TY - JOUR
T1 - Multicenter analysis of immunosuppressive medications on the risk of malignancy following adult solid organ transplantation
AU - Shaw, Reid
AU - Haque, Ali R.
AU - Luu, Tyler
AU - O’Connor, Timothy E.
AU - Hamidi, Adam
AU - Fitzsimons, Jack
AU - Varda, Bianca
AU - Kwon, Danny
AU - Whitcomb, Cody
AU - Gregorowicz, Alex
AU - Roloff, Gregory W.
AU - Bemiss, Bradford C.
AU - Kallwitz, Eric R.
AU - Hagen, Patrick A.
AU - Berg, Stephanie
N1 - Publisher Copyright:
Copyright © 2023 Shaw, Haque, Luu, O’Connor, Hamidi, Fitzsimons, Varda, Kwon, Whitcomb, Gregorowicz, Roloff, Bemiss, Kallwitz, Hagen and Berg.
PY - 2023
Y1 - 2023
N2 - Objective: This study aimed to assess the risk of maintenance immunosuppression on the post-transplant risk of malignancy across all solid organ transplant types. Methods: This is a retrospective cohort study from a multicenter hospital system in the United States. The electronic health record was queried from 2000 to 2021 for cases of solid organ transplant, immunosuppressive medications, and post-transplant malignancy. Results: A total of 5,591 patients, 6,142 transplanted organs, and 517 post-transplant malignancies were identified. Skin cancer was the most common type of malignancy at 52.8%, whereas liver cancer was the first malignancy to present at a median time of 351 days post-transplant. Heart and lung transplant recipients had the highest rate of malignancy, but this finding was not significant upon adjusting for immunosuppressive medications (heart HR 0.96, 95% CI 0.72 – 1.3, p = 0.88; lung HR 1.01, 95% CI 0.77 – 1.33, p = 0.94). Random forest variable importance calculations and time-dependent multivariate cox proportional hazard analysis identified an increased risk of cancer in patients receiving immunosuppressive therapy with sirolimus (HR 1.41, 95% CI 1.05 – 1.9, p = 0.04), azathioprine (HR 2.1, 95% CI 1.58 – 2.79, p < 0.001), and cyclosporine (HR 1.59, 95% CI 1.17 – 2.17, p = 0.007), while tacrolimus (HR 0.59, 95% CI 0.44 – 0.81, p < 0.001) was associated with low rates of post-transplant neoplasia. Conclusion: Our results show varying risks of immunosuppressive medications associated with the development of post-transplant malignancy, demonstrating the importance of cancer detection and surveillance strategies in solid organ transplant recipients.
AB - Objective: This study aimed to assess the risk of maintenance immunosuppression on the post-transplant risk of malignancy across all solid organ transplant types. Methods: This is a retrospective cohort study from a multicenter hospital system in the United States. The electronic health record was queried from 2000 to 2021 for cases of solid organ transplant, immunosuppressive medications, and post-transplant malignancy. Results: A total of 5,591 patients, 6,142 transplanted organs, and 517 post-transplant malignancies were identified. Skin cancer was the most common type of malignancy at 52.8%, whereas liver cancer was the first malignancy to present at a median time of 351 days post-transplant. Heart and lung transplant recipients had the highest rate of malignancy, but this finding was not significant upon adjusting for immunosuppressive medications (heart HR 0.96, 95% CI 0.72 – 1.3, p = 0.88; lung HR 1.01, 95% CI 0.77 – 1.33, p = 0.94). Random forest variable importance calculations and time-dependent multivariate cox proportional hazard analysis identified an increased risk of cancer in patients receiving immunosuppressive therapy with sirolimus (HR 1.41, 95% CI 1.05 – 1.9, p = 0.04), azathioprine (HR 2.1, 95% CI 1.58 – 2.79, p < 0.001), and cyclosporine (HR 1.59, 95% CI 1.17 – 2.17, p = 0.007), while tacrolimus (HR 0.59, 95% CI 0.44 – 0.81, p < 0.001) was associated with low rates of post-transplant neoplasia. Conclusion: Our results show varying risks of immunosuppressive medications associated with the development of post-transplant malignancy, demonstrating the importance of cancer detection and surveillance strategies in solid organ transplant recipients.
KW - cancer
KW - immunosuppression
KW - immunosuppressive therapy
KW - machine learning
KW - malignancy
KW - solid organ transplant
UR - http://www.scopus.com/inward/record.url?scp=85164432938&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85164432938&partnerID=8YFLogxK
U2 - 10.3389/fonc.2023.1146002
DO - 10.3389/fonc.2023.1146002
M3 - Article
C2 - 37397376
AN - SCOPUS:85164432938
SN - 2234-943X
VL - 13
JO - Frontiers in Oncology
JF - Frontiers in Oncology
M1 - 1146002
ER -