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Long‐term efficacy and safety of aerosolized tobramycin 300 mg/4 ml in cystic fibrosis

Aerosolized tobramycin is a standard of care for chronic Pseudomonas aeruginosa (Pa) infection in patients with cystic fibrosis (CF).

Objectives : The long-term safety and efficacy of intermittent (28-day “on”/“off” cycles) inhaled tobramycin nebulization solution 300 mg/4 ml (TNS4, Bramitob®/Bethkis®) was assessed over 56 weeks in CF patients aged ≥6 years having baseline 1 sec forced expiratory volume (FEV1) 40–80% predicted.

Methods : Patients were initially randomized in an 8-week open-label trial (core phase) to compare TNS4 (N = 159) and tobramycin 300 mg/5 ml (TNS5, TOBI®) (N = 165). A subset of patients continued in a 48-week, single-arm extension receiving TNS4 only. The primary endpoint of the core phase was to demonstrate the non-inferiority of TNS4 compared to TNS5 in terms of absolute change from baseline to week 4 in FEV1 % predicted. The assessment of long-term safety was the primary purpose of the extension phase. Throughout all phases of the study, microbiological assessments, adverse events, and audiometry findings were also evaluated.

Results : In the core phase (N = 321), FEV1 (% predicted) increased from baseline (absolute change) following a single on-treatment cycle for both TNS4 (7.0%) and TNS5 (7.5%) and the non-inferiority between treatments was met [difference between treatments of −0.5 (95% CI: −2.6; 1.6)]. These improvements were maintained throughout the extension phase (N = 209), ranging throughout the study between 5.1% (95% CI: 3.2; 6.9) and 8.1% (95% CI: 6.8; 9.4) compared to baseline. Pa sputum count reductions ranged between 0.6 (95% CI: 0.2; 0.9) to 2.3 (95% CI: 2.0; 2.6) log10 CFU/g throughout the 56 weeks. No remarkable safety issues were identified throughout both study phases, with similar percentages of patients reporting adverse events in the two treatment groups during the 8-week core phase [TNS4 (31.4%); TNS5 (28.0%)].

Conclusions : Overall, TNS4 demonstrated short-term clinical benefits similar to TNS5 which were maintained during the long-term use of TNS4 and was also associated with a favorable tolerability profile.

Nodule characterization: subsolid nodules.

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Nodule characterization: subsolid nodules.

Radiol Clin North Am. 2014 Jan;52(1):47-67

Authors: Raad RA, Suh J, Harari S, Naidich DP, Shiau M, Ko JP

Abstract
In this review, we focus on the radiologic, clinical, and pathologic aspects primarily of solitary subsolid pulmonary nodules. Particular emphasis will be placed on the pathologic classification and correlative computed tomography (CT) features of adenocarcinoma of the lung. The capabilities of fluorodeoxyglucose positron emission tomography-CT and histologic sampling techniques, including CT-guided biopsy, endoscopic-guided biopsy, and surgical resection, are discussed. Finally, recently proposed management guidelines by the Fleischner Society and the American College of Chest Physicians are reviewed.

PMID: 24267710 [PubMed - indexed for MEDLINE]

The clinical staging of lung cancer through imaging: a radiologist's guide to the revised staging system and rationale for the changes.

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The clinical staging of lung cancer through imaging: a radiologist's guide to the revised staging system and rationale for the changes.

Radiol Clin North Am. 2014 Jan;52(1):69-83

Authors: Kligerman S

Abstract
In 2009, the International Union Against Cancer and the American Joint Committee on Cancer accepted a revised staging system for the staging of lung cancer. Changes to the staging system were made to correlate patient survival more accurately with characteristics of the primary tumor (T) and presence or extent of nodal (N) and metastatic disease (M). Many changes were made to the staging system, most notably within the tumor (T) and metastases (M) designations. There are many ways to clinical stage lung cancer, but PET-CT remains one of the most accurate noninvasive methods.

PMID: 24267711 [PubMed - indexed for MEDLINE]

The idiopathic interstitial pneumonias: an update and review.

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The idiopathic interstitial pneumonias: an update and review.

Radiol Clin North Am. 2014 Jan;52(1):105-20

Authors: Hobbs S, Lynch D

Abstract
Idiopathic interstitial pneumonias (IIPs) are a group of disorders with distinct histologic and radiologic appearances and no identifiable cause. The IIPs comprise 8 currently recognized entities. Each of these entities demonstrates a prototypical imaging and histologic pattern, although in practice the imaging patterns may overlap, and some interstitial pneumonias are not classifiable. To be considered an IIP, the disease must be idiopathic; however, each pattern may be secondary to a recognizable cause, most notably collagen vascular disease, hypersensitivity pneumonitis, or drug reactions. The diagnosis of IIP requires the correlation of clinical, imaging, and pathologic features.

PMID: 24267713 [PubMed - indexed for MEDLINE]

Thoracic infections in immunocompromised patients.

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Thoracic infections in immunocompromised patients.

Radiol Clin North Am. 2014 Jan;52(1):121-36

Authors: Ahuja J, Kanne JP

Abstract
Infections account for approximately 75% of all pulmonary complications in immunocompromised patients, and early and accurate diagnosis is essential because of associated high morbidity and mortality. The number of immunocompromised patients continues to increase because of greater use of immunosuppressive agents. Certain organisms are likely to cause infection with certain types of immunosuppression and during specific times during the course of immunosuppression. Knowledge of the acuity of the patient's illness, environmental exposures, nature of the underlying immune defect(s), and duration and severity of immunodeficiency can help the radiologist provide a more accurate differential diagnosis for the cause of pulmonary infection.

PMID: 24267714 [PubMed - indexed for MEDLINE]

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