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Association details:
Evidence:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

Evaluation of Cabazitaxel in Patients With Brain Metastasis Secondary to Breast Cancer and NSCLC

Excerpt:
...- Histologically confirmed 1) HER2-negative invasive breast carcinoma or 2) NSCLC...
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Go to data
Title:

Study of Cabazitaxel in Patients With Metastatic Breast Cancer Previously Treated With Taxanes

Excerpt:
...- Diagnosis of HER-2 negative (HER-2 ULN (the same limits also refer to patients with liver metastases)...
Trial ID:
More C2 evidence
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

Study assessing if a chemotherapy drug called Cabazitaxel is effective in Patients with certain type of breast cancer (HER2 negative) that has spread to brain that is un treatable.

Excerpt:
...• First or second line metastatic HER2 negative* breast cancer• Oligometastatic brain disease that is unsuitable for surgical resection and/or stereotactic radiosurgery • Age ≥18 years• ECOG performance status 0-2 • Diagnosis of metastatic HER2-negative breast cancer• At least one measurable target lesion (RECIST 1.0) in the brain (unsuitable for resection) identified by CT scan or MRI within 21 days of registration. ...
Less C2 evidence
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

Phase II study of cabazitaxel as second-line treatment in patients with HER-2 negative metastatic breast cancer previously treated with taxanes.

Published date:
05/16/2018
Excerpt:
...phase II trial was to evaluate the activity and safety of cabazitaxel as 2nd-line treatment, given on day 1 of a 21-day cycle, in patients with HER-2 negative metastatic breast cancer...In the 77 patients with evaluable treatment response, the ORR was 24.7% (1 complete and 18 partial responses). The disease-control rate was 58.4%, while the median DOR was 5.6 months (range 0.7-51.3). Within a median follow-up of 32.2 months, the median PFS was 3.7 months (95% CI 2.23-4.36), whereas the median OS was 15.2 months (95% CI 11.21-21.54).
DOI:
10.1200/JCO.2018.36.15_suppl.1089
Trial ID: