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Use of Everolimus After Multivisceral Transplantation: A Report of Two Cases
B Rao1, M C Segovia2, M Kazimi3
1Department of Internal Medicine, Henry Ford Hospital, Detroit, Michigan.
Abstract:
Inhibitors of mechanistic target of rapamycin are used in solid organ transplant procedures to avoid calcineurin inhibitor complications, including nephrotoxicity and malignancy. We present 2 cases of multivisceral transplantation for neuroendocrine tumor (NET) for which everolimus was implemented for its potential to prevent NET recurrence as well as preserve renal function. The first case was complicated by NET recurrence in the liver before initiation of everolimus. After initiation of everolimus, the patient developed a ventral hernia and elevated aminotransferase levels with nonspecific biopsy findings. The second case was complicated by cytomegalovirus infection with elevated everolimus trough levels as well as acute cellular rejection. Everolimus was reinitiated in both cases in addition to decreasing the dosage of tacrolimus, and there were no further complications. Everolimus was beneficial in stabilizing renal function in both patients and has the theoretical potential to prevent recurrence of NET.
Insights
Mechanistic target of rapamycin inhibitors like everolimus may help preserve kidney function after multivisceral transplants. These agents also show theoretical potential in preventing neuroendocrine tumor recurrence.
Area of Science:
- Transplantation immunology
- Oncology
- Pharmacology
Background:
- Mechanistic target of rapamycin (mTOR) inhibitors are utilized in solid organ transplantation to mitigate calcineurin inhibitor-associated nephrotoxicity and malignancy.
- Neuroendocrine tumors (NETs) pose a recurrence risk post-transplantation, necessitating strategies for both oncologic control and renal preservation.
Observation:
- Two cases of multivisceral transplantation for NETs are presented, where everolimus was administered to prevent tumor recurrence and preserve renal function.
- The first patient experienced NET recurrence prior to everolimus initiation, followed by ventral hernia and elevated aminotransferase levels post-initiation.
- The second patient developed cytomegalovirus infection with supratherapeutic everolimus trough levels and acute cellular rejection.
Findings:
- Everolimus was reinitiated in both cases, alongside reduced tacrolimus dosages, leading to resolution of complications.
- Everolimus demonstrated efficacy in stabilizing renal function in both patients.
- The study highlights the theoretical potential of everolimus in preventing NET recurrence.
Implications:
- Everolimus may offer a dual benefit in multivisceral transplantation for NETs, addressing both oncologic and nephroprotective goals.
- Careful monitoring of everolimus levels and potential side effects is crucial in this patient population.
- Further research is warranted to confirm the efficacy of everolimus in preventing NET recurrence post-transplantation.
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