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Phase II study of teniposide in adenocarcinoma of the lung

Summary

A total of 26 evaluable patients with previously untreated, non-resectable adenocarcinoma of the lung were given 80 mg/m2 i.v. teniposide daily for 5 days every 3 weeks. Three partial responses (11%) were obtained that lasted for 12, 11 and 32 weeks, respectively. Leucopenia was the dose-limiting side effect, with WBC counts of <2×109/l being observed in 42% of patients, resulting in one septic death. At the dose and schedule used in the present study, teniposide showed only limited activity in adenocarcinoma of the lung.

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Correspondence to Jens Benn Sørensen.

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Sørensen, J.B., Bach, F., Dombernowsky, P. et al. Phase II study of teniposide in adenocarcinoma of the lung. Cancer Chemother. Pharmacol. 27, 487–489 (1991). https://doi.org/10.1007/BF00685166

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Keywords

  • Adenocarcinoma
  • Cancer Research
  • Partial Response
  • Evaluable Patient
  • Limited Activity