Original Article
A Randomized Trial of Inhaled Cyclosporine in Lung-Transplant Recipients
N Engl J Med 2006; 354:141-150January 12, 2006
- Abstract
Background
Conventional regimens of immunosuppressive drugs often do not prevent chronic rejection after lung transplantation. Topical delivery of cyclosporine in addition to conventional systemic immunosuppression might help prevent acute and chronic rejection events.
Methods
We conducted a single-center, randomized, double-blind, placebo-controlled trial of inhaled cyclosporine initiated within six weeks after transplantation and given in addition to systemic immunosuppression. A total of 58 patients were randomly assigned to inhale either 300 mg of aerosol cyclosporine (28 patients) or aerosol placebo (30 patients) three days a week for the first two years after transplantation. The primary end point was the rate of histologic acute rejection.
Results
The rates of acute rejection of grade 2 or higher were similar in the cyclosporine and placebo groups: 0.44 episode (95 percent confidence interval, 0.31 to 0.62) vs. 0.46 episode (95 percent confidence interval, 0.33 to 0.64) per patient per year, respectively (P=0.87 by Poisson regression). Survival was improved with aerosolized cyclosporine, with 3 deaths among patients receiving cyclosporine and 14 deaths among patients receiving placebo (relative risk of death, 0.20; 95 percent confidence interval, 0.06 to 0.70; P=0.01). Chronic rejection–free survival also improved with cyclosporine, as determined by spirometric analysis (10 events in the cyclosporine group and 20 events in the placebo group; relative risk of chronic rejection, 0.38; 95 percent confidence interval, 0.18 to 0.82; P=0.01) and histologic analysis (6 vs. 19 events, respectively; relative risk, 0.27; 95 percent confidence interval, 0.11 to 0.67; P=0.005). The risks of nephrotoxic effects and opportunistic infection were similar for patients in the cyclosporine group and the placebo group.
Conclusions
Inhaled cyclosporine did not improve the rate of acute rejection, but it did improve survival and extend periods of chronic rejection–free survival. (ClinicalTrials.gov number, NCT00268515.)
Media in This Article
Figure 1
Study Enrollment and Inclusion in the Intention-to-Treat and Survival Analyses.Figure 2
Kaplan–Meier Estimates of Chronic Rejection on the Basis of Bronchiolitis Obliterans Identified by Spirometric and Histologic Analyses.Article Activity
- Article
Outcomes after lung transplantation are poor as compared with those after heart, kidney, or liver transplantation, with a three-year survival rate of only 55 percent for recipients of lung transplants. Death is commonly due to chronic rejection,1 which presents histologically as bronchiolitis obliterans2-7); the latter is thought to be a complex response to immunologic, ischemic, and infectious injury.8-11 Preventive and therapeutic strategies for this process have been largely unsuccessful.12-14
Since the immunosuppressive effect of cyclosporine is dose-dependent, targeted delivery of this drug might improve efficacy by increasing the concentration of cyclosporine in the allograft. In animal models of lung transplantation, inhaled cyclosporine remains in high concentrations in lung tissue and reduces rejection without toxicity.15-18 Moreover, in human lung-transplant recipients with refractory acute and chronic rejection, open-label rescue treatment with inhaled cyclosporine improves clinical markers of rejection and improves survival.19-25 In light of these findings, we tested whether prophylactic inhaled cyclosporine would improve outcomes after lung transplantation.
Methods
Study Design
A randomized, double-blind, placebo-controlled trial of aerosol cyclosporine inhalation, given in addition to conventional immunosuppression, was conducted at the University of Pittsburgh Medical Center with approval of the institutional review board. Recipients of single or bilateral lung transplants who were at least 18 years of age were eligible. Patients were excluded from the study if they had active fungal or bacterial pneumonia, unresolved diffuse alveolar damage, or untreated bronchial stenosis or if they were receiving mechanical ventilation. From November 1998 to August 2001, patients were offered enrollment if they met the study criteria before day 42 after transplantation and were randomly assigned to a treatment group immediately after the provision of written informed consent. Study treatment began as soon as was practically possible thereafter, but no more than 55 days later.
Because mismatches between donor and recipient with respect to cytomegalovirus (CMV) serologic status are known to have an adverse effect on the outcome of transplantation, the randomization was stratified according to donor–recipient CMV status. The two categories were a primary mismatch (a CMV-positive donor and a CMV-negative recipient) and all other serologic combinations. Patients were then randomly assigned to groups according to permuted blocks of four in a 1:1 ratio to receive either inhaled cyclosporine or placebo for two years. All patients were followed for clinical outcome until the last subject completed the scheduled two-year regimen (August 2003). As a result, follow-up ranged from 24 to 56 months.
Novartis Pharmaceuticals provided cyclosporine powder, which was compounded by the University of Pittsburgh experimental pharmacy. University investigators were solely responsible for the trial design, data accrual, and study management. After completion of the study, Chiron obtained a license agreement for inhaled cyclosporine. The analyses presented in this article are those of the university investigators, unless otherwise noted. The data and safety monitoring board took no action regarding early trial cessation.
Administration of Inhaled Cyclosporine
Patients inhaled cyclosporine mixed in propylene glycol (62.5 mg per milliliter) or placebo (propylene glycol alone) initially for 10 consecutive days, then three times weekly with the use of a jet nebulizer (AeroTech II, CIS-US). Patients were instructed to continue treatment for two years. Patients were premedicated by inhalation of 2 percent lidocaine (3 ml) and 2.5 mg of albuterol by means of a nebulizer (Airlife, Cardinal Health). Inhaled cyclosporine was initiated at a dose of 100 mg and increased by incremental doses of 100 mg up to 300 mg or a maximally tolerated dose or an aerosol equivalent volume of placebo. Aerosols were self-administered by the patients and were temporarily discontinued if the treating physician reported an infection that persisted after antibiotic therapy. A study coordinator contacted the patients at least monthly to verify compliance.
