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Gertz, Morie A.

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

Mayo Clinic

Mayo Clinic

Citations 999

Attitudes about when and how to treat patients with AL amyloidosis: an international survey
Milani, Paolo , Gertz, Morie A. , Merlini, Giampaolo , Dispenzieri, Angela , Gertz, Morie A , Merlini, Giampaolo , Milani, Paolo , Dispenzieri, Angela

Amyloid | August 31, 2017 | Volume: 24 | Issue: 4 | Pages: 213-216

10.1080/13506129.2017.1370421 Get It

Delineation of the timing of second-line therapy post–autologous stem cell transplant in patients with AL amyloidosis
Hwa, Yi L. , Warsame, Rahma , Gertz, Morie A. , Buadi, Francis K. , Lacy, Martha Q. , Kumar, Shaji , Dingli, David , Zeldenrust, Steve R., Hayman, Susanne R., Kapoor, Prashant , Kourelis, Taxiarchis , Russell, Stephen J. , Hobbs, Miriam, Fonder, Amie , Dispenzieri, Angela , Gertz, Morie A , Buadi, Francis K , Russell, Stephen J , Dingli, David , Zeldenrust, Steven R., Leung, Nelson , Gonsalves, Wilson I. , Go, Ronald S. , Rajkumar, S. Vincent , Dispenzieri, Angela

Blood | August 14, 2017 | Volume: 130 | Issue: 13 | Pages: 1578-1584

10.1182/blood-2017-05-783415 Get It

Key Points Organ progression at second-line therapy predicated inferior survival. Patients relapsing from >VGPR had a longer time to develop organ progression.
Efficacy of daratumumab‐based therapies in patients with relapsed, refractory multiple myeloma treated outside of clinical trials
Lakshman, Arjun , Abeykoon, Jithma P. , Kumar, Shaji , Dingli, David , Gonsalves, Wilson I. , Leung, Nelson , Kourelis, Taxiarchis , Go, Ronald S. , Lacy, Martha Q. , Hobbs, Miriam, Lin, Yi , Warsame, Rahma , Lust, John A., Fonder, Amie , Hwa, Yi L. , Hayman, Suzanne R. , Russell, Stephen J. , Kyle, Robert A. , Kapoor, Prashant , Buadi, Francis K. , Gonsalves, Wilson , Leung, Nelson , Kourelis, Taxiarchis V, Go, Ronald S , Warsame, Rahma , Lust, John, Fonder, Amie L, Lakshman, Arjun , Russell, Stephen J , Dingli, David , Lin, Yi , Rajkumar, S. Vincent , Dispenzieri, Angela , Gertz, Morie A.

American Journal of Hematology | August 11, 2017 | Volume: 92 | Issue: 11 | Pages: 1146-1155

10.1002/ajh.24883 Get It

AbstractOutside of clinical trials, experience with daratumumab‐based combination therapies (DCTs) using bortezomib (V)/lenalidomide (R)/pomalidomide (P), and dexamethasone (d) in relapsed/refractory multiple myeloma (RRMM) is limited. We reviewed the outcomes of 126 patients who received ≥ 1 cycle of any DCT. Median age at DCT initiation was 67 (range, 43‐93) years. High‐risk cytogenetics was present in 33% patients. Median number of prior therapies was 4 (range, 1‐14) and time to first DCT from diagnosis was 4.3 years (range, 0.4‐13.0). Seventeen (13%) patients were refractory to single agent daratumumab. Fifty‐two (41%), 34 (27%), 23 (18%), and 17 (14%) received DPd, DRd, DVd and “other” DCTs, respectively. Overall response rate was 47%. Median follow‐up was 5.5 months (95% CI, 4.2‐6.1). Median progression‐free survival (PFS) was 5.5 months (95% CI, 4.2‐7.8). Median overall survival was not reached (NR) with any regimen. Median PFS (months) was worst for penta‐refractory MM (n = 8) vs quadruple refractory MM (n = 18) and others (n = 100) (2.2 [95% CI, 1‐2.4] vs 3.1 [95% CI, 2.1‐NR] vs 5.9 [95% CI, 5.0‐NR]; P < .001); those who were refractory to ≥1 agents used in the DCT vs others (4.9 [95% CI, 3.1‐6.0] vs 8.2 [95% CI, 4.6‐NR]; P = .02); and those who received >2 prior therapies vs others (5.0 months [95% CI, 3.7‐5.9] vs NR [95% CI, NR‐NR]; P = .002). Non‐hematologic toxicities included infections (38%), fatigue (32%), and infusion reactions (18%). Grade 3 or higher hematological toxicities were seen in 41% of patients. DCTs are effective in RRMM. ORR and PFS in heavily pretreated patients are lower than those reported in clinical trials.
Dexamethasone, rituximab and cyclophosphamide for relapsed and/or refractory and treatment‐naïve patients with Waldenstrom macroglobulinemia
Paludo, Jonas , Abeykoon, Jithma P. , Kumar, Shaji , Shreders, Amanda , Kourelis, Taxiarchis , King, Rebecca L. , Reeder, Craig B. , Kyle, Robert A. , Dingli, David , Lacy, Martha Q. , Lin, Yi , Warsame, Rahma , Lust, John A., Ansell, Stephen M. , Kapoor, Prashant , Buadi, Francis K. , Gonsalves, Wilson , Paludo, Jonas , Dingli, David , Lin, Yi , Ailawadhi, Sikander , Gertz, Morie A. , Leung, Nelson , Habermann, Thomas M. , Witzig, Thomas E. , Dispenzieri, Angela , Go, Ronald S. , Gonsalves, Wilson I. , Rajkumar, S. Vincent

