Division of Medical Oncology and Department of Pathology, University of Colorado-Denver, 1665 North Ursula Street, Aurora, CO 80045-0508, USA.
Clin Cancer Res. 2010 Nov 15;16(22):5581-90. doi: 10.1158/1078-0432.CCR-10-0851. Epub 2010 Nov 9.
Anaplastic lymphoma kinase (ALK) rearrangements, associated with sensitivity to an experimental ALK/MET inhibitor, occur in 3% to 5% of non-small cell lung cancers. Intratumoral fluorescence in situ hybridization (FISH) heterogeneity has been reported. We explored the heterogeneity basis, the requirements for accurately determining ALK FISH positivity, and the effect of enriching the tested population using clinical and molecular factors.
Lung cancer patients were screened by ALK and MET FISH and for EGFR and KRAS mutations.
Thirteen ALK-positive cases were identified from 73 screened patients. Gene copy number increases occurred together with classic rearrangements. All positive cases were adenocarcinomas, 12 were EGFR/KRAS wild-type, and 1 had a coexistent EGFR exon 20 mutation. No association with MET amplification occurred. ALK positivity was associated with <10-pack-year smoking status (P = 0.0004). Among adenocarcinomas, without KRAS or EGFR mutations, with <10-pack-year history, 44.8% of cases were ALK positive. ALK FISH positivity was heterogeneous, but mean values in tumor areas from ALK-positive patients (54% of cells; range, 22-87%) were significantly higher than in adjacent normal tissue or tumor/normal areas from ALK-negative patients (mean, 5-7%). Contiguous sliding field analyses showed diffuse heterogeneity without evidence of focal ALK rearrangements. One hundred percent sensitivity and specificity occurred when four or more fields (∼60 cells) were counted.
Intratumoral ALK FISH heterogeneity reflects technique, not biology. The clinical activity of ALK/MET inhibitors in ALK-positive patients probably reflects ALK, but not MET, activity. Prescreening by histology, EGFR/KRAS mutations, and smoking status dramatically increases the ALK-positive hit rate compared with unselected series.
间变性淋巴瘤激酶(ALK)重排与对实验性 ALK/MET 抑制剂的敏感性相关,在 3%至 5%的非小细胞肺癌中发生。已有报道称肿瘤内荧光原位杂交(FISH)存在异质性。我们探讨了异质性的基础、准确确定 ALK FISH 阳性的要求,以及使用临床和分子因素富集检测人群对其的影响。
通过 ALK 和 MET FISH 以及 EGFR 和 KRAS 突变筛选肺癌患者。
从 73 例筛选患者中鉴定出 13 例 ALK 阳性病例。基因拷贝数增加与经典重排同时发生。所有阳性病例均为腺癌,12 例为 EGFR/KRAS 野生型,1 例同时存在 EGFR 外显子 20 突变。未发现与 MET 扩增有关。ALK 阳性与<10 包年吸烟史有关(P = 0.0004)。在腺癌中,无 KRAS 或 EGFR 突变,吸烟史<10 包年,44.8%的病例为 ALK 阳性。ALK FISH 存在异质性,但 ALK 阳性患者肿瘤区域的平均值(54%的细胞;范围,22-87%)明显高于 ALK 阴性患者的相邻正常组织或肿瘤/正常区域(平均值,5-7%)。连续滑动字段分析显示无局灶性 ALK 重排的弥漫性异质性。当计数四个或更多字段(约 60 个细胞)时,可实现 100%的灵敏度和特异性。
肿瘤内 ALK FISH 异质性反映的是技术,而不是生物学。ALK 阳性患者中 ALK/MET 抑制剂的临床活性可能反映的是 ALK 活性,而不是 MET 活性。通过组织学、EGFR/KRAS 突变和吸烟状况进行预筛选,与未筛选的系列相比,显著提高了 ALK 阳性的检出率。