TY - JOUR
T1 - Characteristics of rheumatoid arthritis with immunodeficiency-associated lymphoproliferative disorders to regress spontaneously by the withdrawal of methotrexate and their clinical course
T2 - A retrospective, multicenter, case-control study
AU - Kuramoto, Nobuo
AU - Saito, Shuntaro
AU - Fujii, Takao
AU - Kaneko, Yuko
AU - Saito, Rintaro
AU - Tanaka, Masao
AU - Takada, Hideto
AU - Nakano, Kazuhisa
AU - Saito, Kazuyoshi
AU - Sugimoto, Naoki
AU - Sasaki, Sho
AU - Harigai, Masayoshi
AU - Suzuki, Yasuo
N1 - Funding Information:
Nobuo Kuramoto has received a research grant from Eisai Co., Ltd. Shuntaro Saito has received speaking fees from Chugai Pharmaceutical Co., Ltd., Eisai Co., Ltd., Pfizer Japan Inc., Asahi Kasei Pharma Corporation, Bristol Myers Squibb Co., and Mitsubishi Tanabe Pharma Corporation. Takao Fujii has received speaking fees and/or honoraria from AbbVie GK, Astellas Pharma Inc., Asahi Kasei Pharma Corporation, Chugai Pharmaceutical Co., Ltd., Eli Lilly Japan K.K., Eisai Co., Ltd., Janssen Pharmaceutical K.K., Mitsubishi Tanabe Pharma Corporation, Ono Pharmaceutical Co., Ltd., Pfizer Japan Inc., and UCB Japan Co., Ltd. and has received research grants from AbbVie GK, Ayumi Pharmaceutical Corporation, Asahi Kasei Pharma Corporation, Astellas Pharma Inc., Chugai Pharmaceutical Co., Ltd., Eli Lilly Japan K.K., Eisai Co., Ltd., Mitsubishi Tanabe Pharma Corporation, Pfizer Japan Inc., Ono Pharmaceutical Co., Ltd., and UCB Japan Co., Ltd. Yuko Kaneko has received grants or speaking fees from AbbVie GK, Astellas Pharma Inc., Ayumi Pharmaceutical Corporation, Bristol–Myers Squibb Co., Chugai Pharmaceutical Co., Ltd., Eisai Co., Ltd., Eli Lilly Japan K.K., Hisamitsu Pharmaceutical Co., Inc., Janssen Pharmaceutical, Kissei Pharmaceutical Co., Ltd., Kyowa Kirin Co., Ltd., Pfizer Japan Inc., Sanofi K.K., Takeda Pharmaceutical Co., Ltd. Mitsubishi Tanabe Pharma Corporation, and UCB Japan Co., Ltd. Masao Tanaka is in the endowed chair funded by two local governments in Japan (Nagahama City, Shiga and Toyooka City, Hyogo) and five pharmaceutical companies (Mitsubishi Tanabe Pharma Corporation, Chugai Pharmaceutical Co., Ltd., Ayumi Pharmaceutical Corporation., Asahi Kasei Pharma Corporation, and UCB Japan Co., Ltd.). Masao Tanaka has received research grants and/or speaker fees from AbbVie GK, Asahi Kasei Pharma Corporation, Astellas Pharma Inc., Ayumi Pharmaceutical Corporation, Bristol-Myers Squibb Co., Chugai Pharmaceutical Co., Ltd., Eisai Co., Ltd., Eli Lilly Japan K.K., Pfizer Japan Inc., UCB Japan Co., Ltd., Janssen Pharmaceutical K.K., Mitsubishi Tanabe Pharma Corporation, Novartis Pharma K.K., and Taisho Pharmaceutical Co., Ltd. Kazuhisa Nakano has received research grants from Mitsubishi Tanabe Pharma Corporation, Eisai Co., Ltd., and Eli Lilly Japan K.K. Kazuyoshi Saito has received speaking fees from Eli Lilly Japan K.K. Yasuo Suzuki has received funding from Chugai Pharmaceutical Co., Ltd., Teijin Pharma Limited, and Asahi Kasei Pharma Corporation. and has received speaking fees and/or honoraria from Eisai Co., Ltd., Ono Pharmaceutical Co., Ltd., Mitsubishi Tanabe Pharma Corporation, Ltd, Maruho Co., Ltd, Glaxo Smith Klein K.K, and Pfizer Japan Inc. Masayoshi Harigai has received research grants from AbbVie Japan GK, Asahi Kasei Pharma Corporation, Astellas Pharma Inc., Ayumi Pharmaceutical Corporation, Bristol Myers Squibb Co., Chugai Pharmaceutical Co., Ltd., Daiichi-Sankyo Co., Ltd., Eisai Co., Ltd., Kissei Pharmaceutical Co., Ltd., Mitsubishi Tanabe Pharma Corporation, Nippon Kayaku Co., Ltd., Sekisui Medical, Shionogi & Co., Ltd., Taisho Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co., Ltd., and Teijin Pharma Limited. Masayoshi Harigai has received a speaking fee from AbbVie GK, Ayumi Pharmaceutical Corporation, Nippon Boehringer Ingelheim Co., Ltd., Bristol Myers Squibb Co., Chugai Pharmaceutical Co., Ltd., Eisai Co., Ltd., Eli Lilly Japan K.K., GlaxoSmithKline K.K., Kissei Pharmaceutical Co., Ltd., Pfizer Japan Inc., Takeda Pharmaceutical Co., Ltd., and Teijin Pharma Limited. Masayoshi Harigai is a consultant for AbbVie GK, Nippon Boehringer Ingelheim Co., Ltd., Bristol Myers Squibb Co., Kissei Pharmaceutical Co., Ltd., and Teijin Pharma Limited.