British Journal of Haematology | August 8, 2017 | Volume: 179 | Issue: 1 | Pages: 98-105

10.1111/bjh.14826 Get It

SummaryThe management of Waldenström macroglobulinaemia (WM) relies predominantly on small trials, one of which has demonstrated activity of dexamethasone, rituximab and cyclophosphamide (DRC) in the frontline setting. We report on the efficacy of DRC, focusing on relapsed/refractory (R/R) patients. Ibrutinib, a recently approved agent in WM demonstrated limited activity in patients with MYD88WT genotype. Herein, we additionally report on the activity of DRC based on the MYD88L265P mutation status. Of 100 WM patients evaluated between January 2007 and December 2014 who received DRC, 50 had R/R WM. The overall response rate (ORR) was 87%. The median progression‐free survival (PFS) and time‐to‐next‐therapy (TTNT) were 32 (95% confidence interval [CI]: 15–51) and 50 (95% CI: 35–60) months, respectively. In the previously untreated cohort (n = 50), the ORR was 96%, and the median PFS and TTNT were 34 months (95% CI: 23–not reached [NR]) and NR (95% CI: 37–NR), respectively. Twenty‐five (86%) of 29 genotyped patients harbored MYD88L265P. The response rates and outcomes were independent of MYD88 mutation status. Grade ≥3 adverse effects included neutropenia (20%), thrombocytopenia (7%) and infections (3%). Similar to the frontline setting, DRC is an effective and well‐tolerated salvage regimen for WM. In contrast to ibrutinib, DRC offers a less expensive, fixed‐duration option, with preliminary data suggesting efficacy independent of the patients’ MYD88 status.
Outcomes of Patients With Familial Transthyretin Amyloidosis After Liver Transplantation
Banerjee, Dipti, Roeker, Lindsey E. , Grogan, Martha , Poterucha, John J., Zeldenrust, Steve R., Edwards, Brooks S., Daly, Richard C. , Klarich, Kyle W. , Poterucha, John, Zeldenrust, Steve, Edwards, Brooks, Daly, Richard , Swiecicki, Paul Loren , Heimbach, Julie K. , Zeldenrust, Steven R., Gertz, Morie A. , Dispenzieri, Angela , Roeker, Lindsey

Progress in Transplantation | August 3, 2017 | Volume: 27 | Issue: 3 | Pages: 246-250

