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小(≤2厘米)胰腺癌的长期生存及预后指标

Long-term survival and prognostic indicators in small (<or=2 cm) pancreatic cancer.

作者信息

Pongprasobchai Supot, Pannala Rahul, Smyrk Thomas C, Bamlet William, Pitchumoni Suresh, Ougolkov Andrei, de Andrade Mariza, Petersen Gloria M, Chari Suresh T

机构信息

Division of Gastroenterology, Mayo Clinic, Rochester, MN 55905, USA.

出版信息

Pancreatology. 2008;8(6):587-92. doi: 10.1159/000161009. Epub 2008 Oct 13.

Abstract

OBJECTIVES

In a matched analysis, we investigated clinical, histopathological, and survival characteristics of small (<or=2 cm) pancreatic cancer (PaC) as compared to large PaC.

METHODS

From the Mayo pathology database, we identified 41 consecutive patients with small PaC and 94 matched controls with margin-negative PaC >2 cm. Two experienced pathologists, who were blinded to survival data, independently reviewed tumor stage and differentiation. Kaplan-Meier survival analysis and Cox proportional hazards models were applied for data analyses.

RESULTS

In patients with localized disease (stages I and II), survival was similar in small and large PaC but survival was significantly better in small PaC with regional nodal metastasis (stage III) as compared to similar stage large PaC (5-year survival 44 vs. 7%, median survival 58 vs.18 months, p < 0.001). Well-differentiated small and large PaC had similar median survival (76 vs. 74 months, p = NS). In multivariate analysis, tumor differentiation, not tumor size, was the only independent factor predicting survival in PaC (risk ratio, RR, for moderate vs. well- differentiated: 2.6, 95% confidence interval, CI, 1.5-4.5, and RR for poorly differentiated vs. well-differentiated: 5.0, 95% CI 2.4-10.1).

CONCLUSION

Tumor differentiation may be a better predictor of survival in resectable PaC than tumor stage.

摘要

目的

在一项配对分析中,我们研究了小(≤2 cm)胰腺癌(PaC)与大胰腺癌相比的临床、组织病理学和生存特征。

方法

从梅奥病理数据库中,我们确定了41例连续的小胰腺癌患者和94例配对的切缘阴性的>2 cm胰腺癌对照患者。两名对生存数据不知情的经验丰富的病理学家独立审查肿瘤分期和分化情况。应用Kaplan-Meier生存分析和Cox比例风险模型进行数据分析。

结果

在局限性疾病(I期和II期)患者中,小胰腺癌和大胰腺癌的生存率相似,但与相似分期的大胰腺癌相比,伴有区域淋巴结转移(III期)的小胰腺癌生存率显著更高(5年生存率44%对7%,中位生存期58个月对18个月,p<0.001)。高分化的小胰腺癌和大胰腺癌中位生存期相似(76个月对74个月,p=无显著性差异)。在多变量分析中,肿瘤分化而非肿瘤大小是预测胰腺癌生存的唯一独立因素(中度分化与高分化的风险比,RR:2.6,95%置信区间,CI:1.5 - 4.5,低分化与高分化的RR:5.0,95%CI:2.4 - 10.1)。

结论

对于可切除的胰腺癌,肿瘤分化可能比肿瘤分期更能预测生存。

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