Study to Assess Safety and Efficacy of Atezolizumab (MPDL3280A) Compared to Best Supportive Care Following Chemotherapy in Patients With Lung Cancer [IMpower010]

NCT ID: NCT02486718

Last Updated: 2026-01-14

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

PHASE3

Total Enrollment

1280 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-10-31

Study Completion Date

2027-12-17

Brief Summary

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This is a Phase III, global, multicenter, open-label, randomized study to compare the efficacy and safety of 16 cycles (1 cycle duration=21 days) of atezolizumab (MPDL3280A) treatment compared with best supportive care (BSC) in participants with Stage IB-Stage IIIA non-small cell lung cancer (NSCLC) following resection and adjuvant chemotherapy, as measured by disease-free survival (DFS) as assessed by the investigator and overall survival (OS). Participants, after completing up to 4 cycles of adjuvant cisplatin-based chemotherapy, will be randomized in a 1:1 ratio to receive atezolizumab for 16 cycles or BSC.

Detailed Description

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Conditions

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Non-Small Cell Lung Cancer

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Atezolizumab

Enrollment Phase: Participants will receive four 21-day cycles of cisplatin-based chemotherapy (cisplatin plus either vinorelbine or docetaxel or gemcitabine or pemetrexed \[non-squamous cell NSCLC only\]), unless unacceptable toxicity, disease relapse, or participant's decision to discontinue occur. Randomization Phase: Participants will receive atezolizumab 1200 milligrams (mg) intravenously (IV) every 3 weeks (Q3W) for sixteen 21-day cycles and will undergo periodic chest X-ray and CT scan.

Group Type EXPERIMENTAL

Atezolizumab

Intervention Type DRUG

Participants will receive atezolizumab (1200 mg IV) Q3W for 16 cycles (cycle length=21 days).

Cisplatin

Intervention Type DRUG

Participants will receive cisplatin 75 milligrams per square meter (mg/m\^2) IV on Day 1 of up to four 21-day cycles.

Vinorelbine

Intervention Type DRUG

Participants will receive vinorelbine 30 mg/m\^2 IV on Days 1 and 8 of each of the four 21-day cycles.

Docetaxel

Intervention Type DRUG

Participants will receive docetaxel 75 mg/m\^2 IV on Day 1 of each of the four 21-day cycles.

Gemcitabine

Intervention Type DRUG

Participants will receive gemcitabine 1250 mg/m\^2 IV on Days 1 and 8 of each of the four 21-day cycles.

Pemetrexed

Intervention Type DRUG

Participants will receive pemetrexed 500 mg/m\^2 IV on Day 1 of each of the four 21-day cycles. Pemetrexed will be administered only in participants with non-squamous cell NSCLC.

Best Supportive Care

Enrollment Phase: Participants will receive four 21-day cycles of cisplatin-based chemotherapy (cisplatin plus either vinorelbine or docetaxel or gemcitabine or pemetrexed \[non-squamous cell NSCLC only\]), unless unacceptable toxicity, disease relapse, or participant's decision to discontinue occur. Randomization Phase: After enrollment phase participants will receive only the best supportive care and will undergo periodic chest X-ray and CT scan.

Group Type ACTIVE_COMPARATOR

Cisplatin

Intervention Type DRUG

Participants will receive cisplatin 75 milligrams per square meter (mg/m\^2) IV on Day 1 of up to four 21-day cycles.

Vinorelbine

Intervention Type DRUG

Participants will receive vinorelbine 30 mg/m\^2 IV on Days 1 and 8 of each of the four 21-day cycles.

Docetaxel

Intervention Type DRUG

Participants will receive docetaxel 75 mg/m\^2 IV on Day 1 of each of the four 21-day cycles.

Gemcitabine

Intervention Type DRUG

Participants will receive gemcitabine 1250 mg/m\^2 IV on Days 1 and 8 of each of the four 21-day cycles.

Pemetrexed

Intervention Type DRUG

Participants will receive pemetrexed 500 mg/m\^2 IV on Day 1 of each of the four 21-day cycles. Pemetrexed will be administered only in participants with non-squamous cell NSCLC.

Interventions

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Atezolizumab

Participants will receive atezolizumab (1200 mg IV) Q3W for 16 cycles (cycle length=21 days).

