| Literature DB >> 32134199 |
Vivek Nagaraja1, Marco Matucci-Cerinic2, Daniel E Furst3, Masataka Kuwana4, Yannick Allanore5, Christopher P Denton6, Ganesh Raghu7, Vallerie Mclaughlin1, Panduranga S Rao1, James R Seibold8, John D Pauling9, Michael L Whitfield10, Dinesh Khanna1.
Abstract
Systemic sclerosis (SSc) is an autoimmune rheumatic disease with heterogeneous clinical manifestations and a variable course in which the severity of the pathology dictates the disease prognosis and course. Among autoimmune rheumatic diseases, SSc has the highest mortality rate among all rheumatic diseases, though there are exciting new therapeutic targets that appear to halt the progression of SSc manifestations such as skin or lung fibrosis. In selected patients, high-intensity regimens with autologous stem cell transplantation can favorably modify the course. In what was once thought to be an untreatable disease, targeted therapies have now changed the outlook of SSc to a treatable disorder. Herein, we discuss the targeted therapies modifying the outlook on selected organ involvement and creating opportunities for future treatment. We also present a framework for defining low disease activity in SSc.Entities:
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Year: 2020 PMID: 32134199 PMCID: PMC7329619 DOI: 10.1002/art.41246
Source DB: PubMed Journal: Arthritis Rheumatol ISSN: 2326-5191 Impact factor: 10.995