Abstract |
Twenty-six patients affected by acute leukemia were treated with 4-demethoxydaunorubicin ( idarubicin), a new anthracycline compound which in experimental leukemias showed an antitumoral activity superior to daunorubicin (DNR) and doxorubicin (DX), with a higher ratio of active to cardiotoxic doses. A group of 16 patients in relapse received idarubicin at a dosage of 5-6 mg/m2/day for 3 consecutive days; a second group of 6 relapsing and 4 previously untreated cases was treated with a sequential combination of idarubicin and arabinosyl cytosine. In all patients, a significant fall of bone marrow and peripheral blast cells was obtained. These preliminary results suggest that idarubicin has a therapeutic activity against human acute leukemias usually responsive to DNR or DX. The duration of myelosuppression varied from 7 to 50 days, leading in some cases to a high risk of infections. As regards other toxic effects (gastrointestinal, hepatic and acute cardiac toxicity, alopecia), idarubicin appears to be, in our experience, a well-tolerated drug; however, it is too early to comment on delayed cardiac effects.
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Authors | G Lambertenghi-Deliliers, E Pogliani, A T Maiolo, M A Pacciarini, E E Polli |
Journal | Tumori
(Tumori)
Vol. 69
Issue 6
Pg. 515-9
(Dec 31 1983)
ISSN: 0300-8916 [Print] United States |
PMID | 6582678
(Publication Type: Journal Article)
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Chemical References |
- Cytarabine
- Idarubicin
- Daunorubicin
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Topics |
- Acute Disease
- Adolescent
- Adult
- Aged
- Antineoplastic Combined Chemotherapy Protocols
(therapeutic use)
- Bone Marrow
(drug effects)
- Cytarabine
(administration & dosage)
- Daunorubicin
(adverse effects, analogs & derivatives, therapeutic use)
- Drug Evaluation
- Female
- Humans
- Idarubicin
- Leukemia
(drug therapy)
- Male
- Middle Aged
- Time Factors
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