Citations 1052

The utility of MASS‐FIX to detect and monitor monoclonal proteins in the clinic

American Journal of Hematology | April 25, 2017 | Volume: 92 | Issue: 8 | Pages: 772-779

10.1002/ajh.24772 | PMID 28439985

The detection and quantification of monoclonal‐proteins (M‐proteins) are necessary for the diagnosis and evaluation of response in plasma cell dyscrasias. Immunoglobulin enrichment‐coupled with matrix‐assisted laser desorption ionization time‐of‐flight mass‐spectrometry (MASS‐FIX) is a simple and inexpensive method to identify M‐proteins, but its clinical generalizability has not yet been elucidated. We compared MASS‐FIX to protein electrophoresis (PEL), serum/urine immunofixation‐electrophoresis (IFE), and quantitative serum free‐light chain (FLC) for the identification of M‐proteins in different clinical diagnoses. Paired serum and urine samples from 257 patients were tested. There were six patients for whom s‐IFE and FLC ratio were positive and serum MASS‐FIX was negative, but when serum and urine MASS‐FIX results were combined, only one patient with light chain‐MGUS was missed. Serum/urine‐MASS‐FIX detected M‐proteins in 18 patients with negative serum/urine‐PEL/IFE and serum‐FLC, 10 of whom had multiple myeloma or AL amyloidosis, who were mistakenly thought to have complete hematologic response by serum/urine‐PEL/IFE and serum‐FLC. Nearly half of the AL amyloidosis patients had atypical spectra, which may prove to be a clue to the diagnosis and pathogenesis of the disease. In conclusion, MASS‐FIX has a comparable sensitivity with PEL/IFE/FLC methods and can help inform the clinical diagnosis.
Prevalence and predictors of thyroid functional abnormalities in newly diagnosed AL amyloidosis

Journal of Internal Medicine | April 25, 2017 | Volume: 281 | Issue: 6 | Pages: 611-619

10.1111/joim.12617 | PMID 28439924

AbstractBackgroundData on the effect of systemic immunoglobulin light chain amyloidosis (AL amyloidosis) on thyroid function are limited.ObjectiveTo assess the prevalence of hypothyroidism in AL amyloidosis patients and determine its predictors.Methods1142 newly diagnosed AL amyloidosis patients were grouped based on the thyroid‐stimulating hormone (TSH) measurement at diagnosis: hypothyroid group (TSH above upper normal reference; >5 mIU L−1; n = 217, 19% of study participants) and euthyroid group (n = 925, 81%). Predictors for hypothyroidism were assessed in a binary multivariate model. Survival between groups was compared using the log‐rank test and a multivariate analysis.ResultsPatients with hypothyroidism were older, more likely to present with renal and hepatic involvement and had a higher light chain burden compared to patients in the euthyroid group. Higher proteinuria in patients with renal involvement and lower albumin in patients with hepatic involvement were associated with hypothyroidism. In a binary logistic regression model, age ≥65 years, female sex, renal involvement, hepatic involvement, kappa light chain restriction and amiodarone use were independently associated with hypothyroidism. Ninety‐three per cent of patients in the hypothyroid group with free thyroxine measurement had normal values, consistent with subclinical hypothyroidism. Patients in the hypothyroid group had a shorter survival compared to patients in the euthyroid group (4‐year survival 36% vs 43%; P = 0.008), a difference that was maintained in a multivariate analysis.ConclusionA significant proportion of patients with AL amyloidosis present with hypothyroidism, predominantly subclinical, which carries a survival disadvantage. Routine assessment of TSH in these patients is warranted.
Immunoparesis status in AL amyloidosis at diagnosis affects response and survival by regimen type

Amyloid | April 22, 2017 | Volume: 24 | Issue: sup1 | Pages: 44-45

10.1080/13506129.2017.1281117 | PMID 28434304

Immunoparesis in newly diagnosed AL amyloidosis is a marker for response and survival

Amyloid | April 22, 2017 | Volume: 24 | Issue: sup1 | Pages: 40-41

10.1080/13506129.2016.1277696 | PMID 28434371

First report of MYD88L265P somatic mutation in IgM-associated light chain amyloidosis

Amyloid | April 22, 2017 | Volume: 24 | Issue: sup1 | Pages: 42-43

10.1080/13506129.2016.1272454 | PMID 28434299

Outcome of very young (≤40 years) patients with immunoglobulin light chain (AL) amyloidosis

Amyloid | April 22, 2017 | Volume: 24 | Issue: sup1 | Pages: 50-51

10.1080/13506129.2017.1286584 | PMID 28434368

Recommendations from the Amyloidosis Research Consortium Educational Roundtable at the American College of Cardiology Annual Meeting, 1 April 2016

Amyloid | April 22, 2017 | Volume: 24 | Issue: sup1 | Pages: 165-166

10.1080/13506129.2017.1286582 | PMID 28434366

Feasibility study of cardiac magnetic resonance elastography in cardiac amyloidosis

Amyloid | April 22, 2017 | Volume: 24 | Issue: sup1 | Pages: 161-161

10.1080/13506129.2017.1278689 | PMID 28434361

The yin and yang of autophagy in AL amyloidosis

Blood | April 13, 2017 | Volume: 129 | Issue: 15 | Pages: 2044-2045

10.1182/blood-2017-02-765594 | PMID 28408419

IgM myeloma: A multicenter retrospective study of 134 patients

American Journal of Hematology | April 6, 2017 | Volume: 92 | Issue: 8 | Pages: 746-751

10.1002/ajh.24753 | PMID 28383205

AbstractIgM myeloma is a rare hematologic malignancy for which the clinicopathological features and patient outcomes have not been extensively studied. We carried out a multicenter retrospective study in patients with diagnosis of IgM myeloma defined by >10% marrow involvement by monoclonal plasma cells, presence of an IgM monoclonal paraproteinemia of any size, and anemia, renal dysfunction, hypercalcemia, lytic lesions and/or t(11;14) identified by FISH. A total of 134 patients from 20 centers were included in this analysis. The median age at diagnosis was 65.5 years with a male predominance (68%). Anemia, renal dysfunction, elevated calcium and skeletal lytic lesions were found in 37, 43, 19, and 70%, respectively. The median serum IgM level was 2,895 mg dL−1 with 19% of patients presenting with levels >6,000 mg dL−1. International Staging System (ISS) stages 1, 2, and 3 were seen in 40 (33%), 54 (44%), and 29 (24%) of patients, respectively. The malignant cells expressed CD20 (58%) and cyclin D1 (67%), and t(11;14) was the most common cytogenetic finding (39%). The median overall survival (OS) was 61 months. Higher ISS score was associated with worse survival (P = 0.02). Patients with IgM myeloma present with similar characteristics and outcomes as patients with more common myeloma subtypes.