TY - JOUR
T1 - Clinicopathological features of clinical methotrexate-related lymphoproliferative disorders
AU - Tokuhira, Michihide
AU - Saito, Shuntaro
AU - Suzuki, Katsuya
AU - Higashi, Morihiro
AU - Momose, Shuju
AU - Shimizu, Takayuki
AU - Mori, Takehiko
AU - Kimura, Yuta
AU - Amano, Koichi
AU - Okamoto, Shinichiro
AU - Takeuchi, Tsutomu
AU - Tamaru, Jun Ichi
AU - Kizaki, Masahiro
N1 - Publisher Copyright:
© 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2019/8/24
Y1 - 2019/8/24
N2 - Methotrexate (MTX) is one of the potent drugs for autoimmune diseases (ADs), especially for rheumatoid arthritis. Recent studies suggest that MTX should be immediately withdrawn when patients with AD develop lymphoproliferative disorder (LPD). However, biopsy cannot be performed for diagnosis because LPD regresses quickly after MTX withdrawal, thus making clinical MTX-LPD (c-MTX-LPD) challenging to diagnose. In this study, among the 28 patients with c-MTX-LPD, seven developed a proven LPD (p-LPD) after suspicious LPD (s-LPD) regression, six of which were Hodgkin lymphoma. Four of seven patients with p-LPD + died, whereas all patients with p-LPD– survived. The clinical manifestations indicative of p-LPD include fever, elevated serum C-reactive protein level, and soluble interleukin-2 receptor level. Anti-AD drugs did not appear to affect the pathogenesis of p-LPD development. P-LPD was not observed after 3 years from the time of s-LPD regression.
AB - Methotrexate (MTX) is one of the potent drugs for autoimmune diseases (ADs), especially for rheumatoid arthritis. Recent studies suggest that MTX should be immediately withdrawn when patients with AD develop lymphoproliferative disorder (LPD). However, biopsy cannot be performed for diagnosis because LPD regresses quickly after MTX withdrawal, thus making clinical MTX-LPD (c-MTX-LPD) challenging to diagnose. In this study, among the 28 patients with c-MTX-LPD, seven developed a proven LPD (p-LPD) after suspicious LPD (s-LPD) regression, six of which were Hodgkin lymphoma. Four of seven patients with p-LPD + died, whereas all patients with p-LPD– survived. The clinical manifestations indicative of p-LPD include fever, elevated serum C-reactive protein level, and soluble interleukin-2 receptor level. Anti-AD drugs did not appear to affect the pathogenesis of p-LPD development. P-LPD was not observed after 3 years from the time of s-LPD regression.
KW - Clinical
KW - lymphoproliferative disorders
KW - methotrexate
KW - proven
KW - rheumatoid arthritis
KW - suspicious
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U2 - 10.1080/10428194.2019.1585841
DO - 10.1080/10428194.2019.1585841
M3 - Article
C2 - 30947579
AN - SCOPUS:85063860176
SN - 1042-8194
VL - 60
SP - 2508
EP - 2515
JO - Leukemia and Lymphoma
JF - Leukemia and Lymphoma
IS - 10
ER -