Chapel H M, Lee M, Hargreaves R, Pamphilon D H, Prentice A G
Department of Immunology, John Radcliffe Hospital, Oxford, UK.
Lancet. 1994 Apr 30;343(8905):1059-63. doi: 10.1016/s0140-6736(94)90180-5.
Patients with plateau-phase multiple myeloma have an increased risk of life-threatening bacterial infections and polyclonal humoral immune suppression. We conducted a randomised, double-blind, placebo-controlled, multicentre trial of intravenous immunoglobulin (IVIg) as prophylaxis against infection. 82 patients with stable multiple myeloma received monthly infusions of IVIg at 0.4 g/kg body weight or an equivalent volume of placebo (0.4% albumin) intravenously for 1 year. Other interventions, including chemotherapy, were not affected; no patient received prophylactic antibiotics. There were no differences at entry or on study in clinical or laboratory variables between patients in the two groups. There were no episodes of septicaemia or pneumonia in patients receiving IVIg compared with 10 in placebo patients (p = 0.002). There were 57 serious infections; 38 occurred in 470 patient-months on placebo, compared with 19 in 449 patient-months on IVIg (p = 0.019). IVIg also protected against recurrent infections (p = 0.021) in 60 patients who completed a year. Before treatment, 54 patients were immunised with Pneumovax and specific IgG responses were measured. A poor pneumococcal IgG antibody response (less than 2-fold increase) identified patients who had maximum benefit from IVIg. Mild adverse reactions were noted in 12% of IVIg infusions and 5% of placebo infusions. IVIg can be given safely to plateau-phase myeloma patients. It protects against life-threatening infections and significantly reduces the risk of recurrent infections. The individuals who benefit most can be identified prospectively by measuring IgG antibody responses to pneumococcal immunisation.
处于平台期的多发性骨髓瘤患者发生危及生命的细菌感染和多克隆体液免疫抑制的风险增加。我们进行了一项随机、双盲、安慰剂对照、多中心试验,以研究静脉注射免疫球蛋白(IVIg)预防感染的效果。82例病情稳定的多发性骨髓瘤患者每月接受一次静脉输注,剂量为0.4 g/kg体重的IVIg或等量体积的安慰剂(0.4%白蛋白),持续1年。包括化疗在内的其他干预措施不受影响;没有患者接受预防性抗生素治疗。两组患者在入组时或研究过程中的临床或实验室变量没有差异。接受IVIg治疗的患者未发生败血症或肺炎,而安慰剂组患者中有10例发生(p = 0.002)。共发生57例严重感染;安慰剂组470个患者月中有38例发生,而IVIg组449个患者月中有19例发生(p = 0.019)。IVIg还能预防60例完成一年治疗的患者发生反复感染(p = 0.021)。治疗前,54例患者接种了肺炎球菌疫苗并检测了特异性IgG反应。肺炎球菌IgG抗体反应较差(增加不到2倍)的患者从IVIg治疗中获益最大。IVIg输注的12%和安慰剂输注的5%出现轻度不良反应。IVIg可安全用于平台期骨髓瘤患者。它能预防危及生命的感染,并显著降低反复感染的风险。通过检测对肺炎球菌免疫接种的IgG抗体反应,可以前瞻性地确定最受益的个体。