Association of cetuximab with adverse pulmonary events in cancer patients: A comprehensive review

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Abstract

Compounds derived from biologic sources, or biologicals, are increasingly utilized as therapeutic agents in malignancy. Development of anti-cancer targeted therapies from biologics is increasingly being utilized. Cetuximab, a chimeric monoclonal antibody, is one such anti-cancer targeted therapeutic that has shown efficacy in quelling the rate of patient decline in colorectal, head/neck, and non-small cell lung cancer. However, due to the relatively recent addition of biologic compounds to the therapeutic arsenal, information related to adverse reactions is less well known than those seen in traditional chemotherapeutics. Dermatologic reactions have been demonstrated as the most frequent side effect cited during cetuximab therapy for malignancy; however, other effects may lead to greater morbidity. In general, pulmonary complications of therapeutics can lead to significant morbidity and mortality. The purpose of this review is to compile the various pulmonary side effects seen in patients treated with cetuximab for various malignancies, and to compare the incidence of these adverse reactions to standard therapies. © 2009 Hoag et al; licensee BioMed Central Ltd.

Figures

  • Table 1: Studies included in the analysis including first author, year of publication, type of trial and combined therapy, and pulmonary adverse reactions.
  • Table 1: Studies included in the analysis including first author, year of publication, type of trial and combined therapy, and pulmonary adverse reactions. (Continued)
  • Table 2: Number and type of trials broken into groups according to cancer type.
  • Table 3: Number of patients included by trial type.
  • Table 4: Combined pulmonary adverse events cited in clinical trials.

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CITATION STYLE

APA

Hoag, J. B., Azizi, A., Doherty, T. J., Lu, J., Willis, R. E., & Lund, M. E. (2009). Association of cetuximab with adverse pulmonary events in cancer patients: A comprehensive review. Journal of Experimental and Clinical Cancer Research, 28(1). https://doi.org/10.1186/1756-9966-28-113

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