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在杜克A期和B期结直肠癌中,淋巴结微转移具有临床意义吗?

Are lymph node micrometastases of any clinical significance in Dukes Stages A and B colorectal cancer?

作者信息

Oberg A, Stenling R, Tavelin B, Lindmark G

机构信息

Department of Surgery, Umeå University Hospital, Sweden.

出版信息

Dis Colon Rectum. 1998 Oct;41(10):1244-9. doi: 10.1007/BF02258221.

Abstract

PURPOSE

The aim was to investigate the significance of lymph node micrometastases in Dukes Stages A and B colorectal cancer.

METHODS

Archival specimens were examined from 147 patients (96 colon, 51 rectum; 44 Stage A, 103 Stage B) who had surgery between 1987 and 1994. One lymph node section from each node (colon, 1-11; median, 4; rectum, 1-15; median, 3) was examined with use of an anticytokeratin antibody.

RESULTS

Forty-seven (32 percent) patients had micrometastases. At follow-up in June 1996, 23 patients had died of cancer or with known tumor relapse, after a median time of 28 (range, 5-67) months; 8 of 47 (17 percent) patients had micrometastases, 15 of 100 (15 percent) did not. No statistically significant differences were observed according to micrometastases when the results were analyzed with respect to Dukes stage or survival time. The median survival time of living patients with micrometastases was 48 (range, 18-97) months, and for patients without micrometastases, 48 (range, 19-111) months. Six of 96 living patients had a tumor relapse; three of these displayed micrometastases.

CONCLUSION

Lymph node micrometastases are not a useful prognostic marker in Dukes Stages A and B and do not imply different strategies for additional therapy or follow-up.

摘要

目的

旨在研究淋巴结微转移在杜克A期和B期结直肠癌中的意义。

方法

对1987年至1994年间接受手术的147例患者(96例结肠癌,51例直肠癌;44例A期,103例B期)的存档标本进行检查。使用抗细胞角蛋白抗体对每个淋巴结的一个切片(结肠癌,1至11个;中位数为4个;直肠癌,1至15个;中位数为3个)进行检查。

结果

47例(32%)患者存在微转移。在1996年6月的随访中,23例患者死于癌症或已知肿瘤复发,中位时间为28(范围5至67)个月;47例中有8例(17%)患者存在微转移,100例中15例(15%)没有微转移。根据微转移情况分析结果时,在杜克分期或生存时间方面未观察到统计学上的显著差异。有微转移的存活患者的中位生存时间为48(范围18至97)个月,无微转移的患者为48(范围19至111)个月。96例存活患者中有6例出现肿瘤复发;其中3例显示有微转移。

结论

淋巴结微转移在杜克A期和B期不是一个有用的预后标志物,也不意味着在额外治疗或随访方面需要采取不同策略。

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