Evidence map›Paper›PMID 35763704›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2022

Atezolizumab With Neoadjuvant Anti-Human Epidermal Growth Factor Receptor 2 Therapy and Chemotherapy in Human Epidermal Growth Factor Receptor 2-Positive Early Breast Cancer: Primary Results of the Randomized Phase III IMpassion050 Trial.

Jens Huober, Carlos H Barrios, Naoki Niikura, Michał Jarząb, Yuan-Ching Chang, Shannon L Huggins-Puhalla, José Pedrini, Lyudmila Zhukova, Vilma Graupner, Daniel Eiger and 6 more

Open access · greenAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed, 6 pooled it
11.5field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

84 citing papers in PubMed, 6 syntheses or guidelines pooled it, 112 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Pooled it
  7. Safety and Efficacy of KN046 in Combination with KN026 in Patients with Advanced HER2-Positive Breast Cancer: A Phase II Trial.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Trial
  8. Trial
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  10. Trial
  11. Trial
  12. Review
  13. The immunology of human breast cancer.Nature reviews. Immunology · 2026
    Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Restoring the CD226 in CD8Cell death & disease · 2026
    Article
  19. Article
  20. Article

24 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 11 institutions in 9 countries.

Jens HuoberCantonal Hospital, Breast Center St Gallen, St Gallen, Switzerland.ORCID 0000-0002-8618-1820
Carlos H BarriosCentro de Pesquisa em Oncologia, Hospital São Lucas, PUCRS, Porto Alegre, Brazil.ORCID 0000-0001-6021-667X
Naoki NiikuraDepartment of Breast Oncology, Tokai University School of Medicine, Isehara, Japan.ORCID 0000-0001-6732-8527
Michał JarząbBreast Cancer Unit, Maria Skłodowska-Curie National Research Institute of Oncology, Gliwice Branch, Gliwice, Poland.ORCID 0000-0002-2642-9724
Yuan-Ching ChangDepartment of Surgery, Mackay Memorial Hospital, Taipei, Taiwan.ORCID 0000-0001-7625-606X
Shannon L Huggins-PuhallaUPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, PA.
José PedriniHospital Nossa Senhora da Conceição, Porto Alegre, Brazil.
Lyudmila ZhukovaSBIH Moscow Clinical Scientific and Practical Center named after A.S. Loginov of DHM, Moscow, Russia.
Vilma GraupnerProduct Development Oncology, F. Hoffmann-La Roche Ltd, Basel, Switzerland.
Daniel EigerProduct Development Oncology, F. Hoffmann-La Roche Ltd, Basel, Switzerland.ORCID 0000-0002-9879-6048
Volkmar HenschelProduct Development Data Science, F. Hoffmann-La Roche Ltd, Basel, Switzerland.
Nino GochitashviliProduct Development Safety, Roche Products Limited, Welwyn Garden City, United Kingdom.
Chiara LambertiniOncology Biomarker Development, F. Hoffmann-La Roche Ltd, Basel, Switzerland.
Eleonora RestucciaProduct Development Oncology, F. Hoffmann-La Roche Ltd, Basel, Switzerland.
Hong ZhangDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
IMpassion050 Trial Investigators
Roche (Switzerland) · CHHospital Nossa Senhora da Conceição · BRHospital São Lucas da PUCRS · BRMackay Memorial Hospital · TWMemorial Sloan Kettering Cancer Center · USMoscow Clinical Scientific Center · RURoche (United Kingdom) · GBThe Maria Sklodowska-Curie National Research Institute of Oncology · PLTokai University · JPUniversity of St.Gallen · CHUPMC Hillman Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeCombining standard of care (pertuzumab-trastuzumab [PH], chemotherapy) with cancer immunotherapy may potentiate antitumor immunity, cytotoxic activity, and patient outcomes in high-risk, human epidermal growth factor receptor 2 (HER2)-positive early breast cancer. We report the phase III IMpassion050 primary analysis of neoadjuvant atezolizumab, PH, and chemotherapy in these patients.

methodsPatients with a primary tumor of > 2 cm and histologically confirmed, positive lymph node status (T2-4, N1-3, M0) were randomly assigned 1:1 to atezolizumab/placebo with dose-dense doxorubicin/cyclophosphamide, followed by paclitaxel, and PH. After surgery, patients were to continue atezolizumab/placebo and PH (total: 1 year of HER2-targeted therapy); those with residual disease could switch to ado-trastuzumab emtansine with atezolizumab/placebo. Coprimary efficacy end points were pathologic complete response (pCR; ypT0/is ypN0) rates in intention-to-treat (ITT) and programmed cell death-ligand 1 (PD-L1)-positive populations.

resultsAt clinical cutoff (February 5, 2021), pCR rates in the placebo and atezolizumab groups in the ITT populations were 62.7% (n = 143/228) and 62.4% (n = 141/226), respectively (difference -0.33%; 95% CI, -9.2 to 8.6;

conclusionAtezolizumab with neoadjuvant dose-dense doxorubicin/cyclophosphamide-paclitaxel and PH for high-risk, HER2-positive early breast cancer did not increase pCR rates versus placebo in the ITT or PD-L1-positive populations. PH and chemotherapy remains standard of care; longer follow-up may help to inform the long-term impact of atezolizumab.

Indexed as

Breast NeoplasmsNeoadjuvant TherapyAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsB7-H1 AntigenCyclophosphamideDoxorubicinErb-b2 Receptor Tyrosine KinasesFemaleHumansPaclitaxelTrastuzumabTreatment OutcomeAntibodies, Monoclonal, HumanizedatezolizumabB7-H1 AntigenCyclophosphamideDoxorubicinErb-b2 Receptor Tyrosine KinasesPaclitaxelTrastuzumab

Identifiers

PMID35763704
PMCPMC9426828
OpenAlexW4283713242

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.