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Metronomic Treatment With Daily Oral Vinorelbine as First-line Chemotherapy in Patients With Advanced/Metastatic Hormone Receptor Positive (HR+)/Human Epidermal Growth Factor Receptor 2 Negative (HER2-) Breast Cancer (VinoMetro)

J

Johannes Gutenberg University (JGU)

Status and phase

Completed
Phase 2

Conditions

Metastatic Breast Cancer

Treatments

Drug: Vinorelbine

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT03007992
2015-007

Details and patient eligibility

About

The purpose of the trial is to investigate the efficacy of metronomic treatment with daily oral vinorelbine in terms of clinical benefit rate based on local radiological assessment in patients with advanced/metastatic HR+/HER2- breast cancer resistant to endocrine therapy.

Full description

In terms of the chronic nature of advanced/metastatic breast cancer, there is a high medical need for new treatment options after failure of hormonal treatment that prolong the interval to the start of intensive cytotoxic therapy, which is commonly associated with impaired quality of life (QoL) and potentially serious side effects. In this respect, metronomic treatment with daily administration of oral vinorelbine could provide an efficacious treatment option with limited toxicities.

Accordingly, this national, multi-centre, open-label, single-arm phase II trial aims to investigate a truly metronomic schedule with daily oral vinorelbine in HR+/HER2-patients with metastatic breast cancer resistant to endocrine therapy, by assessing efficacy and safety. Oral vinorelbine will be administered at a daily dose of 30 mg (flat dose without any adaptation to body weight or body surface area) without breaks. Treatment will continue until disease progression, occurrence of unacceptable toxicity, patient's refusal or investigator's decision to stop the treatment.

In the course of the study, the following interim and final analyses will be done:

i) 1st interim analysis (safety): This analysis will be performed on the basis of 10 patients, who were initially included into the study and who are eligible for safety evaluation; frequency statistics of (serious) adverse events will be analysed.

ii) 2nd interim analysis (efficacy): This analysis will be performed at the completion of the 1st Simon stage.

iii) Final analysis (complete): This analysis will be performed after completion of the follow-up phase (6 months of follow-up after Last Patient Last Treatment).

Enrollment

9 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Written (personally dated and signed) informed consent prior to the performance of any trial specific procedure

  2. Absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and/or the follow-up schedule

  3. Female patient ≥ 18 years of age

  4. Eastern Cooperative Oncology Group (ECOG) performance status 0-1, which the investigator assesses as being stable at time of screening

  5. Estimated life expectancy ≥ 16 weeks

  6. Histologically confirmed adenocarcinoma of the breast

  7. Documented locally advanced or metastatic disease, previously untreated by palliative chemotherapy and not amenable to any curative treatment

  8. Hormone receptor positive disease determined by ≥ 1% positive stained cells for oestrogen and/or progesterone receptor by immunohistochemistry on the primary tumour or on a metastatic site

  9. HER2-negative disease assessed by 0-1+ immuno-histochemistry (IHC) or 2+ IHC with negative fluorescence in situ hybridization (FISH) or CISH) on the primary tumour or on a metastatic site

  10. Availability of archival (from the most recently obtained sample) or fresh tumour tissue from patients included in the trial for the analysis of relevant metronomic biomarkers; one tumour block (preferred) or a minimum of 12 (recommended: 15) unstained slides to be provided

  11. Relapse ≤ 12 months from end of adjuvant hormonal therapy or pro¬gres¬sion during/after ≥ 1 line of endocrine therapy in the metastatic set¬ting and/or no longer candidate for further endocrine therapy

  12. Prior (neo-)adjuvant chemotherapy is allowed, if the interval between end of chemotherapy and date of registration is > 12 months

  13. Prior treatment with everolimus and/or palbociclib in the frame of hormonal therapy is allowed

  14. Complete staging before registration (CT/MRI thorax and CT/MRI abdomen/pelvis ≤ 28 days before registration; bone scan ≤ 3 months before registration)