10.1177/1526924817715463 Get It

Background: Familial transthyretin amyloidosis is a disease caused by misfolded transthyretin aggregates that can impair multiple organ systems. Liver transplantation is the first-line treatment for familial transthyretin amyloidosis. Research Question: Our objective is to study outcomes and survival among patients with familial transthyretin amyloidosis after transplantation. Design: All patients undergoing orthotopic liver transplant for familial transthyretin amyloidosis at Mayo Clinic between 1997 and 2012 were reviewed. Baseline clinical characteristics, organs transplanted, and posttransplant clinical course were assessed. Results: Of the 40 patients, 7 patients had the V30M mutation and 33 had other mutations. Nineteen patients received liver only, 19 liver and heart, and 2 combined liver, heart, and kidney transplants. The 5-year overall survival was 85% for those receiving multiple organ transplant and 52% for those receiving liver transplant only ( P = .057). There was no difference in overall survival based on mutation (V30M vs other mutations), but survival was confounded by varied disease involvement and organs transplanted. Those who had early death (≤24 months from liver transplant) had a higher incidence of baseline peripheral neuropathy, autonomic neuropathy, lower modified BMI, and higher alkaline phosphatase. Discussion: Outcomes of orthotopic liver transplant in familial transthyretin amyloidosis are variable due to heterogeneity in mutations and patient status at the time of transplant. Familial transthyretin amyloidosis can progress, despite liver transplantation. Patients receiving combined liver, heart/kidney transplant demonstrated improved survival compared to liver transplant alone.
Elevation of serum lactate dehydrogenase in AL amyloidosis reflects tissue damage and is an adverse prognostic marker in patients not eligible for stem cell transplantation
Muchtar, Eli , Lacy, Martha Q. , Kapoor, Prashant , Hayman, Suzanne R. , Gonsalves, Wilson I. , Warsame, Rahma , Kourelis, Taxiarchis , Chakraborty, Rajshekhar , Russell, Stephen J. , Lust, John A., Lin, Yi , Zeldenrust, Steven R., Dingli, David , Kyle, Robert A. , Kumar, Shaji , Buadi, Francis K. , Gonsalves, Wilson , Kourelis, Taxiarchis V, Russell, Stephen, Zeldenrust, Steven, Kumar, Shaji K , Gertz, Morie A , Dispenzieri, Angela , Go, Ronald S. , Leung, Nelson , Rajkumar, S. Vincent , Gertz, Morie A. , Muchtar, E , Russell, Stephen J , Chakraborty, Rajshekhar , Dingli, David , Lin, Yi

British Journal of Haematology | July 12, 2017 | Volume: 178 | Issue: 6 | Pages: 888-895

10.1111/bjh.14830 Get It

SummaryThe significance of serum lactate dehydrogenase (LDH) in light chain (AL) amyloidosis has not been previously explored. We studied 1019 newly diagnosed patients and correlated the elevation of LDH above the upper limit of normal (ULN) with disease characteristics and outcome. Four hundred and nine patients had an LDH above ULN, representing 40% of the study population. Patients with an elevated LDH were older, were less likely to be male and had more extensive organ involvement compared to patients with a normal LDH. Patients with high LDH had greater cardiac and renal dysfunction. Elevated LDH was an independent prognostic marker for overall survival and for death within 6 months of diagnosis, but this was restricted to patients not eligible for stem cell transplant. Serum LDH may act as a marker for organ damage and should be explored as a potential marker for tissue healing and organ recovery.
Pomalidomide, bortezomib, and dexamethasone for patients with relapsed lenalidomide-refractory multiple myeloma
Paludo, Jonas , LaPlant, Betsy, Halvorson, Alese E. , Kumar, Shaji , Hayman, Suzanne R. , Lust, John A., Kapoor, Prashant , Russell, Stephen J. , Dingli, David , Lin, Yi , Bergsagel, P. Leif , Sher, Taimur , Chanan‐Khan, Asher , Stewart, A. Keith, Reeder, Craig B. , Richardson, Paul G. , Lacy, Martha Q. , Bergsagel, P. Leif , Mikhael, Joseph R., LaPlant, Betsy R, Buadi, Francis K. , Chanan-Khan, Asher A., Mıkhael, Joseph , Gertz, Morie A. , Dispenzieri, Angela , Leung, Nelson , Go, Ronald S. , Gonsalves, Wilson I. , Fonseca, Rafaël , Roy, Vivek , Ailawadhi, Sikander , Richardson, Paul Gerard Guy , Rajkumar, S. Vincent , Paludo, Jonas , Russell, Stephen J , Dingli, David , Lin, Yi

Blood | July 6, 2017 | Volume: 130 | Issue: 10 | Pages: 1198-1204

10.1182/blood-2017-05-782961 Get It

Key Points PVD is an active combination in relapsed lenalidomide-refractory MM patients. PVD with weekly bortezomib offers a simpler, more convenient, and well-tolerated regimen option.
Will we be able to afford a cure in multiple myeloma?
Chakraborty, Rajshekhar , Gertz, Morie A. , Chakraborty, Rajshekhar

Leukemia & Lymphoma | June 20, 2017 | Volume: 59 | Issue: 1 | Pages: 1-2

10.1080/10428194.2017.1339883 Get It

Clinical trials evaluating potential therapies for light chain (AL) amyloidosis
Muchtar, Eli , Gertz, Morie A. , Muchtar, E

Expert Opinion on Orphan Drugs | June 10, 2017 | Volume: 5 | Issue: 8 | Pages: 655-663

10.1080/21678707.2017.1341834 Get It