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排序方式: 共有365条查询结果,搜索用时 78 毫秒
1.
肺癌患者淋巴结微转移灶的检测的预后价值 总被引:1,自引:0,他引:1
目的:通过免疫组化的方法检测非小细胞肺癌患术后常规病理检查阴性的淋巴结的微转移灶,研究其预后价值。方法:用免疫组化角蛋白(CK)染色的方法检测术后常规病理学检查阴性的淋巴结中的微转移灶,以此研究非小细胞肺癌患淋巴结微转移灶的检出和患生存期的关系。结果:在39例患的90枚阴性淋巴结中22例患(56.4%)的26枚淋巴结(28.89%)检出微转移灶。有无复发转移患的淋巴结微转移率有显性差异(81%vs39%,P=0.02);有无微转移灶的患的生存期各为32个月和48个月,3年生存率各为35%和75%(P=0.0178)。结论:淋巴结微转移灶的检测可以作为非小细胞肺癌患手术后的一个重要的预后指标。 相似文献
2.
胃癌患者外周血中CK19,CK20表达的临床研究 总被引:1,自引:2,他引:1
目的:研究胃癌患者外周血CK19、CK20的表达,并探讨其临床意义.方法:用流式细胞术(FCM)方法,检测66例胃癌、7例消化系统良性疾病及21例本院健康职工外周血CK19、CK20的表达.结果:7例消化系统良性患者、21例本院健康职工外周血CK19、CK20无表达.66例胃癌患者CK19、CK20、CK19 CK20阳性表达率分别为53.1%(35/66)、56.1%(37/66)、46.9%(31/66).TNM分期之间比较,Ⅳ期与Ⅰ、Ⅱ、Ⅲ期差异有显著性意义(P<0.01).Ⅰ、Ⅱ、Ⅲ期之间相互比较,差异无显著性意义(P>0.05).转移程度比较,差异有显著性意义(P<0.01).胃癌远处转移诊断敏感度高达90%.结论:胃癌患者外周血CK19、CK20可以作为检测胃癌微转移的指标. 相似文献
3.
目的:探讨早期乳腺癌腋淋巴结转移(ALNM)的相关因素,并对阴性腋淋巴结行角蛋白19(CK19)检测以发现微转移癌.方法:收集乳腺癌病例138例,建立数据库,用Logistic回归进行单因素和多因素分析,并对有意义的指标进行相关分析,对40例患者441枚阴性腋淋巴结再切片,用CK19行免疫组织化学染色.结果:多因素分析显示肿瘤大小、肿瘤部位、癌抗原153(CA153)、人类表皮生长因子受体-2(HER2)4个指标进入Logistic回归方程,40例患者中有3例患者的腋窝淋巴结CK19免疫组织化学染色阳性.结论:肿瘤大小、肿瘤部位、CA153和HER2为乳腺癌患者ALNM的高危因素;CK19免疫组织化学染色可发现乳腺癌腋淋巴结微转移癌. 相似文献
4.
5.
乳腺癌患者外周血、骨髓斯钙素基因检测及其意义 总被引:4,自引:0,他引:4
目的 观察人类斯钙素-1(hSTC-1)基因在原发性乳腺癌患者外周血液及骨髓中的表达,研究将hSTC-1作为一种新的肿瘤分子标记用来检测乳腺癌患者血液及骨髓中的肿瘤微转移情况.方法 采用逆转录-聚合酶链反应(RT-PCR)方法分别检测51例乳腺癌病人的外周血(A组)、8例乳腺癌病人的骨髓(B组)以及30例乳腺癌病人的肿瘤组织(C组)中hSTC-1 mRNA的表达水平.结果 C组标本hSTC-1 mRNA的阳性率为93.3%,A组和B组hSTC-1 mRNA的阳性率分别为37.3%和37.5%.结论 乳腺癌患者外周血、骨髓中检测到hSTC-1基因的表达,说明乳腺癌已发牛血行微转移;hSTC-1可作为检测乳腺癌病人外周血、骨髓微转移新的分子标记. 相似文献
6.
《Cancer radiothérapie》2015,19(4):276-283
In patients with breast cancer, axillary lymph node micrometastasis detection has been more frequent with a better definition since the introduction of the sentinel node procedure. In this review, we focus on pN1mi micrometastasis and review the literature in order to determine factors involved in making the decision of a regional treatment. 相似文献
7.
Tveito S Maelandsmo GM Hoifodt HK Rasmussen H Fodstad O 《Clinical & experimental metastasis》2007,24(5):317-327
Molecular studies of rare cells, such as circulating cancer cells, require efficient pre-enrichment steps to obtain a pure
population of target cells for further characterization. We have developed a two-step approach, starting with immunomagnetic
enrichment, followed by specific isolation of individual, easily identifiable bead-rosetted target cells using a new semi-automated
CellPick system. With this procedure, 1–50 live target cells can now be isolated. As a model system, we spiked a small number
of tumor cells into millions of normal mononuclear cells (MNCs). Efficient isolation of pure target cells was obtained by
use of the CellPick system, and the nature of isolated, bead-rosetted cells was verified by use of FISH. Single breast cancer
cells were picked directly into an RNA preserving lysis buffer, reverse transcribed, and PCR amplified with two cDNA specific
primer sets. With the isolated cells we consistently obtained both ubiquitously expressed and tumor cell specific PCR products.
