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Reductions in immunosuppression after haematological or solid organ cancer diagnosis in kidney transplant recipients
Christopher M Hope1,2, Alice J Krige1, Alex Barratt1
1Central Northern Adelaide Renal and Transplantation Service (CNARTS), Adelaide, SA, Australia.
Abstract:
Few data exist on how immunosuppression is altered in kidney transplant recipients (KTR) following a diagnosis of cancer. This study investigated how immunosuppression was altered in KTR after cancer diagnosis and its effect on patient and graft survival. All KTR diagnosed with cancer at our centre from 1990 to 2012 were assessed. Drug regime and serum creatinine levels were recorded 1 year before, at time of, and 1 year after cancer diagnosis. Of 87 KTR who developed cancer (7.3% of transplanted population, n = 1189), 30 developed haematological malignancies and 57 developed solid organ cancers (SOC). In total, 38% of KTR presented with nodal or metastatic disease and 23 of 87 (26%) KTR died within 6 months of cancer diagnosis. Fifty-five KTR had records of pre- and postcancer diagnosis drug regimes. Thirty-six KTR had a (>50%) dose reduction or cessation of 1 or more immunosuppressive agents, and 19 no reduction in immunosuppression. In total, 2 of 36 (6%) of KTR who underwent a dose reduction suffered acute rejection that was reversed with methylprednisolone. Dose reduction/cessation of immunosuppression did not impair graft function, but also did not affect cancer free survival. Further larger prospective studies are needed to determine whether dose reduction alters relapse free cancer survival in KTR.
Insights
Reducing immunosuppression in kidney transplant recipients (KTR) with cancer did not impair graft function or affect cancer survival. Acute rejection was rare and reversible. Further studies are needed on relapse-free cancer survival.
Area of Science:
- Nephrology
- Oncology
- Immunology
Background:
- Limited data exist on immunosuppression management in kidney transplant recipients (KTR) diagnosed with cancer.
- Cancer is a significant concern for KTR, impacting long-term outcomes.
Purpose of the Study:
- To investigate alterations in immunosuppression following cancer diagnosis in KTR.
- To evaluate the impact of these alterations on patient and graft survival.
Main Methods:
- Retrospective analysis of 87 KTR diagnosed with cancer between 1990 and 2012.
- Recorded drug regimens and serum creatinine levels pre-cancer, at diagnosis, and 1 year post-diagnosis.
- Compared outcomes between KTR with and without immunosuppression dose reduction/cessation.
Main Results:
- 38% of KTR presented with advanced disease; 26% died within 6 months.
- 55 KTR had documented drug regimens; 36 (65%) had dose reduction/cessation.
- Only 2 KTR (6%) with dose reduction experienced acute rejection, successfully treated.
- Dose reduction did not impair graft function or affect cancer-free survival.
Conclusions:
- Immunosuppression dose reduction in KTR with cancer is feasible and safe regarding graft function and overall cancer survival.
- Further prospective research is warranted to explore the impact on cancer relapse-free survival.
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