Junker Klaus, Stachetzki Ulf, Rademacher Daniela, Linder Albert, Macha Hans-Nicol, Heinecke Achim, Müller Klaus-Michael, Thomas Michael
Institute of Pathology, Bergmannsheil-University-Hospital, Bürkle-de-la-Camp-Platz 1, D-44789 Bochum, Germany.
Lung Cancer. 2005 Apr;48(1):59-67. doi: 10.1016/j.lungcan.2004.10.010. Epub 2004 Dec 13.
Expression and amplification of the HER2/neu protooncogene was analyzed in locally advanced NSCLC in a multimodality therapy approach in order to obtain information on the predictive value of HER2/neu for success or failure of neoadjuvant therapy.
In the scope of a prospective randomized phase III-trial, tumor tissue of pre-therapeutically obtained mediastinal lymph node biopsies (n=105) and corresponding post-surgical resection specimens (n=44) was analyzed by means of immunohistochemistry (DAKO-Hercep-Test) and fluorescence in situ hybridization (FISH). In 58 of 105 patients with metastatic mediastinal lymph node disease the extent of therapy-induced tumor regression could be established.
Concerning HER2/neu expression, 16 lymph node biopsies (15.2%) showed 1+, 2+, or 3+ results. Five of these cases revealed amplification in FISH analysis (4.8%). In 44 corresponding resection specimens, Hercep-Test showed 1+, 2+, or 3+ results in 13 tumors (29.5%). Two of these patients revealed HER2/neu amplification in FISH analysis (4.5%). In patients with HER2/neu expressing tumors a trend towards a less extensive therapy-induced tumor regression could be demonstrated. When comparing pre-therapy and post-surgical results, there was a weak trend towards a selection of HER2/neu expressing tumor tissue in the course of neoadjuvant therapy.
Only a limited subcollective of locally advanced NSCLC meets the biological requirements for anti-HER2/neu therapy. HER2/neu positive tumors appeared to be relatively resistant to chemotherapy and radiation treatment, none of these cases having a pathological complete or at least subtotal response in the corresponding resection specimens. This observation requires confirmation in large randomized controlled studies.
为了获取有关HER2/neu对新辅助治疗成败的预测价值的信息,采用多模态治疗方法分析局部晚期非小细胞肺癌(NSCLC)中HER2/neu原癌基因的表达及扩增情况。
在一项前瞻性随机III期试验中,通过免疫组织化学(DAKO-Hercep-Test)和荧光原位杂交(FISH)对治疗前获取的纵隔淋巴结活检组织(n = 105)及相应的手术切除标本(n = 44)的肿瘤组织进行分析。在105例有纵隔淋巴结转移疾病的患者中,有58例可确定治疗引起的肿瘤消退程度。
关于HER2/neu表达,16例淋巴结活检(15.2%)显示为1+、2+或3+结果。其中5例在FISH分析中显示扩增(4.8%)。在44例相应的切除标本中,Hercep-Test显示13例肿瘤(29.5%)为1+、2+或3+结果。其中2例患者在FISH分析中显示HER2/neu扩增(4.5%)。在HER2/neu表达肿瘤的患者中,可证明治疗引起的肿瘤消退程度有较轻的趋势。比较治疗前和手术后的结果,在新辅助治疗过程中有选择HER2/neu表达肿瘤组织的微弱趋势。
只有有限的局部晚期NSCLC亚组符合抗HER2/neu治疗的生物学要求。HER2/neu阳性肿瘤似乎对化疗和放疗相对耐药,在相应的切除标本中这些病例均无病理完全缓解或至少近完全缓解。这一观察结果需要在大型随机对照研究中得到证实。