Literature DB >> 8261579

Pulmonary distribution of vinorelbine in patients with non-small-cell lung cancer.

D Levêque1, E Quoix, P Dumont, G Massard, J G Hentz, A Charloux, F Jehl.   

Abstract

Vinorelbine (Navelbine, NVB) is a new semi-synthetic vinca alkaloid that is currently used in the treatment of advanced breast cancer and advanced non-small-cell lung cancer (NSCLC). In this study we investigated the tumoral and healthy pulmonary tissue concentrations of NVB in previously untreated NSCLC patients undergoing surgery. A total of 13 patients (mean age, 60 years; range, 42-70 years) were included and received NVB (20 mg/m2) at 1 h (mean, 1.1 h; SD, 0.2 h; n = 6 patients) and 3 h (mean, 3.0 h; SD, 0.6 h; n = 7 patients) before tumor resection. A tumoral and adjacent healthy lung-tissue specimen as well as simultaneously sampled serum were analyzed for NVB by high-performance liquid chromatography (HPLC). NVB levels were much higher in tissue than in serum (up to 300-fold). The tissue/serum ratio increased between the 1-h sampling time (range, 0.1-100) and the 3-h time point (range, 10-300). In all patients but two, NVB concentrations were lower in tumors than in healthy lung tissue. The tumor/healthy tissue ratio ranged from 0.06 to 1.3 (median, 0.09) at 1 h and from 0.18 to 1.1 (median, 0.55) at 3 h. This ratio increased between the 1-h sampling time and the 3-h time point as a consequence of increasing tumor levels (median, 50.4 ng/g at 1 h and 278 ng/g at 3 h). In four patients, concentrations could be measured in necrotic and peripheral tumor zones, showing lower values in necrotic areas. Thus, these data indicate that NVB is highly distributed in lung tissue, with the disposition rate being slower in tumor tissue than in healthy parenchyma during the first 3 h.

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Year:  1993        PMID: 8261579     DOI: 10.1007/bf00685338

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


  11 in total

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Journal:  Cancer Chemother Pharmacol       Date:  1990       Impact factor: 3.333

4.  Determination of navelbine and desacetylnavelbine in biological fluids by high-performance liquid chromatography.

Authors:  F Jehl; J Debs; C Herlin; E Quoix; C Gallion; H Monteil
Journal:  J Chromatogr       Date:  1990-01-26

5.  Phase-II study of Navelbine in advanced breast cancer.

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Journal:  Semin Oncol       Date:  1989-04       Impact factor: 4.929

6.  Concentration of vinblastine in human intracerebral tumor and other tissues.

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7.  Clinical pharmacokinetics of vinorelbine alone and combined with cisplatin.

Authors:  D Levêque; F Jehl; E Quoix; F Breillout
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9.  Biliary elimination and pharmacokinetics of vinorelbine in micropigs.

Authors:  D Levêque; M Merle-Melet; L Bresler; J P Didelot; J P Aymard; J Wihlm; F Jehl
Journal:  Cancer Chemother Pharmacol       Date:  1993       Impact factor: 3.333

10.  A phase II study of Navelbine (vinorelbine) in the treatment of non-small-cell lung cancer.

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Authors:  D Levêque; F Jehl
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Authors:  Monique P Curran; Greg L Plosker
Journal:  Drugs Aging       Date:  2002       Impact factor: 3.923

Review 3.  New oral chemotherapeutic agents for lung cancer.

Authors:  E M Bengtson; J R Rigas
Journal:  Drugs       Date:  1999       Impact factor: 9.546

Review 4.  Vinorelbine. A review of its pharmacological properties and clinical use in cancer chemotherapy.

Authors:  K L Goa; D Faulds
Journal:  Drugs Aging       Date:  1994-09       Impact factor: 3.923

Review 5.  Vinorelbine--a clinical review.

Authors:  R K Gregory; I E Smith
Journal:  Br J Cancer       Date:  2000-06       Impact factor: 7.640

  5 in total

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