Transplant Monitoring
Patients followed a typical care regimen for patients after lung transplantation, including surveillance bronchoscopy with transbronchial biopsy and bronchoalveolar lavage, spirometry, blood work, and a complete history and physical examination one month after transplantation and at intervals of approximately three months for the first two postoperative years, then at intervals of four to six months. Histologic rejection was defined according to established criteria.26 Spirometry was performed according to American Thoracic Society standards27 and the results expressed in terms of the percentage of predicted values.28 Because bronchiolitis obliterans is not uniformly detectable by biopsy, spirometry is routinely used as a surrogate marker to diagnose chronic rejection. Airflow measurements were evaluated for criteria of the bronchiolitis obliterans syndrome, which was defined as a sustained decrease in the forced expiratory volume in one second (FEV1) of at least 20 percent from the patient's maximum values in the absence of other causes.29 Cytomegalovirus status was assessed by CMV pp65 antigenemia at weekly intervals for six months after transplantation.
Clinical Management
Both groups received conventional immunosuppression, including tacrolimus (0.06 mg per kilogram of body weight per day), azathioprine (2 mg per kilogram per day), and prednisone (20 mg per day). Subsequent adjustments were made at the discretion of the treating clinician on the basis of lung function and biopsy results. Enhanced immune suppression for treatment of acute rejection (grade 2 or higher), active bronchiolitis obliterans, or both consisted of pulsed corticosteroids (intravenous methylprednisolone at a dose of 1 g per day for 3 days or oral prednisone at a dose of 100 mg tapered to 10 mg over 14 days) or rabbit antithymocyte globulin (Thymoglobulin [SangStat] at a dose of 1.5 mg per kilogram per day for 5 to 7 days). Intravenous ganciclovir was used if the level of antigenemia was more than 10 CMV-positive cells per 2×105 leukocytes.
End Points
The primary end point of the study was the frequency of histologic acute rejection. Secondary end points included chronic rejection–free survival and overall survival. Chronic rejection was identified on the basis of both histologic markers (for bronchiolitis obliterans) and spirometric markers (for the bronchiolitis obliterans syndrome).29
Adverse events were defined as infections requiring treatment, hospitalizations, and symptoms as reported by questionnaire. All evaluations of outcomes were performed in a blinded manner.
Statistical Analysis
Power analysis stipulating a 33 percent difference in the frequency of acute rejection suggested the enrollment of 136 patients on the basis of a two-sided test (α=0.05, β=0.15), an assumed acute-rejection rate of 2.8 events per year, and a dropout rate of 15 percent. The study prespecified a three-year enrollment period. During this time, all qualifying lung-transplant recipients were approached for participation. Enrollment was discontinued after three years, after the accrual of only 58 subjects. The failure to achieve enrollment goals was due to an overestimation of the number of transplantations that would be performed during the accrual period (anticipated number, 180; actual number performed, 121). The study was closed two years after the last subject had been enrolled. All outcome variables were followed until either the death of the patient or the end of the study (in August 2003), independent of the continuation or discontinuation of study medication or the conclusion of the scheduled two-year study-treatment period. Patients were analyzed according to the intention to treat, and no patients were lost to follow-up. Group means were compared with the use of unpaired, two-tailed t-tests or Mann–Whitney tests. All reported P values are two-sided and have not been adjusted for multiple testing.
The frequency of acute rejection was calculated by determining the number of rejection events of grade 2 or higher per year of study time for each subject. Differences between groups were also considered with the use of a Poisson regression model, with covariates including treatment group, CMV mismatch, and the occurrence or nonoccurrence of a rejection episode before the start of the study treatment. The Poisson model was calculated by Chiron.
Log-rank and Cox proportional-hazards analyses were used to compare survival and chronic rejection–free survival. Nonaerosol covariates that were tested in multivariate analyses included CMV-mismatch status, HLA-mismatch status, the age and sex of the recipient, the age and sex of the donor, smoking history of the recipient, diagnosis before transplantation, type of transplantation (single or double), and ischemic time. After closure of the study and unblinding, Chiron performed a follow-up analysis of survival as of June 2004. Statistical analyses were performed with Statview software (SAS).
Results
Characteristics of the Patients
Of the 121 patients who received lung transplants during the enrollment period, 58 were randomly assigned to a study group and 56 received at least one dose of study medication (inhaled cyclosporine, 26; placebo aerosol, 30) (Figure 1Figure 1
Study Enrollment and Inclusion in the Intention-to-Treat and Survival Analyses.). The baseline characteristics and clinical management in the two groups were similar (Table 1Table 1
Characteristics of the Patients.). The CMV-mismatch status, the number of biopsy procedures, the number of spirometric measurements, immunosuppressive-drug regimens, and tacrolimus levels were similar in patients in the two groups (Table 1 and Table 2Table 2
Characteristics of the Patients after Enrollment.).The mean duration of treatment was 400±57 days among patients receiving cyclosporine and 431±50 days among patients receiving placebo. Thirteen of the 28 patients in the cyclosporine group (46 percent) and 13 of the 30 patients in the placebo group (43 percent) completed the two-year inhalation period. Reasons for discontinuation are given in Table 2. Discontinuation that was initiated by patients (i.e., patients tolerated the aerosol administration but withdrew from the study) and concern on the part of investigators regarding infection accounted for most of the discontinuations in the cyclosporine group (43 percent) and the placebo group (37 percent), and there were no significant differences between the groups. Two patients in each group stopped treatment because of symptoms related to aerosol inhalation. Two patients in the placebo group and one in the cyclosporine group with refractory rejection were withdrawn from the study and entered into the separate open-label, “rescue” trial of inhaled cyclosporine. Two additional patients received open-label therapy after study medication was stopped. All data from these five patients after crossover were included in the statistical results in the intention-to-treat analysis.
Acute Rejection
We performed a total of 335 biopsies in patients in the cyclosporine group and 333 biopsies among patients in the placebo group. The mean number of biopsies (5.5 per patient per year) exceeded the minimum protocol requirements. The mean follow-up for acute rejection (mean time from study initiation to the last biopsy) was 2.4±0.2 years for the cyclosporine group and 2.2±0.2 years for the placebo group (P=0.43). The estimated number of acute-rejection episodes of grade 2 or higher per patient per year after the start of study-drug administration was 0.44 (95 percent confidence interval, 0.31 to 0.62) for the cyclosporine group and 0.46 (95 percent confidence interval, 0.33 to 0.64) for the placebo group. In each group, 17 patients had no more than one event per year; 26 patients in the cyclosporine group and 23 patients in the placebo group had no more than two events per year; and 26 patients in each group had no more than three events per year. A Poisson regression model with control for CMV-mismatch status and the occurrence or nonoccurrence of a rejection episode of grade 2 or higher before study-drug administration demonstrated that there was no significant difference between the treatment groups (P=0.87).
Chronic Rejection
Chronic rejection–free survival was improved among patients who were treated with inhaled cyclosporine as determined by spirometric and histologic evaluation. Figure 2AFigure 2
Kaplan–Meier Estimates of Chronic Rejection on the Basis of Bronchiolitis Obliterans Identified by Spirometric and Histologic Analyses. shows the results of a hazards analysis of survival free of the bronchiolitis obliterans syndrome, with 10 events in the cyclosporine group and 20 events in the placebo group (relative risk, 0.38; 95 percent confidence interval, 0.18 to 0.82; P=0.01). Figure 2B shows the results of a similar analysis of survival free of histologic bronchiolitis obliterans, with 6 events among patients in the cyclosporine group and 19 events among patients in the placebo group (relative risk, 0.27; 95 percent confidence interval, 0.11 to 0.67; P=0.005). None of the four patients in the cyclosporine group in whom histologic bronchiolitis obliterans was diagnosed were receiving study drug at the time of diagnosis.There was no significant difference in the number of methylprednisolone pulses or treatments with antilymphocyte globulin between the two groups. However, none of the 28 patients in the cyclosporine group were treated with sirolimus after other therapies for chronic rejection failed (as determined by histologic or spirometric analysis), as compared with 7 of 30 patients in the placebo group (P=0.006). Overall, more patients required treatment for histologic bronchiolitis obliterans in the placebo group (8 of 30 patients) than in the cyclosporine group (2 of 28 patients) (P=0.05).
Survival Analysis
The use of inhaled cyclosporine was associated with a substantial survival advantage (Figure 3Figure 3
Kaplan–Meier Estimates of Overall Survival.). There were 14 deaths (47 percent) in the placebo group, as compared with 3 deaths (11 percent) in the cyclosporine group (P=0.005 by log-rank analysis). Multivariate survival regression confirmed that the risk of death for patients receiving placebo was higher by a factor of 5 (relative risk of death in the cyclosporine group as compared with the placebo group, 0.20; 95 percent confidence interval, 0.06 to 0.70; P=0.01) and revealed no significant effect for CMV strata, transplant type, or HLA mismatch.Ten deaths were attributed to rejection, pneumonia, or sepsis (eight in the placebo group and two in the cyclosporine group). Three other patients with a known previous diagnosis of clinically significant rejection or pneumonia died of either pulmonary embolism (two patients in the placebo group) or congestive heart failure (one in the placebo group). Four patients with a known previous diagnosis of rejection (three with bronchiolitis obliterans) or pneumonia died outside our institution (three in the placebo group and one in the cyclosporine group) without postmortem verification of the cause of death.
A follow-up analysis of survival including all 56 patients who received study medication was conducted during the 10 months that followed the end of the study. During that period, an additional two patients in the cyclosporine group and one patient in the placebo group died. The results of log-rank analysis of survival were similar to those reported at study closure (P=0.02).30
Infection
The pneumonia rate was not significantly different in the two groups (13 patients in the cyclosporine group and 17 patients in the placebo group, P=0.44), and patients receiving aerosol cyclosporine were no more likely to be treated for infection than were patients in the placebo group (2.3±0.4 vs. 3.1±0.6 courses of antibiotic per patient per year, respectively; P=0.29). The risk of CMV pneumonitis was less in the cyclosporine group (3 of 28 patients) than in the placebo group (10 of 30 patients; P=0.04). The difference was confirmed by Cox proportional-hazards analysis with study drug and donor–recipient CMV status as covariates, with a relative risk of assignment to cyclosporine of 0.27 (P=0.05) and of CMV mismatch of 4.33 (P=0.009) among CMV-positive donors with CMV-negative recipients, as compared with all other combinations.
Adverse Events
Both cyclosporine and placebo aerosols were associated with local irritation, including cough, pharyngeal soreness, or dyspnea in 52 percent of study participants on the basis of responses to a questionnaire administered during clinical visits (Table 3Table 3
Adverse Events.). Such symptoms were observed in both groups, were typically transient, and were either mild or moderate in severity. When symptoms occurred, they usually resolved within 30 to 45 minutes after inhalation.Twelve patients were given a diagnosis of cancer (6 of 28 patients in the cyclosporine group and 6 of 30 patients in the placebo group, P=0.89). Although the overall area under the concentration–time curve (AUC) for the mean serum creatinine level was not significantly different in the two groups (1.5±0.1 mg per deciliter in the cyclosporine group and 1.7±0.1 mg per deciliter in the placebo group), a higher proportion of patients in the placebo group had an AUC mean creatinine level that was more than 1 SD above the all-patient mean (0 of 28 patients in the cyclosporine group and 6 of 30 patients in the placebo group, P=0.01). There was no significant difference between the groups in the number of hospital days per patient per year (23±4 in the cyclosporine group and 48±12 in the placebo group, P=0.07) or the number of hospitalizations per patient per year (2.1±0.5 in the cyclosporine group and 3.8±1.0 in the placebo group, P=0.17).
