Gemcitabine‐induced severe pulmonary toxicity

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Abstract
Gemcitabine is a relatively new deoxycytidine analog (2′,2′‐difluorodeoxycytidine) with structural similarities to cytosine arabinoside (Ara‐C). Activity of gemcitabine is demonstrated in the treatment of many solid tumors, like pancreas, ovarian and nonsmall cell lung cancer (NSCLC). Although gemcitabine is considered as a drug with a good safety profile, cases of gemcitabine‐induced severe pulmonary toxicity (GISPT) were reported as for Ara‐C. We performed a systematic review of reported cases on the GISPT. Twenty‐nine clinical trials especially interesting NSCLC patients (21) and 21 reported cases recording 40 patients were analyzed. The incidence of the GISPT varies from 0 to 5%. The clinical presentation is a subacute clinical syndrome and is frequently nonspecific. The predominant radiographic pattern on chest X‐ray are reticulo‐nodular interstitial infiltrates. It was postulated that the physio‐pathological mechanism of the GISPT was an inflammatory reaction of the alveolar capillary wall cytokine‐mediated, which created an abnormal permeability of its membrane. After the differential diagnosis were ruled out, the discontinuation of the drug and the early initiation of steroids and diuretics are the most frequently performed treatments. Under these conditions, the outcome was favorable in a delay of few days generally for a majority of patients but 20% of patients died. Some risk factors, as a previous pulmonary disease or a previous thoracic irradiation, for the occurrence of the GISPT were proposed. GISPT is rare but sometimes fatal. Its a necessity to increase awareness about it to enhanced an early and suitable management of patients developing such a toxicity after gemcitabine administration.