Corticosteroid-responsive pulmonary toxicity associated with fludarabine monophosphate: a case report.

"DISCUSSION: Development of diffuse interstitial changes in the lungs can occur due to various reasons, such as connective tissue diseases, drugs, exposure to occupational and environmental toxins, and inherited conditions [9]. Many diverse etiologies of diffuse interstitial changes in the lungs may produce difficulties to establish the cause of pneumonitis. : Fludarabine monophosphate depletes CD4 cells, altering the CD4:CD8 ratio and producing a syndrome that is clinically and immunologically similar to acquired immunodeficiency [10,11]. The most common infections seen in patients treated with fludarabine are opportunistic infections caused by P. jiroveci, mycobacteria, cytomegalovirus, and Candida spp. [7]. : Interstitial pneumonitis induced by P. jiroveci presents with acute hypoxia, fever, and non-productive cough. : Chest X-ray in such cases shows pulmonary infiltrates and a very low arterial oxygen level. Chest X-ray in the presented patient showed diffuse interstitial changes with fibrotic alterations in the lungs, which are not characteristic of P. jioveci infection, and microbiological cultures of secretions obtained from bronchoscopy didn’t show evidence of P. jiroveci, the arterial oxygen level was 96%, and there was no response to trimethoprim/sulfamethoxazole treatment. The observed diffuse interstitial changes strongly suggested atypical pneumonia caused by M. pneumoniae or viral infection; however, viral infection in the lungs was excluded because it does not cause TLCO reduction. Antibodies against cytomegalovirus were negative. Pneumonitis due to M. pneumoniae was excluded because IgM antibodies were negative and there was no response to clarithromycin therapy. Laboratory data did not support the existence of connective tissue diseases. The patient’s anamnesis was negative for exposure to toxins, such as asbestosis, silica dust, and chest radiotherapy. : The incidence of fludarabine-associated pulmonary toxicity is not known. Helman et al. conducted a retrospective analysis of 105 patients with chronic lymphoproliferative diseases that were treated with fludarabine or fludarabine-containing regimens, and reported an 8.6% incidence of fludarabine-associated pulmonary toxicity [12]. The literature includes several case reports of interstitial pneumonitis related to fludarabine therapy [4,5,6,7,8,13]. In all cases the patients had non-productive cough, dyspnea, and fever, which typically began 1-2 weeks after the last course of chemotherapy. A relationship between the number of chemotherapy cycles and the development of pneumonitis was not established. In the four previous cases patients presented with the certain degree of hypoxia [4,5,8,13]. Garg et al. reported a patient with no signs of hypoxia [7]. In the presented patient pulse oximetry was 96% on room air. Kane et al. reported pneumonitis with severe respiratory failure [5] and Disel et al. reported a case of pneumonitis with rapidly progressing severe dyspnea, cyanosis, and massive pulmonary bleeding [8]. No deaths have been reported. : Radiographic changes consist mostly of diffuse reticular infiltrates, with or without nodularity, usually in the middle or lower zones of the lungs [7,14]. Chest X-ray in the presented patient showed bilateral pneumofibrotic changes and chest CT showed bilateral diffuse interstitial changes with the fibrotic alterations in the lower parts of the lungs. In all reported cases, as in the presented patient, the causes of infection (viral, bacterial, P. jiroveci, fungal) were excluded and antibiotic therapy was ineffective. In the presented patient a lung function test was performed (TLCO) and the result was 45%. The TLCO is a test used to diagnose, grade, and monitor diseases that affect gas transfer at the alveolar-capillary surface area. The test is useful for identification of disorders that affect lung parenchyma, interstitial lung diseases, and anemia that result from pulmonary hemorrhage, as is seen in chronic thromboembolic disease or pulmonary hypertension [15]. In previously reported cases this test was not performed and interstitial pneumonitis was pathologically confirmed via open lung biopsy in only in 1 published case [5]. : In previously reported cases, as in the presented patient, corticosteroids were administrated after excluding causes of infection that could have led to the pneumonitis. All reported patients had clinical response and resolution of radiographic findings. Tapering corticosteroid therapy for pneumonitis resulted in relapse in 1 patient, but after steroids were again administered a secondary response was induced [4]. Following reinstatement of fludarabine therapy recurrence of interstitial pneumonitis was observed in some patients [4,6,16]. : The mechanism of lung injury due to fludarabine is unknown. Response to steroids suggests an immunological mechanism, although direct toxicity cannot be ruled out [7]. Fludarabine therapy can induce pulmonary toxicity, ranging from mild to severe respiratory failure. If symptoms and radiographic findings indicate development of interstitial pneumonitis and possible etiological infections are excluded, fludarabine therapy should be terminated and steroid therapy should be initiated. : Conflict of Interest Statement: The authors of this paper have no conflicts of interest, including specific financial interests, relationships, and/ or affiliations relevant to the subject matter or materials included."