European myeloma network recommendations on diagnosis and management of patients with rare plasma cell dyscrasias

scientific article published on 23 July 2018

European myeloma network recommendations on diagnosis and management of patients with rare plasma cell dyscrasias is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1038/S41375-018-0209-7
P698PubMed publication ID30038381

P50authorHermann EinseleQ1610986
Roman HajekQ63639209
Francesca GayQ79780506
Niels W C J van de DonkQ87712098
Maria GavriatopoulouQ88776018
Ute HegenbartQ89376735
Pieter SonneveldQ90143311
Sonja ZweegmanQ92858507
Christian StrakaQ92973626
Benedetto BrunoQ96123891
Mario BoccadoroQ98568600
Athanasios DimopoulosQ26338766
Giampaolo MerliniQ37839101
Efstathios KastritisQ43187559
Evangelos TerposQ57015797
P2093author name stringMonika Engelhardt
Pellegrino Musto
Jo Caers
P2860cites workParadoxical increases in serum IgM and viscosity levels following rituximab in Waldenstrom's macroglobulinemiaQ80563613
Bendamustine therapy in patients with relapsed or refractory Waldenström's macroglobulinemiaQ83757867
Thalidomide for POEMS syndromeQ83827655
Bevacizumab therapy for POEMS syndromeQ83929768
Maintenance Rituximab is associated with improved clinical outcome in rituximab naïve patients with Waldenstrom Macroglobulinaemia who respond to a rituximab-containing regimenQ84201369
Autologous stem cell transplant for light chain deposition disease: incorporating bortezomib to the induction therapyQ84235764
MYD88 Mutations and Response to Ibrutinib in Waldenström's MacroglobulinemiaQ85732520
Rituximab intolerance in patients with Waldenström macroglobulinaemiaQ86602713
Atrial fibrillation associated with ibrutinib in Waldenström macroglobulinemiaQ87495207
Carfilzomib, rituximab, and dexamethasone (CaRD) treatment offers a neuropathy-sparing approach for treating Waldenström's macroglobulinemiaQ87946433
Treatment of light chain deposition disease with bortezomib and dexamethasoneQ24658325
Molecular Classification and Pharmacogenetics of Primary Plasma Cell Leukemia: An Initial Approach toward Precision MedicineQ26799238
Ibrutinib in previously treated Waldenström's macroglobulinemia.Q27853148
Prognostic markers and criteria to initiate therapy in Waldenstrom's macroglobulinemia: consensus panel recommendations from the Second International Workshop on Waldenstrom's MacroglobulinemiaQ28201685
Immunophenotypic analysis of Waldenstrom's macroglobulinemiaQ28201709
Targeted pharmacological depletion of serum amyloid P component for treatment of human amyloidosisQ28217930
Bendamustine plus rituximab versus CHOP plus rituximab as first-line treatment for patients with indolent and mantle-cell lymphomas: an open-label, multicentre, randomised, phase 3 non-inferiority trialQ28286064
Primary plasma cell leukemia 2.0: advances in biology and clinical management.Q30243927
Improved Outcomes After Autologous Hematopoietic Cell Transplantation for Light Chain Amyloidosis: A Center for International Blood and Marrow Transplant Research StudyQ30278687
Long-term outcomes to fludarabine and rituximab in Waldenström macroglobulinemiaQ33382030
How I treat plasma cell leukemiaQ33402555
Long-term results of the phase II trial of the oral mTOR inhibitor everolimus (RAD001) in relapsed or refractory Waldenstrom MacroglobulinemiaQ33414529
Ibrutinib for patients with rituximab-refractory Waldenström's macroglobulinaemia (iNNOVATE): an open-label substudy of an international, multicentre, phase 3 trial.Q33437577
Outcomes of patients with POEMS syndrome treated initially with radiationQ33794285
First-in-Human Phase I/II Study of NEOD001 in Patients With Light Chain Amyloidosis and Persistent Organ DysfunctionQ33795363
Primary plasma cell leukemia and autologous stem cell transplantationQ33829100
Plasma cell leukemia: consensus statement on diagnostic requirements, response criteria and treatment recommendations by the International Myeloma Working GroupQ33956990
POEMS syndromeQ34006873
Trends in survival of patients with primary plasma cell leukemia: a population-based analysisQ34019590
Treatment recommendations for patients with Waldenström macroglobulinemia (WM) and related disorders: IWWM-7 consensusQ34106817
Long-term follow-up from a phase 1/2 study of single-agent bortezomib in relapsed systemic AL amyloidosisQ34353682
Therapeutic Clearance of Amyloid by Antibodies to Serum Amyloid P ComponentQ34485172
Prognostic impact of circulating plasma cells in patients with multiple myeloma: implications for plasma cell leukemia definition.Q34552588
Common variants in the human platelet PAR4 thrombin receptor alter platelet function and differ by raceQ34580117
