Muñoz Mar, Fernández-Aceñero M Jesús, Martín Silvia, Schneider José
Department of Gynecology and Obstetrics, Hospital of Parla, Madrid, Spain.
Arch Gynecol Obstet. 2009 Jul;280(1):43-8. doi: 10.1007/s00404-008-0867-1. Epub 2008 Dec 11.
Breast carcinoma classification has dramatically changed in recent years following application of molecular techniques. Immunohistochemistry can help select patients for different therapies. The objective of the present report is to determine the prognostic influence of the molecular classification of breast carcinoma with immunohistochemistry.
We have retrospectively selected a cohort of 257 patients with invasive ductal carcinoma NOS diagnosed and treated in the same hospital between 1997 and 2000. We have classified the cases in four tumor types according to the immunohistochemical expression of several markers, as luminal A tumors [estrogen and/or progesterone receptors (ER/PE) positive and Her-2 negative]; luminal B tumors (ER/PR positive and Her-2 positive); Her-2 positive tumors (ER/PR negative with Her-2 positive); and triple negative phenotype (all markers negative).
In our series, 116 patients had tumors of luminal A type (47.93%); 67 (27.68%) were luminal type B; 33 (13.63%) were Her2 positive; and 26 (10.74%) were triple negative. The recurrence rate was 19% for luminal type A tumors, 25.4% for luminal type B, 39.4% for Her2 positive and 30.8% for triple negative lesions. The mean relapse free survival was 79.07, 73.07, 64.3 and 83,5 months for luminal A and B, Her-2 and triple negative lesions, respectively. Mortality rate reached 11.2% for luminal A tumors compared with 19.4, 33.3 and 26.9% for luminal B, Her2 and triple negative tumors, respectively. The mean overall survival for these groups was 88.42, 81.41, 77.62 and 93.6 months.
Molecular classification with immunohistochemistry behaves as a significant prognosticator for breast invasive ductal carcinoma in our series of patients. The worse prognosis observed for Her2 expressing lesions may have changed after trastuzumab use.
近年来,随着分子技术的应用,乳腺癌的分类发生了巨大变化。免疫组织化学有助于为不同治疗方案选择合适的患者。本报告的目的是确定免疫组织化学在乳腺癌分子分类中的预后影响。
我们回顾性选取了1997年至2000年间在同一家医院诊断并接受治疗的257例浸润性导管癌患者。根据几种标志物的免疫组化表达情况,将病例分为四种肿瘤类型,即腔面A型肿瘤(雌激素和/或孕激素受体(ER/PR)阳性且Her-2阴性);腔面B型肿瘤(ER/PR阳性且Her-2阳性);Her-2阳性肿瘤(ER/PR阴性且Her-2阳性);以及三阴性表型(所有标志物均为阴性)。
在我们的研究系列中,116例患者为腔面A型肿瘤(47.93%);67例(27.68%)为腔面B型;33例(13.63%)为Her2阳性;26例(10.74%)为三阴性。腔面A型肿瘤的复发率为19%,腔面B型为25.4%,Her2阳性为39.4%,三阴性病变为30.8%。腔面A、B型、Her-2和三阴性病变的无复发生存期分别为79.07、73.07、64.3和83.5个月。腔面A型肿瘤的死亡率为11.2%,而腔面B型、Her2和三阴性肿瘤的死亡率分别为19.4%、33.3%和26.9%。这些组的平均总生存期分别为88.42、81.41、77.62和93.6个月。
在我们的患者系列中,免疫组织化学分子分类是乳腺浸润性导管癌的一个重要预后指标。使用曲妥珠单抗后,观察到的Her2表达病变预后较差的情况可能已经改变。