Barak V, Kalickman I, Nisman B, Farbstein H, Fridlender Z G, Baider L, Kaplan A, Stephanos S, Peretz T
Department of Oncology and Psychiatry, Hadassah Hebrew University Hospital and Medical School, Jerusalem, Israel.
Cytokine. 1998 Dec;10(12):977-83. doi: 10.1006/cyto.1998.0378.
A clinical randomized study was performed on advanced breast cancer patients who were treated by interferons (IFN) beta and gamma in combination with hormonotherapy (Megace or Tamoxifen). Cytokine levels (IL-1beta, IL-2, IL-6, TNF-alpha, IFN-gamma) and sIL-2R of individual patients before, during (3 months) and after (6 months) therapy were evaluated and correlated to clinical response according to UICC criteria (responder patients-partial or Complete Response versus non-responder patients-Stable/Progression). Decreases in IL-1beta, IL-6 and sIL-2R were associated with clinical response to therapy versus increases in their levels which corresponded to progression of disease. A significant and dramatic increase in IFN-gamma levels was associated with a favourable response to therapy in the IFNs-treated patients, mainly in the group of Tamoxifen. Baseline levels of sIL-2R and of IFN-gamma were prognostic of clinical response and were found to be the most sensitive cytokine parameters for defining the clinical utility of the combination of IFNs and hormonotherapy in breast cancer patients.
对接受干扰素(IFN)β和γ联合激素疗法(甲地孕酮或他莫昔芬)治疗的晚期乳腺癌患者进行了一项临床随机研究。评估了个体患者在治疗前、治疗期间(3个月)和治疗后(6个月)的细胞因子水平(IL-1β、IL-2、IL-6、TNF-α、IFN-γ)和可溶性IL-2受体,并根据国际抗癌联盟(UICC)标准(反应者患者——部分或完全缓解与无反应者患者——病情稳定/进展)将其与临床反应相关联。IL-1β、IL-6和可溶性IL-2受体水平降低与治疗的临床反应相关,而其水平升高则与疾病进展相对应。IFN-γ水平显著且急剧升高与接受IFN治疗的患者对治疗的良好反应相关,主要是在他莫昔芬组。可溶性IL-2受体和IFN-γ的基线水平可预测临床反应,并且被发现是定义IFN与激素疗法联合应用于乳腺癌患者临床效用的最敏感细胞因子参数。