Discussion
Chronic rejection remains the leading cause of death after lung transplantation despite the use of systemic calcineurin inhibitors.31-33 The immunosuppressive effects of cyclosporine have been shown to be dose-dependent. However, high systemic levels of the drug cannot be achieved without significant toxicity, especially to the kidneys. We hypothesized that the inhalation of an aerosol cyclosporine would provide high pulmonary concentrations of the drug with minimal systemic toxicity, resulting in less acute and chronic rejection. This double-blind, placebo-controlled trial of inhaled cyclosporine given in addition to conventional immunosuppression after lung transplantation was negative with respect to its primary end point, since rates of acute rejection were similar in the group receiving cyclosporine and that receiving placebo. However, survival improved significantly with aerosol cyclosporine, as did the rate of chronic rejection–free survival (on the basis of both histologic and spirometric analysis).
In the absence of notable differences in rates of acute rejection, a positive result in terms of chronic rejection was unexpected, since previous studies have linked repeated acute rejection events with chronic rejection.2 Histologically, chronic rejection presents in the airways as bronchiolitis obliterans, whereas acute rejection presents as vasculitis. Bronchioles would have higher local concentrations of a drug as a result of direct aerosol delivery, whereas pharmacokinetic studies suggest a much less substantial vascular concentration of the drug.34-36 Therefore, it is possible that aerosol cyclosporine has a local airway antiinflammatory effect that decreases the likelihood of chronic rejection while having a lesser effect on vascular acute rejection.
The rates of pneumonia were similar in the two groups, as were serum creatinine levels. More than half the study patients had some level of local irritation (pharyngeal soreness, cough, or dyspnea), with no significant differences noted between patients in the two groups. Less than 10 percent of patients in the cyclosporine group withdrew because of symptoms associated with the aerosol. However, supervision during the first several treatments would probably be required, given the tenuous respiratory status of patients soon after transplantation. Many patients who had some initial minor respiratory symptoms developed a tolerance for the medication after a few treatments.
Local cyclosporine treatment had some benefit in this small, single-center trial. Further experience with inhaled cyclosporine is needed to confirm the magnitude and durability of the observed effects in recipients of single-lung and double-lung transplants.
Supported by a grant from the National Institutes of Health (HL059490 01, to Drs. Iacono and Griffith).
A U.S. patent application (20020006901) entitled “Use of Aerosolized Cyclosporine for Prevention and Treatment of Pulmonary Disease” was submitted on February 5, 1999, and assigned to the University of Pittsburgh, with Dr. Iacono listed as inventor. The patent has been licensed by the University of Pittsburgh to Chiron and Novartis Pharmaceuticals. In the event of eventual commercialization of aerosol cyclosporine, a royalty could be paid to the following investigators at the University of Pittsburgh and the State University of New York, Stony Brook: Dr. Iacono, Dr. Dauber, Dr. Smaldone, Dr. Zeevi, and Dr. Burckart. No author reports having any equity interest in either Chiron or Novartis as a stockholder or other related ownership interests. Drs. Iacono, Johnson, and Corcoran report having received consulting fees and Dr. Zeevi lecture fees from Chiron. Dr. McCurry reports having received a grant from Pfizer. Dr. Dauber reports having received lecture fees from and serving on an advisory board for InterMune. No other potential conflict of interest relevant to this article was reported.
We are indebted to Howard E. Rockette of the Department of Biostatistics at the University of Pittsburgh for trial design and for his assistance with statistical analyses; to Laurence S. Magder of the Department of Biostatistics–Informatics at the University of Maryland for his review of statistical analyses; to William B. Capra of Chiron in Emeryville, Calif., for performing the Poisson regression analysis and reviewing statistical analyses performed at the University of Pittsburgh; to Dr. Brack G. Hattler, Carmella R. Campbell, Mary C. Williams, Jan D. Manzetti, and Judi L. Vensak of the University of Pittsburgh Medical Center for their support for this project and assistance with patient care; to Dr. N. Paul Ohori of the Department of Pathology at the University of Pittsburgh for interpretation of lung biopsies; to Frank J. Clementi of the Sunrise Medical Home Healthcare Group, Somerset, Pa., for donating compressors; to Novartis in East Hanover, N.J., for supplying the cyclosporine powder needed to conduct this study; and to Dr. Maria M. Crespo of the Pulmonary Allergy and Critical Care Division, University of Pittsburgh Medical Center, and Dr. Edward P. Ingenito of the Pulmonary and Critical Care Division, Brigham and Women's Hospital, Boston, for their thoughtful review of the manuscript.
Source Information
From the Division of Pulmonary, Allergy and Critical Care Medicine (A.T.I., B.A.J., W.F.G., J.G.Y., T.E.C., D.A.S., J.H.D.), the Department of Pathology (A.Z., S.A.Y.), and the Thomas E. Starzl Transplantation Institute (J.J.F.), University of Pittsburgh Medical Center; and the Division of Cardiothoracic Surgery, University of Pittsburgh (K.R.M.) — all in Pittsburgh; the Division of Pulmonary and Critical Care Medicine, State University of New York at Stony Brook, Stony Brook (G.C.S.); the Department of Pharmacy, University of Southern California, Los Angeles (G.J.B.); and the Division of Cardiothoracic Surgery, University of Maryland, Baltimore (B.P.G.).
Address reprint requests to Dr. Iacono at the Division of Pulmonary Transplantation and Pulmonary and Critical Care Medicine, Medical School Teaching Facility 800, University of Maryland School of Medicine, 10 S. Pine St., Baltimore, MD 21201, or at aiacono@medicine.umaryland.edu.
