National Hospital Organization Kumamoto Minami Hospital, 2338 Toyofuku, Matubase-machi, Kumamoto 869-0593, Japan.
Int J Clin Oncol. 2010 Apr;15(2):145-52. doi: 10.1007/s10147-010-0033-1. Epub 2010 Mar 13.
A recent report showed that oral adjuvant immunochemotherapy with protein-bound polysaccharide K (PSK) and tegafur/uracil (UFT) for stage II and III colorectal cancer improves overall survival compared with UFT alone. PSK has been supposed to improve survival through immunological mechanisms such as induction of cytokines, regulation of Th1/Th2 balance, and inhibition of immunosuppressive molecules.
We investigated the mechanisms by which PSK influences immunological parameters such as Th1 cells (IFN-gamma-positive CD4(+) T cells), Th2 cells (IL-4-positive CD4(+) T cells), Th1/Th2 ratio, NKT cells (CD56(+) T cells and CD57(+) T cells), NK cells, and CD25(+)CD4(+) T cells in stage III gastric cancer patients. Patients were randomly assigned to receive either 3 g PSK plus 300 mg UFT (PSK group) or 300 mg UFT alone (control) orally each day for at least 1 year following their operation.
Twenty-one registered patients with stage III gastric cancer were analyzed. The 3-year overall survival was 62.2% in the PSK group (n = 10) and 12.5% in the control group (n = 11) (P = 0.038). Before operation, there were no significant differences in the proportions of Th1 cells, Th2 cells, Th1/Th2 ratio, CD56(+) T cells, CD57(+) T cells, NK cells, and CD4(+)CD25(+) T cells between PSK and control groups. However, after operation, CD57(+) T cells decreased significantly in the PSK group compared to the control (P = 0.0486). When all patients were analyzed, patients with increased proportion (>18%) of CD57(+) T cells showed worse survival than those with lower (< or = 18%) CD57(+) T cells (3-year survival, 25.0 and 45.7%, respectively; P = 0.046), consistent with our previous report that high CD57(+) is an indicator of poor prognosis in patients with advanced gastric cancer. However, in the group treated with PSK + UFT, 3-year survival of CD57-high patients was as great as that of CD57-low patients (66.7 and 51.4%, respectively; P = 0.67).
The present findings suggest that PSK improves overall survival of stage III gastric cancer patients partly by inhibiting CD57(+) T cells, a proven poor prognostic factor in advanced gastric cancer.
最近的一份报告显示,对于 II 期和 III 期结直肠癌患者,与单独使用替加氟/尿嘧啶(UFT)相比,口服辅助免疫化疗联合蛋白结合型多糖 K(PSK)可提高总生存率。PSK 被认为通过诱导细胞因子、调节 Th1/Th2 平衡和抑制免疫抑制分子等免疫机制来提高生存率。
我们研究了 PSK 影响免疫参数的机制,如 Th1 细胞(IFN-γ阳性 CD4+T 细胞)、Th2 细胞(IL-4 阳性 CD4+T 细胞)、Th1/Th2 比值、NKT 细胞(CD56+T 细胞和 CD57+T 细胞)、NK 细胞和 CD25+CD4+T 细胞在 III 期胃癌患者中的作用。患者随机分为 PSK 组(PSK 组)和对照组(n=11),每天口服 3g PSK 联合 300mg UFT 或单独口服 300mg UFT 治疗至少 1 年。
21 名登记的 III 期胃癌患者进行了分析。PSK 组的 3 年总生存率为 62.2%(n=10),对照组为 12.5%(n=11)(P=0.038)。手术前,PSK 组和对照组 Th1 细胞、Th2 细胞、Th1/Th2 比值、CD56+T 细胞、CD57+T 细胞、NK 细胞和 CD4+CD25+T 细胞的比例无显著差异。然而,手术后,PSK 组 CD57+T 细胞明显减少与对照组(P=0.0486)。当所有患者进行分析时,与 CD57+T 细胞比例较低(<18%)的患者相比,CD57+T 细胞比例升高(>18%)的患者生存情况较差(3 年生存率分别为 25.0%和 45.7%;P=0.046),与我们之前的报告一致,即 CD57+高是晚期胃癌患者预后不良的指标。然而,在 PSK+UFT 治疗组中,CD57 高患者的 3 年生存率与 CD57 低患者相似(分别为 66.7%和 51.4%;P=0.67)。
本研究结果提示 PSK 通过抑制 CD57+T 细胞改善 III 期胃癌患者的总生存率,CD57+T 细胞是晚期胃癌预后不良的已知因素。