Intervention Type DRUG

Cisplatin

Participants will receive cisplatin 75 milligrams per square meter (mg/m\^2) IV on Day 1 of up to four 21-day cycles.

Intervention Type DRUG

Vinorelbine

Participants will receive vinorelbine 30 mg/m\^2 IV on Days 1 and 8 of each of the four 21-day cycles.

Intervention Type DRUG

Docetaxel

Participants will receive docetaxel 75 mg/m\^2 IV on Day 1 of each of the four 21-day cycles.

Intervention Type DRUG

Gemcitabine

Participants will receive gemcitabine 1250 mg/m\^2 IV on Days 1 and 8 of each of the four 21-day cycles.

Intervention Type DRUG

Pemetrexed

Participants will receive pemetrexed 500 mg/m\^2 IV on Day 1 of each of the four 21-day cycles. Pemetrexed will be administered only in participants with non-squamous cell NSCLC.

Intervention Type DRUG

Other Intervention Names

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MPDL3280A; TECENTRIQ

Eligibility Criteria

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Inclusion Criteria

* Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
* Histological or cytological diagnosis of Stage IB (tumors greater than or equal to \[\>/=\] 4 centimeters \[cm\])-IIIA (T2-3 N0, T1-3 N1, T1-3 N2, T4 N0-1) NSCLC (per the Union Internationale Contre le Cancer staging system (UICC)/American Joint Committee on Cancer staging system (AJCC) staging system, 7th edition; Detterbeck et al. 2009)
* Participants must have had complete resection of NSCLC 4-12 weeks (\>/=28 days and less than or equal to \[\</=\] 84 days) prior to enrollment and must be adequately recovered from surgery
* If mediastinoscopy was not performed preoperatively, it is required that, at a minimum, mediastinal lymph node systematic sampling will have occurred. Systematic sampling is defined as removal of at least one representative lymph node at specified levels. MLND entails resection of all lymph nodes at those same levels. For a right thoracotomy, sampling or MLND is required at levels 4 and 7 and for a left thoracotomy, levels 5 and/or 6 and 7. Exceptions will be granted if there is clear documentation in the operative report or in a separately submitted addendum by the surgeon of exploration of the required lymph node areas, the participant will be considered eligible if no lymph nodes are found in those areas; if participants have documented N2 disease in one level (per the UICC/AJCC staging system, 7th edition; Detterbeck et al. 2009), not all levels need to be sampled; if the preoperative staging imaging results (contrast computed tomography \[CT\] and positron emission tomography \[PET\] scans) do not suggest evidence of disease in the mediastinum, the participant will be considered eligible if N2 nodal sampling is not performed per surgeon's decision
* Eligible to receive a cisplatin-based chemotherapy regimen
* Adequate hematologic and end-organ function
* Women who are not postmenopausal (\>/=12 months of non-therapy-induced amenorrhea) or surgically sterile must have a negative serum pregnancy test result within 14 days prior to initiation of cisplatin-based chemotherapy

