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Published on: July 20, 2019
TNF-α blocker therapy and solid malignancy risk in ANCA-associated vasculitis
Francisco Silva1, Marcela Cisternas, Ulrich Specks
1Departamento de Inmunología Clínica y Reumatología, Escuela de Medicina, Facultad de Medicina, Pontificia Universidad Católica de Chile, Marcoleta 352, Santiago, Chile. fsilval@uc.cl
Tumor necrosis factor-alpha (TNF-α) blockers, like etanercept, are used to treat ANCA-associated vasculitides (AAV). Studies suggest a potential link between these biologic therapies and an increased risk of solid malignancies in patients with AAV.
Area of Science:
- Rheumatology
- Immunology
- Oncology
Background:
- ANCA-associated vasculitides (AAV) are serious conditions requiring immunosuppressive therapy.
- Current treatments have significant adverse effects.
- Biologics, including TNF-α blockers, are explored for targeted therapy.
Purpose of the Study:
- To review evidence on the association between TNF-α blockers and solid malignancies in AAV.
- To evaluate the safety profile of etanercept and other TNF-α inhibitors in AAV patients.
Main Methods:
- Review of clinical trial data, including the Wegener's Granulomatosis Etanercept Trial (WGET).
- Analysis of long-term follow-up data regarding malignancy incidence.
- Synthesis of evidence on TNF-α inhibition and cancer risk in AAV.
Main Results:
- Etanercept use in GPA was linked to increased solid malignancy development compared to placebo in the WGET trial.
- A 5-year follow-up indicated a sustained increase in malignancy incidence, not solely attributable to etanercept.
- Concerns regarding the safety of TNF-α blockers in AAV patients have been raised.
Conclusions:
- The use of TNF-α blockers in AAV warrants careful consideration due to potential malignancy risks.
- Further research is needed to fully understand the long-term safety of these biologic agents in AAV.
- Risk-benefit assessment is crucial when considering TNF-α inhibitors for ANCA-associated vasculitides.
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