Skip to main content
Erschienen in: Clinical Rheumatology 7/2023

27.03.2023 | CASE BASED REVIEW

Bortezomib is efficacious in the treatment of severe childhood-onset neuropsychiatric systemic lupus erythematosus with psychosis: a case series and mini-review of B-cell immunomodulation in antibody-mediated diseases

verfasst von: Renee F. Modica, Akaluck Thatayatikom, Denise H. Bell-Brunson, Melissa E. Elder

Erschienen in: Clinical Rheumatology | Ausgabe 7/2023

Einloggen, um Zugang zu erhalten

Abstract

Childhood-onset neuropsychiatric systemic lupus erythematosus (cNPSLE) with psychosis is a challenging manifestation of SLE. Pathogenic long-lived plasma cells (LLPCs) are not specifically targeted by standard immunosuppression and their persistence contributes to chronic autoimmunity. Bortezomib is approved for the treatment of multiple myeloma and has shown benefits in a variety of other antibody-mediated diseases. Bortezomib may be efficacious for severe or treatment-refractory cNPSLE through eradication of LLPCs, decreasing autoantibody production. We describe the first pediatric case series of five patients with unrelenting cNPSLE with psychosis who were treated safely and effectively with bortezomib between 2011 and 2017. Most patients had persistent cNPSLE with psychosis despite aggressive immunosuppression with methylprednisolone, cyclophosphamide, rituximab, and usually plasmapheresis. All patients demonstrated rapid clinical improvement in their psychotic manifestations with the ability to quickly taper immunosuppression after the introduction of bortezomib. No patient had a recurrence of overt psychosis during a follow-up period of 1–10 years. Secondary hypogammaglobulinemia developed in all five patients and required immunoglobulin replacement. No other severe side effects or adverse events were observed. Bortezomib-mediated LLPC depletion is a promising therapy for severe recalcitrant cNPSLE with psychosis when used as adjunctive therapy to conventional immunosuppression, B-cell, and antibody-depleting therapies. After initiation of bortezomib, patients had rapid, demonstrable improvement in psychosis as well as reduction in glucocorticoids and antipsychotics. Further investigation is needed to determine the therapeutic role of bortezomib in severe cNPSLE and cSLE. We present a mini-review of the rationale for bortezomib use and novel B-cell immunomodulation in rheumatic disease.
Literatur
4.
Zurück zum Zitat Giani T, Smith EM, Al-Abadi E, Armon K, Bailey K, Ciurtin C, Davidson J, Gardner-Medwin J, Haslam K, Hawley DP, Leahy A, Leone V, McErlane F, Mewar D, Modgil G, Moots R, Pilkington C, Pregnolato F, Ramanan AV, Rangaraj S, Riley P, Sridhar A, Wilkinson N, Cimaz R, Beresford MW, Hedrich CM (2021) Neuropsychiatric involvement in juvenile-onset systemic lupus erythematosus: data from the UK Juvenile-onset systemic lupus erythematosus cohort study. Lupus 30(12):1955–1965. https://doi.org/10.1177/09612033211045050CrossRefPubMedPubMedCentral Giani T, Smith EM, Al-Abadi E, Armon K, Bailey K, Ciurtin C, Davidson J, Gardner-Medwin J, Haslam K, Hawley DP, Leahy A, Leone V, McErlane F, Mewar D, Modgil G, Moots R, Pilkington C, Pregnolato F, Ramanan AV, Rangaraj S, Riley P, Sridhar A, Wilkinson N, Cimaz R, Beresford MW, Hedrich CM (2021) Neuropsychiatric involvement in juvenile-onset systemic lupus erythematosus: data from the UK Juvenile-onset systemic lupus erythematosus cohort study. Lupus 30(12):1955–1965. https://​doi.​org/​10.​1177/​0961203321104505​0CrossRefPubMedPubMedCentral
8.
Zurück zum Zitat Streicher K, Morehouse CA, Groves CJ, Rajan B, Pilataxi F, Lehmann KP, Brohawn PZ, Higgs BW, McKeever K, Greenberg SA, Fiorentino D, Richman LK, Jallal B, Herbst R, Yao Y, Ranade K (2014) The plasma cell signature in autoimmune disease. Arthritis Rheumatol (Hoboken, NJ) 66(1):173–184. https://doi.org/10.1002/art.38194CrossRef Streicher K, Morehouse CA, Groves CJ, Rajan B, Pilataxi F, Lehmann KP, Brohawn PZ, Higgs BW, McKeever K, Greenberg SA, Fiorentino D, Richman LK, Jallal B, Herbst R, Yao Y, Ranade K (2014) The plasma cell signature in autoimmune disease. Arthritis Rheumatol (Hoboken, NJ) 66(1):173–184. https://​doi.​org/​10.​1002/​art.​38194CrossRef
14.
