TCNU in adenocarcinoma of the lung: A Phase II study with divided doses
- 1 July 1990
- journal article
- research article
- Published by Elsevier in Annals of Oncology
- Vol. 1 (4) , 299-300
- https://doi.org/10.1093/oxfordjournals.annonc.a057753
Abstract
TCNU, a new water soluble nitrosourea, has in preclinical studies shown higher activity when given as divided doses compared with one day single treatment. Accordingly, 38 consecutive patients with non-resectable adenocarcinoma of the lung received TCNU 40 mg/m2 p.o. daily for three days every 4 weeks. The response rate among 37 evaluable patients was 14%, median response duration was 17 weeks (range 5–57+ weeks) and median survival 22 weeks (range 3–96+ weeks). Hematologic toxicity was pronounced, especially thrombocytopenia, and 57% of the patients had WHO grade 3 or 4 WBC or platelet count. Overall, dose reduction or delay of treatment due to hematologic toxicity was necessary in 66% of the patients. This, together with the limited activity, renders TCNU in the present dose and schedule unsuitable for further investigations in this disease entity.Keywords
This publication has 3 references indexed in Scilit:
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- Phase I study of TCNU, a novel nitrosoureaEuropean Journal of Cancer and Clinical Oncology, 1987
- A phase I clinical evaluation of 1-(2-chloroethyl)-3-[2-(dimethylaminosulphonyl)ethyl]-1-nitrosourea (TCNU)European Journal of Cancer and Clinical Oncology, 1987