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p63 expression in Merkel cell carcinoma predicts poorer survival yet may have limited clinical utility.

Merkel细胞癌中p63的表达预示较差的生存时间,但其临床价值有限。

Stetsenko GY,Malekirad J,Paulson KG,Iyer JG,Thibodeau RM,Nagase K,Schmidt M,Storer BE,Argenyi ZB,Nghiem P

Abstract

To determine the clinical utility of p63 expression, which has been identified in several cohorts as a predictor of poorer prognosis in Merkel cell carcinoma (MCC).
Immunohistochemistry was used to determine p63 expression on MCC tumors from 128 patients.
Of the patients, 33% had detectable p63 expression. p63 Positivity was associated with an increased risk of death from MCC (hazard ratio, 2.05; P = .02) in a multivariate Cox regression model considering stage at presentation, age at diagnosis, and sex. Although p63 expression correlated with diminished survival in this largest cohort reported thus far, the effect was weaker than that observed in prior studies. Indeed, within a given stage, p63 status did not predict survival in a clinically or statistically significant manner.
It remains unclear whether this test should be integrated into routine MCC patient management.

摘要

为了确定一直被认为是Merkel细胞癌预后较差(MCC)的预测因子p63表达的临床价值
用免疫组化法确定128例患者MCC肿瘤的p63表达情况。
在这些患者中,33%检测出p63的表达。为了确定一直被认为是Merkel细胞癌预后较差(MCC)的预测因子p63表达的临床价值
用免疫组化法确定128例患者MCC肿瘤的p63表达情况。
在这些患者中,33%检测出p63的表达。在包括了确诊时的疾病分期、年龄和性别的多元Cox回归模型中,p63的阳性率与MCC死亡风险的增加相关(风险比2.05,P=0.02)。尽管在此次目前最大量的病例中,p63表达与存活时间的缩短相关,但其效果比先前研究中的观察结果更弱。事实上,在给定的疾病分期中,p63的状态并不能以临床或统计学显着的方式预测生存时间。
目前还不清楚本次测试是否应纳入MCC病人的常规管理。
在包括了确诊时的疾病分期、年龄和性别的多元Cox回归模型中,p63的阳性率与MCC死亡风险的增加相关(风险比2.05,P=0.02)。尽管在此次目前最大量的病例中,p63表达与存活时间的缩短相关,但其效果比先前研究中的观察结果更弱。事实上,在给定的疾病分期中,p63的状态并不能以临床或统计学显着的方式预测生存时间。
目前还不清楚本次测试是否应纳入MCC病人的常规管理。

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