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Kidney international reports · 2021

Rituximab in Membranous Nephropathy.

СтатьяОбзорНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Gauckler Philipp, Shin Jae Il, Alberici Federico, Audard Vincent, Bruchfeld Annette, Busch Martin, Cheung Chee Kay, Crnogorac Matija, Delbarba Elisa, Eller Kathrin, Faguer Stanislas, Galesic Kresimir, Griffin Siân, van den Hoogen Martijn W F, Hrušková Zdenka, Jeyabalan Anushya, Karras Alexandre, King Catherine, Kohli Harbir Singh, Mayer Gert, Maas Rutger, Muto Masahiro, Moiseev Sergey, Odler Balazs, Pepper Ruth J, Quintana Luis F, Radhakrishnan Jai, Ramachandran Raja, Salama Alan D, Schönermarck Ulf, Segelmark Mårten, Smith Lee, Tesař Vladimír, Wetzels Jack, Willcocks Lisa, Windpessl Martin, Zand Ladan, Zonozi Reza, Kronbichler Andreas, RITERM study group

Аннотация

Membranous nephropathy (MN) is the most common cause of primary nephrotic syndrome among adults. The identification of phospholipase A2 receptor (PLA2R) as target antigen in most patients changed the management of MN dramatically, and provided a rationale for B-cell depleting agents such as rituximab. The efficacy of rituximab in inducing remission has been investigated in several studies, including 3 randomized controlled trials, in which complete and partial remission of proteinuria was achieved in approximately two-thirds of treated patients. Due to its favorable safety profile, rituximab is now considered a first-line treatment option for MN, especially in patients at moderate and high risk of deterioration in kidney function. However, questions remain about how to best use rituximab, including the optimal dosing regimen, a potential need for maintenance therapy, and assessment of long-term safety and efficacy outcomes. In this review, we provide an overview of the current literature and discuss both strengths and limitations of "the new standard."

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

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