Vassilios J Papantoniou, Michael A Souvatzoglou, Varvara J Valotassiou, Androniki N Louvrou, Constantina Ambela, John Koutsikos, Dimitrios Lazaris, Julie K Christodoulidou, Maria G Sotiropoulou, Maria J Melissinou, Aris Perperoglou, Spyridon Tsiouris, Cherry J Zerva
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In addition, by multivariate regression analysis, we further isolated those factors with independent associations with (V)DMSA and/or MIBI uptake in primary breast cancer.</p><p><strong>Methods: </strong>Thirty-four patients with histologically confirmed breast carcinoma underwent preoperative scintimammography with technetium-99m (99mTc)-(V)DMSA and/or 99mTc-MIBI in consecutive sessions 10 and 60 min after administration of 925-1110 MBq of each radiotracer. The tumor-to-background ratio was calculated and correlated with the presence of ER, PR, Ki-67, tumor size, tumor grade, p53, and c-erbB-2. ER, PR, p53, and c-erbB-2 were determined immunohistochemically. The analysis included tumor-to-background ratio of (V)DMSA and MIBI uptake as dependent and all of the other parameters as independent variables.</p><p><strong>Results: </strong>Correlation was positive between Ki-67 and (V)DMSA (r = 0.37 at 10 min, P = 0.038; r = 0.42 at 60 min, P = 0.018) and inverse between PR and (V)DMSA uptake (r = -0.46 at 10 min, P = 0.010; r = -0.51 at 60 min, P = 0.003). Multivariate regression analysis demonstrated a positive correlation between Ki-67 and (V)DMSA at 60 min (P = 0.045). Ki-67 was not significantly correlated with MIBI uptake, whereas tumor size was positively correlated with MIBI uptake at 60 min both in univariate (r = 0.45, P = 0.027) and multivariate analysis (P = 0.024). Negative correlations were observed between (V)DMSA uptake and ER, as well as between ER/PR and MIBI uptake, but these were not significant.</p><p><strong>Conclusion: </strong>Ki-67 appears to represent the major independent factor affecting (V)DMSA uptake in breast cancer. Tumor size was the only independent parameter influencing MIBI uptake in breast cancer. (V)DMSA appears to have an advantage over MIBI in that it can be used to visualize tumors with intense proliferative activity, and thus it can identify those tumors that are more aggressive.</p>","PeriodicalId":9283,"journal":{"name":"Breast Cancer Research : BCR","volume":"6 2","pages":"R56-62"},"PeriodicalIF":0.0000,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/bcr751","citationCount":"44","resultStr":"{\"title\":\"Relationship of cell proliferation (Ki-67) to 99mTc-(V)DMSA uptake in breast cancer.\",\"authors\":\"Vassilios J Papantoniou, Michael A Souvatzoglou, Varvara J Valotassiou, Androniki N Louvrou, Constantina Ambela, John Koutsikos, Dimitrios Lazaris, Julie K Christodoulidou, Maria G Sotiropoulou, Maria J Melissinou, Aris Perperoglou, Spyridon Tsiouris, Cherry J Zerva\",\"doi\":\"10.1186/bcr751\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>The aim of the present study was to identify the relationships between the uptake of radiotracers - namely pentavalent dimercaptosuccinic acid [(V)DMSA] and sestamibi (MIBI) - and the following parameters in primary breast cancer: steroid receptor concentrations (i.e. estrogen receptor [ER] and progesterone receptor [PR]), Ki-67 expression, tumor size, tumor grade, age, and levels of expression of p53 and c-erbB-2. In addition, by multivariate regression analysis, we further isolated those factors with independent associations with (V)DMSA and/or MIBI uptake in primary breast cancer.</p><p><strong>Methods: </strong>Thirty-four patients with histologically confirmed breast carcinoma underwent preoperative scintimammography with technetium-99m (99mTc)-(V)DMSA and/or 99mTc-MIBI in consecutive sessions 10 and 60 min after administration of 925-1110 MBq of each radiotracer. The tumor-to-background ratio was calculated and correlated with the presence of ER, PR, Ki-67, tumor size, tumor grade, p53, and c-erbB-2. ER, PR, p53, and c-erbB-2 were determined immunohistochemically. 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引用次数: 44