Zurück zum Zitat Gomez AM, Willcox N, Vrolix K, Hummel J, Nogales-Gadea G, Saxena A, Duimel H, Verheyen F, Molenaar PC, Buurman WA, De Baets MH, Martinez-Martinez P, Losen M (2014) Proteasome inhibition with bortezomib depletes plasma cells and specific autoantibody production in primary thymic cell cultures from early-onset myasthenia gravis patients. Journal of immunology (Baltimore, Md : 1950) 193(3):1055–1063. https://doi.org/10.4049/jimmunol.1301555CrossRefPubMed Gomez AM, Willcox N, Vrolix K, Hummel J, Nogales-Gadea G, Saxena A, Duimel H, Verheyen F, Molenaar PC, Buurman WA, De Baets MH, Martinez-Martinez P, Losen M (2014) Proteasome inhibition with bortezomib depletes plasma cells and specific autoantibody production in primary thymic cell cultures from early-onset myasthenia gravis patients. Journal of immunology (Baltimore, Md : 1950) 193(3):1055–1063. https://​doi.​org/​10.​4049/​jimmunol.​1301555CrossRefPubMed
17.
Zurück zum Zitat Alexander T, Sarfert R, Klotsche J, Kuhl AA, Rubbert-Roth A, Lorenz HM, Rech J, Hoyer BF, Cheng Q, Waka A, Taddeo A, Wiesener M, Schett G, Burmester GR, Radbruch A, Hiepe F, Voll RE (2015) The proteasome inhibitior bortezomib depletes plasma cells and ameliorates clinical manifestations of refractory systemic lupus erythematosus. Ann Rheum Dis 74(7):1474–1478. https://doi.org/10.1136/annrheumdis-2014-206016CrossRefPubMed Alexander T, Sarfert R, Klotsche J, Kuhl AA, Rubbert-Roth A, Lorenz HM, Rech J, Hoyer BF, Cheng Q, Waka A, Taddeo A, Wiesener M, Schett G, Burmester GR, Radbruch A, Hiepe F, Voll RE (2015) The proteasome inhibitior bortezomib depletes plasma cells and ameliorates clinical manifestations of refractory systemic lupus erythematosus. Ann Rheum Dis 74(7):1474–1478. https://​doi.​org/​10.​1136/​annrheumdis-2014-206016CrossRefPubMed
18.
Zurück zum Zitat Ishii T, Tanaka Y, Kawakami A, Saito K, Ichinose K, Fujii H, Shirota Y, Shirai T, Fujita Y, Watanabe R, Chiu SW, Yamaguchi T, Harigae H (2018) Multicenter double-blind randomized controlled trial to evaluate the effectiveness and safety of bortezomib as a treatment for refractory systemic lupus erythematosus. Mod Rheumatol 28(6):986–992. https://doi.org/10.1080/14397595.2018.1432331CrossRefPubMed Ishii T, Tanaka Y, Kawakami A, Saito K, Ichinose K, Fujii H, Shirota Y, Shirai T, Fujita Y, Watanabe R, Chiu SW, Yamaguchi T, Harigae H (2018) Multicenter double-blind randomized controlled trial to evaluate the effectiveness and safety of bortezomib as a treatment for refractory systemic lupus erythematosus. Mod Rheumatol 28(6):986–992. https://​doi.​org/​10.​1080/​14397595.​2018.​1432331CrossRefPubMed
25.
Zurück zum Zitat Liang MH, Corzillius M, Bae SC, Lew RA, Fortin PR, Gordon C, Isenberg D, Alarcón GS, Straaton KV, Denburg J, Denburg S, Esdaile JM, Glanz BI, Karlson EW, Khoshbin S, Rogers MP, Schur PH, Hanly JG, Kozora E, West S, Lahita RG, Lockshin MD, McCune J, Moore PM, Petri M, Roberts WN, Sanchez-Guerrero J, Veilleux M, Brey R, Cornblath WD, Filley CM, Fisk JD, Harten P, Hay EM, Iverson G, Levine SR, Waterhouse E, Wallace DJ, Winer JB (1999) The American College of Rheumatology nomenclature and case definitions for neuropsychiatric lupus syndromes. Arthritis Rheum 42(4)599–608. https://doi.org/10.1002/1529-0131(199904)42:4<599::Aid-anr2>3.0.Co;2-f Liang MH, Corzillius M, Bae SC, Lew RA, Fortin PR, Gordon C, Isenberg D, Alarcón GS, Straaton KV, Denburg J, Denburg S, Esdaile JM, Glanz BI, Karlson EW, Khoshbin S, Rogers MP, Schur PH, Hanly JG, Kozora E, West S, Lahita RG, Lockshin MD, McCune J, Moore PM, Petri M, Roberts WN, Sanchez-Guerrero J, Veilleux M, Brey R, Cornblath WD, Filley CM, Fisk JD, Harten P, Hay EM, Iverson G, Levine SR, Waterhouse E, Wallace DJ, Winer JB (1999) The American College of Rheumatology nomenclature and case definitions for neuropsychiatric lupus syndromes. Arthritis Rheum 42(4)599–608. https://​doi.​org/​10.​1002/​1529-0131(199904)42:​4<599:​:​Aid-anr2>3.​0.​Co;2-f
26.
Zurück zum Zitat Moreau P, Pylypenko H, Grosicki S, Karamanesht I, Leleu X, Grishunina M, Rekhtman G, Masliak Z, Robak T, Shubina A, Arnulf B, Kropff M, Cavet J, Esseltine DL, Feng H, Girgis S, van de Velde H, Deraedt W, Harousseau JL (2011) Subcutaneous versus intravenous administration of bortezomib in patients with relapsed multiple myeloma: a randomised, phase 3, non-inferiority study. Lancet Oncol 12(5):431–440. https://doi.org/10.1016/s1470-2045(11)70081-xCrossRefPubMed Moreau P, Pylypenko H, Grosicki S, Karamanesht I, Leleu X, Grishunina M, Rekhtman G, Masliak Z, Robak T, Shubina A, Arnulf B, Kropff M, Cavet J, Esseltine DL, Feng H, Girgis S, van de Velde H, Deraedt W, Harousseau JL (2011) Subcutaneous versus intravenous administration of bortezomib in patients with relapsed multiple myeloma: a randomised, phase 3, non-inferiority study. Lancet Oncol 12(5):431–440. https://​doi.​org/​10.​1016/​s1470-2045(11)70081-xCrossRefPubMed
