PMID- 25529354 OWN - NLM STAT- MEDLINE DCOM- 20150409 LR - 20220321 IS - 1934-6638 (Electronic) IS - 1934-662X (Linking) VI - 123 IP - 2 DP - 2015 Feb TI - Detection of ALK rearrangements in malignant pleural effusion cell blocks from patients with advanced non-small cell lung cancer: a comparison of Ventana immunohistochemistry and fluorescence in situ hybridization. PG - 117-22 LID - 10.1002/cncy.21510 [doi] AB - BACKGROUND: Surgical resections or tumor biopsies are often not available for patients with late-stage non-small cell lung cancer (NSCLC). Cytological specimens, such as malignant pleural effusion (MPE) cell blocks, are critical for molecular testing. Currently, diagnostic methods to identify anaplastic lymphoma kinase (ALK) rearrangements include fluorescence in situ hybridization (FISH), real-time reverse transcriptase-polymerase chain reaction (RT-PCR), and immunohistochemistry (IHC). In the current study, the authors compared Ventana ALK IHC assays and ALK FISH to detect ALK rearrangements in MPE cell blocks from patients with advanced NSCLC. METHODS: The ALK IHC assay and ALK FISH were performed on 63 MPE cell blocks. RT-PCR analysis was performed as additional validation in cases in which a discrepancy was observed between the IHC assay and FISH results. RESULTS: The Ventana ALK IHC assay was found to be informative for all 63 samples, and 8 cases were positive. Fifty-eight cases were interpretable for FISH detection, and 6 were positive. The concordance between IHC and FISH was 100% among the 58 cases. Of the 5 uninterpretable ALK FISH cases, 2 cases and 3 cases, respectively, were ALK IHC positive and negative. One of the 2 ALK IHC-positive cases also demonstrated a positive result in the RT-PCR assay and the patient benefited from crizotinib treatment. CONCLUSIONS: MPE cell blocks can be used successfully for the detection of ALK rearrangement when tumor tissue is not available. The Ventana ALK IHC assay is an effective screening method for ALK rearrangement in MPE cell blocks from patients with advanced NSCLC, demonstrating high agreement with FISH results. CI - (c) 2014 American Cancer Society. FAU - Wang, Weiya AU - Wang W AD - Department of Pathology, West China Hospital of Sichuan University, Chengdu, China. FAU - Tang, Yuan AU - Tang Y FAU - Li, Jinnan AU - Li J FAU - Jiang, Lili AU - Jiang L FAU - Jiang, Yong AU - Jiang Y FAU - Su, Xueying AU - Su X LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20141219 PL - United States TA - Cancer Cytopathol JT - Cancer cytopathology JID - 101499453 RN - EC 2.7.10.1 (ALK protein, human) RN - EC 2.7.10.1 (Anaplastic Lymphoma Kinase) RN - EC 2.7.10.1 (Receptor Protein-Tyrosine Kinases) SB - IM MH - Anaplastic Lymphoma Kinase MH - Humans MH - In Situ Hybridization, Fluorescence MH - Lung Neoplasms/*metabolism/pathology MH - Pleural Effusion, Malignant/*metabolism MH - Receptor Protein-Tyrosine Kinases/*metabolism MH - Small Cell Lung Carcinoma/*metabolism/pathology OTO - NOTNLM OT - Ventana immunohistochemistry (IHC) assay OT - anaplastic lymphoma kinase (ALK) OT - cell block OT - fluorescence OT - fluorescence in situ hybridization (FISH) OT - malignant pleural effusion OT - non-small cell lung cancer EDAT- 2014/12/23 06:00 MHDA- 2015/04/10 06:00 CRDT- 2014/12/23 06:00 PHST- 2014/09/10 00:00 [received] PHST- 2014/11/20 00:00 [revised] PHST- 2014/12/01 00:00 [accepted] PHST- 2014/12/23 06:00 [entrez] PHST- 2014/12/23 06:00 [pubmed] PHST- 2015/04/10 06:00 [medline] AID - 10.1002/cncy.21510 [doi] PST - ppublish SO - Cancer Cytopathol. 2015 Feb;123(2):117-22. doi: 10.1002/cncy.21510. Epub 2014 Dec 19.