摘要
本研究的目的是确定原发性乳腺癌中放射性示踪剂(即五价二巯基琥珀酸[(V)DMSA]和赛斯米比(MIBI))的摄取与以下参数之间的关系:类固醇受体浓度(即雌激素受体[ER]和孕激素受体[PR])、Ki-67表达、肿瘤大小、肿瘤分级、年龄以及p53和c-erbB-2的表达水平。此外,通过多变量回归分析,我们进一步分离出与原发性乳腺癌(V)DMSA和/或MIBI摄取独立相关的因素。方法:34例经组织学证实的乳腺癌患者在给予925-1110 MBq放射性示踪剂后连续10分钟和60分钟,行锝-99m (99mTc)-(V)DMSA和/或99mTc- mibi的术前ct检查。计算肿瘤与背景比值,并与ER、PR、Ki-67、肿瘤大小、肿瘤分级、p53和c-erbB-2的存在相关。免疫组织化学检测ER、PR、p53、c-erbB-2。分析包括肿瘤与背景比(V)DMSA和MIBI摄取作为因变量,所有其他参数作为自变量。结果:Ki-67与(V)DMSA呈正相关(10 min r = 0.37, P = 0.038;60 min时r = 0.42, P = 0.018), PR与(V)DMSA摄取呈负相关(10 min时r = -0.46, P = 0.010;r = -0.51, P = 0.003)。多因素回归分析显示Ki-67与60 min时(V)DMSA呈正相关(P = 0.045)。Ki-67与MIBI摄取无显著相关,而肿瘤大小与60 min时的MIBI摄取在单因素分析(r = 0.45, P = 0.027)和多因素分析(P = 0.024)中均呈正相关。(V)DMSA摄取与ER、ER/PR与MIBI摄取呈负相关,但均不显著。结论:Ki-67似乎是影响乳腺癌中(V)DMSA摄取的主要独立因素。肿瘤大小是影响乳腺癌中MIBI摄取的唯一独立参数。DMSA似乎比MIBI有优势,因为它可以用来观察具有强烈增殖活性的肿瘤,因此它可以识别那些更具侵袭性的肿瘤。
Relationship of cell proliferation (Ki-67) to 99mTc-(V)DMSA uptake in breast cancer.
Introduction: The aim of the present study was to identify the relationships between the uptake of radiotracers - namely pentavalent dimercaptosuccinic acid [(V)DMSA] and sestamibi (MIBI) - and the following parameters in primary breast cancer: steroid receptor concentrations (i.e. estrogen receptor [ER] and progesterone receptor [PR]), Ki-67 expression, tumor size, tumor grade, age, and levels of expression of p53 and c-erbB-2. In addition, by multivariate regression analysis, we further isolated those factors with independent associations with (V)DMSA and/or MIBI uptake in primary breast cancer.
Methods: Thirty-four patients with histologically confirmed breast carcinoma underwent preoperative scintimammography with technetium-99m (99mTc)-(V)DMSA and/or 99mTc-MIBI in consecutive sessions 10 and 60 min after administration of 925-1110 MBq of each radiotracer. The tumor-to-background ratio was calculated and correlated with the presence of ER, PR, Ki-67, tumor size, tumor grade, p53, and c-erbB-2. ER, PR, p53, and c-erbB-2 were determined immunohistochemically. The analysis included tumor-to-background ratio of (V)DMSA and MIBI uptake as dependent and all of the other parameters as independent variables.
Results: Correlation was positive between Ki-67 and (V)DMSA (r = 0.37 at 10 min, P = 0.038; r = 0.42 at 60 min, P = 0.018) and inverse between PR and (V)DMSA uptake (r = -0.46 at 10 min, P = 0.010; r = -0.51 at 60 min, P = 0.003). Multivariate regression analysis demonstrated a positive correlation between Ki-67 and (V)DMSA at 60 min (P = 0.045). Ki-67 was not significantly correlated with MIBI uptake, whereas tumor size was positively correlated with MIBI uptake at 60 min both in univariate (r = 0.45, P = 0.027) and multivariate analysis (P = 0.024). Negative correlations were observed between (V)DMSA uptake and ER, as well as between ER/PR and MIBI uptake, but these were not significant.
Conclusion: Ki-67 appears to represent the major independent factor affecting (V)DMSA uptake in breast cancer. Tumor size was the only independent parameter influencing MIBI uptake in breast cancer. (V)DMSA appears to have an advantage over MIBI in that it can be used to visualize tumors with intense proliferative activity, and thus it can identify those tumors that are more aggressive.