Drug-induced Thrombotic Microangiopathy with Concurrent Proteasome Inhibitor Use in the Treatment of Multiple Myeloma: A Case Series and Review of the Literature

2020 ◽  
Vol 20 (11) ◽  
pp. e791-e800
Author(s):  
Bethany E. Monteith ◽  
Christopher P. Venner ◽  
Donna E. Reece ◽  
Andrea K. Kew ◽  
Marc Lalancette ◽  
...  
HemaSphere ◽  
2019 ◽  
Vol 3 (3) ◽  
pp. e192 ◽  
Author(s):  
Víctor Higuero Saavedra ◽  
Verónica González-Calle ◽  
Eduardo Sobejano ◽  
Josefa Sebastiá ◽  
Mónica Cabrero ◽  
...  

2014 ◽  
Vol 25 (2) ◽  
pp. 180-184 ◽  
Author(s):  
Muhammed Sait Dag ◽  
Zeynel Abidin Ozturk ◽  
Irem Akin ◽  
Ediz Tutar ◽  
Oztekin Cikmam ◽  
...  

2021 ◽  
Vol 11 (2) ◽  
pp. 71
Author(s):  
Ogechi Ikediobi ◽  
Jeremy A. Schneider

Severe cutaneous adverse drug reactions (SCAR) such as the Stevens–Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) and drug rash with eosinophilia and systemic symptoms/drug-induced hypersensitivity syndrome (DIHS) can be induced by a plethora of medications. The field of pharmacogenomics aims to prevent severe adverse drug reactions by using our knowledge of the inherited or acquired genetic risk of drug metabolizing enzymes, drug targets, or the human leukocyte antigen (HLA) genotype. Dermatologists are experts in the diagnosis and management of severe cutaneous adverse drug reactions (SCAR) in both the inpatient and outpatient setting. However, most dermatologists in the US have not focused on the prevention of SCAR. Therefore, this paper presents a case series and review of the literature highlighting salient examples of how dermatologists can apply pharmacogenomics in the diagnosis and especially in the prevention of SCAR induced by allopurinol and sulfamethoxazole/trimethoprim, two commonly prescribed medications.


2016 ◽  
Vol 16 (3) ◽  
pp. e39-e45 ◽  
Author(s):  
Artur Jurczyszyn ◽  
Magdalena Olszewska-Szopa ◽  
Adam S. Vesole ◽  
David H. Vesole ◽  
David S. Siegel ◽  
...  

2016 ◽  
Vol 2016 ◽  
pp. 1-5
Author(s):  
Jan Van Keer ◽  
Michel Delforge ◽  
Daan Dierickx ◽  
Kathelijne Peerlinck ◽  
Evelyne Lerut ◽  
...  

Bortezomib is a first-generation proteasome inhibitor used in the treatment of multiple myeloma (MM). A few reports have linked bortezomib exposure with the development of thrombotic microangiopathy (TMA). We describe a case of biopsy-proven renal thrombotic microangiopathy associated with the use of bortezomib in a 51-year-old man with IgG lambda MM. To our knowledge, this is the first biopsy-proven case. In addition, reexposure to bortezomib 18 months later was associated with recurrence of TMA. This supports a possible causal role of bortezomib. The exact mechanisms remain to be elucidated.


2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Michael Rassner ◽  
Rebecca Baur ◽  
Ralph Wäsch ◽  
Mario Schiffer ◽  
Johanna Schneider ◽  
...  

Abstract Background Treatment with proteasome inhibitors like carfilzomib in patients with multiple myeloma (MM) can induce thrombotic microangiopathy (TMA) characterized by neurological symptoms, acute kidney injury, hemolysis and thrombocytopenia. Successful treatment with the monoclonal antibody eculizumab was described for these patients, but reports of ideal management and definitive treatment protocols are lacking. Case Presentation The first case describes a 43-years-old IgG-kappa-MM patient that developed TMA during the first course of carfilzomib-lenalidomide-dexamethasone (KRd) consolidation after autologous stem cell transplantation (ASCT). In the second case, a 59-years-old IgG-kappa-MM patient showed late-onset TMA during the fourth and last cycle of elotuzumab-KRd consolidation within the DSMM XVII study of the German study group MM (DSMM; clinicalTrials.gov Identifier: NCT03948035). Concurrently, he suffered from influenza A/B infection. Both patients had a high TMA-index for a poor prognosis of TMA. Therapeutically, in both patients plasma exchange (TPE) was initiated as soon as TMA was diagnosed. In patient #1, dialysis became necessary. For both patients, only when the complement inhibitor eculizumab was administered, kidney function and blood values impressively improved. Conclusion In this small case series, two patients with MM developed TMA due to carfilzomib treatment (CFZ-TMA), the second patient as a late-onset form. Even though TMA could have been elicited by influenza in the second patient and occurred after ASCT in both patients, with cases of TMA post-transplantation in MM being described, a relation of TMA and carfilzomib treatment was most likely. In both patients, treatment with eculizumab over two months efficiently treated TMA without recurrence and with both patients remaining responsive months after TMA onset. Taken together, we describe two cases of TMA in MM patients on carfilzomib-combination treatment, showing similar courses of this severe adverse reaction, with good responses to two months of eculizumab treatment.


2021 ◽  
Author(s):  
Rachel Hilburg ◽  
Abdallah S. Geara ◽  
Maylene Kefeng Qiu ◽  
Matthew B. Palmer ◽  
Elaine Y. Chiang ◽  
...  

2019 ◽  
Vol 103 (4) ◽  
pp. 307-318 ◽  
Author(s):  
Meera Sridharan ◽  
C. Christopher Hook ◽  
Nelson Leung ◽  
Jeffrey L. Winters ◽  
Ronald S. Go ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document