Clinical of Experimental Onco-Haematology Unit, CRO Aviano National Cancer Institute IRCCS, Aviano (PN), Italy.
Cancer Epidemiology Unit, CRO Aviano National Cancer Institute IRCCS, Aviano (PN), Italy.
Clin Exp Rheumatol. 2018 Mar-Apr;36 Suppl 111(2):107-114. Epub 2018 Feb 13.
To investigate the long-term effects and safety of new direct anti-viral agents (DAAs) in patients with hepatitis C virus (HCV)-related mixed cryoglobulinaemia (MC) without renal involvement.
The study enrolled 22 consecutive patients, 19 received sofosbuvir-based regimen and three patients received other DAAs, individually tailored according to latest guidelines. As of December 2016, the median length of follow-up was 17 months (range 13-21).
Extra-hepatic manifestations at enrollment were: purpura and arthralgia (12 cases), peripheral neuropathy (10 cases) and marginal zone B- lymphomas (2 cases). After a four-week DAA therapy, all patients became HCV- negative. Moreover, after 48 weeks since the beginning of DAA treatment, sustained regression of purpura and arthralgias was observed respectively in eight and in nine cases; peripheral neuropathy improved in seven cases, and cryocrit median values decreased from three (1-20) at baseline to two (1-12) after 48 weeks. Two cases with indolent marginal zone lymphomas did not show any haematological response: size and number of the involved nodes remained unchanged. In addition, the monoclonal B-cell population found in the peripheral blood in four cases did not disappear after recovery from HCV- RNA. Mild side effects occurred in nine patients, but six patients developed ribavirin-related anaemia requiring reduction of ribavirin dose.
DAA therapy is safe and effective to eradicate HCV in MC, but seems associated with satisfactory clinical response in mild or moderate cryoglobulinaemic vasculitis and no response in B-NHL.
研究新的直接抗病毒药物(DAA)在无肾受累的丙型肝炎病毒(HCV)相关混合性冷球蛋白血症(MC)患者中的长期疗效和安全性。
本研究纳入了 22 例连续患者,其中 19 例接受了索非布韦为基础的方案,3 例患者根据最新指南单独接受了其他 DAA 治疗。截至 2016 年 12 月,中位随访时间为 17 个月(范围 13-21 个月)。
入组时的肝外表现为:紫癜和关节炎(12 例)、周围神经病(10 例)和边缘区 B 细胞淋巴瘤(2 例)。在 DAA 治疗四周后,所有患者 HCV 均转为阴性。此外,在 DAA 治疗开始后的 48 周时,分别有 8 例和 9 例患者的紫癜和关节炎持续缓解;7 例患者的周围神经病得到改善,冷球蛋白血症的中位数从基线时的 3(1-20)降至 48 周时的 2(1-12)。2 例惰性边缘区 B 细胞淋巴瘤患者无血液学反应:受累淋巴结的大小和数量无变化。此外,4 例患者外周血中发现的单克隆 B 细胞群在 HCV-RNA 恢复后并未消失。9 例患者出现轻微副作用,但 6 例患者因利巴韦林相关贫血而需要减少利巴韦林剂量。
DAA 治疗可安全有效地清除 MC 中的 HCV,但似乎与轻度或中度冷球蛋白血症性血管炎的良好临床反应相关,而与 B-NHL 无反应相关。