Evidence map›Paper›PMID 32043771›Full record

Observational studyThe oncologist2020

De Novo Versus Recurrent HER2-Positive Metastatic Breast Cancer: Patient Characteristics, Treatment, and Survival from the SystHERs Registry.

Debu Tripathy, Adam Brufsky, Melody Cobleigh, Mohammad Jahanzeb, Peter A Kaufman, Ginny Mason, Joyce O'Shaughnessy, Hope S Rugo, Sandra M Swain, Denise A Yardley and 4 more

Registry-linked trialOpen access · bronzeAbstract readObservational Study
In one paragraph

Observational study in The oncologist, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01615068 (An Observational Cohort Study of Treatment Patterns and Outcomes in Patients With HER2 Positive), which is not on this map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.2field-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.

NCT01615068 completednot on this map

An Observational Cohort Study of Treatment Patterns and Outcomes in Patients With HER2 Positive (HER2+) Metastatic Breast Cancer (SystHERs Registry (Systemic Therapies for HER2+ Metastatic Breast Cancer Study)).

TypeobservationalSponsorGenentech, Inc.Ran2012 to 2017Enrolled1,007ConditionsBreast Cancer
3 · Its place in the literature

Who cites it

39 citing papers in PubMed, 68 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Advances in Targeting HER2 across Cancer Subtypes: A Pan-Tumor Approach.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. HER2-Positive Breast Cancer Treatment and Resistance.Advances in experimental medicine and biology · 2025
    Review
  13. Observational
  14. Article
  15. Article
  16. Personalized treatment approach for HER2-positive metastatic breast cancer.Medical oncology (Northwood, London, England) · 2024
    Review
  17. Article
  18. Review
  19. Article
  20. De Novo Oligometastatic Breast Cancer.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 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

14 authors at 12 institutions in 2 countries.

Debu TripathyDepartment of Breast Medical Oncology, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID 0000-0002-5711-2404
Adam BrufskyHillman Cancer Center, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
Melody CobleighDepartment of Internal Medicine, Rush University Medical Center, Chicago, Illinois, USA.
Mohammad JahanzebFlorida Precision Oncology, a division of 21st Century Oncology, Boca Raton, Florida, USA.
Peter A KaufmanBreast Oncology, Division of Hematology/Oncology, University of Vermont Cancer Center, University of Vermont Medical Center, Burlington, Vermont, USA.
Ginny MasonInflammatory Breast Cancer Research Foundation, West Lafayette, Indiana, USA.
Joyce O'ShaughnessyDepartment of Medical Oncology, Baylor University Medical Center, Texas Oncology and U.S. Oncology, Dallas, Texas, USA.
Hope S RugoHelen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, California, USA.
Sandra M SwainGeorgetown Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.
Denise A YardleySarah Cannon Research Institute and Tennessee Oncology, Nashville, Tennessee, USA.
Laura ChuPersonalized Healthcare, Product Development, Genentech, Inc., South San Francisco, California, USA.
Haocheng LiU.S. Medical Affairs, F. Hoffmann-La Roche, Mississauga, Ontario, Canada.
Vincent AntaoU.S. Medical Affairs, Genentech, Inc., South San Francisco, California, USA.
Sara A HurvitzDavid Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.
21st Century Oncology (United States) · USBreast Cancer Research Foundation · USGeorgetown University · USRoche (Canada) · CARush University Medical Center · USTennessee Oncology · USTexas Oncology · USThe University of Texas MD Anderson Cancer Center · USUCSF Helen Diller Family Comprehensive Cancer Center · USUniversity of California, Los Angeles · USUniversity of Pittsburgh Medical Center · USUniversity of Vermont Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLimited data exist describing real-world treatment of de novo and recurrent HER2-positive metastatic breast cancer (MBC). MATERIALS AND

methodsThe Systemic Therapies for HER2-Positive Metastatic Breast Cancer Study (SystHERs) was a fully enrolled (2012-2016), observational, prospective registry of patients with HER2-positive MBC. Patients aged ≥18 years and ≤6 months from HER2-positive MBC diagnosis were treated and assessed per their physician's standard practice. The primary endpoint was to characterize treatment patterns by de novo versus recurrent MBC status, compared descriptively. Secondary endpoints included patient characteristics, progression-free and overall survival (PFS and OS, by Kaplan-Meier method; hazard ratio [HR] and 95% confidence interval [CI] by Cox regression), and patient-reported outcomes.

resultsAmong 977 eligible patients, 49.8% (n = 487) had de novo and 50.2% (n = 490) had recurrent disease. A higher proportion of de novo patients had hormone receptor-negative disease (34.9% vs. 24.9%), bone metastasis (57.1% vs. 45.9%), and/or liver metastasis (41.9% vs. 33.1%), and a lower proportion had central nervous system metastasis (4.3% vs. 13.5%). De novo patients received first-line regimens containing chemotherapy (89.7%), trastuzumab (95.7%), and pertuzumab (77.8%) more commonly than recurrent patients (80.0%, 85.9%, and 68.6%, respectively). De novo patients had longer median PFS (17.7 vs. 11.9 months; HR, 0.69; 95% CI, 0.59-0.80; p < .0001) and OS (not estimable vs. 44.5 months; HR, 0.55; 95% CI, 0.44-0.69; p < .0001).

conclusionPatients with de novo versus recurrent HER2-positive MBC exhibit different disease characteristics and survival durations, suggesting these groups have distinct outcomes. These differences may affect future clinical trial design. Clinical trial identification number. NCT01615068 (clinicaltrials.gov). IMPLICATIONS FOR PRACTICE: SystHERs was an observational registry of patients with HER2-positive metastatic breast cancer (MBC), which is a large, modern, real-world data set for this population and, thereby, provides a unique opportunity to study patients with de novo and recurrent HER2-positive MBC. In SystHERs, patients with de novo disease had different baseline demographics and disease characteristics, had superior clinical outcomes, and more commonly received first-line chemotherapy and/or trastuzumab versus those with recurrent disease. Data from this and other studies suggest that de novo and recurrent MBC have distinct outcomes, which may have implications for disease management strategies and future clinical study design.

Indexed as

Breast NeoplasmsAdolescentAdultAntineoplastic Combined Chemotherapy ProtocolsErb-b2 Receptor Tyrosine KinasesFemaleHumansNeoplasm MetastasisNeoplasm Recurrence, LocalRegistriesTrastuzumabTreatment OutcomeErb-b2 Receptor Tyrosine KinasesTrastuzumabDe novoHER2-positive metastatic breast cancerRecurrentRegistrySystHERs

Identifiers

PMID32043771
PMCPMC7011632
OpenAlexW2979515484

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.