Exclusion Criteria

* Illness or condition that may interfere with a participant's capacity to understand, follow, and/or comply with study procedures
* Pregnant and lactating women
* Treatment with prior systemic chemotherapy: Chemotherapy for early stage of malignancy with curative intent, provided that the last dose received was more than 5 years prior to enrollment and low-dose chemotherapy for non-malignant conditions may be allowed upon approval by the Medical Monitor
* Hormonal cancer therapy or radiation therapy as prior cancer treatment within 5 years before enrollment
* Treatment with any other investigational agent with therapeutic intent within 28 days prior to enrollment
* Participants with hearing impairment
* Known sensitivity to any component of the chemotherapy regimen the participant will be assigned to, or to mannitol
* Prior treatment with cluster of differentiation (CD) 137 (CD137) agonists or immune checkpoint blockade therapies, anti-programmed death-1 (PD-1), and anti programmed death ligand 1 (PD-L1) therapeutic antibodies
* Malignancies other than NSCLC within 5 years prior to randomization, with the exception of those with a negligible risk of metastasis or death (e.g., expected 5-year OS greater than \[\>\] 90 percent \[%\]) treated with expected curative outcome (such as adequately treated carcinoma in situ of the cervix, basal or squamous cell skin cancer, localized prostate cancer treated surgically with curative intent, ductal carcinoma in situ treated surgically with curative intent)
* History of severe allergic, anaphylactic, or other hypersensitivity reactions to chimeric or humanized antibodies or fusion proteins
* Known hypersensitivity to biopharmaceuticals produced in Chinese hamster ovary cells or any component of the atezolizumab formulation
* History of autoimmune disease, including but not limited to myasthenia gravis, myositis, autoimmune hepatitis, systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, vascular thrombosis associated with antiphospholipid syndrome, Wegener's granulomatosis, Sjögren's syndrome, Guillain-Barré syndrome, multiple sclerosis, vasculitis, or glomerulonephritis
* Positive test for human immunodeficiency virus (HIV)
* Participants with active hepatitis B (chronic or acute; defined as having a positive hepatitis B surface antigen \[HBsAg\] test at screening) or hepatitis C
* Active tuberculosis
* Significant cardiovascular disease, such as New York Heart Association cardiac disease (Class II or greater), myocardial infarction, or cerebrovascular accident within the previous 3 months, unstable arrhythmias, or unstable angina
* History of idiopathic pulmonary fibrosis, organizing pneumonia (e.g., bronchiolitis obliterans), drug-induced pneumonitis, idiopathic pneumonitis, or evidence of active pneumonitis on screening chest CT scan
* Prior allogeneic bone marrow transplantation or solid organ transplant
* Any other diseases, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug or that may affect the interpretation of the results or render the participant at high risk from treatment complications
* Known tumor PD-L1 expression status as determined by an immunohistochemistry (IHC) assay from other clinical studies (e.g., participants whose PD-L1 expression status was determined during screening for entry into a study with anti-PD-1 or anti-PD-L1 antibodies but were not eligible are excluded)

Specific Exclusions for Pemetrexed Treatment

\- Participants with squamous cell histology


* Signs or symptoms of infection within 14 days prior to randomization (severe infection within 28 days prior to randomization), including but not limited to hospitalization for complications of infection, bacteremia, or severe pneumonia
* Received therapeutic oral or intravenous (IV) antibiotics within 14 days prior to randomization
* Major surgical procedure within 28 days prior to randomization or anticipation of need for a major surgical procedure during the course of the study
* Administration of a live, attenuated vaccine within 4 weeks prior to initiation of study treatment or anticipation that such a live attenuated vaccine will be required during the study
* Treatment with systemic immunostimulatory agents (including but not limited to interferons or interleukin-2) within 4 weeks or 5 half-lives of the drug, whichever is longer, prior to randomization: Prior treatment with cancer vaccines is allowed
* Treatment with systemic corticosteroids or other immunosuppressive medications (including but not limited to prednisone, dexamethasone, cyclophosphamide, azathioprine, methotrexate, thalidomide, and anti-tumor necrosis factor \[anti-TNF\] agents) within 14 days prior to randomization
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hoffmann-La Roche

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Clinical Trials

Role: STUDY_DIRECTOR

Hoffmann-La Roche

Locations

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Highlands Oncology Group

Fayetteville, Arkansas, United States

Site Status

California Cancer Associates for Research & Excellence, Inc.

