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Pilot Study of Cabazitaxel and Paclitaxel in HER2 Negative Breast Cancer
Pilot Study of Cabazitaxel and Paclitaxel in HER2 Negative Breast Cancer

NCT03048942

CompletedPhase 2

Sponsor: University Hospitals Bristol and Weston NHS Foundation Trust

Conditions: HER2 Negative Metastatic Breast Cancer

Interventions: Cabazitaxel, Paclitaxel

Countries: United Kingdom

90 patients with HER2 negative breast cancer will be randomised to receive 18 weeks of chemotherapy treatment, either 6 cycles of 3 weekly Cabazitaxel or 6 cycles of weekly Paclitaxel to determine the difference in progression free survival between the 2 groups. If results at that stage suggest a potential benefit then the trial will be developed further to accrue 70 more patients.

Eligibility overview

Sex: FEMALE

Age: 18 Years to 99 Years

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria
Inclusion Criteria:

* Written informed consent
* Metastatic breast cancer fit to receive cytotoxic chemotherapy for metastatic disease
* Measurable disease as per RECIST 1.1
* HER2 negative defined as ICH 0+, 1+ or 2+ and FISH/SISH/CISH(ration\<2.0) in the case of IHC 2+
* ECOG performance status 0 or 1
* ER+ve or ER-ve
* Female age ≥18 years
* Anticipated life expectancy \> 6 months
* Haemoglobin \>10.0g/DL
* Absolute neutrophil count\>1.5 x 10\^9/L
* Platelet count\>100 x 10\^9/L
* ALT/SGPT\<1.5 X ULN
* Serum creatinine \<1.5 x ULN
* Negative pregnancy test for all women of child bearing potential

Exclusion Criteria:

* Grade ≥2 oral mucositis or peripheral or sensory neuropathy
* History of other malignancy
* History of severe hypersensitivity ≥grade 3 to polysorbate 80- containing drugs and taxanes
* Clinically significant cardiovascular disease
* Any acute or chronic medical condition
* Acute infection requiring systemic antibiotics or antifungal medication
* Sex hormones
* Administration of any live vaccine within 8 weeks
* Concurrent or planned treatment with strong inhibitors or strong inducers of cytochrome P450 3A4/5
* Participation in another clinical trial with an investigational drug within 30 days of randomisation
* Pregnant or breast feeding women
* Contraindications to the use of corticosteroid treatment
* HER2 Positive breast cancer
* Previous Paclitaxel chemotherapy in the adjuvant setting
* Previous cytotoxic chemotherapy for metastatic disease
* Palliative radiotherapy for metastatic disease within 4 weeks of randomisation
* Symptomatic brain metastases confirmed with CT/MRI brain
* History of other malignancy
* Grade 2
Locations (13)
  • Bath, United Kingdom
  • Blackpool, United Kingdom
  • Bristol, United Kingdom
  • Cardiff, United Kingdom
  • Exeter, United Kingdom
  • London, United Kingdom
  • London, United Kingdom
  • Newcastle, United Kingdom
  • Nottingham, United Kingdom
  • Plymouth, United Kingdom
  • Taunton, United Kingdom
  • Truro, United Kingdom
  • Worcester, United Kingdom