Therapy of adult acute leukemia with daunorubicin and L-asparaginase
β Scribed by Gerald P. Bodey; James S. Hewlett; Charles A. Coltman Jr; Victorio Rodriguez; Emil J. Freireich
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- English
- Weight
- 425 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0008-543X
No coin nor oath required. For personal study only.
β¦ Synopsis
Fifty-four adults with acute leukemia resistant to other therapies received treatment with Daunorubicin and L-asparaginase. Seventeen (31 %) achieved complete remission. The complete remission rate was higher among the 31 patients receiving simultaneous therapy than among the 23 patients receiving sequential therapy (42% vs. 17%). Patients with acute lymphocytic leukemia had a higher remission rate than patients with acute myelogenous leukemia (38% vs. 20%). The median duration of complete remission was only 12 weeks, and the median duration of survival for responders was 30 weeks.
AUNORUBICIN IS AN ANTITUMOR ANTIBIOTIC
D obtained from Streptomyces peucetius
which inhibits DNA-dependent RNA synthesis.5~8313 It is active against both solid and ascitic forms of a wide variety of animal tumors.6 T h e drug has been used successfully in the treatment of both acute lymphocytic leukemia (ALL) and acute myelogenous leukemia I(AML), producing complete remissions in 20-55% of patients.3~12J7 It has been more effective in patients as primary therapy than when administered to patients who have relapsed following successful remission induction with other agents. Daunorubicin has substantial toxicity which includes myelosuppression, oral ulceration, esophagitis, and alopecia.193J2J' Prolonged therapy may lead to cardiac toxicity, manifested as tachycardia and heart failure and usually irreversible.
π SIMILAR VOLUMES
## Abstract LβAsparaginaseβinduced coagulation abnormalities were observed in all patients receiving this drug. All patients studied demonstrated low factor IX and fibrinogen levels and most (75%) had low levels of factor XI. Disturbances in other factors were much less frequent. Despite the presen
I t is clear that asparaginase will have to be combined with other drugs if it is to significantly affect survival of patients with ALL, in spite of the 50% remissions achieved, since these remissions are of such short duration. We have investigated the combination of asparaginase with the glutamine
One hundred and fourteen patients with acute leukemia, 57 children (10 AML and 47 ALL) and 57 adults (37 AML and 20 ALL) were treated with L-asparaginase (Asnase) 200 or 1000 IU/kg daily for 30 days unless withdrawn on account of side effects. Combinations with other cytotoxic drugs were used in all