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CompletedNCT00706069Updated Dec 15, 2009

Vinorelbine Oral Plus Capecitabine Combination In Metastatic Breast Cancer

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

Phase
Phase 1
Study type
Interventional
Enrollment
40
Allocation
Non-randomized
Ages
18 Years to 75 Years
Sex
Female
01

Study summary

This study will evaluate the toxicity and secondary the efficacy of the combination vinorelbine plus capecitabine in metastatic breast cancer patients

Read the detailed description

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)

02

Conditions studied

  • Metastatic Breast Cancer

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Keywords

  • Metastatic Breast Cancer
  • Vinorelbine oral
  • Capecitabine
03

In context

Breast Neoplasms

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 →

Lead sponsor

Hellenic Oncology Research Group is the lead sponsor of 57 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • Histologically confirmed metastatic breast cancer
  • Age 18-75 years
  • Bidimensionally measurable or evaluable disease
  • Performance status (PS) 0-2 (ECOG)
  • Patients with reproductive potential must use an adequate contraceptive method (e.g., abstinence, intrauterine device, oral contraceptives, barrier device with spermicide, or surgical sterilization) during treatment and for three months after completing treatment
  • Adequate liver (serum bilirubin \<1.5 times the upper normal limit, AST and ALT \<2.5 times the UNL in the absence of demonstrable liver metastases, or \<5 times the upper normal limit in the presence of liver metastases); adequate renal function (serum creatinine \<1.5 times the upper normal limit); and adequate bone marrow function(neutrophils ≥ 1.5x 109 /L, and platelets ≥ 100x 109 /L)
  • At least three weeks from completion of irradiation
  • Life expectancy ≥ 12 weeks
  • Patients able to take oral medication
  • written informed consent

Exclusion criteria

Exclusion Criteria:

  • Active infection
  • Brain metastases
  • History of significant cardiac disease (unstable angina, congestive heart failure, myocardial infarction within the previous 6 months, ventricular arrhythmias)
  • Malnutrition (loss of ≥ 20% of the original body weight)
  • Psychiatric illness or social situation that would preclude study compliance
  • Pregnant or lactating women
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    1

    Vinorelbine oral plus Capecitabine

    Drug: Vinorelbine oral · Drug: Capecitabine

Interventions

  • DrugVinorelbine oral

    Vinorelbine at dose levels of 30mg, 40mg, 50mg, 60mg oral every Monday, Wednesday and Friday

    Also known as: Navelbine oral

  • DrugCapecitabine

    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

06

What researchers measure

Primary outcomes

  1. Maximum Tolerated Dose (MTD) of vinorelbine oral plus capecitabine combination

    Time frame: Toxicity assessment at 1st cycle

  2. Dose Limited Toxicity (DLT) of vinorelbine oral plus capecitabine combination.

    Time frame: Toxicity assessment at 1st cycle

Secondary outcomes

  1. Response Rate

    Time frame: Response evaluation at 3rd and 6th cycle by CT's or MRI

07

Study locations

4 sites
  • University General Hospital of Alexandroupolis, Dept. of Medical Oncology
    Alexandroupolis, Greece
  • "IASO" General Hospital of Athens, 1st Dep of Medical Oncology
    Athens, Greece
  • "Marika Iliadis" Hospital of Athens, Dep of Medical Oncology
    Athens, Greece
  • University Hospital of Crete, Dep of Medical Oncology
    Heraklion, Greece
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 15, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00706069
Lead sponsor
Hellenic Oncology Research Group
Collaborators
University Hospital of Crete
First posted
Jun 27, 2008
Start date
Jun 2008
Primary completion
Jul 2009
Completion
Jul 2009
Last update
Dec 15, 2009

Study contacts

Nikos Malamos, MD
principal investigator · "Marika Iliadis" Hospital of Athens, Dep of Medical Oncology

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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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