- References
References
1
Lin HM ,Kauffman HM ,McBride MA , et al. Center-specific graft and patient survival rates: 1997 United Network for Organ Sharing (UNOS) report. JAMA 1998;280:1153-1160
CrossRef | Web of Science | Medline2
Bando K ,Paradis IL ,Similo S , et al. Obliterative bronchiolitis after lung and heart-lung transplantation: an analysis of risk factors and management. J Thorac Cardiovasc Surg 1995;110:4-13
CrossRef | Web of Science | Medline3
Sharples LD ,Tamm M ,McNeil K ,Higenbottam TW ,Stewart S ,Wallwork J . Development of bronchiolitis obliterans syndrome in recipients of heart-lung transplantation -- early risk factors. Transplantation 1996;61:560-566
CrossRef | Web of Science | Medline4
Hosenpud JD ,Bennett LE ,Keck BM ,Fiol B ,Boucek MM ,Novick RJ . The Registry of the International Society for Heart and Lung Transplantation: fifteenth official report -- 1998. J Heart Lung Transplant 1998;17:656-668
Web of Science | Medline5
Trulock EP . Management of lung transplant rejection. Chest 1993;103:1566-1576
CrossRef | Web of Science | Medline6
Yousem SA . Lymphocytic bronchitis/bronchiolitis in lung allograft recipients. Am J Surg Pathol 1993;17:491-496
CrossRef | Web of Science | Medline7
Yousem SA ,Duncan SR ,Griffith BP . Interstitial and airspace granulation tissue reactions in lung transplant recipients. Am J Surg Pathol 1992;16:877-884
CrossRef | Web of Science | Medline8
Date H ,Lynch JP ,Sundaresan S ,Patterson GA ,Trulock EP . The impact of cytolytic therapy on bronchiolitis obliterans syndrome. J Heart Lung Transplant 1998;17:869-875
Web of Science | Medline9
Tikkanen JM ,Lemstrom KB ,Koskinen PK . Blockade of CD28/B7-2 costimulation inhibits experimental obliterative bronchiolitis in rat tracheal allografts: suppression of helper T cell type 1-dominated immune response. Am J Respir Crit Care Med 2002;165:724-729
Web of Science | Medline10
Duncan SR ,Leonard C ,Theodore J , et al. Oligoclonal CD4(+) T cell expansions in lung transplant recipients with obliterative bronchiolitis. Am J Respir Crit Care Med 2002;165:1439-1444
CrossRef | Web of Science | Medline11
Duncan SR ,Valentine V ,Roglic M , et al. T cell receptor biases and clonal proliferations among lung transplant recipients with obliterative bronchiolitis. J Clin Invest 1996;97:2642-2650
CrossRef | Web of Science | Medline12
Kesten S ,Maidenberg A ,Winton T ,Maurer J . Treatment of presumed and proven acute rejection following six months of lung transplant survival. Am J Respir Crit Care Med 1995;152:1321-1324
Web of Science | Medline13
Trulock EP . Lung transplantation. Am J Respir Crit Care Med 1997;155:789-818
Web of Science | Medline14
Paradis I ,Yousem S ,Griffith B . Airway obstruction and bronchiolitis obliterans after lung transplantation. Clin Chest Med 1993;14:751-763
Web of Science | Medline15
Mitruka SN ,Won A ,McCurry KR , et al. In the lung aerosol cyclosporine provides a regional concentration advantage over intramuscular cyclosporine. J Heart Lung Transplant 2000;19:969-975
CrossRef | Web of Science | Medline16
Muggenberg BA ,Hoover MD ,Griffith BP . Administration of cyclosporine by inhalation: a feasibility study in beagle dogs. J Aerosol Med 1990;3:1-6
CrossRef17
Dowling RD ,Zenati M ,Burckart GJ , et al. Aerosolized cyclosporine as single-agent immunotherapy in canine lung allografts. Surgery 1990;108:198-204
Web of Science | Medline18
Keenan RJ ,Duncan AJ ,Yousem SA , et al. Improved immunosuppression with aerosolized cyclosporine in experimental pulmonary transplantation. Transplantation 1992;53:20-25
CrossRef | Web of Science | Medline19
Iacono AT ,Corcoran TE ,Griffith BP , et al. Aerosol cyclosporin therapy in lung transplant recipients with bronchiolitis obliterans. Eur Respir J 2004;23:384-390
CrossRef | Web of Science | Medline20
Iacono AT ,McCurry KR ,Corcoran TE . Inhalation cyclosporine: a new use in lung transplantation? Curr Opin Organ Transplant 2003;8:327-333
CrossRef21
Iacono AT ,Keenan RJ ,Duncan SR , et al. Aerosolized cyclosporine in lung recipients with refractory chronic rejection. Am J Respir Crit Care Med 1996;153:1451-1455
Web of Science | Medline22
Keenan RJ ,Zeevi A ,Iacono AT , et al. Efficacy of inhaled cyclosporine in lung transplant recipients with refractory rejection: correlation of intragraft cytokine gene expression with pulmonary function and histologic characteristics. Surgery 1995;118:385-391
CrossRef | Web of Science | Medline23
Keenan RJ ,Iacono A ,Dauber JH , et al. Treatment of refractory acute allograft rejection with aerosolized cyclosporine in lung transplant recipients. J Thorac Cardiovasc Surg 1997;113:335-340
CrossRef | Web of Science | Medline24
Iacono A ,Dauber J ,Keenan R , et al. Interleukin 6 and interferon-gamma gene expression in lung transplant recipients with refractory acute cellular rejection: implications for monitoring and inhibition by treatment with aerosolized cyclosporine. Transplantation 1997;64:263-269
CrossRef | Web of Science | Medline25
Iacono AT ,Smaldone GC ,Keenan RJ , et al. Dose-related reversal of acute lung rejection by aerosolized cyclosporine. Am J Respir Crit Care Med 1997;155:1690-1698
Web of Science | Medline26
Yousem SA ,Berry GJ ,Cagle PT , et al. Revision of the 1990 working formulation for the classification of pulmonary allograft rejection: Lung Rejection Study Group. J Heart Lung Transplant 1996;15:1-15
