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Incidence of Pneumonitis in Heart Transplant Patients Started on a Proliferation Signal Inhibitor

R. Levine, J. Patel, M. Levine, M. Kittleson, E. Kransdorf, S. Dimbil, D. Geft, D. Chang, L. Czer, J. Kobashigawa.

Cedars Sinai Medical Center, Los Angeles.

Meeting: 2018 American Transplant Congress

Abstract number: B64

Keywords: Drug interaction, Heart/lung transplantation, Inflammation, Sirolimus (SLR)

Session Information

Session Name: Poster Session B: Heart and VADs: All Topics

Session Type: Poster Session

Date: Sunday, June 3, 2018

Session Time: 6:00pm-7:00pm

 Presentation Time: 6:00pm-7:00pm

Location: Hall 4EF

Purpose: Proliferation signal inhibitors(PSI) have a high discontinuation rate due to side effects. PSI induced pneumonitis has been reported in 14% in renal cell carcinoma and 0-7% in solid-organ transplants. We assessed incidence of pneumonitis in patients(pts) started on a PSI after heart transplantation(Htx) at our large single center.

Methods:Between 2007-15, 282 pts were started on a PSI post-HTx. 4 developed pneumonitis while on a PSI. They were compared 5:1 to a control group matched for age, sex, type of PSI, and time to PSI initiation. Endpoints: subsequent 1-yr survival, freedom from rejection, cardiac allograft vasculopathy (CAV) and non-fatal major adverse cardiac events (NF-MACE: myocardial infarction, heart failure, coronary intervention, pacemaker implant, and stroke). We evaluated possible contributing risk factors (table).

Results:Pts were initiated on a PSI mean 1.9 yrs post-HTx. Incidence of pneumonitis after PSI initiation was 1.4% (n=4), 2 pts each on sirolimus and everolimus. Reasons for initiation: renal sparing, CMV, malignancy, and rejection. There was a significant difference in subsequent 1-yr survival. 3/4 pts developing pneumonitis died from infection and respiratory failure. 3/4 pneumonitis pts had pre-existing lung disease. No significant difference in subsequent 1-yr freedom from CAV, NF-MACE, and rejection.

Conclusion: The incidence of PSI induced pneumonitis after HTx is low but associated with high mortality. Pre-existing lung disease increases risk of pneumonitis post-PSI initiation.

Endpoints at 1-Yr Pneumonitis (n=4) Matched Controls 5:1 (n=20) P-Value
Survival 25% 89.4% 0.001
Freedom from (FF):CAV 100% 95.0% 0.752
FF NF-MACE 100% 84.0% 0.533
FF Any-Treated Rejection 100% 95.0% 0.699
FF Acute Cellular Rejection 100% 95.0% 0.699
FF Antibody-Mediated Rejection 100% 100% 1.000
Risk Factors
Pre-Transplant Lung Disease 75% 25% 0.091
Pre-Transplant Diabetes 75% 45% 0.590
Pre-Transplant Hypertension 75% 50% 0.596
Renal Dysfunction 75% 80% 1.000
ICU Stay 100% 85% 0.412
Ventilator Use 100% 45% 1.000

CITATION INFORMATION: Levine R., Patel J., Levine M., Kittleson M., Kransdorf E., Dimbil S., Geft D., Chang D., Czer L., Kobashigawa J. Incidence of Pneumonitis in Heart Transplant Patients Started on a Proliferation Signal Inhibitor Am J Transplant. 2017;17 (suppl 3).

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To cite this abstract in AMA style:

Levine R, Patel J, Levine M, Kittleson M, Kransdorf E, Dimbil S, Geft D, Chang D, Czer L, Kobashigawa J. Incidence of Pneumonitis in Heart Transplant Patients Started on a Proliferation Signal Inhibitor [abstract]. https://atcmeetingabstracts.com/abstract/incidence-of-pneumonitis-in-heart-transplant-patients-started-on-a-proliferation-signal-inhibitor/. Accessed May 13, 2025.

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