Literature DB >> 206339

Ifosfamide in the treatment of recurrent or disseminated lung cancer: a phase II study of two dose schedules.

J J Costanzi, R Gagliano, D Loukas, F J Panettiere, J A Hokanson.   

Abstract

Ifosfamide was administered to 21 patients with recurrent or disseminated lung cancer at a dose of 4.0 gm/M2 iv every 3 weeks. The response rate was 33% with an additional 14% showing no response or stable disease. At a dose of 1.2 gm/M2 daily for 5 days every 4 weeks, 57% of 14 patients responded with 35% showing no response or stable disease. The majority of the patients (28) had epidermoid carcinoma. Two (7%) had complete response with 9 (32%) showing partial responses. Other responses included 1/2 oat cell carcinomas and 3/6 large cell undifferentiated carcinomas. Toxicity was equal in both regimens for nausea, vomiting, increased serum LDH and neutropenia but the 5 day program had significantly less hemorrhagic cystitis. Survival was greatly influenced by response. There was no statistical difference in overall length of response between responders and the non responding/stable disease patients. But these two groups had a very significant survival advantage when compared to those patients with increasing disease. Similarly, there was a significant improvement in response duration for the low dosage regimen. Therefore, the low dose 5 day regimen is recommended because of its response rate, it has less hemorrhagic cystitis and it has better patient acceptance in that it can be given as an outpatient and does not require a Foley catheter.

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Year:  1978        PMID: 206339     DOI: 10.1002/1097-0142(197805)41:5<1715::aid-cncr2820410510>3.0.co;2-x

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  9 in total

1.  Chemotherapy for lung cancer.

Authors: 
Journal:  Br Med J       Date:  1979-10-06

2.  Prolongation of ifosfamide elimination half-life in obese patients due to altered drug distribution.

Authors:  M J Lind; J M Margison; T Cerny; N Thatcher; P M Wilkinson
Journal:  Cancer Chemother Pharmacol       Date:  1989       Impact factor: 3.333

3.  Failure of response to ifosfamide in squamous cell bronchogenic carcinoma.

Authors:  J Banks; E G Anderson; A P Smith
Journal:  Cancer Chemother Pharmacol       Date:  1989       Impact factor: 3.333

4.  Chemotherapy in non-small cell bronchial carcinoma.

Authors:  R Souhami
Journal:  Thorax       Date:  1985-09       Impact factor: 9.139

5.  Pharmacokinetics of ifosfamide and its enantiomers following a single 1 h intravenous infusion of the racemate in patients with small cell lung carcinoma.

Authors:  S A Corlett; D Parker; H Chrystyn
Journal:  Br J Clin Pharmacol       Date:  1995-04       Impact factor: 4.335

6.  Escalating doses of carboplatin with high-dose ifosfamide using autologous bone marrow as support: a phase I study.

Authors:  A D Elias; L J Ayash; J P Eder; C Wheeler; J Deary; L Weissman; M Hunt; J Critchlow; L Schnipper; E Frei
Journal:  J Cancer Res Clin Oncol       Date:  1991       Impact factor: 4.553

Review 7.  Comparative activity of ifosfamide and cyclophosphamide.

Authors:  W Brade; S Seeber; K Herdrich
Journal:  Cancer Chemother Pharmacol       Date:  1986       Impact factor: 3.333

8.  Mesnum as a protector against kidney and bladder toxicity with high-dose ifosfamide treatment.

Authors:  G Falkson; J J Van Dyk; R Stapelberg; H C Falkson
Journal:  Cancer Chemother Pharmacol       Date:  1982       Impact factor: 3.333

9.  Phase II study of cisplatin, ifosfamide, and irinotecan with rhG-CSF support in patients with stage IIIb and IV non-small-cell lung cancer.

Authors:  A Fujita; T Ohkubo; H Hoshino; H Takabatake; S Tagaki; K Sekine; S Abe
Journal:  Br J Cancer       Date:  2003-09-15       Impact factor: 7.640

  9 in total

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