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Annals of Oncology Advance Access originally published online on November 16, 2005
Annals of Oncology 2006 17(3):372-379; doi:10.1093/annonc/mdj057
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© 2005 European Society for Medical Oncology

review

Pulmonary toxicity from novel antineoplastic agents

I. Dimopoulou1,*, A. Bamias2, P. Lyberopoulos1 and M. A. Dimopoulos2

1 Second Department of Critical Care Medicine, Attikon University Hospital; 2 Department of Clinical Therapeutics, Alexandra Hospital, University of Athens, Medical School, Athens, Greece

* Correspondence to: Dr I. Dimopoulou, 2 Pesmazoglou Street, 14 561 Kifissia, Athens, Greece. Tel: +301-6200-663; Fax: +301-6202-939; E-mail: idimo{at}otenet.gr

Background: The pulmonary side-effects induced by novel antineoplastic agents have not been well characterized.

Methods: To further investigate this topic, relevant English and non-English language studies were identified through Medline. For our search we used the generic names of novel cytotoxic or non-cytotoxic antineoplastic agents and the key phrases pulmonary/lung toxicity, dyspnea, pneumonitis, acute lung injury, acute respiratory distress syndrome and alveolar damage. The references from the articles identified were reviewed for additional sources. Abstracts from International Meetings were also included. Furthermore, information was obtained from the Pneumotox® website, which provides updated knowledge on drug-induced respiratory disease as well as from pharmaceutical websites.

Results: Most novel antineoplastic drugs may induce pulmonary toxicity, which involves mainly the parenchyma, and less frequently the airways, pleura or the pulmonary circulation. Furthermore, a subset of these agents impairs pulmonary function tests. The exact incidence of lung toxicity remains unclear. The most common patterns consist of dyspnea without further details and infiltrative lung disease (ILD), denoting changes in the interstitium or alveoli. The diagnosis is one of exclusion. ILD is usually benign and responds to appropriate treatment; however, fatalities have been reported.

Conclusions: Clinicians should be aware of the potential of most novel antineoplastic agents to cause lung toxicity. A high index of suspicion is required if these are combined with other cytotoxic drugs or radiation.

Key words: acute respiratory distress syndrome, dyspnea, novel antineoplastic agents, pneumonitis, pulmonary function tests, pulmonary toxicity


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