Web of Science | Medline27
Standardization of spirometry, 1994 update: American Thoracic Society. Am J Respir Crit Care Med 1995;152:1107-1136
Web of Science | Medline28
Morris JF . Spirometry in the evaluation of pulmonary function. West J Med 1976;125:110-118
Medline29
Estenne M ,Maurer JR ,Boehler A , et al. Bronchiolitis obliterans syndrome 2001: an update of the diagnostic criteria. J Heart Lung Transplant 2002;21:297-310
CrossRef | Web of Science | Medline30
Iacono AT ,Capra WB ,Shrewsbury SB , et al. Long-term follow-up of a double-blind, randomized, placebo-controlled trial of Cyclosporine Inhalation Solution (CyIS) in lung transplant recipients. J Heart Lung Transplant 2005;24:S82-S83
CrossRef | Web of Science31
Di Padova FE . Pharmacology of cyclosporine (Sandimmune). V. Pharmacological effects on immune function: in vitro studies. Pharmacol Rev 1990;41:373-405
Web of Science | Medline32
Losa Garcia JE ,Mateos Rodriguez F ,Jiminez Lopez A , et al. Effect of cyclosporin A on inflammatory cytokine production by human alveolar macrophages. Respir Med 1998;92:722-728
CrossRef | Web of Science | Medline33
Eickelberg O ,Pansky A ,Koehler E , et al. Molecular mechanisms of TGF-β antagonism by interferon-γ and cyclosporine A in lung fibroblasts. FASEB J 2001;15:797-806
CrossRef | Web of Science | Medline34
Burckart GJ ,Smaldone GC ,Eldon MA , et al. Lung deposition and pharmacokinetics of cyclosporine after aerosolization in lung transplant patients. Pharm Res 2003;20:252-256
CrossRef | Web of Science | Medline35
Corcoran TE ,Smaldone GC ,Dauber JH , et al. Preservation of post-transplant lung function with aerosol cyclosporine. Eur Respir J 2004;23:378-383
CrossRef | Web of Science | Medline36
O'Riordan TG ,Iacono A ,Keenan RJ , et al. Delivery and distribution of aerosolized cyclosporine in lung allograft recipients. Am J Respir Crit Care Med 1995;151:516-521
Web of Science | Medline
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David C. Cipolla, Igor Gonda. (2011) Formulation technology to repurpose drugs for inhalation delivery. Drug Discovery Today: Therapeutic Strategies
CrossRef5
Roger D. Yusen. (2011) Survival and Quality of Life of Patients Undergoing Lung Transplant. Clinics in Chest Medicine 32:2, 253-264
CrossRef6
Timothy Floreth, Sangeeta M. Bhorade, Vivek N. Ahya. (2011) Conventional and Novel Approaches to Immunosuppression. Clinics in Chest Medicine 32:2, 265-277
CrossRef7
Herbert Y. Reynolds. (2011) Bronchoalveolar Lavage and Other Methods to Define the Human Respiratory Tract Milieu in Health and Disease. Lung 189:2, 87-99
CrossRef8
Myrna B Dolovich, Rajiv Dhand. (2011) Aerosol drug delivery: developments in device design and clinical use. The Lancet 377:9770, 1032-1045
CrossRef9
C E Lucid, B N Savani, B G Engelhardt, P Shah, C Clifton, S L Greenhut, L A Vaughan, A Kassim, F Schuening, M Jagasia. (2011) Extracorporeal photopheresis in patients with refractory bronchiolitis obliterans developing after allo-SCT. Bone Marrow Transplantation 46:3, 426-429
CrossRef10
Jonathan E Spahr, Keith C Meyer. 2011. Lung Transplantation. , 205-237.
CrossRef11
Alan B. Watts, Jay I. Peters, Robert L. Talbert, Kevin P. O’Donnell, Jacqueline J. Coalson, Robert O. Williams. (2011) Preclinical evaluation of tacrolimus colloidal dispersion for inhalation. European Journal of Pharmaceutics and Biopharmaceutics 77:2, 207-215
CrossRef12
Ralph W. Niven. (2011) Toward managing chronic rejection after lung transplant: The fate and effects of inhaled cyclosporine in a complex environment. Advanced Drug Delivery Reviews 63:1-2, 88-109
CrossRef13
Fernanda Andrade, Mafalda Videira, Domingos Ferreira, Bruno Sarmento. (2011) Nanocarriers for pulmonary administration of peptides and therapeutic proteins. Nanomedicine 6:1, 123-141
CrossRef14
Don Hayes. (2011) A review of bronchiolitis obliterans syndrome and therapeutic strategies. Journal of Cardiothoracic Surgery 6:1, 92
CrossRef15
Jeffry G. Weers, John Bell, Hak-Kim Chan, David Cipolla, Craig Dunbar, Anthony J. Hickey, Ian J. Smith. (2010) Pulmonary Formulations: What Remains to be Done?. Journal of Aerosol Medicine and Pulmonary Drug Delivery 23:S2, S-5-S-23
CrossRef16
Tammy Abuan, Melissa Yeager, A. Bruce Montgomery. (2010) Inhaled Lidocaine for the Treatment of Asthma: Lack of Efficacy in Two Double-Blind, Randomized, Placebo-Controlled Clinical Studies. Journal of Aerosol Medicine and Pulmonary Drug Delivery 23:6, 381-388
CrossRef17
James C. Lee, Vivek N. Ahya. (2010) Lung Transplantation in Autoimmune Diseases. Clinics in Chest Medicine 31:3, 589-603
CrossRef18
M. Solomon, H. Grasemann, S. Keshavjee. (2010) Pediatric Lung Transplantation. Pediatric Clinics of North America 57:2, 375-391
CrossRef19
Michael Hindle. 2010. Aerosol Drug Delivery. .
CrossRef20
Gary M. Doherty, Paul Aurora. (2010) Update on Paediatric Lung Transplantation. Paediatric Respiratory Reviews 11:1, 54-61
CrossRef21
Soleyah Groves, Marek Galazka, Bruce Johnson, Timothy Corcoran, Avelino Verceles, Edward Britt, Nevins Todd, Bartley Griffith, Gerald C. Smaldone, Aldo Iacono. (2010) Inhaled Cyclosporine and Pulmonary Function in Lung Transplant Recipients. Journal of Aerosol Medicine and Pulmonary Drug Delivery 23:1, 31-39
CrossRef22
Jeremy A. Falk, Scott Oh, C. Joyce Lee, Hari Reddy, George E. Chaux, Michael I. Lewis. 2010. Intermediate and Late Complications of Lung Transplantation. , 335-351.
