Factors Associated with Myelosuppression Related to Low-Dose Methotrexate Therapy for Inflammatory Rheumatic Diseases

被引:49
作者
Mori, Shunsuke [1 ]
Hidaka, Michihiro [2 ]
Kawakita, Toshiro [2 ]
Hidaka, Toshihiko [3 ]
Tsuda, Hiroyuki [4 ]
Yoshitama, Tamami [5 ]
Migita, Kiyoshi [6 ]
Ueki, Yukitaka [7 ]
机构
[1] NHO Kumamoto Saishunsou Natl Hosp, Dept Rheumatol, Clin Res Ctr Rheumat Dis, Kumamoto 8611196, Japan
[2] NHO Natl Kumamoto Med Ctr, Dept Hematol, Kumamoto 8600008, Japan
[3] Zenjinkai Shimin No Mori Hosp, Inst Rheumatol, Miyazaki 8800122, Japan
[4] Kumamoto City Hosp, Dept Hematol & Oncol, Kumamoto 8628505, Japan
[5] Yoshitama Clin Rheumat Dis, Kagoshima 8995117, Japan
[6] NHO Natl Nagasaki Med Ctr, Clin Res Ctr, Omura, Nagasaki 8568652, Japan
[7] Sasebo Chuo Hosp, Rheumat & Collagen Dis Ctr, Sasebo, Nagasaki 8571195, Japan
关键词
MODIFYING ANTIRHEUMATIC DRUGS; LONG-TERM SAFETY; INDUCED PANCYTOPENIA; CLINICAL CHARACTERISTICS; PULSE METHOTREXATE; RISK-FACTORS; ARTHRITIS; TOXICITY; PHARMACOKINETICS; EFFICACY;
D O I
10.1371/journal.pone.0154744
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objective Severe myelosuppression is a serious concern in the management of rheumatic disease patients receiving methotrexate (MTX) therapy. This study was intended to explore factors associated with the development of MTX-related myelosuppression and its disease severity. Methods We retrospectively examined a total of 40 cases of MTX-related myelosuppression that had been filed in the registries of participating rheumatology and hematology divisions. Data before onset were compared with those of 120 controls matched for age and sex. Cytopenia was graded according to the National Cancer Institute criteria for adverse events. Data before and at onset were compared between the severe and non-severe groups. Results Non-use of folic acid supplements, concurrent medications, and low renal function were significantly associated with the development of myelosuppression (p < 0.001, p < 0.001, and p = 0.002, respectively). In addition, significantly lower MTX dosages, higher blood cell counts, and lower hemoglobin levels were seen in the myelosuppression group (p < 0.001). No patients exhibited leukocytopenia, neutropenia, or thrombocytopenia in routine blood monitoring taken within the past month. One-fourth developed myelosuppression within the first two months (an early-onset period). Myelosuppression was severe in approximately 40% of patients. Hypoalbuminemia and non-use of folic acid supplements were significantly associated with the severity of pancytopenia (p = 0.001 and 0.008, respectively). Besides these two factors, early onset and the use of lower doses of MTX were significantly associated with the severity of neutropenia (p = 0.003, 0.007, 0.003, and 0.002, respectively). Conclusions Myelosuppression can occur abruptly at any time during low-dose MTX therapy, but severe neutropenia is more likely to occur in the early-onset period of this therapy. Contrary to our expectations, disease severity was not dependent on MTX doses. Serum albumin levels and folic acid supplementation are the important factors affecting the severity of MTXrelated pancytopenia and neutropenia.
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