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Assessment of renal outcome following therapy in monoclonal immunoglobulin deposition disease: Emphasizing the need for a consensus approach

dc.contributor.authorPianko, Matthew J.
dc.contributor.authorTiutan, Timothy
dc.contributor.authorDerkach, Andriy
dc.contributor.authorFlynn, Jessica
dc.contributor.authorSalvatore, Steven P.
dc.contributor.authorJaffer-Sathick, Insara
dc.contributor.authorRossi, Adriana C.
dc.contributor.authorLahoud, Oscar
dc.contributor.authorHultcrantz, Malin
dc.contributor.authorShah, Urvi A.
dc.contributor.authorMaclachlan, Kylee
dc.contributor.authorChung, David J.
dc.contributor.authorShah, Gunjan L.
dc.contributor.authorLandau, Heather J.
dc.contributor.authorKorde, Neha
dc.contributor.authorMailankody, Sham
dc.contributor.authorLesokhin, Alexander M.
dc.contributor.authorTan, Carlyn
dc.contributor.authorScordo, Michael
dc.contributor.authorJaimes, Edgar A.
dc.contributor.authorGiralt, Sergio A.
dc.contributor.authorUsmani, Saad
dc.contributor.authorHassoun, Hani
dc.date.accessioned2023-03-03T21:07:58Z
dc.date.available2024-04-03 16:07:57en
dc.date.available2023-03-03T21:07:58Z
dc.date.issued2023-03
dc.identifier.citationPianko, Matthew J.; Tiutan, Timothy; Derkach, Andriy; Flynn, Jessica; Salvatore, Steven P.; Jaffer-Sathick, Insara ; Rossi, Adriana C.; Lahoud, Oscar; Hultcrantz, Malin; Shah, Urvi A.; Maclachlan, Kylee; Chung, David J.; Shah, Gunjan L.; Landau, Heather J.; Korde, Neha; Mailankody, Sham; Lesokhin, Alexander M.; Tan, Carlyn; Scordo, Michael; Jaimes, Edgar A.; Giralt, Sergio A.; Usmani, Saad; Hassoun, Hani (2023). "Assessment of renal outcome following therapy in monoclonal immunoglobulin deposition disease: Emphasizing the need for a consensus approach." American Journal of Hematology 98(3): 421-431.
dc.identifier.issn0361-8609
dc.identifier.issn1096-8652
dc.identifier.urihttps://hdl.handle.net/2027.42/175876
dc.description.abstractMonoclonal immunoglobulin deposition disease (MIDD), often associated with plasma cell dyscrasias, predominantly affects the kidneys. In this disease, hematologic response (HR) to treatment can be reliably assessed by International Myeloma Working Group (IMWG) consensus criteria, while uniform criteria for assessing renal response are lacking. We report a retrospective analysis of renal outcomes among 34 patients with MIDD. With most patients treated with bortezomib and autologous stem cell transplantation, 26 of 28 (94%) achieved very good partial HR or better. We demonstrate that both IMWG (based on estimated glomerular filtration rate, eGFR) and amyloid (based on proteinuria) criteria are needed to capture renal response: among 28 evaluable patients, 6 (21%) had isolated proteinuria, while 13 (46%) had isolated decreased eGFR. Using both criteria, which were concordant in patients with both decreased eGFR and proteinuria, 22 of 28 patients (79%) achieved a renal response, including 2 of 7 discontinuing dialyses. All 6 patients (100%) with isolated proteinuria and 7 of 13 (54%) with isolated decreased eGFR achieved renal response, suggesting that isolated proteinuria is an early manifestation of MIDD associated with reversible renal damage. Baseline eGFR predicted renal response (p = .02 by quartile) and survival (p = .02), while HR (CR vs. non-CR) did not, probably because of high HR rate. With a median follow-up of 110 months, the median overall survival was 136 months (95% CI: 79–NR) and median renal survival had not been reached. Prospective studies using uniform renal response criteria are needed to optimize the management of MIDD.
dc.publisherJohn Wiley & Sons, Inc.
