Pediatric lung transplantation: The years 1985 to 1992 and the clinical trial of FK 506

1993 ◽  
Vol 28 (11) ◽  
pp. 1510
Author(s):  
Thomas F. Tracy
1992 ◽  
Vol 103 (6) ◽  
pp. 1127-1135 ◽  
Author(s):  
Takashi Hirai ◽  
Hiromi Wada ◽  
Seiki Hasegawa ◽  
Kenji Inui ◽  
Hiroyasu Yokomise ◽  
...  

Trials ◽  
2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Alberto Benazzo ◽  
Ara Cho ◽  
Anna Nechay ◽  
Stefan Schwarz ◽  
Florian Frommlet ◽  
...  

Abstract Background Long-term outcomes of lung transplantation are severely affected by comorbidities and development of chronic rejection. Among the comorbidities, kidney insufficiency is one of the most frequent and it is mainly caused by the cumulative effect of calcineurin inhibitors (CNIs). Currently, the most used immunosuppression protocols worldwide include induction therapy and a triple-drug maintenance immunosuppression, with one calcineurin inhibitor, one anti-proliferative drug, and steroids. Our center has pioneered the use of alemtuzumab as induction therapy, showing promising results in terms of short- and long-term outcomes. The use of alemtuzumab followed by a low-dose double drug maintenance immunosuppression, in fact, led to better kidney function along with excellent results in terms of acute rejection, chronic lung allograft dysfunction, and survival (Benazzo et al., PLoS One 14(1):e0210443, 2019). The hypothesis driving the proposed clinical trial is that de novo introduction of low-dose everolimus early after transplantation could further improve kidney function via a further reduction of tacrolimus. Based on evidences from kidney transplantation, moreover, alemtuzumab induction therapy followed by a low-dose everolimus and low-dose tacrolimus may have a permissive action on regulatory immune cells thus stimulating allograft acceptance. Methods A randomized prospective clinical trial has been set up to answer the research hypothesis. One hundred ten patients will be randomized in two groups. Treatment group will receive the new maintenance immunosuppression protocol based on low-dose tacrolimus and low-dose everolimus and the control group will receive our standard immunosuppression protocol. Both groups will receive alemtuzumab induction therapy. The primary endpoint of the study is to analyze the effect of the new low-dose immunosuppression protocol on kidney function in terms of eGFR change. The study will have a duration of 24 months from the time of randomization. Immunomodulatory status of the patients will be assessed with flow cytometry and gene expression analysis. Discussion For the first time in the field of lung transplantation, this trial proposes the combined use of significantly reduced tacrolimus and everolimus after alemtuzumab induction. The new protocol may have a twofold advantage: (1) further reduction of nephrotoxic tacrolimus and (2) permissive influence on regulatory cells development with further reduction of rejection episodes. Trial registration EUDRACT Nr 2018-001680-24. Registered on 15 May 2018


1995 ◽  
Vol 60 (3) ◽  
pp. 580-585 ◽  
Author(s):  
Robert J. Keenan ◽  
Heroaki Konishi ◽  
Akihiko Kawai ◽  
Irvin L. Paradis ◽  
David R. Nunley ◽  
...  

2005 ◽  
Vol 24 (5) ◽  
pp. 538-543 ◽  
Author(s):  
Akira Ingu ◽  
Kanshi Komatsu ◽  
Shingo Ichimiya ◽  
Noriyuki Sato ◽  
Yoshitaka Hirayama ◽  
...  

1992 ◽  
Vol 54 (2) ◽  
pp. 205-211 ◽  
Author(s):  
John M. Armitage ◽  
Robert L. Kormos ◽  
Shigeki Morita ◽  
John Fung ◽  
Gary C. Marrone ◽  
...  

CHEST Journal ◽  
1997 ◽  
Vol 112 (5) ◽  
pp. 1175-1179 ◽  
Author(s):  
David J. Ross ◽  
Michael Ian Lewis ◽  
Michelle Kramer ◽  
Ashley Vo ◽  
Robert M. Kass

2018 ◽  
Vol 12 ◽  
pp. 175346661880061 ◽  
Author(s):  
Pilar Rivera-Ortega ◽  
Conal Hayton ◽  
John Blaikley ◽  
Colm Leonard ◽  
Nazia Chaudhuri

Idiopathic pulmonary fibrosis (IPF) is a fibrotic interstitial lung disease associated with significant morbidity and mortality. Previously, IPF has been managed using immunosuppressive therapy; however, it has been shown that this is associated with increased mortality. In the last 5 years, two disease-modifying agents have been licensed for use in IPF, namely pirfenidone and nintedanib. Nintedanib is a tyrosine kinase inhibitor with antifibrotic properties that has also been shown to significantly reduce the progression of the disease. The scientific evidence shows that nintedanib is effective and well tolerated for the treatment of IPF in mild, moderate and severe stages of the disease. Real-world experiences also support the findings of previously conducted clinical trials and show that nintedanib is effective for the management of IPF and is associated with reducing disease progression. Gastrointestinal events, mainly diarrhoea, are the main adverse events caused by the treatment. Recent real-word studies also suggest that nintedanib stabilizes lung function till lung transplantation, with no increased surgical complications or postoperative mortality after lung transplantation. In this review, we will discuss the clinical trial evidence and real-world experience for nintedanib in the management of IPF.


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