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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02913456
Other study ID # MO39146
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 16, 2016
Est. completion date January 31, 2024

Study information

Verified date March 2024
Source Hoffmann-La Roche
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This disease registry is a prospective, multicenter non-interventional study designed to observe anti-cancer treatment regimens and clinical outcomes in participants with HER2-positive unresectable LA/mBC. Diagnosis of unresectable LA or mBC can be up to 6 months old prior to registry enrollment.


Recruitment information / eligibility

Status Completed
Enrollment 629
Est. completion date January 31, 2024
Est. primary completion date January 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Initially diagnosed with HER2-positive unresectable LA/mBC no more than 6 months prior to enrollment, although they can have received anti-cancer treatment during that time Exclusion Criteria: - Not applicable

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Austria Lkh-Univ. Klinikum Graz; Klinik Für Gynäkologie Graz
Austria LKH-UNIV. KLINIKUM GRAZ; Klinische Abteilung für Onkologie Graz
Austria Klinikum Klagenfurt; Abt. f. Hämatologie u. internistische Onkologie Klagenfurt
Austria LKH Hochsteiermark; Abt. für Hämato-Onkologie Leoben
Austria Ordensklinikum Linz Elisabethinen ; I. INTERNE ABT. Linz
Austria A.Ö. Krankenhaus Der Barmherzigen Schwestern Ried; Interne Abtl. Ried-innkreis
Austria A.Ö. Lhk Villach; Abt. Für Gynäkologie Villach
Austria Hanusch-Krankenhaus; Geburtshilfliche und Gynäkologische Abteilung Wien
Austria Medizinische Universität Wien; Univ.Klinik für Frauenheilkunde - Klinik für Gynäkologie Wien
Austria Medizinische Universität Wien; Univ.Klinik für Innere Medizin I Wien
Austria Landesklinikum Wiener Neustadt; Innere Medizin, Hämatologie u. internistische Onkologie Wiener Neustadt
Bulgaria Complex Oncological Center - Plovdiv, EOOD Plovdiv
Bulgaria Multiprofile Hospital for Active Treatment Central Onco Hospital OOD Plovdiv
Bulgaria Mdozs - Russe Ruse
Bulgaria Complex Oncology Center-Burgas; Medical Oncology Sofia
Bulgaria MHAT Nadezhda Sofia
Bulgaria SHATOD - Sofia Sofia
Bulgaria Tokuda Hospital; Medical Oncology Department Sofia
Bulgaria University Multiprofile Hospital for Active Treatment Tsaritsa Yoanna - ISUL EAD Sofia
Bulgaria District Oncology Dispensary; Dept of Chimiotherapy Stara Zagora
Bulgaria District Oncology Dispensary Wit Stationary Varna
Bulgaria Comprehensive Oncology Center - Vratsa Vratza
Italy A.O.U. Ospedali Riuniti Umberto I-G.M.Lancisi-G.Salesi Ancona;S.O.D. MED.Interna-Clinica Oncologica Ancona Marche
Italy RCCS - Centro di Riferimento; Oncologia Medica B Aviano (PN) Friuli-Venezia Giulia
Italy Irccs Ist. Tumori Giovanni Paolo Ii; Dipartimento Oncologia Medica Bari Puglia
Italy Ospedale Barletta - Mons. Dimiccoli; Dip. Oncologia Barletta Puglia
Italy Az. Osp. Spedali Civili; Divisione Di Oncologia - Iii Medicina Brescia Lombardia
Italy Ospedale Civile; Oncologia Medica Camposampiero Veneto
Italy Ospedale Cannizzaro, Oncologia Catania Sicilia
Italy Azienda Ospedaliero Universitaria di Ferrara - U.O. Di Oncologia Cona (FE) Veneto
Italy Azienda Ospedaliero-Universitaria Careggi; SOD Radioterapia Firenze Toscana
Italy Ospedale S. Maria Goretti; Divisione Di Oncologia Medica Latina Lazio
Italy Azienda ULSS 21 Ospedale Mater Salutis; Dip. di Oncologia Legnago (VR) Veneto
Italy Ospedale San Luca; Oncologia Lucca Toscana
Italy A.O. Universitaria Policlinico Di Modena; Oncologia Modena Emilia-Romagna
Italy Casa Di Cura Di Alta Specialita La Maddalena; Dept. Oncologico Di Iii Livello Palermo Sicilia
Italy Ospedale Degli Infermi Di Biella; Reparto Oncologia Medica Ponderano (BI) Piemonte
Italy Azienda Ospedaliera Di Perugia Ospedale s. Maria Della Misericordia; Oncologia Medica Sant'Andrea Delle Fratte (PG) Umbria
Italy Ospedale S.S. Trinità Nuovo; Divisione Oncologia Sora Lazio
Italy A.O.U. Integrata Verona - Policlinico G.B. Rossi; Oncologia Medica - Dip. di Medicina Verona Veneto
Italy Ospedale Belcolle Di Viterbo; Oncologia Viterbo Lazio
Portugal Hospital Garcia de Orta; Servico de Oncologia Medica Almada
Portugal IPO de Coimbra; Servico de Oncologia Medica Coimbra
Portugal Hospital de Santa Maria; Servico de Oncologia Medica Lisboa
Portugal Hospital Santo Antonio dos Capuchos;Servico de Oncologia Medica Lisboa
Portugal Hospital Beatriz Angelo; Departamento de Oncologia Loures
Portugal IPO do Porto; Servico de Oncologia Medica Porto
Romania County Hospital Alba; Oncology Alba Iulia
Romania "Filantropia" Clinical Hospital; Gynecological Oncology Bucharest
Romania Institutul Oncologic Prof. Dr. Al. Trestioreanu Bucuresti Bucuresti
Romania Prof. Dr. I. Chiricuta Institute of Oncology Cluj Napoca
Romania Cluj-Napoca Emergency Clinical County Hospital; Medical Oncology Cluj-Napoca
Romania Centrul de Oncologie Sfantul Nectarie Craiova
Romania Oncomed SRL Timisoara

