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在中重度银屑病患者中,甲氨蝶呤早期应答不良预示着长期结局不佳:来自两项 3 期临床试验的证据。

Poor early response to methotrexate portends inadequate long-term outcomes in patients with moderate-to-severe psoriasis: Evidence from 2 phase 3 clinical trials.

机构信息

Medical College of Wisconsin, Milwaukee, Wisconsin.

Analysis Group Inc, Boston, Massachusetts.

出版信息

J Am Acad Dermatol. 2017 Dec;77(6):1030-1037. doi: 10.1016/j.jaad.2017.08.017. Epub 2017 Oct 6.

Abstract

BACKGROUND

Most methotrexate-treated psoriasis patients do not achieve a long-term PASI75 (75% reduction from baseline Psoriasis Area and Severity Index score) response. Indications of nonresponse can be apparent after only 4 weeks of treatment.

OBJECTIVE

To develop a prediction rule to identify patients unlikely to respond adequately to methotrexate.

METHODS

Patient-level data from CHAMPION (NCT00235820, N = 110) was used to construct a prediction model for week 16 PASI75 by using patient baseline characteristics and week 4 PASI25. A prediction rule was determined on the basis of the sensitivity and specificity and validated in terms of week 16 PASI75 response in an independent validation sample from trial M10-255 (NCT00679731, N = 163).

RESULTS

PASI25 achievement at week 4 (odds ratio = 8.917) was highly predictive of response with methotrexate at week 16. Patients with a predicted response probability <30% were recommended to discontinue methotrexate. The rates of week 16 PASI75 response were 65.8% and 21.1% (P < .001) for patients recommended to continue and discontinue methotrexate, respectively.

LIMITATIONS

The CHAMPION trial excluded patients previously treated with biologics, and the M10-255 trial had no restrictions.

CONCLUSION

A prediction rule was developed and validated to identify patients unlikely to respond adequately to methotrexate. The rule indicates that 4 weeks of methotrexate might be sufficient to predict long-term response with limited safety risk.

摘要

背景

大多数接受甲氨蝶呤治疗的银屑病患者无法实现长期 PASI75(从基线银屑病面积和严重程度指数评分降低 75%)应答。在治疗仅 4 周后即可明显看出无应答的迹象。

目的

制定预测规则以识别不太可能对甲氨蝶呤有充分应答的患者。

方法

使用 CHAMPION(NCT00235820,N=110)的患者水平数据,根据患者基线特征和第 4 周 PASI25,构建第 16 周 PASI75 的预测模型。根据灵敏度和特异性,确定预测规则,并在试验 M10-255(NCT00679731,N=163)的独立验证样本中验证第 16 周 PASI75 应答情况。

结果

第 4 周 PASI25 达标(优势比=8.917)对第 16 周甲氨蝶呤应答具有高度预测性。预测应答概率<30%的患者建议停止使用甲氨蝶呤。建议继续和停止甲氨蝶呤的患者第 16 周 PASI75 应答率分别为 65.8%和 21.1%(P<0.001)。

局限性

CHAMPION 试验排除了既往接受过生物制剂治疗的患者,而 M10-255 试验没有限制。

结论

制定并验证了预测规则,以识别不太可能对甲氨蝶呤有充分应答的患者。该规则表明,4 周的甲氨蝶呤治疗可能足以预测长期应答,且安全性风险有限。

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