ASN's Mission

To create a world without kidney diseases, the ASN Alliance for Kidney Health elevates care by educating and informing, driving breakthroughs and innovation, and advocating for policies that create transformative changes in kidney medicine throughout the world.

learn more

Contact ASN

1401 H St, NW, Ste 900, Washington, DC 20005

email@asn-online.org

202-640-4660

The Latest on X

Kidney Week

Abstract: FR-PO1152

Cancer Incidence and Outcomes in Kidney Transplant Recipients with ANCA-Associated Vasculitis

Session Information

Category: Transplantation

  • 2002 Transplantation: Clinical

Authors

  • Arriola Montenegro, Jose J., Mayo Clinic Division of Nephrology and Hypertension, Rochester, Minnesota, United States
  • Shams, Amir Hossein H., Mayo Clinic Division of Nephrology and Hypertension, Rochester, Minnesota, United States
  • Herrera Hernandez, Loren Paola, Mayo Clinic Minnesota Department of Laboratory Medicine and Pathology, Rochester, Minnesota, United States
  • Fervenza, Fernando C., Mayo Clinic Division of Nephrology and Hypertension, Rochester, Minnesota, United States
  • Bentall, Andrew J., Mayo Clinic Division of Nephrology and Hypertension, Rochester, Minnesota, United States
  • Acuña, Pilar A., Mayo Clinic Division of Nephrology and Hypertension, Rochester, Minnesota, United States
  • Silva, Artur Quintiliano, Mayo Clinic Division of Nephrology and Hypertension, Rochester, Minnesota, United States
Background

Malignancy risk in patients with ANCA-associated vasculitis (AAV) remains incompletely defined, particularly in the transplant setting. We examined cancer incidence in kidney transplant recipients (KTR) with AAV.

Methods

Retrospective study of 81 KTR with AAV at Mayo Clinic (1983–2024). Clinical and transplant data were collected; associations with post-transplant malignancy and survival outcomes were analyzed.

Results

The cohort had high comorbidity burden, with 61.7% extra-renal involvement, low immunologic risk (median cPRA 0% [IQR 0–27]), and 6.2% re-transplantation. Induction therapy was used in 88.9%, and 79% received triple immunosuppression (tacrolimus, prednisone, mycophenolate). One-year rejection occurred in 23.5% (84.2% cellular). Overall, 35.8% developed cancer, most commonly non-melanoma skin (27.6%), melanoma (20.7%), and urothelial (17.8%), with median onset at 60 months (IQR 26–96). Male sex was independently associated with malignancy (OR 6.08; HR 2.82). Thymoglobulin showed a reduced cancer risk signal on time-to-event analysis (HR 0.31), not confirmed in bivariable analysis. AAV therapy and pre-transplant dialysis were not associated with malignancy. At 5 and 10 years, patient survival was 70.4% and 46.9%, graft survival 90% and 77%, and death-censored graft survival 70.4% and 41.5%. Malignancy was not associated with patient or graft survival, and outcomes did not differ by cancer type.

Conclusion

Malignancy is common among KTR with AAV, affecting over one-third of patients. Male sex predicts higher risk, identifying a subgroup for enhanced screening.Despite this burden, graft survival remained relatively preserved, suggesting mortality may be driven by non-graft-related factors. Findings support sex-informed cancer surveillance in AAV transplant recipients.

(A) patient survival, (B) graft survival. (C) death-censored graft survival.