Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster display session: Breast cancer - early stage, locally advanced & metastatic, CNS tumours, Developmental therapeutics, Genitourinary tumours - prostate & non-prostate, Palliative care, Psycho-oncology, Public health policy, Sarcoma, Supportive care

5229 - SAMANTHA: A European Registry Study to Prospectively Observe Treatment Patterns and Outcomes in Participants with HER2-Positive Unresectable Locally Advanced (LA) or Metastatic Breast Cancer (mBC)

Date

22 Oct 2018

Session

Poster display session: Breast cancer - early stage, locally advanced & metastatic, CNS tumours, Developmental therapeutics, Genitourinary tumours - prostate & non-prostate, Palliative care, Psycho-oncology, Public health policy, Sarcoma, Supportive care

Topics

Targeted Therapy

Tumour Site

Breast Cancer

Presenters

Guenther Steger

Citation

Annals of Oncology (2018) 29 (suppl_8): viii90-viii121. 10.1093/annonc/mdy272

Authors

G.G. Steger1, F. Puglisi2, C. Timcheva3, L. Costa4, M. Casa-Nova5, D. Hitzl6, B. Dampier7, N. Lindegger8

Author affiliations

  • 1 Department Of Internal Medicine I, Division Of Oncology And Hematology, Medizinische Universität Wien, 1090 - Vienna/AT
  • 2 Department Of Clinical Oncology, IRCCS CRO di Aviano, National Cancer Institute, 33081 - Aviano/IT
  • 3 Clinic Of Medical Oncology, MHAT for Women Health Nadezhda OOD, 1330 - Sofia/BG
  • 4 Oncology Division, Hospital de Santa Maria, Centro Hospitalar de Lisboa Norte, Lissabon/PT
  • 5 Medical Oncology, Hospital Beatriz Angelo-Loures, 2674-514 - Loures/PT
  • 6 Medical Affairs, Roche Austria GmbH, 1121 - Vienna/AT
  • 7 Medical Affairs, Clinical research Consulting, 1220 - Vienna/AT
  • 8 Global Product Development, F. Hoffmann-La Roche AG - Switzerland, 4070 - Basel/CH

Resources

Login to access the resources on OncologyPRO.

If you do not have an ESMO account, please create one for free.

Abstract 5229

Background

Numerous treatment options are available to patients with HER2-positive (HER2+) breast cancer. The used drugs as well as the sequence in which they are used may vary between countries. Frequently used in unresectable LA/mBC is trastuzumab, usually proposed in various combinations, as well as pertuzumab, trastuzumab-emtasine, and lapatinib. Only limited data are available on the treatment patterns used in clinical practice. This study is part of a global umbrella study and will meet the need for real world data on treatment patterns and outcomes in HER2+ unresectable LA or mBC. A descriptive analysis may identify possible associations between patient characteristics, treatments and outcomes. The study will collect data for up to 8 years, thus as new treatments become available, the study will also offer a unique opportunity to gain insight into evolving treatment options.

Trial design

SAMANTHA is a prospective, multicenter non-interventional post authorization safety study designed to observe anti-cancer treatment regimens and clinical outcomes in participants with HER2+ unresectable LA/mBC for up to 8 years. Diagnosis of unresectable LA or mBC can be up to 6 months old prior to registry enrollment. Enrolled participants will receive treatment and clinical assessments for their HER2+ unresectable LA/mBC as determined by their treating physician, according to the standard of care and routine clinical practice at each site. Primary outcome measures are progression-free survival per anti-cancer treatment regimens assessed according to site-/country-specific medical practice and percentage of participants by different anti-cancer treatment regimens and treatment sequences. Secondary outcome measures include overall survival, duration of response per anti-cancer treatment regimens, percentage of participants with best overall response of complete response or partial response per anti-cancer treatment and total number of treatment regimens received by participants.

Clinical trial identification

NCT02913456, EUPAS22426, MO39146.

Legal entity responsible for the study

F. Hoffmann-La Roche Ltd.

Funding

F. Hoffmann-La Roche Ltd.

Editorial Acknowledgement

Disclosure

G.G. Steger: Honoraria and travel support: Roche Austria. F. Puglisi: Compensation for an advisory board: Roche. C. Timcheva: Travel support: Roche Bulgaria. L. Costa: Honoraria and travel support: Roche Portugal. D. Hitzl: Employee: Roche Austria. B. Dampier: Fees for services: Roche Austria. N. Lindegger: Employee: F.Hoffmann-La Roche. All other authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.