Literature DB >> 3396148

High activity of mitoxantrone in previously untreated low-grade lymphomas.

S W Hansen1, N I Nissen, M M Hansen, K Hou-Jensen, J Pedersen-Bjergaard.   

Abstract

A consecutive series of 21 previously untreated patients with low-grade non-Hodgkin lymphomas were treated with mitoxantrone 5 mg/m2 daily for 3 days every 3 weeks. The cumulative dose did not exceed 165 mg/m2 in any patient. In this group, 7 patients had small lymphocytic lymphomas, 10 patients had follicular small cleaved cell lymphomas, and 4 patients had follicular mixed small- and large-cell lymphomas. Of the 21 patients, 20 obtained remission (complete in 6, partial in 14), and 15 of these are still in remission. Relapse-free survival is 68% at 2 years. None of the patients has died. Nonhematologic toxicity was modest. No severe alopecia was seen, and only 6 patients had nausea and vomiting (WHO grade 1-3). No cardiac toxicity was seen. In conclusion, mitoxantrone is a highly active and well-tolerated drug in this subset of patients. Hematologic toxicity, especially leukopenia, was dose limiting, and a reduction of the dose was necessary in 15 out of the 21 patients.

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Year:  1988        PMID: 3396148     DOI: 10.1007/bf00254186

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  10 in total

1.  Non-Hodgkin's lymphomas. IV. Clinicopathologic correlation in 405 cases.

Authors:  S E Jones; Z Fuks; M Bull; M E Kadin; R F Dorfman; H S Kaplan; S A Rosenberg; H Kim
Journal:  Cancer       Date:  1973-04       Impact factor: 6.860

2.  Mitoxantrone in malignant lymphomas.

Authors:  R A Gams; J W Keller; H M Golomb; J Steinberg; G Dukart
Journal:  Cancer Treat Rev       Date:  1983-12       Impact factor: 12.111

3.  Mitoxantrone in refractory nonHodgkin's lymphoma. A Southwest Oncology Group study.

Authors:  C A Coltman; T M Coltman; S P Balcerzak; F S Morrison; D D Von Hoff
Journal:  Semin Oncol       Date:  1984-09       Impact factor: 4.929

4.  Follicular lymphoma: prognostic factors for response and survival.

Authors:  C J Gallagher; W M Gregory; A E Jones; A G Stansfeld; M A Richards; H S Dhaliwal; J S Malpas; T A Lister
Journal:  J Clin Oncol       Date:  1986-10       Impact factor: 44.544

5.  Phase I trial of dihydroxyanthracenedione.

Authors:  D A Van Echo; M Y Whitacre; J Aisner; P H Wiernik
Journal:  Cancer Treat Rep       Date:  1981 Sep-Oct

6.  Phase I clinical study of dihydroxyanthracenedione administered on a 5-day iv schedule.

Authors:  M Valdivieso; A Y Bedikian; M A Burgess; N Savaraj; W B Jeffers; G P Bodey
Journal:  Cancer Treat Rep       Date:  1981 Sep-Oct

7.  Phase I clinical investigation of 1,4-dihydroxy-5,8-bis (( (2-[(2-hydroxyethyl)amino]ethyl) amino))-9,10-anthracenedione dihydrochloride (NSC 301739), a new anthracenedione.

Authors:  D D Von Hoff; E Pollard; J Kuhn; E Murray; C A Coltman
Journal:  Cancer Res       Date:  1980-05       Impact factor: 12.701

8.  Moderate versus aggressive chemotherapy of nodular lymphocytic poorly differentiated lymphoma.

Authors:  E Z Ezdinli; J R Anderson; F Melvin; J H Glick; T E Davis; M J O'Connell
Journal:  J Clin Oncol       Date:  1985-06       Impact factor: 44.544

9.  Mitoxantrone in malignant lymphoma.

Authors:  R A Gams; J Steinberg; L Posner
Journal:  Semin Oncol       Date:  1984-09       Impact factor: 4.929

Review 10.  Mitoxantrone (novantrone): a review of experimental and early clinical studies.

Authors:  I E Smith
Journal:  Cancer Treat Rev       Date:  1983-06       Impact factor: 12.111

  10 in total
  1 in total

Review 1.  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

  1 in total

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