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Published on: April 12, 2021
Malignancies in transplanted patients: Multidisciplinary evaluation and switch to mTOR inhibitors after kidney
Vivan C Hellström1, Ylva Enström2, Bengt von Zur-Mühlen1
1a Department of Surgical Sciences, Section of Transplantation Surgery , Uppsala University , Uppsala , Sweden ;
Abstract:
Background Solid organ transplant recipients are at increased risk of developing malignancies. The objective of this prospective, observational, one-armed study was to study the feasibility to add a mammalian target of rapamycin (mTOR) inhibitor to the immunosuppressive regimen in transplanted patients with post-transplant malignancies. During the trial the need to improve identification of post-transplant malignancies and to reassure adequate oncological treatment of these patients became evident. Multidisciplinary team (MDT) evaluation of oncological and immunosuppressive treatments was implemented for all patients with malignancies after renal or combined renal and pancreas transplantation because of the trial. Material and methods At Uppsala University Hospital, Sweden, a MDT consisting of transplant surgeons, nephrologists, oncologists and dermatologists evaluated 120 renal or combined renal and pancreas-transplanted recipients diagnosed with malignancies from September 2006 to July 2012. To identify all malignancies, the population was linked to the Regional Tumor Registry (RTR). We recorded to which extent a switch to mTOR inhibitors was possible and how often the originally planned oncological managements were adjusted. All patients were followed for three years. (ClinicalTrials.gov: NCT02241564). Results In 76 of 120 patients (63%) a switch to mTOR inhibitors was possible. Immunosuppression was interrupted in seven patients (6%), reduced in three patients (2%) and remained unchanged in 34 of 120 patients (28%). Identification of post-transplant malignancies increased significantly after linkage to RTR (p = 0.015). The initially recommended oncological treatment was adjusted in 23 of 44 patients (52%) with solid or hematological malignancies; 36 of these patients (82%) were treated according to national guidelines. Conclusion In two thirds of the patients the immunosuppressive treatment could be changed to an mTOR inhibitor with anti-tumor effects in transplanted patients with post-transplant malignancies. The use of regional tumor registers considerably improved the identification of patients with post-transplant malignancies indicating that post-transplant malignancies might be timely underreported in transplant registers.
Insights
Adding mammalian target of rapamycin (mTOR) inhibitors to immunosuppression is feasible in transplant patients with post-transplant malignancies. Regional tumor registries significantly improve malignancy identification, ensuring better oncological treatment adherence.
Area of Science:
- Oncology
- Transplantation Medicine
- Immunosuppression
Background:
- Solid organ transplant recipients face a higher risk of developing malignancies.
- Post-transplant malignancies require careful management of both oncological and immunosuppressive therapies.
Purpose of the Study:
- To assess the feasibility of incorporating mammalian target of rapamycin (mTOR) inhibitors into immunosuppressive regimens for transplant patients with post-transplant malignancies.
- To improve the identification and management of post-transplant malignancies.
Main Methods:
- A prospective, observational study involving 120 renal or combined renal and pancreas transplant recipients with malignancies.
- Utilized multidisciplinary team (MDT) evaluation and linkage to the Regional Tumor Registry (RTR) for comprehensive assessment.
- Monitored switches to mTOR inhibitors, changes in immunosuppression, and oncological treatment adjustments over a three-year follow-up.
Main Results:
- A switch to mTOR inhibitors was possible in 63% of patients.
- Immunosuppression was interrupted or reduced in only 8% of patients.
- Linkage to RTR significantly improved malignancy identification (p=0.015), with 82% of patients receiving guideline-adherent oncological treatment.
Conclusions:
- Switching immunosuppression to mTOR inhibitors is feasible in a majority of transplant patients with post-transplant malignancies.
- Regional tumor registries are crucial for accurate identification of post-transplant malignancies, potentially addressing underreporting.
- MDT evaluation ensures optimized oncological and immunosuppressive treatment strategies.
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