dc.titleAssessment of renal outcome following therapy in monoclonal immunoglobulin deposition disease: Emphasizing the need for a consensus approach
dc.typeArticle
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelOncology and Hematology
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biology
dc.subject.hlbtoplevelHealth Sciences
dc.subject.hlbtoplevelScience
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/175876/1/ajh26801_am.pdf
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/175876/2/ajh26801.pdf
dc.identifier.doi10.1002/ajh.26801
dc.identifier.sourceAmerican Journal of Hematology
dc.identifier.citedreferenceMohan M, Buros A, Mathur P, et al. Clinical characteristics and prognostic factors in multiple myeloma patients with light chain deposition disease. Am J Hematol. 2017; 92 ( 8 ): 739 - 745.
dc.identifier.citedreferenceJoly F, Cohen C, Javaugue V, et al. Randall-type monoclonal immunoglobulin deposition disease: novel insights from a nationwide cohort study. Blood. 2019; 133 ( 6 ): 576 - 587.
dc.identifier.citedreferenceTovar N, Cibeira MT, Rosinol L, et al. Bortezomib/dexamethasone followed by autologous stem cell transplantation as front line treatment for light-chain deposition disease. Eur J Haematol. 2012; 89 ( 4 ): 340 - 344.
dc.identifier.citedreferenceSethi S, Fervenza FC, Rajkumar SV. Spectrum of manifestations of monoclonal gammopathy-associated renal lesions. Curr Opin Nephrol Hypertens. 2016; 25 ( 2 ): 127 - 137.
dc.identifier.citedreferenceLeung N, Bridoux F, Batuman V, et al. The evaluation of monoclonal gammopathy of renal significance: a consensus report of the international kidney and monoclonal gammopathy research group. Nat Rev Nephrol. 2019; 15 ( 1 ): 45 - 59.
dc.identifier.citedreferenceAmaador K, Peeters H, Minnema MC, et al. Monoclonal gammopathy of renal significance (MGRS) histopathologic classification, diagnostic workup, and therapeutic options. Neth J Med. 2019; 77 ( 7 ): 243 - 254.
dc.identifier.citedreferenceLeung N, Bridoux F, Nasr SH. Monoclonal gammopathy of renal significance. N Engl J Med. 2021; 384 ( 20 ): 1931 - 1941.
dc.identifier.citedreferenceLin J, Markowitz GS, Valeri AM, et al. Renal monoclonal immunoglobulin deposition disease: the disease spectrum. J Am Soc Nephrol. 2001; 12 ( 7 ): 1482 - 1492.
dc.identifier.citedreferenceStratta P, Gravellone L, Cena T, et al. Renal outcome and monoclonal immunoglobulin deposition disease in 289 old patients with blood cell dyscrasias: a single center experience. Crit Rev Oncol Hematol. 2011; 79 ( 1 ): 31 - 42.
dc.identifier.citedreferenceNasr SH, Valeri AM, Cornell LD, et al. Renal monoclonal immunoglobulin deposition disease: a report of 64 patients from a single institution. Clin J Am Soc Nephrol. 2012; 7 ( 2 ): 231 - 239.
dc.identifier.citedreferenceSayed RH, Wechalekar AD, Gilbertson JA, et al. Natural history and outcome of light chain deposition disease. Blood. 2015; 126 ( 26 ): 2805 - 2810.
dc.identifier.citedreferenceKourelis TV, Nasr SH, Dispenzieri A, et al. Outcomes of patients with renal monoclonal immunoglobulin deposition disease. Am J Hematol. 2016; 91 ( 11 ): 1123 - 1128.
dc.identifier.citedreferenceLi XM, Rui HC, Liang DD, et al. Clinicopathological characteristics and outcomes of light chain deposition disease: an analysis of 48 patients in a single Chinese center. Ann Hematol. 2016; 95 ( 6 ): 901 - 909.
dc.identifier.citedreferenceKastritis E, Migkou M, Gavriatopoulou M, Zirogiannis P, Hadjikonstantinou V, Dimopoulos MA. Treatment of light chain deposition disease with bortezomib and dexamethasone. Haematologica. 2009; 94 ( 2 ): 300 - 302.
dc.identifier.citedreferenceJimenez-Zepeda VH, Trudel S, Winter A, Reece DE, Chen C, Kukreti V. Autologous stem cell transplant for light chain deposition disease: incorporating bortezomib to the induction therapy. Am J Hematol. 2012; 87 ( 8 ): 822 - 823.
