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This observational study will evaluate the efficacy and safety of Avastin (bevacizumab) in combination with fluoropyrimidine-based chemotherapy in elderly patients (>/= 65 years of age) with newly diagnosed metastatic colorectal cancer. Patients will be followed until disease progression, death, withdrawal of consent, discontinuation of physician-patient relationship or study closure, whichever comes first.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Cohort |
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| Measure | Description | Time Frame |
|---|---|---|
| Median progression-free survival | approximately 3.5 years |
| Measure | Description | Time Frame |
|---|---|---|
| Overall response rate (complete response + partial response) | approximately 3.5 years | |
| Clinical benefit rate (complete response + partial response + stable disease) | approximately 3.5 years | |
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Inclusion Criteria:
Exclusion Criteria:
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Elderly patients (\
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| Name | Affiliation | Role |
|---|---|---|
| Clinical Trials | Hoffmann-La Roche | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Budapest | 1145 | Hungary |
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| ID | Term |
|---|---|
| D015179 | Colorectal Neoplasms |
| ID | Term |
|---|---|
| D007414 | Intestinal Neoplasms |
| D005770 | Gastrointestinal Neoplasms |
| D004067 | Digestive System Neoplasms |
| D009371 | Neoplasms by Site |
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| Metastasectomy rate |
| approximately 3.5 years |
| Mean duration of Avastin treatment | approximately 3.5 years |
| Safety: Incidence of adverse events | approximately 3.5 years |
| Median progression-free survival in subgroup receiving Avastin plus fluorouracil monotherapy | approximately 3.5 years |
| Median progression-free survival according to age group (65-74 years; >/= 75 years) | approximately 3.5 years |
| D009369 | Neoplasms |
| D004066 | Digestive System Diseases |
| D005767 | Gastrointestinal Diseases |
| D003108 | Colonic Diseases |
| D007410 | Intestinal Diseases |
| D012002 | Rectal Diseases |