Study on Atezolizumab and Trastuzumab Emtansine for Patients with HER2-Positive Breast Cancer at High Risk of Recurrence After Preoperative Therapy

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What is this study about?

This clinical trial is focused on studying HER2-positive breast cancer, a type of breast cancer that tests positive for a protein called human epidermal growth factor receptor 2, which promotes the growth of cancer cells. The study is evaluating the effectiveness and safety of two treatments: atezolizumab and trastuzumab emtansine. Atezolizumab, also known by its code name RO5541267, is a medication that helps the immune system fight cancer. Trastuzumab emtansine is a combination of two drugs that work together to target and kill cancer cells. The study also includes a comparison with a placebo, which is a substance with no active medication.

The purpose of the study is to determine how well atezolizumab works when given with trastuzumab emtansine, compared to trastuzumab emtansine alone. Participants in the study will receive one of these treatments after they have completed their initial therapy for breast cancer. The study will monitor participants over a period of time to assess their health and any changes in their condition. This will help researchers understand the potential benefits and risks of the treatments.

Participants will be randomly assigned to receive either the combination of atezolizumab and trastuzumab emtansine, trastuzumab emtansine with a placebo, or other variations as part of the study. The treatments will be administered through an infusion, which is a method of delivering medication directly into the bloodstream. The study aims to provide valuable information on the effectiveness of these treatments in preventing the recurrence of breast cancer in patients who are at high risk.

1 joining the study

Upon joining the study, eligibility is confirmed based on specific criteria, including a diagnosis of HER2-positive breast cancer and completion of preoperative therapy.

The interval between primary surgery and randomization must not exceed 12 weeks.

2 randomization

Participants are randomly assigned to receive either the study medication or a placebo.

This process ensures that the study results are unbiased and reliable.

3 treatment phase

Participants receive trastuzumab emtansine and either atezolizumab or a placebo.

Trastuzumab emtansine is administered as an IV infusion.

Atezolizumab or placebo is also administered as an IV infusion.

The specific dosage and frequency of administration are determined by the study protocol.

4 monitoring and assessments

Regular monitoring is conducted to assess the effectiveness and safety of the treatment.

Participants undergo various assessments, including blood tests and imaging studies, to evaluate their response to the treatment.

5 follow-up

After completing the treatment phase, participants enter a follow-up period.

During this time, ongoing assessments are conducted to monitor for any recurrence of cancer and to evaluate overall health.

6 study completion

The study is estimated to conclude by June 29, 2035.

Final results will be analyzed to determine the efficacy and safety of the treatment.

Who Can Join the Study?

  • The patient must have a confirmed diagnosis of invasive breast cancer. This means that cancer cells have spread beyond the original site in the breast.
  • There must be evidence of remaining cancer in the breast or nearby lymph nodes after surgery, following initial treatment. If the cancer was initially found in certain stages (cT1-3/N0-1/M0), there must be cancer left in the lymph nodes.
  • The breast cancer must be HER2-positive, which is a specific type of breast cancer that has more of a protein called HER2. The status of hormone receptors and a protein called programmed death ligand 1 must also be checked through a special test on a tumor sample.
  • The patient must have completed chemotherapy and treatment targeting HER2 before surgery.
  • All visible cancer in the breast and lymph nodes must have been surgically removed.
  • There should be no more than 12 weeks between the main surgery and the start of the trial.
  • The trial is open to both female and male patients.

Who Cannot Join the Study?

  • Patients with other types of cancer besides HER2 positive breast cancer cannot participate. HER2 positive breast cancer is a type of breast cancer that has a higher amount of a protein called HER2, which can make cancer grow faster.
  • Patients who have had previous treatment with the study drugs, atezolizumab or trastuzumab emtansine, are not eligible. Atezolizumab is a medicine that helps the immune system fight cancer, and trastuzumab emtansine is a drug that targets cancer cells with the HER2 protein.
  • Patients with severe or uncontrolled medical conditions that could interfere with the study are excluded. This means if someone has a serious health problem that is not well-managed, they cannot join the study.
  • Pregnant or breastfeeding women cannot participate in the study to ensure the safety of the baby.
  • Patients who are participating in another clinical trial at the same time are not allowed to join this study.
  • Patients with known allergies to the study drugs or their ingredients are excluded to prevent allergic reactions.
  • Patients with a history of certain heart problems may not be eligible, as these conditions could be worsened by the study drugs.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Other Sites