Encinitas, California, United States

Site Status

Compassionate Cancer Care Medical Group, Inc

Fountain Valley, California, United States

Site Status

University of California Los Angeles

Los Angeles, California, United States

Site Status

Kaiser Permanente

Vallejo, California, United States

Site Status

Kaiser Permanente - Walnut Creek

Walnut Creek, California, United States

Site Status

Eastern Connecticut Hematology and Oncology Associates

Norwich, Connecticut, United States

Site Status

Lynn Cancer Institute - West

Boca Raton, Florida, United States

Site Status

University of Miami School of Medicine - Sylvester at Deerfield

Deerfield Beach, Florida, United States

Site Status

SCRI Florida Cancer Specialists North

St. Petersburg, Florida, United States

Site Status

Lewis Hall Singletary Oncology Center

Thomasville, Georgia, United States

Site Status

University of Illinois at Chicago

Chicago, Illinois, United States

Site Status

Illinois Cancer Care

Peoria, Illinois, United States

Site Status

Norton Cancer Institute

Louisville, Kentucky, United States

Site Status

St. Luke's Cancer Institute

Kansas City, Missouri, United States

Site Status

Hematology Oncology Associates of Northern New Jersey

Florham Park, New Jersey, United States

Site Status

Saint Barnabas Medical Center

Livingston, New Jersey, United States

Site Status

Valley Hospital

Paramus, New Jersey, United States

Site Status

Overlook Medical Center

Summit, New Jersey, United States

Site Status

Clinical Research Alliance

Lake Success, New York, United States

Site Status

Weill Cornell Medical College

New York, New York, United States

Site Status

Presbyterian Hospital

Charlotte, North Carolina, United States

Site Status

University of Cincinnati

Cincinnati, Ohio, United States

Site Status

Oncology Hematology Care - SCRI

Cincinnati, Ohio, United States

Site Status

Oregon Health and Science University

Portland, Oregon, United States

Site Status

University Oncology Associates

Chattanooga, Tennessee, United States

Site Status

Houston Methodist Cancer Center

Houston, Texas, United States

Site Status

Wellmont Medical Associates

Bristol, Virginia, United States

Site Status

Hematology Oncology Associates of Fredericksburg, Inc.

Fredericksburg, Virginia, United States

Site Status

MultiCare Regional Cancer Center - Auburn

Auburn, Washington, United States

Site Status

Providence Everett Med Ctr

Everett, Washington, United States

Site Status

Swedish Medical Center

Seattle, Washington, United States

Site Status

Townsville Hospital

Douglas, Queensland, Australia

Site Status

Cabrini Hospital Malvern

Malvern, Victoria, Australia

Site Status

Cliniques Universitaires St-Luc

Brussels, , Belgium

Site Status

CHU de Liège (Sart Tilman)

Liège, , Belgium

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Cancer Institute and Hospital Chinese Academy of Medical Sciences

Beijing, , China

Site Status

The First Affiliated Hospital of Guangzhou Medical University

Guangzhou, , China

Site Status

Zhejiang Cancer Hospital

Hangzhou, , China

Site Status

Anhui Province Cancer Hospital

Hefei, , China

Site Status

Shanghai Chest Hospital

Shanghai, , China

Site Status

Shanghai Pulmonary Hospital

Shanghai, , China

Site Status

Liaoning Provincial Cancer Hospital

Shengyang, , China

Site Status

First Hospital of China Medical University

Shenyang, , China

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First Affiliated Hospital of Soochow University

Suzhou, , China

Site Status

Centre Hospitalier de Mont de Marsan - Hopital Layne

Mont-de-Marsan, , France

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Clinique Clémentville

Montpellier, , France

Site Status

Centre Regional de Lutte contre le Cancer Val d Aurelle - Paul Lamarque

Montpellier, , France

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Centre René Gauducheau Centre de Lutte Contre Le Cancer Nantes Atlantique

Nantes, , France

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Centre Hospitalier Regional Sud Reunion

Saint-Pierre, , France

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Centre Hospitalier de Saint-Quentin

Saint-Quentin, , France

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Hopital d Instruction des Armees de Sainte Anne

Toulon, , France

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Ev.Krankenhaus Bielefeld gGmbH

Bielefeld, North Rhine-Westphalia, Germany

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Evang. Lungenklinik Berlin Klinik für Pneumologie

Berlin, , Germany

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Stadtisches Klinikum Braunschweig

Braunschweig, , Germany

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Klinikum Chemnitz gGmbH

Chemnitz, , Germany

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Krankenhaus Nordwest

Frankfurt am Main, , Germany

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LungenClinic Grosshansdorf GmbH

Großhansdorf, , Germany

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Lungenklinik Hemer

Hemer, , Germany

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Universität Des Saarlandes

Homburg, , Germany

Site Status

Fachklinik für Lungenerkrankungen

Immenhausen, , Germany

Site Status

Vincentius-Diakonissen-Kliniken gAG

Karlsruhe, , Germany

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Katholisches Klinikum Marienhof

Koblenz Am Rhein, , Germany

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Klinikum Bogenhausen

München, , Germany

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Gemeinschaftspraxis für Hämatologie und Onkologie

Münster, , Germany

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Pius-Hospital Oldenburg

Oldenburg, , Germany

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Krankenhaus Barmherzige Bruder Regensburg

Regensburg, , Germany

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Prince of Wales Hosp

Shatin, , Hong Kong

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University of Pecs, I st Dept of Internal Medicine

Pécs, , Hungary

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Jasz-Nagykun-Szolnok Megyei Hetenyi Geza Korhaz-Rend.Int.

