Sustained effect of leukocytapheresis/granulocytapheresis versus anti-human TNF-α monoclonal antibody on ulcerative colitis: A 2-year retrospective study

Author:

Sakai Masahiro1ORCID,Hayashi Koichi2,Ito Tomoyuki3,Otani Haruka3,Mori Yuya3,Ito Shinsuke1,Endo Keita1,Matsuda Hiroto4,Yoshino Kaede1,Kitamura Koichi1,Kubota Eiji5,Motomura Yasuaki6,Suzuki Yasuhiro7,Fujitani Shigeki8,Suzuki Toshihiko1ORCID

Affiliation:

1. Department of Nephrology, Endocrinology and Diabetes, Tokyo Bay Urayasu Ichikawa Medical Center, Urayasu, Chiba, Japan

2. Department of Emergency and Critical Care Medicine, St. Marianna University Yokohama Seibu Hospital, Yokohama, Kanagawa, Japan

3. Department of Pharmacy, Tokyo Bay Urayasu Ichikawa Medical Center, Urayasu, Chiba, Japan

4. Department of Nephrology and Hypertension, Keiyu Hospital, Yokohama, Kanagawa, Japan

5. Department of Nephrology and General Medicine, Shizuoka Red Cross Hospital, Shizuoka, Shizuoka, Japan

6. Department of Gastroenterology, Tokyo Bay Urayasu Ichikawa Medical Center, Urayasu, Chiba, Japan

7. Department of Medical Engineering, Tokyo Bay Urayasu Ichikawa Medical Center, Urayasu, Chiba, Japan

8. Department of Emergency and Critical Care Medicine, St. Marianna University School of Medicine, Kawasaki, Kanagawa, Japan.

Abstract

Although anti-tumor necrosis factor-α monoclonal antibody biological preparations (BP) agents are widely used as an established treatment tool for refractory ulcerative colitis (UC), whether leukocytapheresis/granulocytapheresis (L/G-CAP) has similar beneficial impact on the disease activity remains undetermined. Furthermore, the costs defrayed for the treatment with these 2 modalities have not been compared. We retrospectively evaluated whether L/G-CAP offered sustained beneficial effects over 2-year period. The patients who had moderately to severely active UC (Rachmilewitz clinical activity index (CAI) ≧ 5) and were treated with a series (10 sessions) of L/G-CAP (n = 19) or BP (n = 7) as an add-on therapy to conventional medications were followed. Furthermore, the cost-effectiveness pertaining to the treatment with L/G-CAP and BP was assessed over 12 months. At baseline, L/G-CAP and BP groups manifested similar disease activity (CAI, L/G-CAP; 7.0 [6.0–10.0], BP; 10.0 [6.0–10.0],P= .207). The L/G-CAP and BP treatment suppressed the activity, with CAI 1 or less attained on day 180. When the L/G-CAP group was dichotomized into L/G-CAP-high and L/G-CAP-low group based on CAI values (≥3 or < 3) on day 365, CAI was gradually elevated in L/G-CAP-high group but remained suppressed in L/G-CAP-low group without additional apheresis for 2 years. Anemia was corrected more rapidly and hemoglobin levels were higher in BP group. The cost of the treatment with L/G-CAP over 12 months was curtailed to 76% of that with BP (1.79 [1.73–1.92] vs 2.35 [2.29–3.19] million yen,P= .028). L/G-CAP is as effective as BP in a substantial number of patients over 2 years. The cost for the treatment of UC favors L/G-CAP although the correction of anemia may prefer BP. Thus, L/G-CAP can effectively manage the disease activity with no additional implementation for 2 years although further therapeutic modalities might be required in a certain population with high CAI observed on day 365.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

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