Ogawa Yasuhiro, Nishioka Akihito, Kubota Kei, Kariya Shinji, Yoshida Shoji, Maeda Hironori, Tanaka Yosuke, Moriki Toshiaki, Tochika Naoshige
Department of Radiology, Kochi Medical School, Kochi-Prefecture 783-8505, Japan.
Oncol Rep. 2003 Sep-Oct;10(5):1411-5.
In breast cancer patients, several regimens of neoadjuvant chemotherapy have been developed in order to achieve prognostic advantages for individual patients. Though some percentages of breast cancer patients show clinically complete response to neoadjuvant chemotherapy, the histopathological specimens of these patients demonstrate a considerably high frequency of the existence of residual disease. In this study, we aimed to evaluate the therapeutic effect of neoadjuvant chemotherapy for breast cancer patients showing clinically complete response (cCR) to neoadjuvant chemotherapy, using thin-section (5 mm) helical CT (prone position) with bolus injection of contrast agent. Between April 1994 and March 2002, 9 patients with breast cancer showing cCR to the neoadjuvant chemotherapy, who had undergone thin-section CT study both before and following neoadjuvant chemotherapy, enrolled in the study. The mean age of the patients was 46.2 years and all of them were female. The clinical stages were, 8 patients in stage II, and one in stage IIIA. In the CT evaluation, residual disease was visualized in 5 out of the 9 patients. Histopathological examination disclosed the existence of residual cancers in 6 out of the 9 patients, but only non-invasive cancer was revealed in 1 out of the 6. As patients having residual disease composed only of non-invasive cancer are classified into the pathologically complete response group according to the WHO classification, 4 out of these 9 patients showing clinically complete response to the neoadjuvant chemotherapy were classified into pCR (pathologically complete response) group, and another 5 were classified into the pPR (pathologically partial response) group. As a result, the diagnostic accuracy of the second CT study performed after neoadjuvant chemotherapy was evaluated as 77.8%, with a sensitivity of 80.0%, a specificity of 75.0%, a positive predictive value (PPV) of 80.0%, and a negative predictive value (NPV) of 75.0%. Therefore, for precise evaluation of the neoadjuvant chemotherapeutic effect for breast cancer, thin-section CT studies are considered to be essential.
在乳腺癌患者中,已开发出几种新辅助化疗方案,以便为个体患者实现预后优势。尽管一些乳腺癌患者对新辅助化疗表现出临床完全缓解,但这些患者的组织病理学标本显示残留疾病的存在频率相当高。在本研究中,我们旨在使用薄层(5毫米)螺旋CT(俯卧位)并静脉注射造影剂,评估对新辅助化疗表现出临床完全缓解(cCR)的乳腺癌患者的新辅助化疗疗效。1994年4月至2002年3月期间,9例对新辅助化疗表现出cCR的乳腺癌患者纳入研究,这些患者在新辅助化疗前后均接受了薄层CT检查。患者的平均年龄为46.2岁,均为女性。临床分期为,II期8例,IIIA期1例。在CT评估中,9例患者中有5例发现残留疾病。组织病理学检查显示9例患者中有6例存在残留癌,但6例中只有1例为非浸润性癌。由于仅由非浸润性癌组成残留疾病的患者根据WHO分类被归类为病理完全缓解组,因此这9例对新辅助化疗表现出临床完全缓解的患者中有4例被归类为pCR(病理完全缓解)组,另外5例被归类为pPR(病理部分缓解)组。结果,新辅助化疗后进行的第二次CT检查的诊断准确性评估为77.8%,敏感性为80.0%,特异性为75.0%,阳性预测值(PPV)为80.0%,阴性预测值(NPV)为75.0%。因此,为了精确评估乳腺癌的新辅助化疗效果,薄层CT检查被认为是必不可少的。