  15. Presence of ≥ 1 measurable lesion as per RECIST 1.1, which has not been previously irradiated

  16. Adequate bone marrow, hepatic and renal function as defined by the following laboratory values:

    • Absolute neutrophil count (ANC) ≥ 1,500/mm3
    • Platelet count ≥ 100,000/mm3
    • Haemoglobin ≥ 10 g/dL
    • Total serum bilirubin ≤ 1.5 x upper limit of normal (ULN) (≤ 3 x ULN in case of liver metasta¬s¬es)
    • Liver transaminases ≤ 2.5 x ULN (≤ 5 x ULN in case of liver metasta¬s¬es)
    • Alkaline phosphatase ≤ 5 x ULN
    • Creatinine ≤ 1.5 x ULN (creatinine clearance should be assessed based on the Cockcroft-Gault-formula in case of borderline values and should then be ≥ 50 ml/min)
  17. Women of childbearing potential must be using a medically accepted method of contraception to avoid pregnancy during 2 months preceding registration, throughout the study period and up to 3 months after last dose of study treatment in such a manner that the risk of pregnancy is minimised; reliable contraception comprises sexual abstinence, male sterilization or double barrier methods (e.g. a combination of male condom with diaphragm).

  18. Women of childbearing potential must have a negative serum or urine pregnancy test within 72 hours prior to start of study treatment

  19. Ability of the patient to understand the character and the individual consequences of this clinical trial.

Exclusion criteria

  1. No recovery to ≤ Grade (G)1 side effects (exception: alopecia) of any prior anti-neoplastic treatment

  2. Aggressive locally advanced or metastatic breast cancer disease requiring systemic combination therapy

  3. Known or suspected central nervous system (CNS) and/or leptomeningeal involvement

  4. Current peripheral neuropathy ≥ G2

  5. Dysphagia or inability to swallow oral medication

  6. Malabsorption syndrome or disease significantly affecting GI-function or major resection of the stomach or proximal small bowel that could affect absorption of oral vinorelbine

  7. Other serious illness or medical condition, such as but not limited to:

    • Clinically significant cardiac disease or impaired cardiac function (such as: congestive heart failure requiring treatment (NYHA ≥ II); eft ventricular ejection fraction (LVEF) < 50%; significant cardiac arrhythmia; atrial fibrillation; conduction abnormality such as congenital long QT syndrome or high grade/complete atrioventricular (AV)-blockage; acute coronary syndrome including myocardial infarction, unstable angina pectoris, coronary artery bypass graft, coronary angioplasty or stenting, if < 3 months prior to registration; QTcF > 480 msec at screening)
    • Uncontrolled hypertension (> 140/100 mmHg at rest (average of 3 consecutive readings))
    • Unstable diabetes mellitus
    • Uncontrolled hypercalcemia
    • Clinically significant active infections (current or within the last 2 weeks prior to registration)
    • Previous organ allograft
  8. Prior treatment with vinorelbine or other vinca alkaloids

  9. Concomitant endocrine therapy (e.g. tamoxifen, aromatase inhibitors, fulvestrant) for advanced breast cancer

  10. Concomitant use of yellow-fever vaccination or other attenuated life vaccine

  11. Concomitant treatment with strong CYP3A4-inhibitors or strong CYP3A4-inducers (discontinuation before registration is acceptable, if medically feasible and ethically acceptable)

  12. Necessity to undergo long-term oxygen therapy

  13. Major surgery ≤ 28 days prior to registration and/or no recovery from side effects of such therapy to baseline condition or ≤ G1

  14. Radiotherapy ≤ 28 days prior to registration, no recovery from side effects of such therapy to baseline condition or ≤ G1 and/or irradiation of ≥ 30% of bone marrow

  15. Known hypersensitivity to vinca alkaloids, soy, peanut or any of the excipients contained in the oral vinorelbine capsules

  16. Participation in another clinical trial with any investigational drug ≤ 30 days prior to registration

  17. History of another malignancy within the past 5 years prior to registration, except cured basal cell carcinoma of the skin or cured in-situ carcinoma of the cervix

  18. Pregnant or nursing (lactating) woman

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

9 participants in 1 patient group

Vinorelbine Oral
Experimental group
Description:
Test product: Navelbine® 20 mg / 30 mg soft capsules
Treatment:
Drug: Vinorelbine

Trial contacts and locations

8

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Data sourced from clinicaltrials.gov

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