TY - JOUR
T1 - Withdrawal of thiopurines in Crohn’s disease treated with scheduled adalimumab maintenance
T2 - a prospective randomised clinical trial (DIAMOND2)
AU - DIAMOND2 Study Group
AU - Hisamatsu, Tadakazu
AU - Kato, Shingo
AU - Kunisaki, Reiko
AU - Matsuura, Minoru
AU - Nagahori, Masakazu
AU - Motoya, Satoshi
AU - Esaki, Motohiro
AU - Fukata, Norimasa
AU - Inoue, Satoko
AU - Sugaya, Takeshi
AU - Sakuraba, Hirotake
AU - Hirai, Fumihito
AU - Watanabe, Kenji
AU - Kanai, Takanori
AU - Naganuma, Makoto
AU - Nakase, Hiroshi
AU - Suzuki, Yasuo
AU - Watanabe, Mamoru
AU - Hibi, Toshifumi
AU - Nojima, Masanori
AU - Matsumoto, Takayuki
AU - Endo, Katsuya
AU - Hanai, Hiroyuki
AU - Kobayashi, Taku
AU - Hiraoka, Sakiko
AU - Hisamatsu, Tadakazu
AU - Honda, Yutaka
AU - Inoue, Takuya
AU - Inoue, Shuji
AU - Ishida, Tetsuya
AU - Ito, Hiroaki
AU - Iwakiri, Ryuichi
AU - Izumi, Motoyoshi
AU - Kagaya, Takashi
AU - Kamata, Noriko
AU - Naganawa, Yumiko
AU - Kaneto, Hiroyuki
AU - Kani, Kazuhito
AU - Kinjyo, Fukunori
AU - Yasaka, Hiroki
AU - Kurahara, Koichi
AU - Kyouwon, Lee
AU - Yano, Yutaka
AU - Matsui, Toshiyuki
AU - Tanaka, Hiroki
AU - Munemoto, Yoshinori
AU - Naito, Yuji
AU - Nakagawa, Tomoo
AU - Yokoyama, Yoko
AU - Nakamura, Shiro
N1 - Publisher Copyright:
© 2019, Japanese Society of Gastroenterology.
PY - 2019/10/1
Y1 - 2019/10/1
N2 - Background: The risk:benefit ratio of concomitant use of thiopurines with scheduled adalimumab (ADA) maintenance therapy for Crohn’s disease is controversial. The aim of this study is to identify the influence of withdrawal of thiopurines in patients in remission with combination therapy in an open-label, randomised, controlled trial (DIAMOND2; UMIN000009596). Methods: Patients in corticosteroid-free clinical remission (CFCR) for ≥ 6 months with ADA (40 mg, s.c., every other week) scheduled maintenance combined with thiopurines were randomised into two groups, “continue” (Con) or “discontinue” (Dis) group of thiopurines, whereas all other patients kept receiving scheduled ADA maintenance therapy for 52 weeks. The primary endpoint was the proportion of patients in CFCR at week 52. Secondary endpoints were endoscopic remission (ER), trough levels of ADA in serum, and safety. Results: Fifty patients were randomised to Con or Dis groups. Characteristics of patients were not significantly different between the groups. CFCR and ER prevalence at week 52 were not significantly different between groups (log rank, P = 0.704, P = 1.000, respectively). Trough levels of ADA were not significantly different between groups (P = 0.515). The proportion of patients with AAA positivity at week 52 was not significantly different (P = 0.437). ER at week 0 was involved in ER and triple remission at week 52. No serious adverse effects were observed in either group. Conclusion: Continuation of thiopurines > 6 months offers no clear benefit over scheduled ADA monotherapy. CFCR, ER, and ADA trough level at week 52 were not significantly different between groups. ER at week 0 may be involved in better long-term clinical outcomes.
AB - Background: The risk:benefit ratio of concomitant use of thiopurines with scheduled adalimumab (ADA) maintenance therapy for Crohn’s disease is controversial. The aim of this study is to identify the influence of withdrawal of thiopurines in patients in remission with combination therapy in an open-label, randomised, controlled trial (DIAMOND2; UMIN000009596). Methods: Patients in corticosteroid-free clinical remission (CFCR) for ≥ 6 months with ADA (40 mg, s.c., every other week) scheduled maintenance combined with thiopurines were randomised into two groups, “continue” (Con) or “discontinue” (Dis) group of thiopurines, whereas all other patients kept receiving scheduled ADA maintenance therapy for 52 weeks. The primary endpoint was the proportion of patients in CFCR at week 52. Secondary endpoints were endoscopic remission (ER), trough levels of ADA in serum, and safety. Results: Fifty patients were randomised to Con or Dis groups. Characteristics of patients were not significantly different between the groups. CFCR and ER prevalence at week 52 were not significantly different between groups (log rank, P = 0.704, P = 1.000, respectively). Trough levels of ADA were not significantly different between groups (P = 0.515). The proportion of patients with AAA positivity at week 52 was not significantly different (P = 0.437). ER at week 0 was involved in ER and triple remission at week 52. No serious adverse effects were observed in either group. Conclusion: Continuation of thiopurines > 6 months offers no clear benefit over scheduled ADA monotherapy. CFCR, ER, and ADA trough level at week 52 were not significantly different between groups. ER at week 0 may be involved in better long-term clinical outcomes.
KW - Adalimumab
KW - Crohn’s disease
KW - Thiopurines
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U2 - 10.1007/s00535-019-01582-w
DO - 10.1007/s00535-019-01582-w
M3 - Article
C2 - 31041545
AN - SCOPUS:85065229696
SN - 0944-1174
VL - 54
SP - 860
EP - 870
JO - Journal of gastroenterology
JF - Journal of gastroenterology
IS - 10
ER -