The role of radiotherapy in the management of POEMS syndromeQ34620383
Treatment of POEMS syndrome with bevacizumabQ34714907
Japanese POEMS syndrome with Thalidomide (J-POST) Trial: study protocol for a phase II/III multicentre, randomised, double-blind, placebo-controlled trialQ34903868
Kidney dysfunction during lenalidomide treatment for AL amyloidosis.Q35025410
Combination of melphalan and dexamethasone for patients with newly diagnosed POEMS syndromeQ35067588
Clinicopathological definition of Waldenstrom's macroglobulinemia: consensus panel recommendations from the Second International Workshop on Waldenstrom's MacroglobulinemiaQ35116840
A comparison of immunohistochemistry and mass spectrometry for determining the amyloid fibril protein from formalin-fixed biopsy tissueQ35552353
Polyneuropathy improvement following autologous stem cell transplantation for POEMS syndrome.Q35611648
Hematopoietic cell transplantation for primary plasma cell leukemia: results from the Center for International Blood and Marrow Transplant ResearchQ35742685
Peripheral blood stem cell transplantation in 16 patients with POEMS syndrome, and a review of the literatureQ35848803
Serum cardiac troponins and N-terminal pro-brain natriuretic peptide: a staging system for primary systemic amyloidosisQ35886289
Activity of pomalidomide in patients with immunoglobulin light-chain amyloidosisQ36015183
Primary plasma cell leukemia: clinical and laboratory presentation, gene-expression profiling and clinical outcome with Total Therapy protocolsQ36185955
Dangerous small B-cell clones.Q36516158
Natural history and outcome of light chain deposition diseaseQ36519972
Revised prognostic staging system for light chain amyloidosis incorporating cardiac biomarkers and serum free light chain measurementsQ36910372
Coexistent multiple myeloma or increased bone marrow plasma cells define equally high-risk populations in patients with immunoglobulin light chain amyloidosisQ36938784
Proliferative glomerulonephritis with monoclonal IgG deposits.Q37330535
Genetic aberrations and survival in plasma cell leukemiaQ37486780
Oral melphalan and dexamethasone grants extended survival with minimal toxicity in AL amyloidosis: long-term results of a risk-adapted approach.Q37676296
Clinical outcomes of patients with plasma cell leukemia in the era of novel therapies and hematopoietic stem cell transplantation strategies: a single-institution experienceQ37911050
Monoclonal gammopathy of renal significance: when MGUS is no longer undetermined or insignificantQ38050703
Therapeutic advances in the treatment of primary plasma cell leukemia: a focus on hematopoietic cell transplantation.Q38082246
Lenalidomide/melphalan/dexamethasone in newly diagnosed patients with immunoglobulin light chain amyloidosis: results of a prospective phase 2 study with long-term follow up.Q38376616
How I treat extramedullary myelomaQ38672673
Primary Plasma Cell Leukemia: Identity Card 2016.Q38781794
Lenalidomide is safe and active in Waldenström macroglobulinemia.Q38973119
Improved outcomes for newly diagnosed AL amyloidosis between 2000 and 2014: cracking the glass ceiling of early deathQ40362742
Outcomes of patients with renal monoclonal immunoglobulin deposition diseaseQ40533557
Efficacy and long-term toxicity of the rituximab-fludarabine-cyclophosphamide combination therapy in Waldenstrom's macroglobulinemiaQ40773209
Bortezomib, Doxorubicin, Cyclophosphamide, Dexamethasone Induction Followed by Stem Cell Transplantation for Primary Plasma Cell Leukemia: A Prospective Phase II Study of the Intergroupe Francophone du Myélome.Q40781792
A practical approach to the diagnosis of systemic amyloidoses.Q41505050
Unexpected bone marrow finding in a patient with pancytopenia after hematopoietic stem cell transplantationQ42065087
Encouraging impact of doxycycline on early mortality in cardiac light chain (AL) amyloidosisQ42292795
Lenalidomide in combination with melphalan and dexamethasone in patients with newly diagnosed AL amyloidosis: a multicenter phase 1/2 dose-escalation studyQ42931881
Cyclophosphamide-bortezomib-dexamethasone (CyBorD) produces rapid and complete hematologic response in patients with AL amyloidosis.Q43050098
Bortezomib with or without dexamethasone in primary systemic (light chain) amyloidosisQ43189700
Primary therapy of Waldenstrom macroglobulinemia (WM) with weekly bortezomib, low-dose dexamethasone, and rituximab (BDR): long-term results of a phase 2 study of the European Myeloma Network (EMN).Q43923016
Lenalidomide and low-dose dexamethasone for newly diagnosed primary plasma cell leukemiaQ44404066
Long-term outcomes after autologous stem cell transplantation for patients with POEMS syndrome (osteosclerotic myeloma): a single-center experienceQ44507982