CrossRef23
Selim M Arcasoy. (2009) Editorial introduction: current state of lung transplantation. Current Opinion in Organ Transplantation 14:5, 463-465
CrossRef24
Michael Rosenblum, Mark J. van der Laan. (2009) Using Regression Models to Analyze Randomized Trials: Asymptotically Valid Hypothesis Tests Despite Incorrectly Specified Models. Biometrics 65:3, 937-945
CrossRef25
Isabel P Neuringer, Peadar Noone, Rebecca K Cicale, Ken Davis, Robert M Aris. (2009) Managing complications following lung transplantation. Expert Review of Respiratory Medicine 3:4, 403-423
CrossRef26
Juergen Behr, Gregor Zimmermann, Rainer Baumgartner, Hanno Leuchte, Claus Neurohr, Peter Brand, Christine Herpich, Kurt Sommerer, Jochen Seitz, Gerhard Menges, Sascha Tillmanns, Manfred Keller. (2009) Lung Deposition of a Liposomal Cyclosporine A Inhalation Solution in Patients after Lung Transplantation. Journal of Aerosol Medicine and Pulmonary Drug Delivery 22:2, 121-130
CrossRef27
Stephan Korom, Annette Boehler, Walter Weder. (2009) Immunosuppressive therapy in lung transplantation: state of the art. European Journal of Cardio-Thoracic Surgery 35:6, 1045-1055
CrossRef28
Gerrit S. Zijlstra, Joske Wolting, Jochum Prop, Arjen H. Petersen, Wouter L.J. Hinrichs, Donald R.A. Uges, Huib A.M. Kerstjens, Wim van der Bij, Henderik W. Frijlink. (2009) Efficacy of a New Pulmonary Cyclosporine A Powder Formulation for Prevention of Transplant Rejection in Rats. The Journal of Heart and Lung Transplantation 28:5, 486-492
CrossRef29
(2009) Terapias respiratorias. Archivos de Bronconeumología 45, 2-28
CrossRef30
Alexander S Krupnick, Xue Lin, Wenjun Li, Mikio Okazaki, Jiaming Lai, Seiichiro Sugimoto, Steven B Richardson, Christopher G Kornfeld, Joel R Garbow, G Alexander Patterson, Andrew E Gelman, Daniel Kreisel. (2008) Orthotopic mouse lung transplantation as experimental methodology to study transplant and tumor biology. Nature Protocols 4:1, 86-93
CrossRef31
Jasmine M. Tam, Jason T. McConville, Robert O. Williams, Keith P. Johnston. (2008) Amorphous cyclosporin nanodispersions for enhanced pulmonary deposition and dissolution. Journal of Pharmaceutical Sciences 97:11, 4915-4933
CrossRef32
Beatrice Trammer, Annette Amann, Eleonore Haltner-Ukomadu, Sascha Tillmanns, Manfred Keller, Petra Högger. (2008) Comparative permeability and diffusion kinetics of cyclosporine A liposomes and propylene glycol solution from human lung tissue into human blood ex vivo. European Journal of Pharmaceutics and Biopharmaceutics 70:3, 758-764
CrossRef33
J.-C. Dubus, S. Ravilly. (2008) Aérosolthérapie dans la mucoviscidose. Revue des Maladies Respiratoires 25:8, 989-998
CrossRef34
Herbert Chiou, Hak-Kim Chan, Desmond Heng, Robert K. Prud’homme, Judy A. Raper. (2008) A novel production method for inhalable cyclosporine A powders by confined liquid impinging jet precipitation. Journal of Aerosol Science 39:6, 500-509
CrossRef35
Brian E. Gilbert, Matthew T. McLeay. (2008) MegaRibavirin aerosol for the treatment of influenza A virus infections in mice. Antiviral Research 78:3, 223-229
CrossRef36
Masaaki Sato, Shaf Keshavjee. (2008) Bronchiolitis Obliterans Syndrome: Alloimmune-Dependent and -Independent Injury with Aberrant Tissue Remodeling. Seminars in Thoracic and Cardiovascular Surgery 20:2, 173-182
CrossRef37
M. Galazka, S. Groves, T. Corcoran, B. Johnson, A. Suffredini, E. Britt, B. Sherman, S. Augustine, S. Moainie, N. Todd, B. Griffith, A. Iacono. (2008) 403: Preservation of Pulmonary Function by Inhaled Cyclosporine in Lung Transplant Recipients. The Journal of Heart and Lung Transplantation 27:2, S206
CrossRef38
A. Bergeron, S. Feuillet, V. Meignin, G. Socie, A. Tazi. (2008) Les complications pulmonaires tardives non infectieuses après allogreffe de cellules souches hématopoïétiques. Revue des Maladies Respiratoires 25:2, 173-183
CrossRef39
J Michael Tredger, Nigel W Brown, Anil Dhawan. (2008) Calcineurin Inhibitor Sparing in Paediatric Solid Organ Transplantation. Drugs 68:10, 1385-1414
CrossRef40
Rees L. Lee, Carl W. White. 2008. Bronchiolitis Obliterans. , 1031-1038.
