Standish Leanna J, Torkelson Carolyn, Hamill Frank A, Yim Daesong, Hill-Force Alicia, Fitzpatrick Annette, Olsen Monica, Schildt Sandi, Sweet Erin, Wenner Cynthia A, Martzen Mark R
Department of Research, Bastyr University, Kenmore, WA 98028, USA.
J Soc Integr Oncol. 2008 Summer;6(3):110-21.
The purpose of this study was to evaluate the immune status of women with stage I-III breast cancer after receiving external beam radiotherapy (RT). Fourteen stage I-III, estrogen or progesterone receptor-positive or-negative (FER/PR +-), postsurgical breast cancer patients undergoing a standard course of chemotherapy and radiation were studied. Complete blood counts (CBC) with differential, phagocytic activity, natural killer (NK) cell functional activity, and tumor necrosis factor-alpha (TNF-alpha) and interferon-gamma cytokine activity were measured immediately before and for the six weeks following the completion of radiation therapy. Fatigue levels after completion of RT were measured using the Functional Assessment of Chronic Illness Therapy (FACIT)-Fatigue scale. Nonparametric statistical methods (Wilcoxon rank and Spearman correlations) were used to analyze the data. Compared with postchemotherapy, following the completion of RT, these breast cancer patients showed lymphopenia, low functional activity of natural killer lymphocytes, decreased monocyte phagocytic activity, and decreased TNF-alpha production but no neutropenia, no anemia, and no change in interferon-gamma production. Lymphocyte count did not return to normal by the end of the 6-week post-RT observation period. The severity of lymphopenia and low natural killer cell activity was related to RT area but not radiation dose. Patients did not report significant fatigue levels for the 6 weeks after completing RT. Significant decreases in the numbers and functions of cells from both the innate and adaptive immune system were detected following a standard course of radiation therapy for the treatment of breast cancer. Immune deficits in lymphocyte populations and TNF-alpha production, should they persist, may have consequences for immune response to residual or recurrent malignancy following completion of conventional treatment. The use of adjunctive immune therapies which target these specific defects may be warranted in the post-treatment period.
本研究的目的是评估接受外照射放疗(RT)后I - III期乳腺癌女性的免疫状态。对14例I - III期、雌激素或孕激素受体阳性或阴性(FER/PR +-)、接受标准化化疗和放疗疗程的术后乳腺癌患者进行了研究。在放疗完成前及完成后的六周内,测量全血细胞计数(CBC)及分类、吞噬活性、自然杀伤(NK)细胞功能活性、肿瘤坏死因子-α(TNF-α)和干扰素-γ细胞因子活性。使用慢性病治疗功能评估(FACIT)-疲劳量表测量放疗完成后的疲劳水平。采用非参数统计方法(Wilcoxon秩和检验及Spearman相关性分析)分析数据。与化疗后相比,放疗完成后,这些乳腺癌患者出现淋巴细胞减少、自然杀伤淋巴细胞功能活性降低、单核细胞吞噬活性降低以及TNF-α产生减少,但未出现中性粒细胞减少、贫血,且干扰素-γ产生无变化。放疗后6周观察期结束时,淋巴细胞计数未恢复正常。淋巴细胞减少的严重程度和自然杀伤细胞活性降低与放疗区域有关,而非辐射剂量。患者在放疗完成后的6周内未报告明显的疲劳水平。在乳腺癌的标准化放疗疗程后,检测到先天性和适应性免疫系统的细胞数量和功能均显著下降。淋巴细胞群体和TNF-α产生方面的免疫缺陷若持续存在,可能会对传统治疗完成后对残留或复发性恶性肿瘤的免疫反应产生影响。在治疗后期,可能有必要使用针对这些特定缺陷的辅助免疫疗法。