A Phase 1 interventional study of Vinorelbine oral and Capecitabine in Metastatic Breast Cancer, sponsored by Hellenic Oncology Research Group. Completed at 4 sites in Greece. Open to female participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2009-12-15.
Sponsored by Hellenic Oncology Research Group · Phase 1, Interventional, and Treatment
This study will evaluate the toxicity and secondary the efficacy of the combination vinorelbine plus capecitabine in metastatic breast cancer patients
The combination capecitabine-vinorelbine, with iv administration of vinorelbine, has been studied in a phase [I]/[II], with favourable profile of toxicity in pretreated patients with anthracyclines and/or taxanes (Oncology News International vol 12, no 3, suppl 2, 2003).
In a study of toxicity and effectiveness, Vanhopher reported objective response rates (PR) in 21 from 45 patients (47%) and stabilization of disease (SD) in 16 patients (36%). Severe leucopenia (grade 4), was reported in 5% of patients (Borquez D, et al: Proc Am Soc Clin Oncol 19: Abstract 420, 2000)
12,544 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.
This study's planned enrollment of 40 is below the median of 72 across 9,303 interventional studies indexed under Breast Neoplasms.
Browse Breast Neoplasms studies →Hellenic Oncology Research Group is the lead sponsor of 57 studies on the registry; none are open to participants now.
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Exclusion Criteria:
Vinorelbine oral plus Capecitabine
Drug: Vinorelbine oral · Drug: Capecitabine
Vinorelbine at dose levels of 30mg, 40mg, 50mg, 60mg oral every Monday, Wednesday and Friday
Also known as: Navelbine oral
Capecitabine at dose levels of 800 mg/m2, 950mg/m2, 1100mg/m2, 1250mg/m2 per os from day 1 to day 14 every 21 days
Also known as: Xeloda
Maximum Tolerated Dose (MTD) of vinorelbine oral plus capecitabine combination
Time frame: Toxicity assessment at 1st cycle
Dose Limited Toxicity (DLT) of vinorelbine oral plus capecitabine combination.
Time frame: Toxicity assessment at 1st cycle
Response Rate
Time frame: Response evaluation at 3rd and 6th cycle by CT's or MRI
This study is completed, as verified in Dec 2009. You cannot join it, but the record below documents what was studied.
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Hellenic Oncology Research Group