Literature DB >> 1967666

Comparison of short-term and continuous chemotherapy (mitozantrone) for advanced breast cancer.

A L Harris1, B M Cantwell, J Carmichael, R Wilson, J Farndon, P Dawes, S Ghani, R G Evans.   

Abstract

132 patients with advanced recurrent breast cancer were treated with four courses of mitozantrone 14 mg/m2 intravenously every 3 weeks (9 weeks). Patients showing disease stabilisation or objective response were randomised to stop chemotherapy or to continue until disease progression. At that stage 27% showed partial responses, 3% complete responses, and 10% disease stabilisation. 22 patients were randomised to continue chemotherapy and 21 to stop. There was no difference in time to disease progression, response duration, or survival between the two groups. Toxicity was mild during the first four courses of therapy. Thus, short courses of single-agent chemotherapy can produce similar therapeutic results to long-term chemotherapy, which has major implications for cost, resource allocation, and toxicity of therapy. Stopping chemotherapy early in responders did not cause rapid relapse. Since drug resistance apparently develops early during therapy, new approaches to modify resistance should be more useful than continuous chemotherapy.

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Year:  1990        PMID: 1967666     DOI: 10.1016/0140-6736(90)90277-c

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  13 in total

1.  Survival in metastatic breast cancer after combination of radio-chemotherapy and hyperthermia.

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2.  Extending the duration of first-line chemotherapy in metastatic breast cancer: a perspective review.

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Review 3.  General surgery.

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Journal:  Postgrad Med J       Date:  1991-10       Impact factor: 2.401

4.  Primary medical treatment in breast cancer.

Authors:  Z Rayter; R F Phipps
Journal:  BMJ       Date:  1991-01-05

5.  Does induction chemotherapy with a mitoxantrone/vinorelbine regimen allow a breast-conservative treatment in patients with operable locoregional breast cancer? A French Northern Oncology Group trial in 105 patients. French Northern Oncology Group.

Authors:  A Adenis; L Vanlemmens; C Fournier; B Hecquet; J Bonneterre
Journal:  Breast Cancer Res Treat       Date:  1996       Impact factor: 4.872

Review 6.  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

7.  Weekly low-dose mitoxantrone plus doxorubicin as second-line chemotherapy for advanced breast cancer.

Authors:  M Bontenbal; A S Planting; C J Rodenburg; A Dees; J Verweij; C C Bartels; J Alexieva-Figusch; W L van Putten; J G Klijn
Journal:  Breast Cancer Res Treat       Date:  1992       Impact factor: 4.872

8.  Results of chemotherapy using ifosfamide with doxorubicin in advanced breast cancer.

Authors:  M Millward; M Lind; L Gumbrell; A Robinson; T Lennard; B Cantwell
Journal:  Breast Cancer Res Treat       Date:  1994       Impact factor: 4.872

Review 9.  Management of metastatic breast cancer.

Authors:  K Wong; I C Henderson
Journal:  World J Surg       Date:  1994 Jan-Feb       Impact factor: 3.352

10.  A randomised trial of second-line hormone vs single agent chemotherapy in tamoxifen resistant advanced breast cancer.

Authors:  A R Dixon; L Jackson; S Chan; J Haybittle; R W Blamey
Journal:  Br J Cancer       Date:  1992-08       Impact factor: 7.640

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