JGH Open (Jul 2024)

Comparison of early versus late addition of granulocyte and monocyte adsorption for incomplete remission induction in ulcerative colitis

  • Keiichi Tominaga,
  • Mimari Kanazawa,
  • Shoko Watanabe,
  • Takanao Tanaka,
  • Shunsuke Kojimahara,
  • Satoshi Masuyama,
  • Keiichiro Abe,
  • Akira Kanamori,
  • Akira Yamamiya,
  • Takeshi Sugaya,
  • Kenichi Goda,
  • Yuji Fujita,
  • Shigemi Yoshihara,
  • Yasuo Haruyama,
  • Atsushi Irisawa

DOI
https://doi.org/10.1002/jgh3.70012
Journal volume & issue
Vol. 8, no. 7
pp. n/a – n/a

Abstract

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Abstract Background and aim Ulcerative colitis (UC) is characterized by repeated relapse and remission. Because no fundamental therapeutic strategy has been established, the treatment goal is generally to maintain the remission phase for a long period after rapid remission induction. Granulocyte and monocyte adsorption (GMA) for UC is reportedly quite safe because it does not affect immunosuppression. Moreover, it is useful in combination with other remission induction therapy. The aim of this study was to evaluate the difference in efficacy by the timing of the addition of GMA with corticosteroids, calcineurin inhibitors, and anti‐cytokine therapy for active UC. Methods The study included 59 patients. Patients who started GMA of 5–11 days were in the early GMA combination group. Patients who started GMA 12 days or more were in the late GMA combination group. The primary endpoint was difference in the effect of additional GMA according to the timing of the intervention. The secondary endpoint was difference in the time to remission induction between the two groups. Results Of the 32 early GMA group patients, 24 achieved remission induction. Of the 27 late group patients, 18 achieved remission induction. No significant difference in induction rates was found (P = 0.481). The early group had shorter mean time to remission induction (P < 0.001). Conclusions In conclusion, results suggest that early addition of GMA might lead to earlier remission in patients who have had an inadequate response to remission induction therapy with corticosteroids, calcineurin inhibitors, and anti‐cytokine therapy.

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