Evidence map›Paper›PMID 29253081›Full record

Trial reportAnnals of oncology : official journal of the European Society for Medical Oncology2018

Pertuzumab, trastuzumab, and standard anthracycline- and taxane-based chemotherapy for the neoadjuvant treatment of patients with HER2-positive localized breast cancer (BERENICE): a phase II, open-label, multicenter, multinational cardiac safety study.

S M Swain, M S Ewer, G Viale, S Delaloge, J-M Ferrero, M Verrill, R Colomer, C Vieira, T L Werner, H Douthwaite and 6 more

Registry-linked trialOpen access · bronzeAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Annals of oncology : official journal of the European Society for Medical Oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02132949 (A Multicenter, Multinational, Phase II Study to Evaluate Perjeta in Combination With Herceptin and Standard Neoadjuvant Anthracycline-Based Chemotherapy in Patients With HER2-Positive, Locally Advanced, Inflammatory, or Early-Stage Breast Cancer), which is not on this map. Cited by 138 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
138citing papers in PubMed, 7 pooled it
6.6field-weighted citation impact, top 2% 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.

NCT02132949 phase2completednot on this map

A Multicenter, Multinational, Phase II Study to Evaluate Perjeta in Combination With Herceptin and Standard Neoadjuvant Anthracycline-Based Chemotherapy in Patients With HER2-Positive, Locally Advanced, Inflammatory, or Early-Stage Breast Cancer

TypeinterventionalSponsorHoffmann-La RocheRan2014 to 2020Enrolled401ConditionsBreast CancerArms5-Fluorouracil, Cyclophosphamide, Docetaxel, Doxorubicin, Epirubicin
3 · Its place in the literature

Who cites it

138 citing papers in PubMed, 7 syntheses or guidelines pooled it, 238 citations in OpenAlex.

  1. Exercise and pathologic complete response to cancer treatment: a systematic review and meta-analysis.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
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78 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 7 countries.

S M SwainGeorgetown University Medical Center, Lombardi Comprehensive Cancer Center, Washington, USA. Electronic address: sandra.swain@georgetown.edu.
M S EwerDepartment of Cardiology, The University of Texas MD Anderson Cancer Center, Houston, USA.
G VialeDepartment of Pathology, European Institute of Oncology, University of Milan, Milan, Italy.
S DelalogeDepartment of Medical Oncology, Institut Gustave Roussy, Villejuif.
J-M FerreroClinical Research Department, Centre Antoine Lacassagne, Nice, France.
M VerrillMedical Oncology Department, Northern Centre for Cancer Care, Newcastle upon Tyne, UK.
R ColomerMedical Oncology Department, Hospital Universitario La Princesa, Madrid, Spain.
C VieiraMedical Oncology, Instituto Português de Oncologia Francisco Gentil (IPOFG) Porto, Porto, Portugal.
T L WernerHuntsman Cancer Institute, University of Utah, Salt Lake City, USA.
H DouthwaiteBiostatistics, Product Development, Roche Products Ltd, Welwyn Garden City, UK.
D BradleyClinical Science, Global Product Development, Roche Products Ltd, Welwyn Garden City, UK.
M Waldron-LynchClinical Science, Global Product Development, Roche Products Ltd, Welwyn Garden City, UK.
A KiermaierOncology Biomarker Development (OBD), F. Hoffmann-La Roche Ltd, Basel, Switzerland.
J Eng-WongProduct Development - Oncology, Genentech, Inc., South San Francisco.
C DangDepartment of Medicine, Breast Medicine Service, Memorial Sloan Kettering Cancer Center, New York, USA.
BERENICE Study Group
Roche (United Kingdom) · GBCentre Antoine Lacassagne · FRGeorgetown University · USHospital Universitario de La Princesa · ESInstitut Gustave Roussy · FRInstituto Português de Oncologia Francisco Gentil · PTMemorial Sloan Kettering Cancer Center · USRoche (Switzerland) · CHThe University of Texas MD Anderson Cancer Center · USUniversity of Milan · ITUniversity of Utah · 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

Background: Anti-HER2 therapies are associated with a risk of increased cardiac toxicity, particularly when part of anthracycline-containing regimens. We report cardiac safety of pertuzumab, trastuzumab, and chemotherapy in the neoadjuvant treatment of HER2-positive early breast cancer. Patients and methods: BERENICE (NCT02132949) is a nonrandomized, phase II, open-label, multicenter, multinational study in patients with normal cardiac function. In the neoadjuvant period, cohort A patients received four cycles of dose-dense doxorubicin and cyclophosphamide, then 12 doses of standard paclitaxel plus four standard trastuzumab and pertuzumab cycles. Cohort B patients received four standard fluorouracil/epirubicin/cyclophosphamide cycles, then four docetaxel cycles with four standard trastuzumab and pertuzumab cycles. The primary end point was cardiac safety during neoadjuvant treatment, assessed by the incidence of New York Heart Association class III/IV heart failure and of left ventricular ejection fraction declines (≥10 percentage-points from baseline and to a value of <50%). The main efficacy end point was pathologic complete response (pCR, ypT0/is ypN0). Results are descriptive. Results: Safety populations were 199 and 198 patients in cohorts A and B, respectively. Three patients [1.5%; 95% confidence interval (CI) 0.31% to 4.34%] in cohort A experienced four New York Heart Association class III/IV heart failure events. Thirteen patients (6.5%; 95% CI 3.5% to 10.9%) in cohort A and four (2.0%; 95% CI 0.6% to 5.1%) in cohort B experienced at least one left ventricular ejection fraction decline. No new safety signals were identified. pCR rates were 61.8% and 60.7% in cohorts A and B, respectively. The highest pCR rates were in the HER2-enriched PAM50 subtype (75.0% and 73.7%, respectively). Conclusion: Treatment with pertuzumab, trastuzumab, and common anthracycline-containing regimens for the neoadjuvant treatment of early breast cancer resulted in cardiac and general safety profiles, and pCR rates, consistent with prior studies with pertuzumab. Clinical Trial Information: NCT02132949.

Indexed as

AdultAgedAnthracyclinesAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsCardiotoxicityChemotherapy, AdjuvantCyclophosphamideDoxorubicinErb-b2 Receptor Tyrosine KinasesFemaleHumansIncidenceMiddle AgedNeoadjuvant TherapyAnthracyclinesAntibodies, Monoclonal, HumanizedCyclophosphamideDoxorubicinERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesPaclitaxelpertuzumabTaxoidsTrastuzumab

Identifiers

PMID29253081
PMCPMC5888999
OpenAlexW2791139688

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

Registered trials

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.