28.
Zurück zum Zitat Fowler NH (2011) Role of maintenance rituximab (rituxan) therapy in the treatment of follicular lymphoma. P t 36(9):590–598PubMedPubMedCentral Fowler NH (2011) Role of maintenance rituximab (rituxan) therapy in the treatment of follicular lymphoma. P t 36(9):590–598PubMedPubMedCentral
29.
Zurück zum Zitat Brunner HI, Higgins GC, Klein-Gitelman MS, Lapidus SK, Olson JC, Onel K, Punaro M, Ying J, Giannini EH (2010) Minimal clinically important differences of disease activity indices in childhood-onset systemic lupus erythematosus. Arthritis Care Res (Hoboken) 62(7):950–959. https://doi.org/10.1002/acr.20154CrossRefPubMed Brunner HI, Higgins GC, Klein-Gitelman MS, Lapidus SK, Olson JC, Onel K, Punaro M, Ying J, Giannini EH (2010) Minimal clinically important differences of disease activity indices in childhood-onset systemic lupus erythematosus. Arthritis Care Res (Hoboken) 62(7):950–959. https://​doi.​org/​10.​1002/​acr.​20154CrossRefPubMed
31.
35.
Zurück zum Zitat (2022) Benlysta (belimumab) [package insert]. GlaxoSmithKline, Philadelphia, PA (2022) Benlysta (belimumab) [package insert]. GlaxoSmithKline, Philadelphia, PA
38.
Zurück zum Zitat Alexander T, Cheng Q, Klotsche J, Khodadadi L, Waka A, Biesen R, Hoyer BF, Burmester GR, Radbruch A, Hiepe F (2018) Proteasome inhibition with bortezomib induces a therapeutically relevant depletion of plasma cells in SLE but does not target their precursors. Eur J Immunol 48(9):1573–1579. https://doi.org/10.1002/eji.201847492CrossRefPubMed Alexander T, Cheng Q, Klotsche J, Khodadadi L, Waka A, Biesen R, Hoyer BF, Burmester GR, Radbruch A, Hiepe F (2018) Proteasome inhibition with bortezomib induces a therapeutically relevant depletion of plasma cells in SLE but does not target their precursors. Eur J Immunol 48(9):1573–1579. https://​doi.​org/​10.​1002/​eji.​201847492CrossRefPubMed
39.
Zurück zum Zitat (2022) Velcade (bortezomib) [package insert]. Takeda Pharmaceuticals America Inc, Lexington, MA (2022) Velcade (bortezomib) [package insert]. Takeda Pharmaceuticals America Inc, Lexington, MA
45.
Zurück zum Zitat Taddeo A, Khodadadi L, Voigt C, Mumtaz IM, Cheng Q, Moser K, Alexander T, Manz RA, Radbruch A, Hiepe F, Hoyer BF (2015) Long-lived plasma cells are early and constantly generated in New Zealand Black/New Zealand White F1 mice and their therapeutic depletion requires a combined targeting of autoreactive plasma cells and their precursors. Arthritis Res Ther 17(1):39. https://doi.org/10.1186/s13075-015-0551-3CrossRefPubMedPubMedCentral Taddeo A, Khodadadi L, Voigt C, Mumtaz IM, Cheng Q, Moser K, Alexander T, Manz RA, Radbruch A, Hiepe F, Hoyer BF (2015) Long-lived plasma cells are early and constantly generated in New Zealand Black/New Zealand White F1 mice and their therapeutic depletion requires a combined targeting of autoreactive plasma cells and their precursors. Arthritis Res Ther 17(1):39. https://​doi.​org/​10.​1186/​s13075-015-0551-3CrossRefPubMedPubMedCentral
48.
Zurück zum Zitat Ostendorf L, Burns M, Durek P, Heinz GA, Heinrich F, Garantziotis P, Enghard P, Richter U, Biesen R, Schneider U, Knebel F, Burmester G, Radbruch A, Mei HE, Mashreghi MF, Hiepe F, Alexander T (2020) Targeting CD38 with daratumumab in refractory systemic lupus erythematosus. N Engl J Med 383(12):1149–1155. https://doi.org/10.1056/NEJMoa2023325CrossRefPubMed Ostendorf L, Burns M, Durek P, Heinz GA, Heinrich F, Garantziotis P, Enghard P, Richter U, Biesen R, Schneider U, Knebel F, Burmester G, Radbruch A, Mei HE, Mashreghi MF, Hiepe F, Alexander T (2020) Targeting CD38 with daratumumab in refractory systemic lupus erythematosus. N Engl J Med 383(12):1149–1155. https://​doi.​org/​10.​1056/​NEJMoa2023325CrossRefPubMed
Metadaten
Titel
Bortezomib is efficacious in the treatment of severe childhood-onset neuropsychiatric systemic lupus erythematosus with psychosis: a case series and mini-review of B-cell immunomodulation in antibody-mediated diseases
verfasst von
Renee F. Modica
Akaluck Thatayatikom
Denise H. Bell-Brunson
Melissa E. Elder
Publikationsdatum
27.03.2023
Verlag
Springer International Publishing
Erschienen in
Clinical Rheumatology / Ausgabe 7/2023
Print ISSN: 0770-3198
Elektronische ISSN: 1434-9949
DOI
https://doi.org/10.1007/s10067-023-06559-y

