Second Report of the American Intestinal Transplant Working Group: New Insights Into Risk Factors, Treatment Regimens, and Outcomes of Malignancy After Intestinal Transplantation
Recommended Citation
Chiu CEN, Fujiki M, Truong R, Marquez JM, Venick R, Feist S, Jafri SM, Aburumman R, Di Cocco P, Alaniz MJ, Merola J, Garcia J, Selvaggi G, Merani S, Farell A, Cruz RJ, Ganoza A, Mazariegos G, Sudan D, Segovia MC, Sanha V, Kroemer A, Matsumoto C, Alemayehu C, Patil D, Muralidaran V, Pahl E, Weiner J. Second Report of the American Intestinal Transplant Working Group: New Insights Into Risk Factors, Treatment Regimens, and Outcomes of Malignancy After Intestinal Transplantation. Transplantation. 2026;110(9):1916.
Document Type
Article
Publication Date
9-1-2026
Publication Title
Transplantation
Keywords
Humans, Risk Factors, Retrospective Studies, Immunosuppressive Agents, Female, Male, United States, Intestines, Incidence, Middle Aged, Treatment Outcome, Neoplasms, Adult, Tacrolimus, Organ Transplantation, Graft Rejection, Time Factors, Postoperative Complications
Abstract
BACKGROUND: Intestinal transplantation requires high levels of long-term immunosuppression, putting recipients at high risk of developing malignancies. Factors influencing the incidence and outcomes of these malignancies remain poorly understood.
METHODS: We conducted a retrospective multicenter study surveying 11 of 15 intestinal transplantation (ITx) centers in the United States, including 336 of 451 transplants performed between 2020 and 2025.
RESULTS: Forty-four patients developed de novo malignancies, including 34 posttransplant lymphoproliferative disorder, 5 skin carcinomas and 5 other carcinomas. Malignancy incidence was 13.1% at a mean follow-up time of 2.33 y. Overall survival did not significantly differ between all intestinal transplant recipients and those who developed malignancies. Malignancy incidence was significantly influenced by maintenance immunosuppression: tacrolimus + Steroids was associated with increased odds of malignancy and tacrolimus + mycophenolate mofetil + steroids with decreased odds. Subsequently reducing immunosuppression did not impact the incidence or severity of rejection. However, concurrent infection-especially opportunistic infection-was associated with higher mortality in the malignancy group.
CONCLUSIONS: Malignancy after ITx is likely related to greater T-cell immunosuppression with increased incidence associated with tacrolimus-predominant maintenance regimens and improved outcomes with multimodal regimens and the absence of infections. Our results suggest that reduced T-cell suppression and maintenance of some level of immunocompetence may decrease the incidence, morbidity, and mortality of malignancy after ITx without increasing rejection rates.
Medical Subject Headings
Humans; Risk Factors; Retrospective Studies; Immunosuppressive Agents; Female; Male; United States; Intestines; Incidence; Middle Aged; Treatment Outcome; Neoplasms; Adult; Tacrolimus; Organ Transplantation; Graft Rejection; Time Factors; Postoperative Complications
PubMed ID
42319222
ePublication
ePub ahead of print
Volume
110
Issue
9
First Page
1916
Last Page
1916
