Journal of Clinical Oncology, Vol 16, 3524-3527, Copyright © 1998 by American Society of Clinical Oncology
Tirapazamine with cisplatin in patients with advanced non-small-cell lung cancer: a phase II study
J Treat, E Johnson, C Langer, C Belani, B Haynes, R Greenberg, R Rodriquez, P Drobins, W Miller Jr, L Meehan, A McKeon, J Devin, R von Roemeling and J Viallet
Allegheny University of the Health Sciences, Hahnemann Division, Philadelphia, PA 19104, USA.
PURPOSE: A phase II study was conducted to evaluate the safety and efficacy
of tirapazamine combined with cisplatin for the treatment of patients with
advanced non-small-cell lung cancer (NSCLC). PATIENTS AND METHODS:
Forty-four patients with stage IIIB/IV NSCLC were treated with a
combination of tirapazamine and cisplatin. Patients received tirapazamine
260 mg/m2 administered intravenously over 2 hours, followed 1 hour later by
cisplatin 75 mg/m2 administered over an additional hour, repeated every 21
days. The duration of therapy was meant to be limited to four cycles for
nonresponders and eight cycles for responders. RESULTS: Ten of 44 patients
(23%) showed a partial response. The estimated median survival for all
patients was 37 weeks. Toxicities were treatable and included grade 3
nausea or vomiting (25%), fatigue (27.3%), and muscle cramps (4.5%). No
dose reductions were necessary. CONCLUSION: The results show that
tirapazamine can safely be added to cisplatin. Both the median survival and
response rate observed strongly suggest that tirapazamine with cisplatin is
more active than cisplatin alone.
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