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Clinical Trial Summary

Vecchione et al showed that suppression of RANBP2 results in mitotic defects only in BRAF-like colon cancer (CC) cells, which leads to cell death. Mechanistically, RANBP2 silencing reduces microtubule outgrowth from the kinetochores, thereby inducing spindle perturbations, providing an explanation for the observed mitotic defects. Vinorelbine mimics RANPB2 silencing in BRAF-like and BRAFV600E CC cell lines.

These preclinical data represent a strong rationale to also explore the anti-tumor activity of vinorelbine in patients with advanced BRAF-like (both BRAFm and BRAF wild type) CC. Tumors having this gene signature are referred to as "BRAF-like" and have a similar poor prognosis irrespective of the presence of BRAF(V600E) mutation. Since vinorelbine is standard of care in advanced breast and NSCLC, there is ample experience with the dose and schedule as well as with the safety profile and supportive measures required to prevent side-effects.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03482362
Study type Interventional
Source The Netherlands Cancer Institute
Contact N Steeghs, MD, PhD
Phone +31(0)20-5129111
Email n.steeghs@nki.nl
Status Recruiting
Phase Phase 2
Start date March 1, 2018
Completion date March 1, 2020

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