Valavaara R, Tuominen J, Toivanen A
Department of Radiotherapy, University of Turku, Finland.
Cancer Immunol Immunother. 1990;31(6):381-6. doi: 10.1007/BF01741410.
The immune status of breast cancer patients was followed during antiestrogen treatment for at least 1 year or until progression of the disease. Twelve post-menopausal women with advanced estrogen-receptor-positive breast cancer were treated with a novel antiestrogen, toremifene. Immune functions were determined before the start of the treatment and at 3, 6, and 12 months. For NK cell cytotoxicity testing there were 74 healthy controls and for T cell subset measurements 28 healthy controls. No statistically significant changes in the T cell subsets or NK cell cytotoxicity were observed during treatment. However, throughout toremifene treatment patients had fewer CD4 cells (T helper lymphocytes) than did the controls. Cancer patients had higher pretreatment B cell values than the controls, P = 0.01, but during the first months of toremifene treatment B cell values decreased and remained within the normal range thereafter. A positive effect on mitogen-stimulation tests with phytohemagglutinin (PHA) and concanavalin A (ConA) was observed during the first months of treatment (P = 0.01 for PHA and 0.03 for log [ConA] and a stabilization at the higher level thereafter. These results indicate that toremifene has a stimulatory effect on cell-mediated immunity in breast cancer patients.
在抗雌激素治疗期间,对乳腺癌患者的免疫状态进行了至少1年的跟踪,或直至疾病进展。12名绝经后晚期雌激素受体阳性乳腺癌女性患者接受了新型抗雌激素药物托瑞米芬治疗。在治疗开始前以及治疗3个月、6个月和12个月时测定免疫功能。进行自然杀伤(NK)细胞细胞毒性测试时有74名健康对照者,进行T细胞亚群测量时有28名健康对照者。治疗期间未观察到T细胞亚群或NK细胞细胞毒性有统计学显著变化。然而,在整个托瑞米芬治疗期间,患者的CD4细胞(辅助性T淋巴细胞)比对照组少。癌症患者治疗前的B细胞值高于对照组,P = 0.01,但在托瑞米芬治疗的头几个月,B细胞值下降,此后保持在正常范围内。在治疗的头几个月观察到对植物血凝素(PHA)和刀豆球蛋白A(ConA)的丝裂原刺激试验有积极影响(PHA为P = 0.01,log[ConA]为0.03),此后稳定在较高水平。这些结果表明,托瑞米芬对乳腺癌患者的细胞介导免疫有刺激作用。