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Trial record 1 of 1 for:    NCT01615068
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An Observational Study in Patients With HER2 Positive Metastatic Breast Cancer (SystHERs Registry)

This study is ongoing, but not recruiting participants.
Sponsor:
Information provided by (Responsible Party):
Genentech, Inc.
ClinicalTrials.gov Identifier:
NCT01615068
First received: June 6, 2012
Last updated: June 29, 2017
Last verified: June 2017
June 6, 2012
June 29, 2017
June 5, 2012
August 28, 2020   (Final data collection date for primary outcome measure)
Distribution of patients receiving unique treatment regimen/sequence of treatment regimens [ Time Frame: Up to 8 years ]
Same as current
Complete list of historical versions of study NCT01615068 on ClinicalTrials.gov Archive Site
  • Progression-free survival (PFS) [ Time Frame: Up to 8 years ]
  • Overall survival (OS) [ Time Frame: Up to 8 years ]
  • Post-progression survival (PPS) [ Time Frame: Up to 8 years ]
  • Time-to-treatment failure (TTF) [ Time Frame: Up to 8 years ]
  • Response rate (RR) [ Time Frame: Up to 8 years ]
  • Safety: Incidence of adverse events [ Time Frame: Up to 8 years ]
  • Patient-reported outcome assessment (PRO) [ Time Frame: Up to 8 years ]
Same as current
Not Provided
Not Provided
 
An Observational Study in Patients With HER2 Positive Metastatic Breast Cancer (SystHERs Registry)
An Observational Cohort Study Of Treatment Patterns And Outcomes In Patients With HER2 Positive (Her2+) Metastatic Breast Cancer (SystHERs Registry (Systematic Therapies for HER2+ Metastatic Breast Cancer Study)).
This multi-center, prospective observational study will evaluate the treatment patterns, and the safety in patients with HER2-positive (HER2+) metastatic breast cancer (MBC). Eligible patients will have an initial metastatic breast cancer diagnosis that has not been previously treated with systemic therapy; patients may be enrolled up to 6 months after the diagnosis. Data will be collected for up to 8 years.
Not Provided
Observational
Observational Model: Cohort
Time Perspective: Prospective
Not Provided
Retention:   Samples With DNA
Description:
Tissue and whole blood samples
Probability Sample
Patients with HER2 positive (HER2+) metastatic breast cancer
Breast Cancer
Not Provided
Cohort
Tripathy D, Rugo HS, Kaufman PA, Swain S, O'Shaughnessy J, Jahanzeb M, Mason G, Beattie M, Yoo B, Lai C, Masaquel A, Hurvitz S. The SystHERs registry: an observational cohort study of treatment patterns and outcomes in patients with human epidermal growth factor receptor 2-positive metastatic breast cancer. BMC Cancer. 2014 May 2;14:307. doi: 10.1186/1471-2407-14-307.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
1007
August 28, 2020
August 28, 2020   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Adult patients, >/=18 years of age
  • Initial diagnosis of HER2+ MBC, as diagnosed by the treating physician, no more than 6 months prior to study enrollment
  • Availability of cancer-specific historical data points in the patient's medical records

Exclusion Criteria:

  • Any inability to provide informed consent
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
United States
India
 
NCT01615068
ML28257
Not Provided
Not Provided
Not Provided
Genentech, Inc.
Genentech, Inc.
Not Provided
Study Director: Clinical Trials Genentech, Inc.
Genentech, Inc.
June 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP