Clinical trial · Interventional
Adjuvant Capecitabine in Elderly Patients With Breast Cancer: a Phase II Study
NCT00263705CI-TRIAL-00004462completedPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Determination of guidelines regarding the use of adjuvant chemotherapy for early breast cancer in this population of Patients over 70 years old.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Elderly Patients | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Adjuvant capecitabine | Drug | — | UNRESOLVED |
| capecitabine in aduvant setting | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- capecitabine
- description
- capecitabine 2000 mg/m² daily
- interventionNames
- Drug: Adjuvant capecitabine
- Drug: capecitabine in aduvant setting
Primary outcomes (1)
- measure
- safety of capecitabine in ederly
- timeFrame
- 1 year
- description
- safety of capecitabine in ederly
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria:
1. Women aged ³70 years
2. Histologic diagnosis of early breast cancer for which the treating physician considers adjuvant chemotherapy to be beneficial. Recommended situations are for example:
* endocrine non responsive (ER- and PgR -) and pT\>1 cm, any T if N+ OR
* endocrine responsiveness doubtful (ER and/or PgR- or poor \[3 to-5 according to Harvey score (12) or £ 30% of positive cells by immunohistochemistry) and other risk factors (pT³2 cm or N+ or G3 or Her-2/neu positive, etc.) OR
* endocrine responsive (ER and PgR \> 5 according to Harvey score or \> 30% of positive cells by immunohistochemistry) and at least two risk factors (pT³ 2 cm, N+, G3, Her-2/neu positive, etc.) OR
* Very high risk (N\>3) any ER/PgR.
3. ECOG Performance status £ 1
4. No previous exposition to chemotherapy in the neoadjuvant setting
5. Adequate organ function including:
1. neutrophils ³ 1.5 x 109 /l
2. platelets ³100 x 109 / l
3. bilirubin \< 1.25 x upper normal limit for the institution
4. transaminases \< 2.5 x upper normal limit for the institution
5. calculated creatinine clearance of \> 30ml/min (using the Crockoft and Gault formula)
6. absence of
* symptomatic ventricular arrhythmias;
* clinically significant Congestive Heart Failure;
* clinical and/or ECG evidence of myocardial infarction within the last 12 months;
* Coronary artery disease requiring medication.
6. Absence of any psychological, familial or sociological condition or comorbidities that may affect compliance
7. Written informed consent obtained according to local ethics committee guidelines -
Exclusion Criteria:
N/A-References
Publications (0)
Data not yet available
No reference posted for this study.