Breast Cancer Clinical Trial
Official title:
A Retrospective, Observational Molecular Epidemiology Study of HER2 Expression in Patients With Early / Metastatic Breast Cancer in Saudi Arabia
| NCT number | NCT02954471 |
| Other study ID # | ML29903 |
| Secondary ID | |
| Status | Completed |
| Phase | |
| First received | |
| Last updated | |
| Start date | October 21, 2016 |
| Est. completion date | September 17, 2019 |
| Verified date | September 2019 |
| Source | Hoffmann-La Roche |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
This is a retrospective, multicenter study, consisting of chart review of Saudi Arabian participants diagnosed with breast cancer between 2007 and 2013 and with available human epidermal growth factor receptor 2 (HER2) testing. Data on survival will be collected through 2015.
| Status | Completed |
| Enrollment | 351 |
| Est. completion date | September 17, 2019 |
| Est. primary completion date | September 17, 2019 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Initially diagnosed with breast cancer - Has a proven result of HER2 testing by immunohistochemistry (IHC), fluorescent in situ hybridization (FISH) or any other in situ hybridization (ISH) method - Alive or not alive Exclusion Criteria: - Inconclusive, equivocal or unavailable result of HER2/neu overexpression by IHC and FISH |
| Country | Name | City | State |
|---|---|---|---|
| Saudi Arabia | King Fahad Specialist Hospital; Oncology | Dammam | |
| Saudi Arabia | King Faisal Specialist Hospital & Research Centre | Jeddah | |
| Saudi Arabia | National Guard King Abdulaziz Medical City; Oncology | Riyadh |
| Lead Sponsor | Collaborator |
|---|---|
| Hoffmann-La Roche |
Saudi Arabia,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Percentage of Participants With Positive HER2 Test Result | From January 2007 to December 2013 (Up to 7 years; assessed retrospectively) | ||
| Secondary | Percentage of Participants With Estrogen Receptor/Progesterone Receptor Positive Breast Cancer | From January 2007 to December 2013 (Up to 7 years; assessed retrospectively) | ||
| Secondary | Percentage of Participants by Type of First-line and Subsequent Treatment Regimens Used | From January 2007 to December 2013 (Up to 7 years; assessed retrospectively) | ||
| Secondary | Kaplan-Meier Estimate of Overall Survival (OS) | From January 2007 to December 2015 (Up to 9 years; assessed retrospectively) | ||
| Secondary | Kaplan-Meier Estimates of Progression-free Survival (PFS) as Assessed Using Response Evaluation Criteria in Solid Tumors (RECIST) | From January 2007 to December 2013 (Up to 7 years; assessed retrospectively) | ||
| Secondary | Percentage of Participants With Complete Response as Assessed Using RECIST | From January 2007 to December 2013 (Up to 7 years; assessed retrospectively) | ||
| Secondary | Percentage of Participants With Partial Response as Assessed Using RECIST | From January 2007 to December 2013 (Up to 7 years; assessed retrospectively) | ||
| Secondary | Percentage of Participants With Progressive Disease as Assessed Using RECIST | From January 2007 to December 2013 (Up to 7 years; assessed retrospectively) | ||
| Secondary | Percentage of Participants with Stable Disease as Assessed Using RECIST | From January 2007 to December 2013 (Up to 7 years; assessed retrospectively) | ||
| Secondary | Percentage of Participants With Adverse Events | From January 2007 to December 2013 (Up to 7 years; assessed retrospectively) |
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