Literature DB >> 7803948

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

K L Goa1, D Faulds.   

Abstract

Vinorelbine is a semisynthetic vinca alkaloid with a broad spectrum of antitumour activity. The drug is effective as a single agent in inoperable/advanced non-small cell lung cancer (NSCLC), producing objective response rates of about 15 to 30%, and as first-line or later chemotherapy for metastatic spread in advanced breast cancer. Combining vinorelbine with standard chemotherapeutic regimens improves response rates in these indications compared with vinorelbine monotherapy: in NSCLC response rates increase to 30 to 50% when vinorelbine is administered with cisplatin. Importantly, survival was prolonged by a further 9 weeks with this combination in a trial in > 600 patients with NSCLC. Comparative trials evaluating vinorelbine in women with advanced breast cancer are few at present. However, results suggest greater efficacy for vinorelbine than for melphalan as second-line chemotherapy, and similar efficacy for vinorelbine plus doxorubicin compared with doxorubicin plus 2 other drugs as first-line chemotherapy. Vinorelbine has tended to yield superior response rates when compared with vindesine, and appears to have greater haematological toxicity (i.e. granulocytopenia) but less neurological toxicity (peripheral neuropathy, constipation, loss of deep tendon reflexes) than this agent. Myelosuppression is the most frequent cause of vinorelbine treatment delay or dose reduction. Other consequences of vinorelbine therapy are those typically seen with antineoplastic agents, such as diarrhoea, nausea and vomiting, and alopecia. However, these are rarely severe. Early clinical investigations indicate that the antitumour effects of vinorelbine in other malignancies including ovarian carcinoma, lymphoma and head and neck cancer warrant further exploration, as does the efficacy of the drug relative to standard approaches and its possible beneficial effects on quality of life of cancer patients. Clarification is also required of the feasibility of an oral dosage form, which in preliminary investigations has shown some efficacy in NSCLC, but a variable response rate and high incidence of gastrointestinal disturbances in women with breast cancer. Thus, vinorelbine as a single agent or combined palliative therapy is effective against advanced NSCLC, and as first- or second-line chemotherapy in advanced breast cancer. This semisynthetic vinca alkaloid has a manageable tolerability profile and potential for use in other malignancies and as an oral formulation. With these attributes, vinorelbine is a valuable option which extends the range of treatments available for these difficult-to-treat malignancies.

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Year:  1994        PMID: 7803948     DOI: 10.2165/00002512-199405030-00006

Source DB:  PubMed          Journal:  Drugs Aging        ISSN: 1170-229X            Impact factor:   3.923


  81 in total

1.  Antiproliferative activity of vinorelbine (Navelbine) against six human melanoma cell lines.

Authors:  A Photiou; M N Sheikh; D Bafaloukos; S Retsas
Journal:  J Cancer Res Clin Oncol       Date:  1992       Impact factor: 4.553

2.  The synthesis of Navelbine prototype of a new series of vinblastine derivatives.

Authors:  P Potier
Journal:  Semin Oncol       Date:  1989-04       Impact factor: 4.929

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

Authors:  L Canobbio; F Boccardo; G Pastorino; F Brema; C Martini; M Resasco; L Santi
Journal:  Semin Oncol       Date:  1989-04       Impact factor: 4.929

4.  [Clinical pharmacokinetics of navelbine after oral administration, in vitro metabolism and interindividual variability].

Authors:  Z Sahnoun; X J Zhou; P Bore; S Monjanel; R Favre; A Durand; R Rahmani
Journal:  Bull Cancer       Date:  1990       Impact factor: 1.276

5.  Effective second line chemotherapy of advanced breast cancer with navelbine and mitomycin C.

Authors:  W Scheithauer; G Kornek; K Haider; W Kwasny; T Schenk; R Pirker; D Depisch
Journal:  Breast Cancer Res Treat       Date:  1993       Impact factor: 4.872

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

Authors:  D Levêque; F Jehl; E Quoix; F Breillout
Journal:  J Clin Pharmacol       Date:  1992-12       Impact factor: 3.126

7.  In vivo study of vinorelbine associations with cisplatin, 5-fluorouracil or actinomycin D relative to a non-small-cell lung carcinoma (NSCLCN6-L16).

