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接受丙磺舒或肠胃外金制剂治疗的类风湿性关节炎患者的癌症发病率。

Cancer morbidity in rheumatoid arthritis patients treated with Proresid or parenteral gold.

作者信息

Bendix G, Bjelle A, Holmberg E

机构信息

Department of Rheumatology, University of Gothenburg, Sweden.

出版信息

Scand J Rheumatol. 1995;24(2):79-84. doi: 10.3109/03009749509099289.

DOI:10.3109/03009749509099289
PMID:7747148
Abstract

The cancer risk was studied by comparison of 305 rheumatoid arthritis (RA) patients exposed to Proresid during a mean time of 22 months and 305 RA patients exposed to sodium aurothiomalate during a mean time of 19 months with the regional cancer register. The mean observation time was 6.9 years (2,117 person-years) for the Proresid-treated and 7.5 years (2,293 person-years) for the gold-treated patients. No increased risk of total malignancies was observed for either group. However, looking at separate tumours, an increased risk of lymphoma and leukemia was found although only significant in the gold-treated group. It was not correlated to dosage or duration of either therapy. The increased risk is consistent with earlier reports of an increased risk of hematopoietic malignancies in RA patients. Marginal over and underreporting, particularly of hematopoietic malignancies, were observed, mainly due to clinicians' failure to report and to recall false reports.

摘要

通过将305名平均暴露于丙磺舒22个月的类风湿性关节炎(RA)患者和305名平均暴露于硫代苹果酸金钠19个月的RA患者与地区癌症登记处进行比较,研究了癌症风险。丙磺舒治疗组的平均观察时间为6.9年(2117人年),金制剂治疗组为7.5年(2293人年)。两组均未观察到总恶性肿瘤风险增加。然而,在单独分析肿瘤时,发现淋巴瘤和白血病风险增加,尽管仅在金制剂治疗组中具有统计学意义。它与任何一种治疗的剂量或持续时间均无关联。风险增加与先前关于RA患者造血系统恶性肿瘤风险增加的报道一致。观察到报告略有高估和低估,尤其是造血系统恶性肿瘤,主要是由于临床医生未报告以及错误报告的回忆。

相似文献

1
Cancer morbidity in rheumatoid arthritis patients treated with Proresid or parenteral gold.接受丙磺舒或肠胃外金制剂治疗的类风湿性关节炎患者的癌症发病率。
Scand J Rheumatol. 1995;24(2):79-84. doi: 10.3109/03009749509099289.
2
Proresid therapy in rheumatoid arthritis. A comparison with injectable gold using life-table analysis.
Scand J Rheumatol. 1993;22(2):77-82. doi: 10.3109/03009749309095119.
3
Proresid in the long-term treatment of rheumatoid arthritis.Proresid用于类风湿关节炎的长期治疗。 (注:Proresid可能是特定药物名称,此处直接保留英文未翻译,因为不确定其准确的中文译名)
Scand J Rheumatol. 1988;17(6):465-8. doi: 10.3109/03009748809098808.
4
Treatment of rheumatoid patients with Proresid.用Proresid治疗类风湿患者。
Scand J Rheumatol. 1990;19(2):170. doi: 10.3109/03009749009102123.
5
Proresid--a valuable and well-tolerated drug?原药——一种有价值且耐受性良好的药物?
Scand J Rheumatol. 1989;18(4):245. doi: 10.3109/03009748909099938.
6
Cushingoid picture with Proresid.出现类库欣面容伴普乐可复。
Br J Rheumatol. 1994 Dec;33(12):1198. doi: 10.1093/rheumatology/33.12.1198.
7
Side effects of Proresid in the treatment of chronic arthritis.丙磺舒治疗慢性关节炎的副作用。
Scand J Rheumatol. 1988;17(1):63-6. doi: 10.3109/03009748809098762.
8
A randomized controlled trial of parenteral methotrexate compared with sodium aurothiomalate (Myochrysine) in the treatment of rheumatoid arthritis.一项比较胃肠外注射甲氨蝶呤与金硫葡糖(金诺芬)治疗类风湿关节炎的随机对照试验。
J Rheumatol. 1988;15(5):753-6.
9
Parenteral methotrexate or gold for rheumatoid arthritis: a follow up.用于类风湿性关节炎的肠胃外注射甲氨蝶呤或金制剂:一项随访研究
Clin Exp Rheumatol. 1990 Mar-Apr;8(2):163-6.
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Auranofin and sodium aurothiomalate in the treatment of rheumatoid arthritis. A double-blind, comparative multicenter study.金诺芬和硫代苹果酸金钠治疗类风湿性关节炎。一项双盲、对比性多中心研究。
J Rheumatol Suppl. 1982 Jul-Aug;8:184-9.

引用本文的文献

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[Gold as an alternative in the treatment of RA patients with malignancies].[黄金作为类风湿关节炎合并恶性肿瘤患者治疗的替代方案]
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Haematopoietic malignancies in rheumatoid arthritis: lymphoma risk and characteristics after exposure to tumour necrosis factor antagonists.类风湿关节炎中的血液系统恶性肿瘤:接触肿瘤坏死因子拮抗剂后的淋巴瘤风险及特征
Ann Rheum Dis. 2005 Oct;64(10):1414-20. doi: 10.1136/ard.2004.033241. Epub 2005 Apr 20.
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Risks of solid cancers in patients with rheumatoid arthritis and after treatment with tumour necrosis factor antagonists.
类风湿关节炎患者及使用肿瘤坏死因子拮抗剂治疗后的实体癌风险。
Ann Rheum Dis. 2005 Oct;64(10):1421-6. doi: 10.1136/ard.2004.033993. Epub 2005 Apr 13.
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Chromosomal changes in rheumatoid arthritis patients treated with CPH82.接受CPH82治疗的类风湿性关节炎患者的染色体变化
Clin Rheumatol. 1996 Nov;15(6):584-9. doi: 10.1007/BF02238548.