Treatment with bortezomib-based regimens improves overall response and predicts for survival in patients with primary or secondary plasma cell leukemia: Analysis of the Greek myeloma study groupQ44559311
Frontline chemotherapy with bortezomib-containing combinations improves response rate and survival in primary plasma cell leukemia: a retrospective study from GIMEMA Multiple Myeloma Working PartyQ44962191
Fludarabine, cyclophosphamide, and rituximab in salvage therapy of Waldenström's macroglobulinemia.Q44991602
Bortezomib and dexamethasone consolidation following risk-adapted melphalan and stem cell transplantation for patients with newly diagnosed light-chain amyloidosisQ46251291
Bortezomib produces high hematological response rates with prolonged renal survival in monoclonal immunoglobulin deposition diseaseQ46538650
Bortezomib in the treatment of AL amyloidosis: targeted therapy?Q46892406
The role of frontline autologous stem cell transplantation for primary plasma cell leukemia: a retrospective multicenter study (KMM160).Q47140962
Management of relapsed and refractory multiple myeloma: novel agents, antibodies, immunotherapies and beyondQ47283493
Long-term outcome of patients with AL amyloidosis treated with high-dose melphalan and stem cell transplantation: 20-year experienceQ48123471
Combination therapy incorporating Bcl-2 inhibition with Venetoclax for the treatment of refractory primary plasma cell leukemia with t (11;14).Q48137388
Daratumumab yields rapid and deep hematologic responses in patients with heavily pretreated AL amyloidosis.Q48276787
Doxycycline disrupts transthyretin amyloid: evidence from studies in a FAP transgenic mice model.Q50743781
Translocation t(11;14) is associated with adverse outcome in patients with newly diagnosed AL amyloidosis when treated with bortezomib-based regimens.Q50851104
Plasma cell leukemia: update on biology and therapy.Q52838137
Progress in the Treatment of Primary Plasma Cell Leukemia.Q53781542
Immunohistochemistry in the classification of systemic forms of amyloidosis: a systematic investigation of 117 patients.Q54337852
Renal Monoclonal Immunoglobulin Deposition Disease: A Report of 64 Patients from a Single InstitutionQ56658531
High-Dose Melphalan versus Melphalan plus Dexamethasone for AL AmyloidosisQ57218202
Dexamethasone, rituximab, and cyclophosphamide as primary treatment of Waldenstrom macroglobulinemia: final analysis of a phase 2 studyQ57904277
Hematologic Response and Stabilization of Renal Function in a Patient With Light Chain Deposition Disease After Lenalidomide Treatment: A Novel Therapeutic Approach?Q57904322
A phase 1/2 study of lenalidomide with low-dose oral cyclophosphamide and low-dose dexamethasone (RdC) in AL amyloidosisQ57904446
Melphalan and dexamethasone with or without bortezomib in newly diagnosed AL amyloidosis: a matched case–control study on 174 patientsQ58029880
Salvage therapy with lenalidomide and dexamethasone in patients with advanced AL amyloidosis refractory to melphalan, bortezomib, and thalidomideQ58030111
Identification of Amyloidogenic Light Chains Requires the Combination of Serum-Free Light Chain Assay with Immunofixation of Serum and UrineQ58030328
Cytogenetic and therapeutic characterization of primary plasma cell leukemia: the IFM experienceQ58051878
Gain of chromosome 1q21 is an independent adverse prognostic factor in light chain amyloidosis patients treated with melphalan/dexamethasoneQ58136617
The role of minor salivary gland biopsy in the diagnosis of systemic amyloidosis: results of a prospective study in 62 patientsQ58190652
Cyclophosphamide, bortezomib, and dexamethasone therapy in AL amyloidosis is associated with high clonal response rates and prolonged progression-free survivalQ58853078
A matched comparison of cyclophosphamide, bortezomib and dexamethasone (CVD) versus risk-adapted cyclophosphamide, thalidomide and dexamethasone (CTD) in AL amyloidosisQ61657837
P433issue9
P304page(s)1883-1898
P577publication date2018-07-23
P1433published inLeukemiaQ6534498
P1476titleEuropean myeloma network recommendations on diagnosis and management of patients with rare plasma cell dyscrasias
P478volume32

Reverse relations

cites work (P2860)
Q61454609Cardiovascular adverse events in multiple myeloma patients
Q64257450Germline Risk Contribution to Genomic Instability in Multiple Myeloma
Q60949296How I treat elderly patients with plasma cell dyscrasias
Q96348701The BLIMP1-EZH2 nexus in a non-Hodgkin lymphoma
Q97545594Upfront Daratumumab With Lenalidomide and Dexamethasone for POEMS Syndrome

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