All content on this site is intended for healthcare professionals only. By acknowledging this message and accessing the information on this website you are confirming that you are a healthcare professional.
The SOT Hub website uses a third-party service provided by Google that dynamically translates web content. Translations are machine generated, so may not be an exact or complete translation, and the SOT Hub cannot guarantee the accuracy of translated content. The SOT Hub and its employees will not be liable for any direct, indirect, or consequential damages (even if foreseeable) resulting from use of the Google Translate feature. For further support with Google Translate, visit Google Translate Help.
The SOT Hub is an independent medical education platform, supported through a founding grant from Therakos. Funders are allowed no direct influence on our content. The levels of sponsorship listed are reflective of the amount of funding given. View funders.
Now you can support HCPs in making informed decisions for their patients
Your contribution helps us continuously deliver expertly curated content to HCPs worldwide. You will also have the opportunity to make a content suggestion for consideration and receive updates on the impact contributions are making to our content.
Find out more
Create an account and access these new features:
Bookmark content to read later
Select your specific areas of interest
View solid organ transplantation content recommended for you
Results from a multi-institutional retrospective study, evaluating conversion to belatacept, a co-stimulation blocker, as a calcineurin inhibitor (CNI)-sparing therapy in adult lung transplant recipients, were published in Transplant Immunology by Younis et al. The analysis compared patients who received belatacept (n = 170) with contemporaneous controls (n = 288). The primary outcome was change in estimated glomerular filtration rate (eGFR) following belatacept initiation.
Key data: In the belatacept group, median eGFR was 43 mL/min/1.73 m² at initiation, 46 mL/min/1.73 m² at 6 months, and 43 mL/min/1.73 m² at 1 year following belatacept initiation, with an overall change of 0 mL/min/1.73 m² (interquartile range [IQR], −21 to 52; p = 0.21). Median eGFR in the control group declined from 60 mL/min/1.73 m² at transplant to 57 mL/min/1.73 m² at 6 months and 48 mL/min/1.73 m² at 1 year, with an overall change of −18 mL/min/1.73 m² (IQR, −30 to −5; p < 0.0001). There were no significant differences between groups in rates of chronic lung allograft dysfunction (CLAD), acute cellular rejection, antibody-mediated rejection, de novo donor-specific antibodies, forced expiratory volume in 1 second, infections, or malignancy.
Key learning: Belatacept-based immunosuppression was associated with stabilization of renal function without increased rates of rejection, CLAD, or malignancy, supporting consideration of belatacept as a CNI-sparing strategy in lung transplant recipients.
References
Please indicate your level of agreement with the following statements:
The content was clear and easy to understand
The content addressed the learning objectives
The content was relevant to my practice
I will change my clinical practice as a result of this content