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


Journal

The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837

Informations de publication

Date de publication:
02 2020
Historique:
received: 12 06 2019
accepted: 20 09 2019
entrez: 12 2 2020
pubmed: 12 2 2020
medline: 22 6 2021
Statut: ppublish

Résumé

Limited data exist describing real-world treatment of de novo and recurrent HER2-positive metastatic breast cancer (MBC). The 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. Among 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). Patients 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). 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.

Sections du résumé

BACKGROUND
Limited data exist describing real-world treatment of de novo and recurrent HER2-positive metastatic breast cancer (MBC).
MATERIALS AND METHODS
The 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.
RESULTS
Among 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).
CONCLUSION
Patients 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.

Identifiants

pubmed: 32043771
doi: 10.1634/theoncologist.2019-0446
pmc: PMC7011632
doi:

Substances chimiques

Receptor, ErbB-2 EC 2.7.10.1
Trastuzumab P188ANX8CK

Banques de données

ClinicalTrials.gov
['NCT01615068']

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e214-e222

Informations de copyright

© 2019 The Authors. The Oncologist published by Wiley Periodicals, Inc. on behalf of AlphaMed Press.

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Auteurs

Debu Tripathy (D)

Department of Breast Medical Oncology, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.

Adam Brufsky (A)

Hillman Cancer Center, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Melody Cobleigh (M)

Department of Internal Medicine, Rush University Medical Center, Chicago, Illinois, USA.

Mohammad Jahanzeb (M)

Florida Precision Oncology, a division of 21st Century Oncology, Boca Raton, Florida, USA.

Peter A Kaufman (PA)

Breast Oncology, Division of Hematology/Oncology, University of Vermont Cancer Center, University of Vermont Medical Center, Burlington, Vermont, USA.

Ginny Mason (G)

Inflammatory Breast Cancer Research Foundation, West Lafayette, Indiana, USA.

Joyce O'Shaughnessy (J)

Department of Medical Oncology, Baylor University Medical Center, Texas Oncology and U.S. Oncology, Dallas, Texas, USA.

Hope S Rugo (HS)

Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, California, USA.

Sandra M Swain (SM)

Georgetown Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.

Denise A Yardley (DA)

Sarah Cannon Research Institute and Tennessee Oncology, Nashville, Tennessee, USA.

Laura Chu (L)

Personalized Healthcare, Product Development, Genentech, Inc., South San Francisco, California, USA.

Haocheng Li (H)

U.S. Medical Affairs, F. Hoffmann-La Roche, Mississauga, Ontario, Canada.

Vincent Antao (V)

U.S. Medical Affairs, Genentech, Inc., South San Francisco, California, USA.

Sara A Hurvitz (SA)

David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.

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