Schmidt R E, Hartlapp J H, Niese D, Illiger H J, Stroehmann I
Infection. 1984 May-Jun;12(3):167-70. doi: 10.1007/BF01640891.
Thirty-two patients with small cell carcinoma of the lung received intensive induction chemoradiotherapy. In a randomized prospective study, we compared the outcome of patients who received 30 g immunoglobulin i.v. divided into three doses per therapy course for infection prophylaxis (Group A) with patients undergoing the same anti-tumor therapy (Group B). All patients were prospectively randomized to one of two groups in order to evaluate the role of intravenous immunoglobulin therapy for infection prophylaxis. Group A received 30 g intravenous immunoglobulin during each course of chemotherapy. Group B was a control group that received identical chemoradiotherapy but did not receive any immunoglobulin therapy. All patients had a severely impaired cellular immune response. IgG serum concentrations were significantly higher in group A. Patients who received intravenous immunoglobulin had significantly fewer infections during the entire treatment period than patients who did not receive prophylactic treatment.
32例肺小细胞癌患者接受了强化诱导放化疗。在一项随机前瞻性研究中,我们将接受30g静脉注射免疫球蛋白(每次治疗疗程分三剂)预防感染的患者(A组)与接受相同抗肿瘤治疗的患者(B组)的结局进行了比较。所有患者均被前瞻性随机分为两组,以评估静脉注射免疫球蛋白治疗在预防感染中的作用。A组在每个化疗疗程中接受30g静脉注射免疫球蛋白。B组为对照组,接受相同的放化疗,但未接受任何免疫球蛋白治疗。所有患者的细胞免疫反应均严重受损。A组的血清IgG浓度显著更高。接受静脉注射免疫球蛋白的患者在整个治疗期间的感染明显少于未接受预防性治疗的患者。