Second symptomatic COVID-19 infections in patients with an underlying monoclonal gammopathy
Year: 2022
Type: article
Abstract: Patients with hematologic malignancies, including multiple myeloma (MM), light chain (AL) amyloidosis, smoldering MM (SMM) and monoclonal gammopathy of undetermined significance (MGUS), have disproportionately high rates of COVID-19 infection and associated mortality [ 1 , 2 ]. Immune paresis is a common feature in dysproteinemias and has been demonstrated to be an independent risk factor for severity of COVID-19 infection in patients with MGUS [ 3 ]. In a matched control study of patients with MM and MGUS compared with healthy controls, the risk of breakthrough infections after completion of vaccination was around 3% [ 4 ]. Ongoing myeloma-directed treatment further induces immune suppression increasing the risk for severe COVID-19 infections [ 5 , 6 , 7 ]. While inferior immune response to COVID-19 vaccination have been described in patients with monoclonal gammopathies [ 8 ], information on the rate and severity of COVID-19 infections in patients who do demonstrate immunogenicity post infection or vaccination is limited. Additionally, rates and clinical course of second symptomatic COVID-19 infections in patients with monoclonal gammopathy in relation to prior antibody testing has been previously described.
Source: Blood Cancer Journal
Authors: Saurabh Zanwar, Matthew Ho, Francis K. Buadi, Sikander Ailawadhi, Jeremy Larsen, Leif Bergsagel, Moritz Binder, Asher Chanan-Khan, David Dingli, Angela Dispenzieri, Rafael Fonseca, Morie A. Gertz, Wilson Gonsalves, Ronald S. Go, Suzanne Hayman, Prashant Kapoor, Taxiarchis Kourelis, Martha Q. Lacy, Nelson Leung, Yi Lin, Eli Muchtar, Vivek Roy, Taimur Sher, Rahma Warsame, Amie Fonder, Miriam Hobbs, Yi L. Hwa, Robert A. Kyle, S. Vincent Rajkumar, Shaji Kumar
Language: English
Subfield: Hematology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $4,590
Funder: National Cancer Institute
Award: G1016754749
OpenAlex ID: W4309899864
