Literature DB >> 24381657

Taxanes: vesicants, irritants, or just irritating?

Meagan S Barbee1, Taofeek K Owonikoko2, R Donald Harvey2.   

Abstract

Several classes of antineoplastic agents are universally referred to as vesicants with ample supporting literature. However, the literature surrounding the taxanes is controversial. While the American Society of Clinical Oncology and Oncology Nursing Society Chemotherapy Administration Safety Standards and the Chemotherapy and Biotherapy Guidelines and Recommendations for Practice identify the risks of extravasation and the parameters surrounding the infusion of known vesicants, recommend administration sites for known agents, and recommend antidotes for particular extravasation cases, they fail to provide specific recommendations for the administration of individual taxanes, or a classification system for antineoplastic agents as vesicants, irritants, or inert compounds. There is also a lack of prescribing information regarding such recommendations. The lack of a formal classification system further complicates the accurate delineation of vesicant antineoplastic agents and subsequent appropriate intravenous administration and extravasation management. There are several factors that make the classification of taxanes as vesicants or irritants challenging. Comprehensive preclinical data describing potential mechanisms of tissue damage or vesicant-like properties are lacking. Furthermore, most case reports of taxane extravasation fail to include the parameters surrounding administration, such as the concentration of medication and duration of infusion, making it difficult to set parameters for vesicant potential. Subsequently, many practitioners default to central venous administration of taxanes without evidence that such administration minimizes the risk of extravasation or improves outcomes thereof. Here, we review briefly the data surrounding taxane extravasation and potential vesicant or irritant properties, classify the taxanes, and propose a spectrum for antineoplastic agent potential to cause tissue injury that warrants clinical intervention if extravasation occurs.

Entities:  

Keywords:  cabazitaxel; docetaxel; extravasation; irritant; paclitaxel; taxane; vesicant

Year:  2014        PMID: 24381657      PMCID: PMC3866993          DOI: 10.1177/1758834013510546

Source DB:  PubMed          Journal:  Ther Adv Med Oncol        ISSN: 1758-8340            Impact factor:   8.168


  17 in total

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Review 2.  Vesicant extravasation part II: Evidence-based management and continuing controversies.

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Review 3.  Vesicant extravasation part I: Mechanisms, pathogenesis, and nursing care to reduce risk.

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Journal:  Oncol Nurs Forum       Date:  2006-11-27       Impact factor: 2.172

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Authors:  P Berghammer; R Pöhnl; M Baur; C Dittrich
Journal:  Support Care Cancer       Date:  2001-03       Impact factor: 3.603

6.  Action of bis(betachloroethyl)sulphide (BCES) on human epidermis reconstituted in culture: Morphological alterations and biochemical depletion of glutathione.

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7.  The First Description of Docetaxel-Induced Recall Inflammatory Skin Reaction After Previous Drug Extravasation.

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Journal:  Ann Pharmacother       Date:  2011-02       Impact factor: 3.154

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Authors:  Esther Uña; Fernando Cuadrillero; Francisco López-Lara
Journal:  BMJ Case Rep       Date:  2009-04-14

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Journal:  Cancer       Date:  1996-07-01       Impact factor: 6.860

Review 10.  A review of clinical experience with paclitaxel extravasations.

Authors:  Brad L Stanford; Fred Hardwicke
Journal:  Support Care Cancer       Date:  2003-03-27       Impact factor: 3.603

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  6 in total

Review 1.  Overview, prevention and management of chemotherapy extravasation.

Authors:  Firas Y Kreidieh; Hiba A Moukadem; Nagi S El Saghir
Journal:  World J Clin Oncol       Date:  2016-02-10

Review 2.  Dermatological adverse events with taxane chemotherapy.

Authors:  Vincent Sibaud; Nicole R Lebœuf; Henri Roche; Viswanath R Belum; Laurence Gladieff; Marion Deslandres; Marion Montastruc; Audrey Eche; Emmanuelle Vigarios; Florence Dalenc; Mario E Lacouture
Journal:  Eur J Dermatol       Date:  2016-10-01       Impact factor: 3.328

3.  Docetaxel Accumulates in Lymphatic Circulation Following Subcutaneous Delivery Compared to Intravenous Delivery in Rats.

Authors:  Deanna R Worley; Ryan J Hansen; Luke A Wittenburg; Laura S Chubb; Daniel L Gustafson
Journal:  Anticancer Res       Date:  2016-10       Impact factor: 2.480

4.  A Polymer Prodrug Strategy to Switch from Intravenous to Subcutaneous Cancer Therapy for Irritant/Vesicant Drugs.

Authors:  Alexandre Bordat; Tanguy Boissenot; Nada Ibrahim; Marianne Ferrere; Manon Levêque; Léa Potiron; Stéphanie Denis; Sébastien Garcia-Argote; Olivia Carvalho; Jérôme Abadie; Catherine Cailleau; Grégory Pieters; Nicolas Tsapis; Julien Nicolas
Journal:  J Am Chem Soc       Date:  2022-10-04       Impact factor: 16.383

5.  New cutaneous toxicities with generic docetaxel: are the excipients guilty?

Authors:  Margarita Garrido-Siles; Jose Javier Arenas-Villafranca; Elísabeth Pérez-Ruiz; M Francisca de Linares Fernández; Begoña Tortajada; Francisco Rivas-Ruiz; Vicente Faus; Antonio Rueda
Journal:  Support Care Cancer       Date:  2014-12-10       Impact factor: 3.603

6.  Subcutaneous administration of paclitaxel in dogs with cancer: A preliminary study.

Authors:  Daniella M Silva; Aline I Franciosi; Paula C F Pezzini; Simone D Guérios
Journal:  Can Vet J       Date:  2015-08       Impact factor: 1.008

  6 in total

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