Szolnok, , Hungary

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Rambam Medical Center

Haifa, , Israel

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Edith Wolfson Medical Center

Holon, , Israel

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Meir Medical Center

Kfar Saba, , Israel

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Tel Aviv Sourasky Medical Ctr

Tel Aviv, , Israel

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Chaim Sheba Medical Center

Tel Litwinsky, , Israel

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Ospedale Clinicizzato SS Annunziata

Chieti, Abruzzo, Italy

Site Status

Azienda per l'Assistenza Sanitaria N° 5 - Friuli Occidentale

Pordenone, Friuli Venezia Giulia, Italy

Site Status

Policlinico Universitario Campus Biomedico Di Roma

Rome, Lazio, Italy

Site Status

Asst Papa Giovanni XXIII

Bergamo, Lombardy, Italy

Site Status

ASST Spedali Civili di Brescia

Brescia, Lombardy, Italy

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Azienda Sanitaria Ospedaliera S Luigi Gonzaga

Orbassano, Piedmont, Italy

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Azienda Ospedaliera Città della Salute e della Scienza di Torino

Turin, Piedmont, Italy

Site Status

Azienda Ospedaliera Di Rilievo Nazionale E Di Alta Specializzazione Garibaldi

Catania, Sicily, Italy

Site Status

Ospedale Santa Chiara

Trento, Trentino-Alto Adige, Italy

Site Status

Azienda Ospedaliero Universitaria Pisana

Pisa, Tuscany, Italy

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Ospedale Silvestrini

Perugia, Umbria, Italy

Site Status

Azienda Ospedaliera Universitaria Integrata Verona

Verona, Veneto, Italy

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Aichi Cancer Center Hospital

Aichi, , Japan

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Hyogo Cancer Center

Akashi, , Japan

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Juntendo University Hospital

Bunkyō City, , Japan

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Tokyo Metropolitan Cancer and Infectious diseases Center Komagome Hospital

Bunkyō City, , Japan

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National Cancer Center Hospital

Chūō, , Japan

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Kyushu University Hospital

Fukuoka, , Japan

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Hiroshima University Hospital

Hiroshima, , Japan

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Saitama Cancer Center

Kitaadachi-gun, , Japan

Site Status

Hospital of the University of Occupational and Environmental Health,Japan

Kitakyushu-shi, , Japan

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Kumamoto University Hospital

Kumamoto, , Japan

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Kyoto University Hospital

Kyoto, , Japan

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Shikoku Cancer Center

Matsuyama, , Japan

Site Status

Kyorin University Hospital

Mitaka-shi, , Japan

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Niigata Cancer Center Hospital

Niigata, , Japan

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Okayama University Hospital

Okayama, , Japan

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National Hospital Organization Hokkaido Cancer Center

Sapporo, , Japan

Site Status

Toranomon Hospital

Tokyo, , Japan

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Tokyo Medical University Hospital

Tokyo, , Japan

Site Status

Kanagawa Cancer Center

Yokohama-shi, Asahi-ku, , Japan

Site Status

Jeroen Bosch Ziekenhuis

's-Hertogenbosch, North Brabant, Netherlands

Site Status

St. Antonius Ziekenhuis Nieuwegein

Nieuwegein, , Netherlands

Site Status

Mazowieckie Centrum Leczenia Chorob Pluc i Gruzlicy

Otwock, , Poland

Site Status

Wielkopolskie Centrum Pulmonologii i Torakochirurgii w Poznaniu

Poznan, , Poland

Site Status

Centro Hospitalar E Universitário de Coimbra EPE

Coimbra, , Portugal

Site Status

Instituto Portugues de Oncologia Do Porto Francisco Gentil Epe

Porto, , Portugal

Site Status

Hospital de Sao Joao

Porto, , Portugal

Site Status

Oncology Center Sf. Nectarie

Craiova, , Romania

Site Status

Principal Military Clinical Hospital n.a. N.N. Burdenko

Moscow, Moscow Oblast, Russia

Site Status

Leningrad Regional Clinical Hospital

Saint Petersburg, Sankt-Peterburg, Russia

Site Status

GBUZ Saint Petersburg Clinical Research Center of Specialized Types of Care (Oncology)

