Annals of Oncology 7:867-869, 1996
© 1996 European Society for Medical Oncology
brief-report |
Phase II study on mitoxantrone in adenoid cystic carcinomas of the head and neck
1Department of Medical Oncology, Rotterdam Cancer Institute (Daniel den Hoed Kliniek) and University Hospital Rotterdam
2University Hospital St. Radboud Nijmegen
3University Hospital Utrecht
4University Hospital Vrije Universiteit Amsterdam, The Netherlands
5University Hospital St. Raphael Louvain
6Institute Jules Bordet Brussels, Belgium
7Netherlands Cancer Institute Amsterdam, The Netherlands
8Istituto Regina Elena Rome, Italy
9EORTC Data Center Brussels, Belgium
10Centre Oscar Lambret Lille, France
Correspondence to: Jaap Verweij, MD, PhD Department of Medical Oncology Rotterdam Cancer Institute Dr. Daniel den Hoed Kliniek Groene Hilledijk 301 3075 EA Rotterdam The Netherlands
BACKGROUND:: Based on activity in a case report, mitoxantrone was studied in a phase II study in adenoid cystic carcinoma.
PATIENTS AND METHODS:: Patients with symptomatic and/or rapidly progressive metastatic or recurrent adenoid cystic carcinoma were eligible for this study. They were treated with mitoxantrone given intravenously by bolus injection at a dose of 14 mg/m2, cycles repeated every 3 weeks.
RESULTS:: Thirty-six chemotherapy-naive patients entered on trial, 4 were ineligible. A median of 6 cycles per patient were given. Leucocytopenia (in 97% of patients) was the most important side effect and tended to be cumulative. Other side effects were mainly mild to moderate and consisted of nausea (62%), vomiting (29%), alopecia (53%) and mucositis (41%). Four of 32 patients had a partial response (12%; 95% CI 4%29%) lasting 313 months, 22 patients (69%) had a stable disease.
CONCLUSIONS:: Mitoxantrone at this dose and schedule has modest activity in adenoid cystic carcinomas.
adenoid cystic carcinoma, mitoxantrone, phase II study
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