We also performed a successful mutation analysis of single cells using PCR and cycling temperature capillary electrophoresis
(CTCE). This may have significant clinical implications in cancer and in other diseases, e.g. in characterizing micrometastatic
cancer cells in blood and lymph nodes to help identifying patients who most likely will respond to therapies like tyrosine
kinase inhibitors and compounds targeting specific mutations. By use of the CellPick system it is possible to specifically
isolate bead-rosetted or otherwise labelled target cells from a heterogeneous cell population for further molecular characterization. 相似文献
8.
Hitoshi Shiozaki Yoshiyuki Fujiwara Toshihiro Hirai Hisahiro Matsubara Masaki Mori Tsutomu Nakamura Yukihiro Nakanishi Shoji Natsugoe Tsuyoshi Noguchi Soji Ozawa Yutaka Shimada Seiji Udagawa Hideaki Yamana Masahiko Yano Takushi Yasuda Akio Yanagisawa 《Esophagus》2007,4(1):35-39
Background In esophageal carcinoma, the clinical significance of immunohistochemically (IHC)-detected lymph node (LN) micrometastasis
is still controversial. We designed this multicenter study to determine the clinical significance of IHC-detected LN micrometastasis
in esophageal carcinoma.
Methods The subjects were 164 patients with histopathologically confirmed LN-negative esophageal carcinoma from eight hospitals. A
similar IHC technique was used in all institutions, and micrometastasis was diagnosed by a researcher at each hospital as
well as independently by pathologists with special interest in esophageal carcinoma.
Results IHC-related micrometastasis in LN was considered positive in 51 (31%) patients by the researchers and in 25 (15%) by the pathologists.
The latter micrometastases were further classified into a single (n = 13) and clusters (n = 12) of immunopositive-LN. Kaplan–Meier analysis showed that researcher-based diagnosis of micrometastasis had no significant
impact on prognosis whereas the cluster-type micrometastasis diagnosed by pathologists had a significant impact on prognosis.
Conclusions We speculate that the inconsistent results of IHC analyses reported in the literature are caused by the use of different definitions
of micrometastasis and the subjective nature of diagnosis of micrometastasis, i.e., dependence on the examiner. Our multiinstitutional
study also indicates that the morphological aspects of immunostained cells should be considered when assessing micrometastasis
in LN by IHC and that only LN with clusters of IHC-positive cells are prognostically significant in esophageal carcinoma. 相似文献
9.
Perez RO Habr-Gama A Nishida Arazawa ST Rawet V Coelho Siqueira SA Kiss DR Gama-Rodrigues JJ 《International journal of colorectal disease》2005,20(5):434-439
Objective The objective was to determine the presence and frequency of micrometastasis in lymph nodes of patients with rectal cancer treated by preoperative chemoradiation followed by curative resection.Patients and methods All 56 patients included were treated with 5-FU and leucovorin plus 5,040 cGy, followed by radical surgery and were diagnosed with stage II distal rectal adenocarcinoma after complete pathological examination (ypT3-4N0M0). Immunohistochemistry was assessed with cytokeratin monoclonal antibody AE1/AE3. Three 4-m paraffin sections were obtained from each lymph node, cut at 50 m apart from each other. The results were reviewed by two independent pathologists.Results Mean number of lymph nodes was 9.6 per patient. Four patients (7%) and seven lymph nodes (1.35%) were positive for micrometastasis. Three patients had pT3 and one a pT4 tumor. One of the patients had positive micrometastasis and the presence of mucinous deposits. One other patient had mucinous deposits without any micrometastasis. All four patients are alive with no evidence of recurrent disease. Fourteen patients negative for micrometastasis had recurrent disease (25%), eight systemic (14.7%) and six locoregional (10.3%). There were two cancer-related deaths. The mean follow-up period was 39 months.Conclusion Patients with rectal cancer treated by preoperative chemoradiation showed a surprisingly low rate of micrometastasis detection (7%), even in high-risk patients (T3 and T4 tumors). Lymph node micrometastasis was not associated with decreased overall or disease-free survival. The identification of mucinous deposits on lymph nodes with no viable tumor cells may be direct evidence of lymph node downstaging. The downstaging effect of preoperative chemoradiation therapy may be significant in reducing even micrometastasis detection in low rectal cancer managed by this treatment strategy. 相似文献
10.
目的:建立兔舌癌哨位淋巴结(sentinel lymph node,SLN)微转移模型,为进一步研究舌癌区域淋巴结转移的发生、发展机制及防治提供实验平台。方法:先正位、多循环移植Vx-2癌瘤于兔舌,每次8只兔,筛选出高淋巴转移潜力移植瘤;再将其移植到40只兔的舌部,分别于移植后第8、10、12、14和16天各随机处死8只,取出兔舌Vx-2移植瘤SLN,经连续切片和免疫组织化学检测其微转移形成情况。应用SPSS 17.0软件包对结果进行统计学分析。结果:经3次正位循环移植后,所得Vx-2移植瘤舌移植后SLN转移率达100%(8/8);该高淋巴转移潜力移植瘤移植兔舌后10~12 d,所获移植瘤SLN微转移发生率为100%(8/8)。结论:应用本研究筛选的高淋巴转移潜力Vx-2瘤移植兔舌后10~12 d,可获得较稳定的兔舌癌SLN微转移模型。 相似文献