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Mitoxantrone and high‐dose cytosine arabinoside in refractory acute myelogenous leukemia
Author(s) -
Walters Ronald S.,
Kantarjian Hagop M.,
Keating Michael J.,
Plunkett William K.,
Estey Elihu H.,
Andersson Borje,
Beran Miloslav,
McCredie Kenneth B.,
Freireich Emil J
Publication year - 1988
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/1097-0142(19880815)62:4<677::aid-cncr2820620405>3.0.co;2-b
Subject(s) - mitoxantrone , medicine , gastroenterology , refractory (planetary science) , cytarabine , leukemia , regimen , population , chemotherapy , toxicity , surgery , physics , environmental health , astrobiology
Forty‐four patients with a diagnosis of refractory or relapsed acute myelogenous leukemia received salvage chemotherapy with high‐dose cytosine arabinosine 3 g/m 2 intravenously over 2 hours every 12 hours for six doses and mitoxantrone 5 mg/m 2 intravenously daily for 5 days. Overall 16 patients (36%) had a complete remission; 16 patients (36%) had resistant disease; and 12 (27%) died during induction therapy. The most significant predictive factor for remission was the duration of first remission: the response rate was 17% for patients whose first remission duration was shorter than 12 months (including those who did not achieve a first remission), 45% for those with a first remission lasting between 12 to 18 months, and 69% for those with longer remission durations (P = 0.008). Other predictive factors for higher response rates were a younger age group, a good performance status, and a favorable or diploid karyotype. The median survival from start of therapy was 4 months for the total population and 10 months for patients with remission. Serious side effects including pulmonary toxicity and neurotoxicity occurred in less than 10% of patients. This incidence was significantly lower than previous high‐dose cytosine arabinoside schedules of 3 g/m 2 for nine to 12 doses (total dose, 27 to 36 g per course). Significant granulocytopenia and thrombocytopenia were universal resulting in fever or documented infections in 98% of patients. We conclude that the combination of high‐dose cytosine arabinoside and mitoxantrone is an effective antileukemic regimen with acceptable toxicity. Future studies should incorporate it as part of the frontline induction or maintenance strategies in newly diagnosed patients with acute myelogenous leukemia.