Phase II trial of esorubicin (4′deoxydoxorubicin, DxDx) in patients with small cell lung cancer
✍ Scribed by James R. Rigas; Mark G. Kris; Richard J. Gralla; Robert T. Heelan; Linda D. Marks
- Publisher
- Springer US
- Year
- 1991
- Tongue
- English
- Weight
- 264 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0167-6997
No coin nor oath required. For personal study only.
✦ Synopsis
Esorubicin (4'-deoxydoxorubicin or DxDx) is an analog of doxorubicin with preclinical antitumor activity and no significant cardiotoxicity in model systems. Eleven patients with small cell lung cancer who had previously received chemotherapy were given esorubicin (25 mg/m 2 intravenously) every 3 weeks. No major objective responses were observed (95% confidence limits: 0-25%). Nine of the 11 patients had grade 2 or greater toxicity, with 55~ of the patients experiencing grade 3 or greater toxicity [myelosuppression (4/11), anemia (2/11) or elevated liver enzymes (3/11)]. Nausea, vomiting, alopecia and intravenous site phlebitis were also seen. Three of the 11 patients received 3 or more course of esorubicin without evidence of significant cardiotoxicity. At this dose and shedule, no significant antitumor response were seen in this population of patients. Esorubicin, with this low response rate and significant toxicity, appears to be of limited utility in this disease.
📜 SIMILAR VOLUMES
A phase II trial of 4' Deoxydoxorubicin (DXDX) was conducted in unresectable previously untreated non-small cell lung cancer patients. DXDX was administered every 3 weeks by short intravenous infusion at a starting dose of 30 mg/m2, with dose escalation to 40 mg/m2 toxicity permitting. Four response