Evidence map›Paper›PMID 36291835›Full record

ArticleCancers2022

Event-Free Survival in Patients with Early HER2-Positive Breast Cancer with a Pathological Complete Response after HER2-Targeted Therapy: A Pooled Analysis.

Sandra M Swain, Harrison Macharia, Javier Cortes, Chau Dang, Luca Gianni, Sara A Hurvitz, Christian Jackisch, Andreas Schneeweiss, Dennis Slamon, Pinuccia Valagussa and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Cancers · 2023
    Article
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

15 authors at 8 institutions in 5 countries.

Sandra M SwainLombardi Comprehensive Cancer Center, Georgetown University Medical Center, MedStar Health, Washington, DC 20057, USA.ORCID 0000-0002-1320-3830
Harrison MachariaF. Hoffmann-La Roche Ltd., 4070 Basel, Switzerland.
Javier CortesQuirónsalud Group, IOB Institute of Oncology, Madrid and Barcelona, 08023 Barcelona, Spain.ORCID 0000-0001-7623-1583
Chau DangDepartment of Medicine, Breast Medicine Service, Memorial Sloan Kettering Cancer Center, New York, NY 10013, USA.ORCID 0000-0001-5133-2265
Luca GianniFondazione Michelangelo, 20121 Milano, Italy.
Sara A HurvitzDavid Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 94720, USA.
Christian JackischSana Klinikum Offenbach, 63069 Offenbach, Germany.
Andreas SchneeweissNational Center for Tumor Diseases (NCT), 69120 Heidelberg, Germany.
Dennis SlamonDavid Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 94720, USA.
Pinuccia ValagussaFondazione Michelangelo, 20121 Milano, Italy.ORCID 0000-0003-3590-7916
Yolande du ToitGenentech, Inc., South San Francisco, CA 94080, USA.ORCID 0000-0002-2526-9503
Dominik HeinzmannF. Hoffmann-La Roche Ltd., 4070 Basel, Switzerland.
Adam KnottF. Hoffmann-La Roche Ltd., 4070 Basel, Switzerland.
Chunyan SongGenentech, Inc., South San Francisco, CA 94080, USA.
Patricia CortazarGenentech, Inc., South San Francisco, CA 94080, USA.
Roche (Switzerland) · CHFondazione Michelangelo · ITUniversity of California, Los Angeles · USGeorgetown University · USHospital Quirónsalud Barcelona · ESMemorial Sloan Kettering Cancer Center · USNational Center for Tumor Diseases · DESana Klinikum Offenbach · DE

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
F. Hoffmann-La Roche n/aNCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

The standard-of-care for patients with pathological complete response (pCR) after neoadjuvant human epidermal growth factor receptor 2 (HER2)-targeted therapy plus chemotherapy is continuation of HER2-targeted therapy in the adjuvant setting. Our objective was to evaluate risk of recurrence or death in these patients and determine if outcomes differed by the HER2-targeted regimen received in each setting. We analyzed patient-level data from five randomized trials evaluating trastuzumab, pertuzumab, or both as part of systemic neoadjuvant and adjuvant therapy for HER2-positive early breast cancer, and assessed event-free survival (EFS) in 1763 patients. Patients with pCR had decreased risk of an EFS event versus those with residual disease (unadjusted hazard ratio [HR] = 0.35; 95% confidence interval [CI]: 0.27-0.46). Regardless of pCR status, after adjusting for baseline factors, reduction in EFS event risk was greater in patients administered pertuzumab/trastuzumab in both settings versus those administered only trastuzumab in both settings (HR = 0.36; 95% CI: 0.26-0.49), or pertuzumab/trastuzumab in the neoadjuvant setting and only trastuzumab in the adjuvant setting (HR = 0.67; 95% CI: 0.47-0.96). Patients with pCR had longer EFS than those with residual disease. Patients treated with pertuzumab/trastuzumab in both the neoadjuvant and adjuvant settings had the lowest risk of breast cancer recurrence.

Indexed as

dual HER2 targetingearly breast cancerevent-free survivalHER2pathologic complete responsepertuzumabtrastuzumab

Identifiers

PMID36291835
PMCPMC9599862
OpenAlexW4306367129

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.