Literature DB >> 6385264

Mitoxantrone as a single agent and in combination chemotherapy in patients with refractory acute leukemia.

P A Paciucci, J Cuttner, J F Holland.   

Abstract

A total of 47 patients with relapsed or primarily refractory leukemia were treated with mitoxantrone alone or in combination with vincristine sulfate and prednisone or cytarabine. Eligible patients included those with adequate renal and hepatic function, normal left ventricular ejection fraction, and those who had received previous treatment. When mitoxantrone was given alone in a once daily times five schedule, 5 of 12 acute lymphoblastic leukemia patients achieved complete remission; 4 of these patients had been refractory to reinduction and 1 to induction chemotherapy with anthracycline-containing treatments. Four of these patients had progressive disease, and three died during induction. Of 12 patients with acute myeloid leukemia, 1 had a complete remission, 1 had a partial remission, 8 had progressive disease, and 2 died during induction. Mitoxantrone was also found to be active in two patients in the blastic transformation of chronic myeloid leukemia with a response in one patient lasting 17 weeks. Combinations of mitoxantrone with vincristine sulfate and prednisone resulted in complete remission in four of nine acute lymphoblastic leukemia patients and one of four patients with Tdt-positive chronic myeloid leukemia in blast crisis. Three of these patients had not experienced a prior remission following anthracycline-containing treatments. Partial remission occurred in two of the acute lymphoblastic leukemia patients and one of the Tdt-positive chronic myeloid leukemia patients. Two of this latter group of patients died in induction. Treatment with mitoxantrone and cytarabine resulted in two acute myeloid leukemia patients achieving complete remission and one a partial remission; two patients had progressive disease, and one died in induction. No response was seen in a patient with Tdt-negative chronic myeloid leukemia after two courses of treatment. One patient with acute leukemia in the course of myelofibrosis died in induction. All the patients achieving complete remission are alive and have been in complete remission from 2 to 12 months. Side effects included mild nausea and vomiting in 9 of 13 patients treated with the mitoxantrone-vincristine sulfate-prednisone combination, and in 3 of 8 patients treated with the mitoxantrone-cytarabine combination. Other side effects of the combination treatments include drug-induced oral mucositis (of a lesser degree than with mitoxantrone alone), transient hepatic abnormalities, and infectious complications, such as sepsis, Candida sp colonization of the upper digestive tract, and soft tissue cellulitis, in a few patients.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1984        PMID: 6385264

Source DB:  PubMed          Journal:  Semin Oncol        ISSN: 0093-7754            Impact factor:   4.929


  10 in total

1.  Evaluation of incorporation characteristics of mitoxantrone into unilamellar liposomes and analysis of their pharmacokinetic properties, acute toxicity, and antitumor efficacy.

Authors:  R A Schwendener; H H Fiebig; M R Berger; D P Berger
Journal:  Cancer Chemother Pharmacol       Date:  1991       Impact factor: 3.333

Review 2.  Mitoxantrone. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in the chemotherapy of cancer.

Authors:  D Faulds; J A Balfour; P Chrisp; H D Langtry
Journal:  Drugs       Date:  1991-03       Impact factor: 9.546

Review 3.  Design of preparative regimens for stem cell transplantation in breast cancer.

Authors:  G Spitzer; D Adkins; F Dunphy; P Petruska; V Spencer; W Velasquez
Journal:  Breast Cancer Res Treat       Date:  1993       Impact factor: 4.872

4.  Mitoxantrone-induced DNA damage in leukemia cells is enhanced by treatment with high-dose arabinosylcytosine.

Authors:  V Heinemann; D Murray; R Walters; R E Meyn; W Plunkett
Journal:  Cancer Chemother Pharmacol       Date:  1988       Impact factor: 3.333

5.  Toxicity evaluation of dihydroxyanthracenedione (DHAD) in combination with cytosine arabinoside (Ara-C).

Authors:  C P Steuber; V J Land; C I Civin; A H Ragab; J Krischer; T J Vietti
Journal:  Invest New Drugs       Date:  1987-12       Impact factor: 3.850

6.  Mitoxantrone in the treatment of acute leukemia.

Authors:  D A Vorobiof; G Falkson; M A Coccia-Portugal; A P Terblanche
Journal:  Invest New Drugs       Date:  1987-12       Impact factor: 3.850

7.  The effect of mitoxantrone treatment in beagle dogs previously treated with minimally cardiotoxic doses of doxorubicin.

Authors:  P Tham; W Dougherty; M J Iatropoulos; G Gordon; V C James; C Hall; J F Noble
Journal:  Am J Pathol       Date:  1987-07       Impact factor: 4.307

8.  Novantrone for childhood malignant solid tumors. A pediatric oncology group phase II study.

Authors:  C B Pratt; T J Vietti; E Etcubanas; C Sexauer; R A Krance; D H Mahoney; R B Patterson
Journal:  Invest New Drugs       Date:  1986       Impact factor: 3.850

9.  A randomized study of mitoxantrone plus cytarabine versus daunomycin plus cytarabine in the treatment of previously untreated adult patients with acute nonlymphocytic leukemia.

Authors:  S Pavlovsky; J Gonzalez Llaven; M A Garcia Martinez; P Sobrevilla; M Eppinger-Helft; A Marin; M López-Hernández; I Fernandez; M E Rubio; S Ibarra
Journal:  Ann Hematol       Date:  1994-07       Impact factor: 3.673

Review 10.  Mitochondrial metabolism as a target for acute myeloid leukemia treatment.

Authors:  Svetlana B Panina; Jingqi Pei; Natalia V Kirienko
Journal:  Cancer Metab       Date:  2021-04-21
  10 in total

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