitätsklinik für Frauenheilkunde Medizinische Universität Wien / AKH
Vienna
Germany
Klinik für Gynäkologie am Campus Charité Mitte (CCM)
Berlin
Department of Gynecology and Obstetrics, Marienhospital
Bottrop
Klinikum Coburg, Frauenklinik
Coburg
St Johannes Hospital
Dortmund
Klinik und Poliklinik für Frauenheilkunde und Geburtshilfe - Universitätsklinikum Carl Gustav Carus
Dresden
Markus Krankenhaus - Klinik für Gynäkologie und Geburtshilfe
Frankfurt
SRH Waldklinikum
Gera
Universitätsklinikum Greifswald, Frauenklinik
Greifswald
Klinik und Poliklinik für Gynäkologie am Universitätsklinikum (Saale)
Halle
Gynäkologisch-Onkologische Praxis
Hanover
NCT Nationales Zentrum für Tumorerkrankungen Gynäkologische Onkologie, Frauenklinik
Heidelberg
St. Marien-Klinik GmbH Frauenklinik der St. Vincentius-Kliniken gAG - Gynäkologisches Krebszentrum Karlsruhe - Brustzentrum Karlsruhe
Karlsruhe
Städtisches Klinikum Magdeburg - Klinik für Allgemein - und Viszeralchirurgie
Magdeburg
Am Schillerhain 1-8
Marktredwitz
Klinikum Nürnberg Nord
Nuremberg
Onkologische Praxis Velbert
Velbert
Marien Hospital Witten
Witten
Italy
Ospedale Papa Giovanni XXIII
Bergamo
Presidio Ospedaliero Di Summa-Perrino
Brindisi
Dipartimento di Oncologia Medica AUSL della Romagna
Faenza
IST San Martino
Genova
Istituto Scientifico Romagnolo per lo studio e la cura dei tumori
Meldola
Fondazione IRCCS Istituto Nazionale dei Tumori
Milan
Istituto Europeo di Oncologia
Milan
Ospedale Luigi Sacco
Milan
Ospedale San Raffaele
Milan
AO Universitaria Policlinico di Modena
Modena
Ospedale Sacro Cuore - Don Calabria
Negrar
Fondazione Salvatore Maugeri
Pavia
Azienda Ospedaliero Universitaria Pisana Ospedale S. Chiara
Pisa
Arcispedale Santa Maria Nuova - A.O. Reggio Emilia
Reggio Emilia
Ospedale Infermi AUSL della Romagna
Rimini
Istituto Nazionale Tumori - Regina Elena
Roma
Ospedale Santa Maria della Misericordia
Udine
Spain
Centro Oncologico de Galicia
A Coruña
Hospital Virgen de Los Lirios
Alcoy
Hospital General Unv. Alicante
Alicante
Hospital Infanta Cristina de Badajoz (CICAB - Centro de Investigación Clínica del Área de Salud de Badajoz)
Badajoz
Hospital Clinic Provincial
Barcelona
Hospital de la Santa Creu i Sant Pau
Barcelona
Hospital del Mar - IMAS
Barcelona
Hospital de Basurto
Bilbao
Hospital San Pedro de Alcantara
Cáceres
Hospital Virgen de la Nieves
Granada
Hospital Juan Ramón Jimenez
Huelva
Hospital Clinico San Carlos
Madrid
Hospital de Fuenlabrada
Madrid
Hospital Gregorio Marañon
Madrid
Hospital Unv. Fundación Jimenez Diaz
Madrid
MD Anderson Cancer Center
Madrid
Complejo Hospitalario de Especialidades Virgen de la Victoria
Málaga
Hospital General Universitario Morales Meseguer
Murcia
Clinica Universitaria de Navarra
Pamplona
Complejo Hospitalario de Salamanca
Salamanca
Hospital de Donostia
San Sebastián
Hospital Onkologikoa
San Sebastián
Hospital Clinico Unv. de Santiago
Santiago De Compostela
Hospital Virgen de la Salud de Toledo
Toledo
Hospital Clínico Universitario de Valencia
Valencia
Hospital Lozano Blesa
Zaragoza
Hospital Miguel Servet
Zaragoza
Time Frame
Start Date: 2018-09-07
Completion Date: 2027-03-15
Participants
Target number of participants: 650
Treatments
Active_comparator: HPCT
Patients will receive a combination of trastuzumab, pertuzumab, carboplatin and paclitaxel as neoadjuvant therapy for 6 cycles every 3 weeks. Trastuzumab (H) will be delivered on day 1 at the dose of 8 mg/kg loading dose i.v., then 6 mg/kg i.v. Pertuzumab (P) will be delivered on day 1 at the dose of 840 mg loading dose i.v., then 420 mg i.v. Carboplatin (C) will be administered at AUC 2 i.v. on day 1 and day 8. Paclitaxel (T) will be given at 90 mg/m2 i.v. on day 1 and day 8. Definite surgery will be performed not later than 4 weeks after the last dose of neoadjuvant therapy. Trastuzumab and pertuzumab will then be delivered for 12 additional cycles as adjuvant therapy.
Experimental: ACy followed by HPCT and atezolizumab
Patients will receive a combination of doxorubicin (A, 60 mg/m2 i.v.), cyclophosphamide (C, 600 mg/m2 i.v.) and atezolizumab (1200 mg i.v.) on day 1 every 3 week for 3 cycles. Subsequently they will be given trastuzumab on day 1 (H, at the loading dose of 8 mg/kg i.v. then 6 mg/kg i.v.), pertuzumab on day 1 (P, at the loading dose of 840 mg .v., then 420 mg i.v.), carboplatin (C) at AUC 2 i.v. on day 1 and day 8, paclitaxel (T) at 90 mg/m2 i.v. on day 1 and day 8, and atezolizumab 1200 mg i.v. on day 1 for 3 cycles every 3 weeks. Definite surgery will be performed not later than 4 weeks after the last dose of neoadjuvant therapy. Trastuzumab and pertuzumab will then be delivered for 15 additional cycles and atezolizumab for 12 additional cycles as adjuvant therapy.
Experimental: HPCT and atezolizumab
Patients will receive a combination of trastuzumab, pertuzumab, carboplatin, paclitaxel and atezolizumab as neoadjuvant therapy for 6 cycles every 3 weeks. Trastuzumab (H) will be delivered on day 1 at the dose of 8 mg/kg loading dose i.v., then 6 mg/kg i.v. Pertuzumab (P) will be delivered on day 1 at the dose of 840 mg loading dose i.v., then 420 mg i.v. Carboplatin (C) will be administered at AUC 2 i.v. on day 1 and day 8; paclitaxel (T) will be given at 90 mg/m2 i.v. on day 1 and day 8; atezolizumab at the dose of 1200 mg i.v. on day 1. Definite surgery will be performed not later than 4 weeks after the last dose of neoadjuvant therapy. Trastuzumab, pertuzumab and atezolizumab will then be delivered for 12 additional cycles as adjuvant therapy.
Sponsors
Collaborators: Hoffmann-La Roche
Leads: Fondazione Michelangelo

This content was sourced from clinicaltrials.gov