Literature DB >> 481319

Inapparent infiltrations associated with vindesine administration.

R T Dorr, S E Jones.   

Abstract

Vindesine is des-acetyl vinblastine amide sulfate (Eldisine, Eli Lilly and Co), an investigational derivative of the vinca alkaloid, vinblastine. Initial phase I results with vindesine have determined that myelotoxicity is dose-limiting and that, contrary to preclinical studies in animals [1], a neurotoxic potential is indeed present [2]. Another phase I study also observed a rather high incidence of phlebitis (16%) and of cellulitis (10%), however, myelosuppression remained the dose-limiting toxicity [3]. Because good clinical responses have been noted in lymphomas, leukemias [4] and some solid tumors including breast cancer [5], the drug has a potential for wide utility. However, while we have noted several clinical responses with vindesine, injections of the drug have been complicated by serious infiltration with atypically delayed presentation. The purpose of this communication is to briefly describe the incidence and course of these infiltrations.

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Year:  1979        PMID: 481319     DOI: 10.1002/mpo.2950060403

Source DB:  PubMed          Journal:  Med Pediatr Oncol        ISSN: 0098-1532


  4 in total

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Authors:  M L Brigden; L N Hughes; J B Barnett
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2.  Extravasation injury potential of CI-980, a novel synthetic mitotic inhibitor.

Authors:  J R MacDonald; D G Pegg
Journal:  Cancer Chemother Pharmacol       Date:  1993       Impact factor: 3.333

3.  Lack of experimental vesicant activity for the anticancer agents cisplatin, melphalan, and mitoxantrone.

Authors:  R T Dorr; D S Alberts; M Soble
Journal:  Cancer Chemother Pharmacol       Date:  1986       Impact factor: 3.333

4.  Antidote studies of vinorelbine-induced skin ulceration in the mouse.

Authors:  R T Dorr; K L Bool
Journal:  Cancer Chemother Pharmacol       Date:  1995       Impact factor: 3.333

  4 in total

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