Dergiler / Turkish Journal of Medical Sciences / 2020 / Cilt: 50 - Sayı: 1

Anti-interleukin-6 (tocilizumab) therapy in Takayasu’s arteritis: a real life experience

Sayfa
31–36
Yayın Tarihi
2022-11-05
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

All patients tolerated tocilizumabwell.Conclusion: Based on retrospective real life data, anti-IL-6 (tocilizumab) appears to be an effective and tolerable treatment option inrefractory TA patients.

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Amaç & Hipotez:Background/aim: Tumour necrosis factor inhibitors and anti-interleukin-6 (anti-IL-6) therapies are increasingly being used inTakayasu’s arteritis (TA) patients who are unresponsive to corticosteroids ± conventional immunosuppressive agents.
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Temel Bulgular & Veri:The aim of thisstudy is to assess the efficacy and safety of anti-IL-6 (tocilizumab) therapy in refractory TA patients in real life.Materials and methods: Fifteen TA patients (86.7% were female) who received at least 3 cycles of tocilizumab therapy were retrospectivelyassessed by clinical, laboratory, and radiological evaluations before and after tocilizumab therapy.Results: The median (min–max) age of the patients at evaluation was 35 (20–58) years and the median disease duration from diagnosiswas 24 (12–168) months.
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Sonuç & Katkı:All patients tolerated tocilizumabwell.Conclusion: Based on retrospective real life data, anti-IL-6 (tocilizumab) appears to be an effective and tolerable treatment option inrefractory TA patients.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Abstract

Background/aim: Tumour necrosis factor inhibitors and anti-interleukin-6 (anti-IL-6) therapies are increasingly being used inTakayasu’s arteritis (TA) patients who are unresponsive to corticosteroids ± conventional immunosuppressive agents. The aim of thisstudy is to assess the efficacy and safety of anti-IL-6 (tocilizumab) therapy in refractory TA patients in real life.Materials and methods: Fifteen TA patients (86.7% were female) who received at least 3 cycles of tocilizumab therapy were retrospectivelyassessed by clinical, laboratory, and radiological evaluations before and after tocilizumab therapy.Results: The median (min–max) age of the patients at evaluation was 35 (20–58) years and the median disease duration from diagnosiswas 24 (12–168) months. The median (min.–max.) duration of follow-up after tocilizumab was 15 (3–42) months. There was a significantdecrease in erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and patient global visual analogue scale (VAS) scores ofpatients after tocilizumab therapy. The median (min.–max.) ESR was 26 (5–119) vs. 3 (2–49) mm/h, P = 0.02; CRP was 39.8 (2.4–149.0)vs. 7.9 (0–92.9) mg/L, P = 0.017; and patient global VAS was 50 (0–90) vs. 30 (0–60), P = 0.027, respectively. In 8 patients, ESR and CRPlevels were in the normal range in the last control. Imaging modality results after tocilizumab were available for 9 patients; 8 patientswere radiologically stable and regression was seen in 1 patient. Comparable imaging modality results before and after tocilizumab wereavailable for 5 patients; 4 patients were radiologically stable and regression was seen in 1 patient. Radiological findings were consistentwith laboratory responses. Glucocorticoid dosages decreased from a mean dosage of 16.2 (9.1) mg/day at baseline to 7.1 (3.8) mg/day (P= 0.001) at the last follow-up visit. There was no increase in the steroid dosage in any of the patients. All patients tolerated tocilizumabwell.Conclusion: Based on retrospective real life data, anti-IL-6 (tocilizumab) appears to be an effective and tolerable treatment option inrefractory TA patients.

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Bu Makaleye Atıf Yap

FIRAT, E., ERDEN, A., ARMAĞAN, B., KILIÇ, L., BİLGEN, Ş. A., SARI, A., KALYONCU, U., KİRAZ, S., KARADAĞ, Ö., YARDIMCI, G. K., ERTENLİ, İ., AKDOĞAN, A. (2022). Anti-interleukin-6 (tocilizumab) therapy in Takayasu’s arteritis: a real life experience. Turkish Journal of Medical Sciences, Cilt: 50 - Sayı: 1, 31–36. https://ajindex.com/articles/609682

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Kaynakça (4)

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