Site Name City Country Status
Orszagos Onkologiai Intezet Budapest Hungary
Centro Di Riferimento Oncologico Di Aviano Aviano Italy
Centre Hospitalier Universitaire De Nimes Nimes France
IRCCS Istituto Nazionale Tumori Fondazione Pascale Naples Italy
Centre Hospitalier Universitaire De Poitiers Poitiers France
Azienda Ospedaliero Universitaria Di Modena Modena Italy
Staedtisches Klinikum Lueneburg gGmbH Lueneburg Germany
Universitaetsklinikum Schleswig-Holstein AöR Kiel Germany
Leopoldina-Krankenhaus der Stadt Schweinfurt GmbH Schweinfurt Germany
Klinikum Ernst von Bergmann gGmbH Potsdam Germany
Hospital General Universitario Gregorio Maranon Madrid Spain
Hospital De Santa Maria E.P.E. Lisbon Portugal
Hospital Del Mar Barcelona Spain
Masarykuv Onkologicky Ustav Brno-Stred Czechia
Instituto Portugues De Oncologia Do Porto Francisco Gentil E.P.E. Porto Portugal
Wielkopolskie Centrum Onkologii Im. Marii Sklodowskiej-Curie Poznan Poland
Centre Hospitalier Universitaire Dinant Godinne Sainte-Elisabeth-UCL-Namur Namur Belgium
Hospital Universitario De Jaen Jaen Spain
Hospital Beatriz Angelo Loures Portugal
Radiotherapy Center Cluj S.R.L. Floresti Romania
SCRI CCCIT Ges.m.b.H. Salzburg Austria
University General Hospital Of Heraklion Heraklion Greece
Hospital Universitario Basurto Bilbao Spain
Hospital Universitario Dr Peset Aleixandre Valencia Spain
Institut Sainte Catherine Avignon France
Complex Oncological Center Plovdiv EOOD Plovdiv Bulgaria
Bialostockie Centrum Onkologii Im. Marii Sklodowskiej-Curie W Bialymstoku Bialystok Poland
AORN San Giuseppe Moscati Avellino Avellino Italy
Spitalul Clinic Filantropia Bucharest Romania
Praxis Fuer Interdisziplinaere Onkologie And Haematologie GbR Freiburg Im Breisgau Germany
Staedtisches Klinikum Dessau Dessau-Roßlau Germany
Gesundheitszentrum Wetterau gGmbH Bad Nauheim Germany
Marienhospital Bottrop gGmbH Bottrop Germany
Saint Savvas Oncology Hospital Athens Greece
General University Hospital Of Larissa Larissa Greece
Mbal Za Zhensko Zdrave Nadezhda OOD Sofia Bulgaria
Centrul De Oncologie SF Nectarie S.R.L. Craiova Romania
University Of Debrecen Debrecen Hungary
Metropolitan General Hospital/Healthcare Facilities Operation And Management Single Member S.A Cholargos Greece
Virgen del Rocío University Hospital Sevilla Spain
Ospedale San Raffaele S.r.l. Milan Italy
Alexandra Hospital Athens Greece
Hospital Clinic De Barcelona Barcelona Spain
Fakultni Nemocnice Hradec Kralove Novy Hradec Kralove Czechia
Hospital Universitario Quironsalud Madrid Pozuelo De Alarcon Spain
Universita’ Di Pisa Pisa Italy
Sygehus Lillebaelt Vejle Sygehus Vejle Denmark
Universidade De Santiago De Compostela Santiago De Compostela Spain
Samodzielny Publiczny Zaklad Opieki Zdrowotnej Szpital Uniwersytecki W Krakowie Cracow Poland
Uniteversity Muliprofile Hospital For Active Treatment Tsaritsa Yoanna-Isul EAD Sofia Bulgaria
Jessa Ziekenhuis Hasselt Belgium
Nemocnice AGEL Novy Jicin a.s. Novy Jicin Czechia
Oncomed S.R.L. Timisoara Romania
Institute Of Oncology Prof. Dr. Ion Chiricuta Cluj-Napoca Cluj Napoca Romania
Hospital Cuf Tejo S.A. Lisbon Portugal
Azienda Ospedaliero-Universitaria Maggiore Della Carita Novara Italy
Vseobecna Fakultni Nemocnice V Praze Prague Czechia
University Hospital Olomouc Olomouc Czechia
Groupe Hospitalier Diaconesses Croix Saint Simon Paris France
Hospital Universitario De Canarias La Laguna Spain
Polyclinique Bordeaux Nord Aquitaine Bordeaux France
Hospital Alvaro Cunqueiro Vigo Spain
Universita Degli Studi Di Brescia Brescia Italy
Fondazione I.R.C.C.S. Istituto Neurologico Besta Milan Italy
Budapesti Szent Margit Korhaz Budapest Hungary
Fakultni Thomayerova nemocnice Prague Czechia
Centre Francois Baclesse Caen France
Agaplesion Frankfurter Diakonie Kliniken gGmbH Frankfurt Germany
Hospital Universitario Virgen De La Victoria Malaga Spain
Metropolitan Hospital Athens Greece
Onkologische Schwerpunktpraxis Kurfuerstendamm Berlin Germany
Cpzypuvwi Ujmncozlsfbshl Sxsxteipd Woluwe-Saint-Lambert Belgium
Cdwyaw Luty Bxqklb Lyon France
Oupdkcoohboxud Lzck Gjkj Linz Austria
Uficmyojxamzzcdembzht Aeqtrtcz Augsburg Germany
Mdz Msrjgej Clyseb Dbmaljqanhf Gfrq Duesseldorf Germany
Diq Aiba Mwjrmupcawba Vwymkhqtrx Gnrj Erfurt Germany
Dqaucgtnm Hgfrfqvasmbzyxg Hanover Germany
Gqnawq Hivqobsjkjd Pcdltu Dw Sjt Dy L Oupu Creil France
Pijj Tkjwf Hmevbfsn Uwscdekdhfwv Sabadell Spain
Ajajied Uvd Tuafvwe nlkt oterr Leghorn Italy
Bbksnbzh Urogvntlpk Huqmudsk Coioos Besançon France
Gojzabaprtcngrdh Zseolfo Bmih Bonn Germany
Adntwp Mderuaj Csdfgs Sodg Thessaloniki Greece
Nkazwczi Ipjhlqgb Ovfukuvty Iej Msnnj Sxmromwauehrwdxxqblxomwcwhwn Iinsvcpm Bzwrkvuu Cracow Poland
Gkobbs Ubvvbcwuej Fzyczobsf Frankfurt Germany
Klcilsfl dai Uginqymwnyto Myyudndx Aln Munich Germany
Uiqgmqlqkcansg Cakpvnp Kgswbeoyj Gdansk Poland
Ibbyibhg Cpwgza Dgdvqiowgokrnjwky L'hospitalet De Llobregat Spain
Kjpnrusw Etwcfpflejhmmettcvblvwat Hcwaabvrkidxhdhsw Essen Germany
Hueasyan Vfdf dqwibadk Barcelona Spain
Hjfwxqcl Uemerjznmubep dz A Cdtjov A Coruna Galicia Spain
Iybvmjos Cbpce Paris France

