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Phase 3 Completed N=770 Randomized Treatment

Trial of Vinflunine Plus Capecitabine in Advanced Breast Cancer

Source: ClinicalTrials.gov NCT01095003 ↗
Enrolled (actual)
770
Serious AEs
25.1%
Results posted
Sep 2019
Primary outcomePrimary: Progression Free Survival — 5.6; 4.3 Months — p=0.0426
◆ Published Evidence
Emerging
12citations · ~2 / year
Randomised phase III trial of vinflunine plus capecitabine versus capecitabine alone in patients with advanced breast cancer previously treated with an anthracycline and resistant to taxane.
Annals of oncology : official journal of the European Society for Medical Oncology · 2018 · Open access · Likely link

Summary

The increasing use of anthracyclines and taxanes in the adjuvant, neoadjuvant and first-line metastatic settings, led to a raise of patients presenting with metastatic breast cancer after treatment with these agents. Options for the treatment of patients who have progressed after an anthracycline and a taxane are limited. The high level of in-vitro synergy of vinflunine combined with 5-fluorouracil (5-FU) together with the good tolerance and the encouraging response rate observed while combining IV vinflunine to oral capecitabine make it a promising combination to investigate further in a phase III trial. This phase III trial will evaluate the effectiveness and the safety profile of such combination for the treatment of patient with advanced breast cancer previously treated with or resistant to anthracycline and taxane resistant.

Linked Publications

  • Randomised phase III trial of vinflunine plus capecitabine versus capecitabine alone in patients with advanced breast cancer previously treated with an anthracycline and resistant to taxane.
    Annals of oncology : official journal of the European Society for Medical Oncology · 2018 · 12 citations · Open access · Likely link

Outcome Measures

OutcomeResultp-value
PRIMARY
Progression Free Survival
5.6; 4.3 0.0426 sig
SECONDARY
Overall Survival
13.9; 11.7 0.7657
SECONDARY
Overall Response Rate (ORR)
22.9; 17.9 0.103
SECONDARY
Disease Control Rate
57.3; 47.9 0.0089 sig
SECONDARY
Duration of Response
57.3; 47.9

Eligibility Criteria

Inclusion Criteria

  • female patients
  • 21 years of age or older
  • histologically/cytologically confirmed carcinoma of the breast
  • documented locally recurrent or metastatic disease not amenable to curative surgery or radiotherapy
  • either one, two or three prior chemotherapy regimens
  • prior treatments including both an anthracycline and a taxane and patient no longer candidate for these drugs
  • measurable or non-measurable disease according to RECIST 1.1
  • Karnofsky performance score of at least 70 %
  • adequate haematological, hepatic and renal functions
  • ECG without clinically relevant abnormality

Exclusion Criteria

  • known or clinical evidence of brain metastasis or leptomeningeal involvement
  • pulmonary lymphangitis or symptomatic pleural effusion
  • any serious, concurrent uncontrolled medical disorder
  • history of second primary malignancy
  • preexisting motor/sensory peripheral neuropathy
  • known history of HIV infection
  • prior therapy with capecitabine and/or vinca-alkaloids
  • history of severe hypersensitivity to vinca alkaloids and/or to fluoropyrimidine or contra indication to any of these drugs
  • known or suspected dihydropyrimidine dehydrogenase (DPD) deficiency
  • pregnancy or breast feeding
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01095003) and the linked publication. Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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