Kidney Transplantation in Patients With Monoclonal Gammopathy of Renal Significance (MGRS)–Associated Lesions: A Case Series

Data on kidney transplantation outcomes among patients with monoclonal gammopathy of renal significance (MGRS) are lacking. Case series of patients with MGRS, some of whom received clone-directed therapies before kidney transplantation. 28 patients who underwent kidney transplantation from 1987 thro...

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Veröffentlicht in:American journal of kidney diseases 2022-02, Vol.79 (2), p.202-216
Hauptverfasser: Heybeli, Cihan, Alexander, Mariam Priya, Bentall, Andrew J., Amer, Hatem, Buadi, Francis K., Dean, Patrick G., Dingli, David, Dispenzieri, Angela, El Ters, Mireille, Gertz, Morie A., Issa, Naim S., Kapoor, Prashant, Kourelis, Taxiarchis, Kukla, Aleksandra, Kumar, Shaji, Lacy, Martha Q., Lorenz, Elizabeth C., Muchtar, Eli, Murray, David L., Nasr, Samih H., Prieto, Mikel, Rajkumar, S. Vincent, Schinstock, Carrie A., Stegall, Mark D., Warsame, Rahma, Leung, Nelson
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container_issue 2
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container_title American journal of kidney diseases
container_volume 79
creator Heybeli, Cihan
Alexander, Mariam Priya
Bentall, Andrew J.
Amer, Hatem
Buadi, Francis K.
Dean, Patrick G.
Dingli, David
Dispenzieri, Angela
El Ters, Mireille
Gertz, Morie A.
Issa, Naim S.
Kapoor, Prashant
Kourelis, Taxiarchis
Kukla, Aleksandra
Kumar, Shaji
Lacy, Martha Q.
Lorenz, Elizabeth C.
Muchtar, Eli
Murray, David L.
Nasr, Samih H.
Prieto, Mikel
Rajkumar, S. Vincent
Schinstock, Carrie A.
Stegall, Mark D.
Warsame, Rahma
Leung, Nelson
description Data on kidney transplantation outcomes among patients with monoclonal gammopathy of renal significance (MGRS) are lacking. Case series of patients with MGRS, some of whom received clone-directed therapies before kidney transplantation. 28 patients who underwent kidney transplantation from 1987 through 2016 after diagnosis with MGRS-associated lesions including light-chain deposition disease (LCDD), C3 glomerulopathy with monoclonal gammopathy (C3G-MG), and light-chain proximal tubulopathy (LCPT). Of the 19 patients with LCDD, 10 were treated before kidney transplantation and 9 were treatment-naive. Among the treated patients with LCDD, 3 (30%) experienced histologic recurrence, 2 (20%) grafts failed, and 2 (20%) died during a median follow-up of 70 (range, 3-162) months after transplant. In the treatment-naive LCDD group, 8 (89%) had histologic recurrence, 6 (67%) grafts failed, and 4 (44%) patients died during a median follow-up of 60 (range, 35-117) months. Of the 5 patients who had a complete response before transplant, none died, and only 1 experienced graft failure, 162 months after transplant. Of 5 patients with C3G-MG, 3 were treatment-naive before transplant. Both patients who were treated before transplant had histologic recurrence, and 1 experienced graft failure and died. Among the 3 patients with treatment-naive C3G-MG, histologic recurrence occurred in all, and graft loss and death were observed in 2 and 1, respectively. In the LCPT group (n=4), histologic recurrence was observed in all 3 patients who did not receive clone-directed therapies before transplant, and 2 of these patients died, 1 with a functioning kidney. The 1 patient with LCPT who received therapy before transplant did not have histologic recurrence or graft loss and survived. Small sample size, nonstandardized clinical management, retrospective design. Recurrence is very common in all MGRS-associated lesions after kidney transplant. Achieving a complete hematologic response may reduce the risks of recurrence, graft loss, and death. More studies are needed to determine the effects of hematologic response on outcomes for each MGRS-associated lesion.
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Case series of patients with MGRS, some of whom received clone-directed therapies before kidney transplantation. 28 patients who underwent kidney transplantation from 1987 through 2016 after diagnosis with MGRS-associated lesions including light-chain deposition disease (LCDD), C3 glomerulopathy with monoclonal gammopathy (C3G-MG), and light-chain proximal tubulopathy (LCPT). Of the 19 patients with LCDD, 10 were treated before kidney transplantation and 9 were treatment-naive. Among the treated patients with LCDD, 3 (30%) experienced histologic recurrence, 2 (20%) grafts failed, and 2 (20%) died during a median follow-up of 70 (range, 3-162) months after transplant. In the treatment-naive LCDD group, 8 (89%) had histologic recurrence, 6 (67%) grafts failed, and 4 (44%) patients died during a median follow-up of 60 (range, 35-117) months. Of the 5 patients who had a complete response before transplant, none died, and only 1 experienced graft failure, 162 months after transplant. Of 5 patients with C3G-MG, 3 were treatment-naive before transplant. Both patients who were treated before transplant had histologic recurrence, and 1 experienced graft failure and died. Among the 3 patients with treatment-naive C3G-MG, histologic recurrence occurred in all, and graft loss and death were observed in 2 and 1, respectively. In the LCPT group (n=4), histologic recurrence was observed in all 3 patients who did not receive clone-directed therapies before transplant, and 2 of these patients died, 1 with a functioning kidney. The 1 patient with LCPT who received therapy before transplant did not have histologic recurrence or graft loss and survived. Small sample size, nonstandardized clinical management, retrospective design. Recurrence is very common in all MGRS-associated lesions after kidney transplant. Achieving a complete hematologic response may reduce the risks of recurrence, graft loss, and death. 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subjects case series
graft loss
hematologic response
Humans
Kidney
Kidney Diseases
kidney transplantation
Kidney Transplantation - adverse effects
Monoclonal gammopathy of renal significance (MGRS)
Monoclonal Gammopathy of Undetermined Significance
Paraproteinemias - complications
plasma cell disorder
recurrence
renal transplant
Retrospective Studies
title Kidney Transplantation in Patients With Monoclonal Gammopathy of Renal Significance (MGRS)–Associated Lesions: A Case Series
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