Literature DB >> 91430

Role of single-breath carbon monoxide-diffusing capacity in monitoring the pulmonary effects of bleomycin in germ cell tumor patients.

R L Comis, M S Kuppinger, S J Ginsberg, S T Crooke, R Gilbert, J H Auchincloss, A W Prestayko.   

Abstract

Serial pulmonary function tests including single-breath carbon monoxide-diffusing capacity (DLCO), forced vital capacity (FVC), and forced expiratory volume in 1 sec were performed in a relatively homogeneous group of male patients with germ cell tumors treated with vinblastine, bleomycin, and cis-diamminedichloroplatinum. Of the pulmonary function tests used, the DLCO was shown to be the most sensitive indicator of subclinical bleomycin pulmonary effects. Decreases in DLCO were both total dose and schedule dependent. Patients receiving their total dose of bleomycin at a rate of 25 +/- 2 (S.D.) units/week developed a linear decrease in DLCO with increasing total doses of bleomycin. Changes in FVC did not correlate with bleomycin total dose. Although both the mean DLCO and FVC decreased after completion of bleomycin therapy, the mean FVC returned to base-line levels rapidly, whereas the decrease in mean DLCO was persistent for several months. When routine volumetric tests (FVC and forced expiratory volume in 1 sec) and DLCO are used in a systematic manner, DLCO is the most sensitive indicator of the subclinical pulmonary effects of bleomycin in germ cell tumor patients treated with vinblastine, bleomycin, and cis-diamminedichloroplatinum.

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Year:  1979        PMID: 91430

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  12 in total

1.  Reversal of bleomycin lung toxicity with corticosteroids.

Authors:  J Kozielski
Journal:  Thorax       Date:  1994-03       Impact factor: 9.139

2.  Changes in pulmonary function during and after bleomycin treatment in patients with testicular carcinoma.

Authors:  P W van Barneveld; G Veenstra; D T Sleijfer; T W van der Mark; N H Mulder; H Schraffordt Koops; H J Sluiter; R Peset
Journal:  Cancer Chemother Pharmacol       Date:  1985       Impact factor: 3.333

3.  Development of acute lung injury after the combination of intravenous bleomycin and exposure to hyperoxia in rats.

Authors:  J G Hay; P L Haslam; A Dewar; B Addis; M Turner-Warwick; G J Laurent
Journal:  Thorax       Date:  1987-05       Impact factor: 9.139

Review 4.  The correlation of lung structure with function.

Authors:  N Berend
Journal:  Lung       Date:  1982       Impact factor: 2.584

5.  The single-breath carbon monoxide transfer test 25 years on: a reappraisal. 2--Clinical considerations.

Authors:  C Ogilvie
Journal:  Thorax       Date:  1983-01       Impact factor: 9.139

Review 6.  Therapeutic drug monitoring in oncology. Problems and potential in antineoplastic therapy.

Authors:  M J Moore; C Erlichman
Journal:  Clin Pharmacokinet       Date:  1987-10       Impact factor: 6.447

7.  High-performance liquid chromatography assay of bleomycin in human plasma and rat hepatocytes in culture.

Authors:  R Mahdadi; A Kenani; N Pommery; J Pommery; J P Hénichart; M Lhermitte
Journal:  Cancer Chemother Pharmacol       Date:  1991       Impact factor: 3.333

Review 8.  Clinical pharmacokinetics of commonly used anticancer drugs.

Authors:  F M Balis; J S Holcenberg; W A Bleyer
Journal:  Clin Pharmacokinet       Date:  1983 May-Jun       Impact factor: 6.447

9.  Severe vascular toxicity associated with vinblastine, bleomycin, and cisplatin chemotherapy.

Authors:  B L Samuels; N J Vogelzang; B J Kennedy
Journal:  Cancer Chemother Pharmacol       Date:  1987       Impact factor: 3.333

Review 10.  Chemotherapy for Good-Risk Nonseminomatous Germ Cell Tumors: Current Concepts and Controversies.

Authors:  Gino In; Tanya Dorff
Journal:  Urol Clin North Am       Date:  2015-08       Impact factor: 2.766

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