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芦可替尼与最佳可用疗法治疗真性红细胞增多症的疗效和安全性:一项更新的系统评价和荟萃分析。

Efficacy and safety of ruxolitinib vs best available therapy for polycythemia vera: An updated systematic review and meta-analysis.

机构信息

International University of Catalonia, Barcelona, Spain.

Faisalabad Medical University, Faisalabad, Pakistan.

出版信息

APMIS. 2024 Nov;132(11):775-786. doi: 10.1111/apm.13472. Epub 2024 Oct 8.

DOI:10.1111/apm.13472
PMID:39377511
Abstract

Ruxolitinib, a JAK1/JAK2 inhibitor, has been shown to have lower thromboembolism rates compared to placebo in polycythemia vera (PV) patients. This meta-analysis evaluates ruxolitinib's efficacy and safety against best available therapy (BAT) in patients with PV and in hydroxyurea-resistant/intolerant PV patients. A comprehensive literature search was conducted up to November 2023. We compared ruxolitinib and BAT for efficacy and safety endpoints. Six studies involving 1061 patients were analyzed, with 620 on BAT and 441 on ruxolitinib. Ruxolitinib showed higher hematocrit control (p = 0.015) and treatment response (p = 0.04) compared to BAT. It also significantly improved Myeloproliferative Neoplasms-Symptom Assessment Form scores (MPN-SAF) (p < 0.01). Additionally, patients with PV treated with ruxolitinib had higher rates of nonmelanoma skin cancer (p < 0.01). In subgroup analyses focusing on patients resistant or intolerant to hydroxyurea, ruxolitinib maintained its efficacy, significantly improving treatment response (p < 0.01) and significant improvements in MPN-SAF (p = 0.02) score when compared to BAT. The safety profile was consistent with the overall analyses, showing significantly reduced thromboembolism rates (p = 0.04), increased rates of anemia (p = 0.01), and increased herpes zoster infections (p = 0.02). Ruxolitinib outperforms BAT in PV and patients with PV-resistant or intolerant to hydroxyurea, offering better hematocrit control and reducing symptomatic burden and thromboembolism risk. Yet, it is associated with higher rates of anemia, herpes infection, and skin cancer.

摘要

芦可替尼是一种 JAK1/JAK2 抑制剂,与安慰剂相比,在真性红细胞增多症(PV)患者中显示出较低的血栓栓塞率。这项荟萃分析评估了芦可替尼在 PV 患者和对羟基脲耐药/不耐受的 PV 患者中的疗效和安全性。我们进行了全面的文献检索,截至 2023 年 11 月。我们比较了芦可替尼和最佳可用治疗(BAT)在疗效和安全性终点方面的疗效。共分析了 6 项涉及 1061 名患者的研究,其中 620 名患者接受 BAT,441 名患者接受芦可替尼。芦可替尼在控制血细胞比容(p=0.015)和治疗反应(p=0.04)方面优于 BAT。它还显著改善了骨髓增殖性肿瘤症状评估表(MPN-SAF)评分(p<0.01)。此外,接受芦可替尼治疗的 PV 患者中非黑色素瘤皮肤癌的发生率更高(p<0.01)。在针对对羟基脲耐药或不耐受的患者的亚组分析中,芦可替尼保持其疗效,与 BAT 相比,显著改善治疗反应(p<0.01)和 MPN-SAF 评分的显著改善(p=0.02)。安全性概况与总体分析一致,显示血栓栓塞率显著降低(p=0.04),贫血发生率增加(p=0.01),带状疱疹感染增加(p=0.02)。芦可替尼在 PV 和对羟基脲耐药或不耐受的 PV 患者中优于 BAT,提供更好的血细胞比容控制,减轻症状负担和血栓栓塞风险。然而,它与更高的贫血、疱疹感染和皮肤癌发生率相关。

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