Chavez-Blanco Alma, Perez-Sanchez Victor, Gonzalez-Fierro Aurora, Vela-Chavez Teresa, Candelaria Myrna, Cetina Lucely, Vidal Silvia, Dueñas-Gonzalez Alfonso
Unidad de Investigación Biomédica en Cáncer, Instituto Nacional de Cancerología-Instituto de Investigaciones Biomédicas, UNAM, Av, San Fernando No, 22, Tlalpan 14080, Mexico City, USA.
BMC Cancer. 2004 Sep 1;4:59. doi: 10.1186/1471-2407-4-59.
Trastuzumab, a humanized monoclonal antibody against the HER2 receptor is currently being used in breast and other tumor types. Early studies have shown that a variable proportion of cervical carcinoma tumors overexpress the HER2 receptor as evaluated by diverse techniques and antibodies. Currently it is known that a tumor response to trastuzumab strongly correlates with the level of HER2 expression evaluated by the Hercep Test, thus, it seems desirable to evaluate the status of expression of this receptor using the FDA-approved Hercep Test and grading system to gain insight in the feasibility of using trastuzumab in cervical cancer patients.
We analyzed a series of cervical cancer cell lines, the primary tumors of 35 cases of cervical cancer patients and four recurrent cases, with the Hercep Test in order to establish whether this tumor type overexpress HER2 at level of 2+/3+ as trastuzumab is currently approved for breast cancer having such level of expression.
The results indicate that only 1 out of 35 primary tumors cases overexpress the receptor at this level, however, two out of four recurrent tumors that tested negative at diagnosis shifted to Hercep Test 2+ and 3+ respectively.
The low frequency of expression in primary cases suggests that trastuzumab could have a limited value for the primary management of cervical cancer patients, however, the finding of "conversion" to Hercep Test 2+ and 3+ of recurrent tumors indicates the need to further evaluate the expression of HER2 in the metastatic and recurrent cases.
曲妥珠单抗是一种针对HER2受体的人源化单克隆抗体,目前用于乳腺癌和其他肿瘤类型。早期研究表明,通过多种技术和抗体评估,不同比例的宫颈癌肿瘤过度表达HER2受体。目前已知,肿瘤对曲妥珠单抗的反应与通过赫赛汀检测评估的HER2表达水平密切相关,因此,似乎有必要使用FDA批准的赫赛汀检测和分级系统来评估该受体的表达状态,以深入了解在宫颈癌患者中使用曲妥珠单抗的可行性。
我们使用赫赛汀检测分析了一系列宫颈癌细胞系、35例宫颈癌患者的原发性肿瘤以及4例复发性病例,以确定这种肿瘤类型是否像目前曲妥珠单抗被批准用于具有这种表达水平的乳腺癌那样,在2+/3+水平过度表达HER2。
结果表明,35例原发性肿瘤病例中只有1例在此水平过度表达该受体,然而,4例复发性肿瘤中有2例在诊断时检测为阴性,分别转变为赫赛汀检测2+和3+。
原发性病例中低表达频率表明曲妥珠单抗对宫颈癌患者的原发性治疗价值有限,然而,复发性肿瘤“转变”为赫赛汀检测2+和3+的发现表明需要进一步评估HER2在转移性和复发性病例中的表达。