Phase I study of 21 days continuous infusion with vindesine
1989

Continuous Infusion of Vindesine for 21 Days

Sample size: 4 publication Evidence: low

Author Information

Author(s): E.G.E. de Vries, E.F. Smit, D.E.M.M. Vendrig, J.J.M. Holthuis, N.H. Mulder

Primary Institution: University Hospital Groningen

Hypothesis

Can continuous infusion of vindesine improve therapeutic outcomes without increasing toxicity?

Conclusion

The study concluded that vindesine cannot be safely administered for 21 days at the low dose of 0.2 mg/m²/day due to severe neurotoxicity.

Supporting Evidence

  • Neurotoxicity was the major complication leading to drug withdrawal in three patients.
  • Patients experienced pain and muscle weakness during treatment.
  • After stopping the treatment, muscle strength was regained in all patients.

Takeaway

Doctors tried giving a cancer drug called vindesine continuously for 21 days, but it made some patients very sick, so they decided it wasn't safe.

Methodology

The study involved a 21-day continuous infusion of vindesine using an ambulatory pump, with toxicity evaluated at multiple time points.

Limitations

The study had a small sample size and was limited to patients who met specific eligibility criteria.

Participant Demographics

Patients aged 21-75 years with no prior treatment with vinca alkaloids.

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication