Back to Authors

Gertz, Morie A.

https://orcid.org/0000-0002-3853-5196

Mayo Clinic

Mayo Clinic

Citations 999

Diagnosis and management of smoldering multiple myeloma: the razor’s edge between clonality and cancer
Muchtar, Eli , Kumar, Shaji , Magen, Hila , Gertz, Morie A. , Kumar, Shaji K , Gertz, Morie A , Muchtar, E

Leukemia & Lymphoma | June 8, 2017 | Volume: 59 | Issue: 2 | Pages: 288-299

10.1080/10428194.2017.1334124 Get It

The prognostic significance of polyclonal bone marrow plasma cells in patients with relapsing multiple myeloma
Ghosh, Toshi, Gonsalves, Wilson I. , Jevremović, Dragan , Dingli, David , Timm, Michael, Morice, William G. , Kapoor, Prashant , Kourelis, Taxiarchis , Lacy, Martha Q. , Hayman, Suzanne R. , Lin, Yi , Russell, Stephen J. , Lust, John A., Zeldenrust, Steven R., Warsame, Rahma , Hwa, Yi L. , Kyle, Robert A. , Kumar, Shaji , Timm, Michael M, Kourelis, Taxiarchis V, Buadi, Francis K. , Leung, Nelson , Go, Ronald S , Warsame, Rahma , Dispenzieri, Angela , Morice, William George , Leung, Nelson , Go, Ronald S. , Gertz, Morie A. , Rajkumar, S. Vincent , Gonsalves, Wilson , Russell, Stephen J , Jevremovic, Dragan , Dingli, David , Lin, Yi

American Journal of Hematology | June 1, 2017 | Volume: 92 | Issue: 9 | Pages: No page available

10.1002/ajh.24807 Get It

AbstractPrior studies have revealed that the presence of increasing number of polyclonal plasma cells (pPCs) in the bone marrow (BM) are associated with better outcomes in newly diagnosed multiple myeloma (MM) patients. This effect has not been studied in patients with MM at the time of disease relapse. We determined the prognostic value of depletion of pPCs in the BM by 7‐color multiparameter flow cytometry in a series of 174 relapsing MM patients. The time to next therapy (TTNT) in those with <5% pPCs was 9.4 months versus 13.9 months in those with ≥5% pPCs (P = .0091). The median overall survival (OS) in those with <5% pPCs was 21.4 months, while the median OS was not reached in those patients with ≥5% pPCs (P = .019). Of the 109 patients with standard risk cytogenetics, the median OS of those with <5% pPCs was 28.4 months, while the median OS was not reached in those with ≥5% pPCs (P = .033). As such, <5% pPCs in the BM appears to have prognostic utility in identifying a subset of relapsing MM patients, even with standard‐risk cytogenetics, who have a particularly adverse outcome.
Management of macroglobulinaemia
Gertz, Morie A.

British Journal of Haematology | May 9, 2017 | Volume: 177 | Issue: 5 | Pages: 669-671

10.1111/bjh.14742 Get It

Prevalence and predictors of thyroid functional abnormalities in newly diagnosed AL amyloidosis
Muchtar, Eli , Dean, Diana S., Dingli, David , Lacy, Martha Q. , Hayman, Suzanne R. , Kapoor, Prashant , Russell, Stephen J. , Lust, John A., Lin, Yi , Warsame, Rahma , Kourelis, Taxiarchis , Chakraborty, Rajshekhar , Zeldenrust, Steven R., Kyle, Robert A. , Kumar, Shaji , Muchtar, E , Dispenzieri, Angela , Buadi, Francis K. , Leung, Nelson , Gonsalves, Wilson I. , Go, Ronald S. , Rajkumar, S. Vincent , Gertz, Morie A. , Russell, Stephen J , Chakraborty, Rajshekhar , Dingli, David , Lin, Yi

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

10.1111/joim.12617 Get It

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.
High prevalence of monoclonal gammopathy among patients with warm autoimmune hemolytic anemia
Ravindran, Aishwarya , Sankaran, Janani , Jacob, Eapen K., Kreuter, Justin D. , Hook, C. Christopher , Call, Timothy G. , Pruthi, Rajiv K. , Litzow, Mark R. , Wolanskyj, Alexandra P. , Ashrani, Aneel A. , Begna, Kebede H. , Marshall, Ariela L. , Kyle, Robert A. , Gertz, Morie A. , Hogan, William J. , Kay, Neil E. , Go, Ronald S. , Ravindran, Aishwarya , Marshall, Ariela , Wolanskyj-Spinner, Alexandra P

American Journal of Hematology | April 24, 2017 | Volume: 92 | Issue: 8 | Pages: No page available

10.1002/ajh.24765 Get It

First report of MYD88L265P somatic mutation in IgM-associated light chain amyloidosis
Chakraborty, Rajshekhar , Novak, Anne J. , Ansell, Stepen M., Muchtar, Eli , Kapoor, Prashant , Hayman, Suzanne R. , Lacy, Martha Q. , King, Rebecca L. , Chakraborty, Rajshekar, Buadi, Francis K. , Dispenzieri, Angela , Gertz, Morie A. , Muchtar, E , Chakraborty, Rajshekhar

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

10.1080/13506129.2016.1272454 Get It

Outcome of very young (≤40 years) patients with immunoglobulin light chain (AL) amyloidosis
Abeykoon, Jithma P. , Dingli, David , Baudi, Francis K., Kyle, Robert A. , Lacy, Martha Q. , Hayman, Suzanne R. , Kourelis, Taxiarchis , Kumar, Shaji , Kapoor, Prashant , Paludo, Jonas , Dispenzieri, Angela , Gertz, Morie A. , Gonsalves, Wilson I. , Leung, Nelson , Rajkumar, S. Vincent , Dingli, David

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

10.1080/13506129.2017.1286584 Get It

IgM myeloma: A multicenter retrospective study of 134 patients
Castillo, Jorge J. , Brožová, Lucie , Czepiel, Jacek , Dávila, Julio , Ghobrial, Irene M. , Gozzetti, Alessandro , Gustine, Joshua , Hájek, Roman , Jayabalan, David , Laubach, Jacob P. , Lewicka, Barbara , Maisnar, Vladimír , Manasanch, Elisabet E. , Moreau, Philippe , Nahi, Hareth , Niesvizky, Rubén, Paba‐Prada, Claudia E., Pika, Tomáš, Pour, Luděk , Reagan, John L. , Richardson, Paul G. , Shah, Jatin J., Špıčka, Ivan , Vij, Ravi , Jurczyszyn, Artur , Crusoé, Edvan de Queiroz , Dispenzieri, Angela , Eveillard, Marion , Fiala, Mark A. , Hungria, Vânia , Jarkovský, Jiří , Morgan, Elizabeth A. , Richardson, Paul Gerard Guy , Waszczuk‐Gajda, Anna , Gertz, Morie A. , Hajek, Roman , Moreau, Philippe , Castillo, Jorge J , Ghobrial, Irene M , Gozzetti, Alessandro , Nahi, Hareth

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

10.1002/ajh.24753 Get It

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.