Weitere Artikel der Ausgabe 7/2023

Clinical Rheumatology 7/2023 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Hodgkin Lymphom: BrECADD-Regime übertrifft die Erwartungen

05.06.2024 ASCO 2024 Kongressbericht

Das Kombinationsregime BrECADD mit Brentuximab vedotin ermöglichte in der Studie HD21 beim fortgeschrittenen klassischen Hodgkin-Lymphom eine unerwartet hohe progressionsfreie Überlebensrate von 94,3% nach vier Jahren. Gleichzeitig war das Regime besser tolerabel als der bisherige Standard eBEACOPP.

Antikörper-Drug-Konjugat verdoppelt PFS bei Multiplem Myelom

05.06.2024 ASCO 2024 Nachrichten

Zwei Phase-3-Studien deuten auf erhebliche Vorteile des Antikörper-Wirkstoff-Konjugats Belantamab-Mafodotin bei vorbehandelten Personen mit Multiplem Myelom: Im Vergleich mit einer Standard-Tripeltherapie wurde das progressionsfreie Überleben teilweise mehr als verdoppelt.

Neuer TKI gegen CML: Höhere Wirksamkeit, seltener Nebenwirkungen

05.06.2024 Chronische myeloische Leukämie Nachrichten

Der Tyrosinkinasehemmer (TKI) Asciminib ist älteren Vertretern dieser Gruppe bei CML offenbar überlegen: Personen mit frisch diagnostizierter CML entwickelten damit in einer Phase-3-Studie häufiger eine gut molekulare Response, aber seltener ernste Nebenwirkungen.

Hereditäres Angioödem: Tablette könnte Akuttherapie erleichtern

05.06.2024 Hereditäres Angioödem Nachrichten

Medikamente zur Bedarfstherapie bei hereditärem Angioödem sind bisher nur als Injektionen und Infusionen verfügbar. Der Arzneistoff Sebetralstat kann oral verabreicht werden und liefert vielversprechende Daten.

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.