Saint Petersburg, Sankt-Peterburg, Russia

Site Status

Scientific Research Institute of Oncology n.a. N.N. Petrov

Saint Petersburg, Sankt-Peterburg, Russia

Site Status

City Clinical Hospital #1

Novosibirsk, , Russia

Site Status

Volgograd Regional Clinical Oncology Dispensary

Volgograd, , Russia

Site Status

Regional Clinical Oncology Hospital

Yaroslavl, , Russia

Site Status

Chonnam National University Hwasun Hospital

Jeonnam, , South Korea

Site Status

The Catholic University of Korea St. Vincent's Hospital

Suwon, , South Korea

Site Status

Hospital Universitario Marques de Valdecilla

Santander, Cantabria, Spain

Site Status

Consorcio Hospitalario Provincial de Castellon

Castellon, Castellon, Spain

Site Status

Hospital Universitario Virgen de La Arrixaca

El Palmar, Murcia, Spain

Site Status

Hospital Universitario de Canarias

San Cristóbal de La Laguna, Tenerife, Spain

Site Status

Hospital del Mar

Barcelona, , Spain

Site Status

Hospital Santa Creu i Sant Pau

Barcelona, , Spain

Site Status

Vall d'Hebron Institute of Oncology (VHIO), Barcelona

Barcelona, , Spain

Site Status

C.H. Regional Reina Sofia

Córdoba, , Spain

Site Status

Complejo Hospitalario de Jaen

Jaén, , Spain

Site Status

Hospital Lucus Augusti

Lugo, , Spain

Site Status

Hospital Universitario La Paz

Madrid, , Spain

Site Status

Hospital Universitario HM Sanchinarro-CIOCC

Madrid, , Spain

Site Status

Hospital Universitari i Politecnic La Fe de Valencia

Valencia, , Spain

Site Status

Hosp Clinico Univ Lozano Blesa

Zaragoza, , Spain

Site Status

Changhua Christian Hospital

Changhua, , Taiwan

Site Status

Chang Gung Memorial Hospital Chiayi

Putzui City, , Taiwan

Site Status

Taichung Veterans General Hospital

Taichung, , Taiwan

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Taipei Veterans General Hospital

Taipei, , Taiwan

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Chang Gung Medical Foundation Linkou Branch

Taoyuan, , Taiwan

Site Status

MI Dnipropetrovsk City Multifield Clinical Hospital 4 of Dnipropetrovsk Regional Council

Dnipropetrovsk, Katerynoslav Governorate, Ukraine

Site Status

Communal Non profit Enterprise Regional Center of Oncology

Kharkiv, Kharkiv Governorate, Ukraine

Site Status

Municipal Institution Odesa Regional Oncology Dispensary

Odesa, KIEV Governorate, Ukraine

Site Status

Municipal Institution SubCarpathian ClinicalOncological Centre

Ivano-Frankivsk, Poltava Governorate, Ukraine

Site Status

Communal Nonprofit Enterprise Podilsky Regional Center Of Oncology OfTheVinnytsia Regional Council

Vinnytsia, Vinnytsia Oblast, Ukraine

Site Status

CE Kryvyi Rih Oncology Dispensary of Dnipropetrovsk Regional Council

Kryvyi Rih, , Ukraine

Site Status

Kyiv City Clinical Oncological Center

Kyiv, , Ukraine

Site Status

Regional Municipal Institution Sumy Regional Clinical Oncology Dispensary

Sumy, , Ukraine

Site Status

MI Zaporizhzhia Regional Clinical Oncological Dispensary Zaporizhzhia SMU Ch of Oncology

Zaporizhzhya, , Ukraine

Site Status

Colchester General Hospital

Colchester, Essex, , United Kingdom

Site Status

St Bartholomew's Hospital

London, , United Kingdom

Site Status

Countries

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United States Australia Belgium China France Germany Hong Kong Hungary Israel Italy Japan Netherlands Poland Portugal Romania Russia South Korea Spain Taiwan Ukraine United Kingdom

References

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Okada M, Sugawara S, Watanabe Y, Saito H, Chen-Yoshikawa TF, Goto Y, Nishio W, Nakagawa S, Hayashi M, Kenmotsu H. IMpower010: 5-Year Outcomes of Atezolizumab in Japanese Patients With Resected Stage IB-IIIA Non-Small Cell Lung Cancer. Cancer Sci. 2025 Dec 19. doi: 10.1111/cas.70297. Online ahead of print.

