Wu L J, Chen K Y, Chi K H, Chen S Y, Liang M J, Shiau C Y, Wang L W, Liu Y M, Chow K C, Yen S H
Cancer Center, Veterans General Hospital-Taipe, Taiwan.
Jpn J Clin Oncol. 1998 Dec;28(12):729-32. doi: 10.1093/jjco/28.12.729.
Soluble interleukin-2 receptor alpha (sIL-2R alpha) is a well-known indicator of T-cell activation noted to be increasing in nasopharyngeal cancer. However, the significance of sIL-2R alpha in monitoring disease relapse is unclear. This study was initiated to address this issue.
Serum of 56 patients with NPC, which underwent either primary, salvage, or palliative treatments, from 1992 to 1993 at the Cancer Center, Veterans General Hospital-Taipei, were collected from our serum bank. According to their disease status at the time of study, at least two years after last treatments, the 56 patients were divided into four groups. The remission group represented those in remission at the time of study (n = 24). The metastasis group represented those with distant metastasis present at the time of study (n = 17). The recurrence group represented those with locoregional recurrence present at the time of study (n = 11). The combined group represented those with locoregional recurrence as well as distant metastasis (n = 4). The seral sIL-2R alpha concentrations of the 56 NPC patients were determined with enzyme-linked immunoabsorbent assay. The combined group was excluded in our statistical analysis. We performed statistical analysis on the differences of paired serum sIL-2R alpha concentrations between different periods of the diseases. The first analysis was on the differences of sIL-2R alpha concentrations between diagnosis and post-radiotherapy periods for 13 out of 24 patients in the remission group and 7 out of 11 patients in the recurrence group. The second analysis was on the differences of sIL-2R alpha concentration between follow-up before detection-of-relapse and after detection-of-relapse for 5 out of 17 patients in the metastasis group and six out of 11 patients in the recurrence group.
The first statistical analysis revealed no significant differences of sIL-2R alpha concentrations for the remission group (P = 0.946) and the recurrence group (P = 0.156) between diagnosis and post-radiotherapy periods. The second statistical analysis revealed no significant differences of sIL-2R alpha concentrations between before and after detection-of-relapse for the recurrence group, neither (P = 0.438). The results for the metastasis group were different. The sIL-2R alpha concentrations were shown to increase after the detection of metastasis for the 5 paired samples from the metastasis group, although the Wilcoxon signed ranks test on the differences only showed borderline significance (P = 0.063).
Our findings show that sIL-2R alpha would be of no value in monitoring the development of locoregional recurrence but might be useful in monitoring distant metastasis. Although our current limited data did not provide strong support for the role of sIL-2R alpha in monitoring metastasis, it might be delineated in the future by collecting more data.
可溶性白细胞介素-2受体α(sIL-2Rα)是一种众所周知的T细胞活化指标,在鼻咽癌中呈升高趋势。然而,sIL-2Rα在监测疾病复发中的意义尚不清楚。本研究旨在解决这一问题。
收集1992年至1993年在台北荣民总医院癌症中心接受初次、挽救或姑息治疗的56例鼻咽癌患者的血清,这些血清来自我们的血清库。根据研究时的疾病状态,即最后一次治疗至少两年后,将这56例患者分为四组。缓解组代表研究时处于缓解状态的患者(n = 24)。转移组代表研究时存在远处转移的患者(n = 17)。复发组代表研究时存在局部区域复发的患者(n = 11)。联合组代表存在局部区域复发以及远处转移的患者(n = 4)。采用酶联免疫吸附测定法测定56例鼻咽癌患者血清中sIL-2Rα的浓度。联合组被排除在我们的统计分析之外。我们对疾病不同时期配对血清sIL-2Rα浓度的差异进行了统计分析。第一次分析是针对缓解组24例患者中的13例以及复发组11例患者中的7例,分析诊断期和放疗后期sIL-2Rα浓度的差异。第二次分析是针对转移组17例患者中的5例以及复发组11例患者中的6例,分析复发检测前和复发检测后sIL-2Rα浓度的差异。
第一次统计分析显示,缓解组(P = 0.946)和复发组(P = 0.156)在诊断期和放疗后期sIL-2Rα浓度无显著差异。第二次统计分析显示,复发组在复发检测前后sIL-2Rα浓度也无显著差异(P = 0.438)。转移组的结果不同。转移组5对配对样本在检测到转移后sIL-2Rα浓度升高,尽管对差异进行的Wilcoxon符号秩检验仅显示临界显著性(P = 0.063)。
我们的研究结果表明,sIL-2Rα在监测局部区域复发的进展方面无价值,但可能有助于监测远处转移。尽管我们目前有限的数据并未为sIL-2Rα在监测转移中的作用提供有力支持,但未来通过收集更多数据可能会明确其作用。