Sponsors (1)

Lead Sponsor Collaborator
Hoffmann-La Roche

Countries where clinical trial is conducted

Austria,  Bulgaria,  Italy,  Portugal,  Romania, 

Outcome

Type Measure Description Time frame Safety issue
Primary Progression-free Survival per Anti-cancer Treatment Regimens Assessed According to Site-/Country-Specific Medical Practice Baseline up to 8 years
Primary Percentage of Participants by Different Anti-cancer Treatment Regimens and Treatment Sequences Baseline up to 8 years
Secondary Overall Survival Baseline up to 8 years
Secondary Duration of Response per Anti-cancer Treatment Regimens Assessed According to Site-/Country-Specific Medical Practice Baseline up to 8 years
Secondary Percentage of Participants with Best Overall Response of Complete Response (CR) or Partial Response (PR) per Anti-cancer Treatment Regimens Assessed According to Site-/Country-Specific Medical Practice Baseline up to 8 years
Secondary Total Number of Treatment Regimens Received by Participants Baseline up to 8 years
Secondary Percentage of Participants with Adverse Events (AEs), Serious AEs, and Protocol-defined AEs of Special Interest Baseline up to 8 years
Secondary Percentage of Participants with HER2 Re-testing of Metastases Baseline up to 8 years
Secondary Percentage of Participants with Change in HER2 Status Baseline up to 8 years
Secondary Percentage of Participants by Type of HER2 Testing (Immunohistochemistry and/or Fluorescence In situ Hybridization [FISH]) Baseline up to 8 years
Secondary Percentage of Participants with Different Anti-Cancer Treatment Regimens by Country Baseline up to 8 years
Secondary Percentage of Participants with History of Breast Cancer by Different Anti-Cancer Treatment Regimens Baseline up to 8 years
Secondary EuroQol 5-Dimensions Questionnaire (EQ-5D) Score Baseline up to 8 years
Secondary Functional Assessment of Cancer Therapy-Breast (FACT-B) Questionnaire Score Baseline up to 8 years
Secondary Total Healthcare Cost Baseline up to 8 years
Secondary Cost of Treating Associated AEs Baseline up to 8 years
Secondary Resource Utilization: Percentage of Participants with Breast Cancer Associated Procedures Baseline up to 8 years
Secondary Resource Utilization: Percentage of Participants with Hospitalization Baseline up to 8 years
Secondary Resource Utilization: Percentage of Participants with Emergency Room Attendances and Outpatient Visits Baseline up to 8 years
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