Literature DB >> 7882459

Continuous mitoxantrone infusion in pretreated epithelial ovarian cancer.

M O Nicoletto1, R Padrini, H Koussis, A Rosabian, S Aversa, L Endrizzi, P Azzoni, M Palumbo, M V Fiorentino.   

Abstract

Mitoxantrone has shown moderate activity in advanced epithelial ovarian cancer following intermittent i.v. administration. Experiments and clinical data suggest that long-term continuous drug infusion may achieve a better therapeutic result with less toxicity. This hypothesis was tested in patients with advanced ovarian cancer who had been pretreated with other agents. Mitoxantrone was infused continuously in 21-day courses beginning every 6 weeks. If severe toxicity did not occur, the infusion rate was increased by 0.1-0.2 mg/m2 per day. The mitoxantrone solution proved to be stable over the 21-day infusion period. For ethical reasons an optimal two-stage design was employed. The trial was interrupted at the end of the first recruitment stage because the target of 3 responses out of 13 patients had not been achieved (only 1 patient had a partial response). Hematologic toxicity was observed in 11 patients, and 2 of them had a catheter occlusion. In conclusion, we found that 21-day of infusion of mitoxantrone apparently has no clinical benefit as compared with bolus administration in patients with advanced ovarian cancer.

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Year:  1995        PMID: 7882459     DOI: 10.1007/BF00686836

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


  16 in total

1.  Optimal two-stage designs for phase II clinical trials.

Authors:  R Simon
Journal:  Control Clin Trials       Date:  1989-03

2.  A phase I pharmacokinetic study of 21-day continuous infusion mitoxantrone.

Authors:  J Greidanus; E G de Vries; N H Mulder; D T Sleijfer; D R Uges; B Oosterhuis; P H Willemse
Journal:  J Clin Oncol       Date:  1989-06       Impact factor: 44.544

3.  The prognostic and therapeutic value of second-look laparotomy in advanced ovarian cancer.

Authors:  K Bertelsen; M K Hansen; P H Pedersen; G Larsen; M Nyland; M Jacobsen; J E Andersen
Journal:  Br J Obstet Gynaecol       Date:  1988-12

4.  Continuous infusion mitoxantrone in relapsed acute nonlymphocytic leukemia.

Authors:  L S Kaminer; K E Choi; K M Daley; R A Larson
Journal:  Cancer       Date:  1990-06-15       Impact factor: 6.860

5.  Comparative cytotoxicity of bisantrene, mitoxantrone, ametantrone, dihydroxyanthracenedione, dihydroxyanthracenedione diacetate, and doxorubicin on human cells in vitro.

Authors:  B Drewinko; L Y Yang; B Barlogie; J M Trujillo
Journal:  Cancer Res       Date:  1983-06       Impact factor: 12.701

6.  Phase I clinical and pharmacokinetic study of mitoxantrone given to patients by intraperitoneal administration.

Authors:  D S Alberts; E A Surwit; Y M Peng; T McCloskey; R Rivest; V Graham; L McDonald; D Roe
Journal:  Cancer Res       Date:  1988-10-15       Impact factor: 12.701

7.  Escalating dose regimen of intraperitoneal mitoxantrone: phase I study--clinical and pharmacokinetic evaluation.

Authors:  B Blöchl-Daum; H G Eichler; H Rainer; R Jakesz; H Salzer; G Steger; J Schüller; E Günther; B Proksch; G Ehninger
Journal:  Eur J Cancer Clin Oncol       Date:  1988-07

8.  Phase I-II intraperitoneal mitoxantrone in advanced pretreated ovarian cancer.

Authors:  M O Nicoletto; R Padrini; E Ferrazzi; O Nascimben; E Visonà; S Tumolo; M Palumbo; L Costa; O Vinante; S Monfardini
Journal:  Eur J Cancer       Date:  1993       Impact factor: 9.162

9.  Phase II study of mitoxantrone in epithelial ovarian cancer.

Authors:  F Lawton; G Blackledge; J Mould; T Latief; R Watson; A D Chetiyawardana
Journal:  Cancer Treat Rep       Date:  1987-06

10.  A radioimmunoassay using a monoclonal antibody to monitor the course of epithelial ovarian cancer.

Authors:  R C Bast; T L Klug; E St John; E Jenison; J M Niloff; H Lazarus; R S Berkowitz; T Leavitt; C T Griffiths; L Parker; V R Zurawski; R C Knapp
Journal:  N Engl J Med       Date:  1983-10-13       Impact factor: 91.245

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