Gross N J, Eddie-Quartey A C
Am Rev Respir Dis. 1976 Apr;113(4):457-64. doi: 10.1164/arrd.1976.113.4.457.
Immunotherapy with bacille Calmette-Guérin (BCG) was administered according to a standard regimen to 23 patients with primary lung cancer who had completed conventional treatment, including surgery and/or radiation therapy. Five additional patients did not receive BCG. Skin tests and in vitro lymphocyte studies were performed serially at intervals for 12 months or until death. The aggregate of skin responses to nonmycobacterial antigens and lymphocyte responses to phytohemagglutinin and recall antigens increased only in the group of 7 patients with no clinically evident disease 12 months after the start of BCG administration. The group of 5 patients who did not receive BCG, but who remained clinically disease free, did not experience immunoenhancement, nor did BCG-treated patients with residual or recurrent malignancy. Patients who had received radiation therapy before BCG also did not experience immunoenhancement, but these patients also had recurrent or persistent disease. Enhancement of certain aspects of the immune response to within 1 SD of the response of a group of subjects with nonmalignant pulmonary disease was prognostic of a favorable clinical outcome at 12 months.
采用标准方案对23例已完成包括手术和/或放疗在内的常规治疗的原发性肺癌患者进行卡介苗(BCG)免疫治疗。另外5例患者未接受BCG治疗。在12个月内或直至死亡,定期进行皮肤试验和体外淋巴细胞研究。仅在开始BCG治疗12个月后,7例无临床明显疾病的患者组中,对非分枝杆菌抗原的皮肤反应以及对植物血凝素和回忆抗原的淋巴细胞反应的总和有所增加。5例未接受BCG治疗但临床上无疾病的患者组未出现免疫增强,接受BCG治疗的有残留或复发性恶性肿瘤的患者也未出现免疫增强。在接受BCG治疗前接受过放疗的患者也未出现免疫增强,但这些患者也有复发或持续性疾病。免疫反应某些方面增强至一组非恶性肺部疾病受试者反应的1个标准差范围内,预示着12个月时临床结局良好。