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Austria Austria
Not recruiting
17.05.2021
Belgium Belgium
Not recruiting
17.05.2021
Bulgaria Bulgaria
Not recruiting
17.05.2021
Czechia Czechia
Not recruiting
17.05.2021
Denmark Denmark
Not recruiting
17.05.2021
France France
Not recruiting
17.05.2021
Germany Germany
Not recruiting
17.05.2021
Greece Greece
Not recruiting
17.05.2021
Hungary Hungary
Not recruiting
17.05.2021
Italy Italy
Not recruiting
17.05.2021
Poland Poland
Not recruiting
17.05.2021
Portugal Portugal
Not recruiting
17.05.2021
Romania Romania
Not recruiting
17.05.2021
Spain Spain
Not recruiting
17.05.2021

Trial locations

Atezolizumab is a medication used in this trial to help the immune system attack cancer cells. It is being tested to see if it can improve the treatment of HER2-positive breast cancer, which is a type of breast cancer that has a higher risk of coming back after initial treatment.

Trastuzumab Emtansine is a medication that combines two different types of cancer treatments. It targets HER2-positive breast cancer cells and delivers a chemotherapy drug directly to them. This helps to kill the cancer cells while minimizing damage to healthy cells. The trial is testing its effectiveness when used with atezolizumab.

Investigated diseases:

Early Human Epidermal Growth Factor Receptor 2 (HER2) Positive Breast Cancer – This is a type of breast cancer characterized by the overexpression of the HER2 protein, which promotes the growth of cancer cells. It is considered an early stage when the cancer is confined to the breast or nearby lymph nodes and has not spread to distant parts of the body. The disease progresses as the cancer cells grow and potentially spread to other areas, which can lead to more advanced stages if not managed. HER2-positive breast cancer tends to grow and spread more aggressively than other types of breast cancer. The progression of the disease can vary, with some cases remaining localized while others may advance more rapidly. Understanding the specific characteristics of HER2-positive breast cancer is crucial for determining appropriate management strategies.

Trial ID:
2023-503568-18-00
Protocol code:
WO42633
Trial Phase:
Therapeutic confirmatory (Phase III)

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