Authors:  C Roussakis; Y F Pouchus; C Gratas; D Riou; P Dimou; G Dabouis; S Merle; J F Verbist
Journal:  Anticancer Drug Des       Date:  1993-04

8.  Determination of vinorelbine (Navelbine) in tumour cells by high-performance liquid chromatography.

Authors:  V Debal; H Morjani; J M Millot; J F Angiboust; B Gourdier; M Manfait
Journal:  J Chromatogr       Date:  1992-10-02

9.  Biochemical effects of Navelbine on tubulin and associated proteins.

Authors:  A Fellous; R Ohayon; T Vacassin; S Binet; H Lataste; A Krikorian; J P Couzinier; V Meininger
Journal:  Semin Oncol       Date:  1989-04       Impact factor: 4.929

Review 10.  Anthracycline antibiotics in cancer therapy. Focus on drug resistance.

Authors:  D J Booser; G N Hortobagyi
Journal:  Drugs       Date:  1994-02       Impact factor: 9.546

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  16 in total

1.  Cost utility in second-line metastatic breast cancer.

Authors:  G Berdeaux; P Hurteloup
Journal:  Pharmacoeconomics       Date:  1997-05       Impact factor: 4.981

2.  Efficacy of vinorelbine-based neoadjuvant chemotherapy in breast cancer: A systematic review and meta-analysis of randomized controlled trials.

Authors:  Hui Gao; Qiuyun Li; Wei Wei; Y I Jiang; Huawei Yang; Jianlun Liu
Journal:  Mol Clin Oncol       Date:  2015-06-09

3.  Monitoring Tumor Response after Liposomal Doxorubicin in Combination with Liposomal Vinorelbine Treatment Using 3'-Deoxy-3'-[18F]Fluorothymidine PET.

Authors:  Chun-Yi Wu; Jo-Hsin Tang; Pei-Chia Chan; Jia-Je Li; Ming-Hsien Lin; Chih-Chieh Shen; Ren-Shyan Liu; Hsin-Ell Wang
Journal:  Mol Imaging Biol       Date:  2017-06       Impact factor: 3.488

4.  Inoperable stage III non-small cell lung cancer: Current treatment and role of vinorelbine.

Authors:  Mariano Provencio; Dolores Isla; Antonio Sánchez; Blanca Cantos
Journal:  J Thorac Dis       Date:  2011-09       Impact factor: 2.895

Review 5.  Clinical pharmacokinetics of vinorelbine.

Authors:  D Levêque; F Jehl
Journal:  Clin Pharmacokinet       Date:  1996-09       Impact factor: 6.447

6.  Vinorelbine in advanced non-small cell lung cancer. A pharmacoeconomic review.

Authors:  A J Coukell; S Noble; D Faulds
Journal:  Pharmacoeconomics       Date:  1999-04       Impact factor: 4.981

7.  Drug-resistant T-lymphoid tumors undergo apoptosis selectively in response to an antimicrotubule agent, EM011.

Authors:  Ritu Aneja; Jun Zhou; Surya N Vangapandu; Binfei Zhou; Ramesh Chandra; Harish C Joshi
Journal:  Blood       Date:  2005-11-10       Impact factor: 22.113

Review 8.  Vinorelbine: a review of its use in elderly patients with advanced non-small cell lung cancer.

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

Review 9.  Toxicity patterns of cytotoxic drugs.

Authors:  Etienne Chatelut; Jean-Pierre Delord; Pierre Canal
Journal:  Invest New Drugs       Date:  2003-05       Impact factor: 3.850

10.  Cisplatin plus oral vinorelbine as first-line treatment for advanced non-small-cell lung cancer: a prospective study confirming that the day-8 hemogram is unnecessary.

Authors:  M Provencio; A Sánchez; A Artal; J M Sánchez Torres; Ramón García Gómez; Manuel Constenla; J de Castro; M Dómine; N Viñolas; A Sánchez; F J Pérez
Journal:  Clin Transl Oncol       Date:  2013-01-29       Impact factor: 3.405

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