Publisher Copyright:
© 2021 Japan College of Rheumatology.
PY - 2022/1/1
Y1 - 2022/1/1
N2 - Objective: To investigate clinical characteristics and time course of lymphoproliferative disorders (LPDs) in rheumatoid arthritis (RA) patients after methotrexate (MTX) discontinuation, in those who achieved spontaneous regression (SR). Methods: We retrospectively reviewed clinical data from RA patients with LPDs obtained from eight institutions between 2000 and 2017 and compared clinical and pathological findings between SR and non-SR groups. Results: Among 232 RA patients with LPDs, 216 were treated with MTX at the onset of LPD and 144 (66.7%) achieved SR after MTX discontinuation. Higher MTX doses, high titers of anti-CCP antibodies (>13.5 U/mL), and lower LDH and soluble IL-2 receptor levels were associated with SR. Lymphocyte count was decreased at LPD onset and increased at 2 weeks after MTX discontinuation in the SR group. Epstein-Barr virus-positive mucocutaneous ulcer, reactive lymphoid hyperplasia and unclassifiable B-cell lymphoma, were more frequent in the SR than in the non-SR group. In multivariable analysis, diffuse large B-cell lymphomas was an independent predictive factor for non-SR. In the patients with SR, 73.9% achieved partial or complete regression as early as 2 weeks after MTX discontinuation. Conclusion: SR and non-SR in RA patients with LPDs after MTX discontinuation were associated with certain clinical characteristics.
AB - Objective: To investigate clinical characteristics and time course of lymphoproliferative disorders (LPDs) in rheumatoid arthritis (RA) patients after methotrexate (MTX) discontinuation, in those who achieved spontaneous regression (SR). Methods: We retrospectively reviewed clinical data from RA patients with LPDs obtained from eight institutions between 2000 and 2017 and compared clinical and pathological findings between SR and non-SR groups. Results: Among 232 RA patients with LPDs, 216 were treated with MTX at the onset of LPD and 144 (66.7%) achieved SR after MTX discontinuation. Higher MTX doses, high titers of anti-CCP antibodies (>13.5 U/mL), and lower LDH and soluble IL-2 receptor levels were associated with SR. Lymphocyte count was decreased at LPD onset and increased at 2 weeks after MTX discontinuation in the SR group. Epstein-Barr virus-positive mucocutaneous ulcer, reactive lymphoid hyperplasia and unclassifiable B-cell lymphoma, were more frequent in the SR than in the non-SR group. In multivariable analysis, diffuse large B-cell lymphomas was an independent predictive factor for non-SR. In the patients with SR, 73.9% achieved partial or complete regression as early as 2 weeks after MTX discontinuation. Conclusion: SR and non-SR in RA patients with LPDs after MTX discontinuation were associated with certain clinical characteristics.
KW - Rheumatoid arthritis
KW - lymphoproliferative disorder
KW - methotrexate
KW - prognostic factors
KW - spontaneous regression
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U2 - 10.1080/14397595.2021.1879362
DO - 10.1080/14397595.2021.1879362
M3 - Article
C2 - 33496194
AN - SCOPUS:85102178543
SN - 1439-7595
VL - 32
SP - 24
EP - 31
JO - Modern rheumatology
JF - Modern rheumatology
IS - 1
ER -