Reference Type DERIVED
PMID: 41416818 (View on PubMed)

Felip E, Altorki N, Zhou C, Vallieres E, Csoszi T, Vynnychenko IO, Goloborodko O, Rittmeyer A, Reck M, Martinez-Marti A, Kenmotsu H, Chen YM, Chella A, Sugawara S, Fu C, Ballinger M, Deng Y, Srivastava MK, Bennett E, Gitlitz BJ, Wakelee HA; IMpower010 Study Investigators. Five-Year Survival Outcomes With Atezolizumab After Chemotherapy in Resected Stage IB-IIIA Non-Small Cell Lung Cancer (IMpower010): An Open-Label, Randomized, Phase III Trial. J Clin Oncol. 2025 Jul 20;43(21):2343-2349. doi: 10.1200/JCO-24-01681. Epub 2025 May 30.

Reference Type DERIVED
PMID: 40446184 (View on PubMed)

Zhou C, Srivastava MK, Xu H, Felip E, Wakelee H, Altorki N, Reck M, Liersch R, Kryzhanivska A, Oizumi S, Tanaka H, Hamm J, McCune SL, Bennett E, Gitlitz B, McNally V, Ballinger M, McCleland M, Zou W, Das Thakur M, Novello S. Comparison of SP263 and 22C3 immunohistochemistry PD-L1 assays for clinical efficacy of adjuvant atezolizumab in non-small cell lung cancer: results from the randomized phase III IMpower010 trial. J Immunother Cancer. 2023 Oct;11(10):e007047. doi: 10.1136/jitc-2023-007047.

Reference Type DERIVED
PMID: 37903590 (View on PubMed)

Felip E, Altorki N, Zhou C, Vallieres E, Martinez-Marti A, Rittmeyer A, Chella A, Reck M, Goloborodko O, Huang M, Belleli R, McNally V, Srivastava MK, Bennett E, Gitlitz BJ, Wakelee HA. Overall survival with adjuvant atezolizumab after chemotherapy in resected stage II-IIIA non-small-cell lung cancer (IMpower010): a randomised, multicentre, open-label, phase III trial. Ann Oncol. 2023 Oct;34(10):907-919. doi: 10.1016/j.annonc.2023.07.001. Epub 2023 Jul 17.

Reference Type DERIVED
PMID: 37467930 (View on PubMed)

Mohindra NA, Patel JD. Top advances in lung cancer, 2021. Cancer. 2022 Oct 1;128(19):3434-3437. doi: 10.1002/cncr.34406. Epub 2022 Aug 10.

Reference Type DERIVED
PMID: 35947027 (View on PubMed)

Felip E, Altorki N, Zhou C, Csoszi T, Vynnychenko I, Goloborodko O, Luft A, Akopov A, Martinez-Marti A, Kenmotsu H, Chen YM, Chella A, Sugawara S, Voong D, Wu F, Yi J, Deng Y, McCleland M, Bennett E, Gitlitz B, Wakelee H; IMpower010 Investigators. Adjuvant atezolizumab after adjuvant chemotherapy in resected stage IB-IIIA non-small-cell lung cancer (IMpower010): a randomised, multicentre, open-label, phase 3 trial. Lancet. 2021 Oct 9;398(10308):1344-1357. doi: 10.1016/S0140-6736(21)02098-5. Epub 2021 Sep 20.

Reference Type DERIVED
PMID: 34555333 (View on PubMed)

Provided Documents

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Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

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Other Identifiers

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2014-003205-15

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

2023-505981-26-00

Identifier Type: REGISTRY

Identifier Source: secondary_id

GO29527

Identifier Type: -

Identifier Source: org_study_id

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