dc.identifier.citedreferenceZiogas DC, Kastritis E, Terpos E, et al. Hematologic and renal improvement of monoclonal immunoglobulin deposition disease after treatment with bortezomib-based regimens. Leuk Lymphoma. 2017; 58 ( 8 ): 1832 - 1839.
dc.identifier.citedreferenceRoyer B, Arnulf B, Martinez F, et al. High dose chemotherapy in light chain or light and heavy chain deposition disease. Kidney Int. 2004; 65 ( 2 ): 642 - 648.
dc.identifier.citedreferenceWeichman K, Dember LM, Prokaeva T, et al. Clinical and molecular characteristics of patients with non-amyloid light chain deposition disorders, and outcome following treatment with high-dose melphalan and autologous stem cell transplantation. Bone Marrow Transplant. 2006; 38 ( 5 ): 339 - 343.
dc.identifier.citedreferenceLorenz EC, Gertz MA, Fervenza FC, et al. Long-term outcome of autologous stem cell transplantation in light chain deposition disease. Nephrol Dial Transplant. 2008; 23 ( 6 ): 2052 - 2057.
dc.identifier.citedreferenceHassoun H, Flombaum C, D’Agati VD, et al. High-dose melphalan and auto-SCT in patients with monoclonal Ig deposition disease. Bone Marrow Transplant. 2008; 42 ( 6 ): 405 - 412.
dc.identifier.citedreferenceBrioli A, Zamagni E, Pasquali S, et al. Long-term follow-up after autologous stem cell transplantation for light- and heavy-chain deposition disease. Bone Marrow Transplant. 2012; 47 ( 9 ): 1248 - 1249.
dc.identifier.citedreferenceBatalini F, Econimo L, Quillen K, et al. High-dose melphalan and stem cell transplantation in patients on dialysis due to immunoglobulin light-chain amyloidosis and monoclonal immunoglobulin deposition disease. Biol Blood Marrow Transplant. 2018; 24 ( 1 ): 127 - 132.
dc.identifier.citedreferenceKastritis E, Theodorakakou F, Roussou M, et al. Daratumumab-based therapy for patients with monoclonal gammopathy of renal significance. Br J Haematol. 2021; 193 ( 1 ): 113 - 118.
dc.identifier.citedreferenceKumar S, Paiva B, Anderson KC, et al. International myeloma working group consensus criteria for response and minimal residual disease assessment in multiple myeloma. Lancet Oncol. 2016; 17 ( 8 ): e328 - e346.
dc.identifier.citedreferenceKumar SK, Callander NS, Adekola K, et al. Multiple myeloma, version 3.2021, NCCN clinical practice guidelines in oncology. J Natl Compr Canc Netw. 2020; 18 ( 12 ): 1685 - 1717.
dc.identifier.citedreferenceDimopoulos MA, Sonneveld P, Leung N, et al. International myeloma working group recommendations for the diagnosis and Management of Myeloma-Related Renal Impairment. J Clin Oncol. 2016; 34 ( 13 ): 1544 - 1557.
dc.identifier.citedreferenceGertz MA, Comenzo R, Falk RH, et al. Definition of organ involvement and treatment response in immunoglobulin light chain amyloidosis (AL): a consensus opinion from the 10th international symposium on amyloid and amyloidosis, Tours, France, 18–22 April 2004. Am J Hematol. 2005; 79 ( 4 ): 319 - 328.
dc.identifier.citedreferencePalladini G, Hegenbart U, Milani P, et al. A staging system for renal outcome and early markers of renal response to chemotherapy in AL amyloidosis. Blood. 2014; 124 ( 15 ): 2325 - 2332.
dc.identifier.citedreferenceJain A, Ramasamy K. Time to redefine risk-stratification and response criteria in immunoglobulin light chain amyloidosis? Clin Lymphoma Myeloma Leuk. 2020; 20 ( 10 ): e769 - e776.
dc.identifier.citedreferenceRajkumar SV, Dimopoulos MA, Palumbo A, et al. International myeloma working group updated criteria for the diagnosis of multiple myeloma. Lancet Oncol. 2014; 15 ( 12 ): e538 - e548.
dc.identifier.citedreferenceKastritis E, Gavriatopoulou M, Roussou M, et al. Renal outcomes in patients with AL amyloidosis: prognostic factors, renal response and the impact of therapy. Am J Hematol. 2017; 92 ( 7 ): 632 - 639.
dc.working.doiNOen
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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