CrossRef41
Tao Wang, Sarah Noonberg, Ronald Steigerwalt, Maryellen Lynch, Rosemary A. Kovelesky, Carlos A. Rodríguez, Katherine Sprugel, Nancy Turner. (2007) Preclinical Safety Evaluation of Inhaled Cyclosporine in Propylene Glycol. Journal of Aerosol Medicine 20:4, 417-428
CrossRef42
Allan L. Coates, Maria Green, Kitty Leung, Emily Louca, Markus Tservistas, Jeffrey Chan, Nancy Ribeiro, Martin Charron. (2007) The Challenges of Quantitative Measurement of Lung Deposition Using 99m Tc-DTPA from Delivery Systems with Very Different Delivery Times. Journal of Aerosol Medicine 20:3, 320-330
CrossRef43
J.E. Spahr, R.B. Love, M. Francois, K. Radford, K.C. Meyer. (2007) Lung transplantation for cystic fibrosis: Current concepts and one center's experience. Journal of Cystic Fibrosis 6:5, 334-350
CrossRef44
Satoshi Yoshihara, Gregory Yanik, Kenneth R. Cooke, Shin Mineishi. (2007) Bronchiolitis Obliterans Syndrome (BOS), Bronchiolitis Obliterans Organizing Pneumonia (BOOP), and Other Late-Onset Noninfectious Pulmonary Complications following Allogeneic Hematopoietic Stem Cell Transplantation. Biology of Blood and Marrow Transplantation 13:7, 749-759
CrossRef45
S. Schrepfer, T. Deuse, H. Reichenspurner, J. Hoffmann, M. Haddad, J. Fink, M. P. Fischbein, R. C. Robbins, M. P. Pelletier. (2007) Effect of Inhaled Tacrolimus on Cellular and Humoral Rejection to Prevent Posttransplant Obliterative Airway Disease. American Journal of Transplantation 7:7, 1733-1742
CrossRef46
Gerrit S. Zijlstra, Michiel Rijkeboer, Dirk Jan Drooge, Marc Sutter, Wim Jiskoot, Marco Weert, Wouter L. J. Hinrichs, Henderik W. Frijlink. (2007) Characterization of a cyclosporine solid dispersion for inhalation. The AAPS Journal 9:2, E190-E199
CrossRef47
Tobias Deuse, Sonja Schrepfer, Hermann Reichenspurner, Grant Hoyt, Michael P. Fischbein, Robert C. Robbins, Marc P. Pelletier. (2007) Techniques for experimental heterotopic and orthotopic tracheal transplantations — When to use which model?. Transplant Immunology 17:4, 255-261
CrossRef48
William J. Steinbach, Jennifer L. Reedy, Robert A. Cramer, John R. Perfect, Joseph Heitman. (2007) Harnessing calcineurin as a novel anti-infective agent against invasive fungal infections. Nature Reviews Microbiology 5:6, 418-430
CrossRef49
S. M. Palmer, W. Klimecki, L. Yu, N. L. Reinsmoen, L. D. Snyder, T. M. Ganous, L. Burch, D. A. Schwartz. (2007) Genetic Regulation of Rejection and Survival Following Human Lung Transplantation by the Innate Immune Receptor CD14. American Journal of Transplantation 7:3, 693-699
CrossRef50
Babith Mankidy, Ramesh B Kesavan, Yavuz S Silay, Tarik J Haddad, Harish Seethamraju. (2007) Emerging drugs in lung transplantation. Expert Opinion on Emerging Drugs 12:1, 61-73
CrossRef51
Noboru Ide, Takeshi Nagayasu, Keitarou Matsumoto, Tsutomu Tagawa, Kenji Tanaka, Tsunenori Taguchi, Yorihisa Sumida, Mikiro Nakashima. (2007) Efficacy and safety of inhaled tacrolimus in rat lung transplantation. The Journal of Thoracic and Cardiovascular Surgery 133:2, 548-553
CrossRef52
Paul S Myles, Greg I Snell, Glen P Westall. (2007) Lung transplantation. Current Opinion in Anaesthesiology 20:1, 21-26
CrossRef53
Rukia Marijani, Madhu Sudhan Shaik, Abhijit Chatterjee, Mandip Singh, Rukia Marijani, Madhu Sudhan Shaik, Abhijit Chatterjee, Mandip Singh. (2007) Evaluation of metered dose inhaler (MDI) formulations of ciclosporin. Journal of Pharmacy and Pharmacology 59:1, 15-21
CrossRef54
J.R. Maurer. (2007) A Randomized Trial of Inhaled Cyclosporine in Lung-Transplant Recipients. Yearbook of Pulmonary Disease 2007, 223-224
CrossRef55
T. E. Corcoran, R. Venkataramanan, K. M. Mihelc, A. L. Marcinkowski, J. Ou, B. M. McCook, L. Weber, M.-E. Carey, D. L. Paterson, J. M. Pilewski, K. R. McCurry, S. Husain. (2006) Aerosol Deposition of Lipid Complex Amphotericin-B (Abelcet) in Lung Transplant Recipients. American Journal of Transplantation 6:11, 2765-2773
CrossRef56
H. Mal. (2006) Transplantation pulmonaire. Revue des Maladies Respiratoires 23:5, 178-179
CrossRef57
T.E. Corcoran. (2006) Inhaled delivery of aerosolized cyclosporine. Advanced Drug Delivery Reviews 58:9-10, 1119-1127
CrossRef58
P H Tan. (2006) World Transplant Congress. Expert Opinion on Biological Therapy 6:10, 1061-1065
CrossRef59
Martin Carby, Haifa Lyster. (2006) A novel approach to immunosuppression: targeting the alloimmune mechanisms of graft rejection. Current Opinion in Organ Transplantation 11:5, 496-501
CrossRef60
Jagdish L. Italia, Vivekanand Bhardwaj, M.N.V. Ravi Kumar. (2006) Disease, destination, dose and delivery aspects of ciclosporin: the state of the art. Drug Discovery Today 11:17-18, 846-854
CrossRef61
Gilbert J Burckart. (2006) Ciclosporin aerosol in lung transplantation. Expert Opinion on Investigational Drugs 15:8, 981-986
CrossRef62
(2006) Inhaled Cyclosporine in Lung Transplantation. New England Journal of Medicine 354:16, 1752-1753
Full Text63
G J Burckart, I V Hutchinson, A Zeevi. (2006) Pharmacogenomics and lung transplantation: clinical implications. The Pharmacogenomics Journal
CrossRef64
Gerald C. Smaldone. (2006) Advances in Aerosols: Adult Respiratory Disease. Journal of Aerosol Medicine 19:1, 36-46
CrossRef65
DeCamp, Malcolm M. Jr., . (2006) Inhaled Cyclosporine — A Breath of Fresh Air?. New England Journal of Medicine 354:2, 191-193
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