Pectasides D, Gaglia A, Arapantoni-Dadioti P, Bobota A, Valavanis C, Kostopoulou V, Mylonakis N, Karabelis A, Pectasides M, Economopoulos T
Second Department of Internal Medicine-Propaedeutic, Oncology Section, Attikon University Hospital, Athens, Greece.
Anticancer Res. 2006 Jan-Feb;26(1B):647-53.
The aim of this prospective study was to investigate whether there were changes in HER-2/neu status in newly-developed metastatic lesions following treatment with trastuzumab in advanced breast cancer patients overexpressing HER-2/neu. The utility of serological assays for HER-2/neu in such patients was also studied.
Sixteen patients with HER-2/neu-overexpressing tumors (15 were 3+ by immunohistochemistry (IHC) and one 2+ by IHC and positive by the chromogenic in situ hybridization (CISH) test) were included in the study. Fourteen patients underwent biopsy and 2 patients fine-needle aspiration (FNA) of newly-developed metastatic lesions following trastuzumab treatment. All samples were assayed for HER-2 by IHC and by the CISH test. Serial serum HER-2/neu (S-HER-2) levels were measured prior to (baseline values) and during trastuzumab-based treatment by enzyme-linked immunosorbent assay (ELISA) (cut-off point: 10 ng/ml) in all patients. The patients were divided into 2 groups: those with "altered HER-2/neu status" and those with "conserved HER-2/neu status" in the metastatic region.
Six out of the 16 (37%) ("altered HER-2/neu status") newly-developed metastatic lesions lost their HER-2/neu overexpression and scored 0 or +1 by IHC or negative on the CISH test, while in the remaining cases (10/16, 62.5%) ("conserved HER-2/neu status"), the HER-2/neu status was unchanged (+3 by IHC or a positive CISH test). Baseline S-HER-2 levels were elevated in 5 out of 16 patients (3 of "altered HER-2/neu status", 2 of "conserved HER-2/neu status"). The serum HER-2 (S-HER-2) levels declined and returned within the normal ranges in all these 5 patients as a response to trastuzumab treatment. Following the disease progression, the S-HER-2 levels of the 3 patients with "altered HER-2/neu status" remained normal, while those of 2 with "conserved HER-2/neu status" increased. There was no statistically significant difference in the number of chemotherapeutic treatments or the median time of treatment with trastuzumab or chemotherapy between the 2 groups. Time to tumor progression (TTP) was significantly shorter in the "altered HER-2/neu status" patients (median TTP for "altered HER-2/neu status": 9.5 months, and for "conserved HER-2/neu status": 12 months; p <0.001).
These data suggest that, for most patients with metastatic breast cancer treated with trastuzumab, the HER-2/neu expression as measured by IHC and/or CISH in newly-developed metastatic lesions was unchanged. However, a remarkable percentage of cases lost HER-2/neu overexpression. It is not clear whether this finding implies resistance or sensitivity to trastuzumab.
本前瞻性研究的目的是调查在接受曲妥珠单抗治疗的HER-2/neu过表达晚期乳腺癌患者中,新出现的转移病灶的HER-2/neu状态是否发生变化。同时也研究了此类患者血清学检测HER-2/neu的实用性。
本研究纳入了16例HER-2/neu过表达肿瘤患者(15例免疫组化(IHC)评分为3+,1例IHC评分为2+且显色原位杂交(CISH)检测为阳性)。14例患者接受了活检,2例患者在曲妥珠单抗治疗后对新出现的转移病灶进行了细针穿刺抽吸(FNA)。所有样本均通过IHC和CISH检测进行HER-2检测。所有患者在曲妥珠单抗治疗前(基线值)和治疗期间通过酶联免疫吸附测定(ELISA)(临界值:10 ng/ml)检测血清HER-2/neu(S-HER-2)水平。患者被分为两组:转移灶中HER-2/neu状态“改变”的患者和HER-2/neu状态“保持不变”的患者。
16例新出现的转移病灶中有6例(37%)(HER-2/neu状态“改变”)失去了HER-2/neu过表达,免疫组化评分为0或+1,或CISH检测为阴性,而其余病例(10/16,62.5%)(HER-2/neu状态“保持不变”)中,HER-2/neu状态未改变(免疫组化评分为+3或CISH检测为阳性)。16例患者中有5例(HER-2/neu状态“改变”的3例,HER-2/neu状态“保持不变”的2例)基线S-HER-2水平升高。作为对曲妥珠单抗治疗的反应,这5例患者的血清HER-2(S-HER-2)水平均下降并恢复到正常范围内。疾病进展后,3例HER-2/neu状态“改变”患者的S-HER-2水平保持正常,而2例HER-2/neu状态“保持不变”患者的S-HER-2水平升高。两组之间的化疗次数、曲妥珠单抗或化疗的中位治疗时间无统计学显著差异。HER-2/neu状态“改变”的患者的肿瘤进展时间(TTP)显著缩短(HER-2/neu状态“改变”的患者中位TTP为9.5个月,HER-2/neu状态“保持不变”的患者为12个月;p<0.001)。
这些数据表明,对于大多数接受曲妥珠单抗治疗的转移性乳腺癌患者,通过IHC和/或CISH检测新出现的转移病灶中的HER-2/neu表达未发生变化。然而,有相当比例的病例失去了HER-2/neu过表达。尚不清楚这一发现是否意味着对曲妥珠单抗耐药或敏感。