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      Inconsistent Intersample ALK FISH Results in Patients with Lung Cancer: Analysis of Potential Causes

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          Abstract

          ALK FISH analyses of multiple specimens occasionally yield inconsistent intersample results in lung cancer patients, posing clinical challenges requiring intensive analysis of all potential causative pre- and post- analytic factors. In this study, 19 patients (8M/11F) with inconsistent intersample ALK FISH results were analyzed, representing 4.9% of patients assessed ≥ twice in our institution. Fifteen patients received ALK tyrosine kinase inhibitor(s) (TKIs). Nine patients died, and ten were alive for 8 to 74-month follow-ups (median, 40 months). Through strict and stringent laboratory and case-review policies, all postanalytic factors were excluded. Correlating clinical information, ALK results obtained by RNA sequencing (RNA-seq) and other concurrent tests, several pre-analytic factors were determined. A suboptimal specimen was likely the cause in three patients, supported by the failure of one or more concurrent tests or discrepant results between FISH and RNA-seq. ALK inhibition by TKIs might have been responsible for the change of ALK status from positive to negative in eight patients. Other potential explanations include the existence of multiple primary lung cancer lesions, tumor heterogeneity, and the clonal evolution of tumor cells, related or not to ALK TKI therapy. This study is helpful for both pathologists and clinicians encountering inconsistent and/or discrepant intersample results.

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          Most cited references21

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          Brigatinib versus Crizotinib in ALK-Positive Non–Small-Cell Lung Cancer

          Brigatinib, a next-generation anaplastic lymphoma kinase (ALK) inhibitor, has robust efficacy in patients with ALK-positive non-small-cell lung cancer (NSCLC) that is refractory to crizotinib. The efficacy of brigatinib, as compared with crizotinib, in patients with advanced ALK-positive NSCLC who have not previously received an ALK inhibitor is unclear.
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            Resensitization to Crizotinib by the LorlatinibALKResistance Mutation L1198F

            In a patient who had metastatic anaplastic lymphoma kinase (ALK)-rearranged lung cancer, resistance to crizotinib developed because of a mutation in the ALK kinase domain. This mutation is predicted to result in a substitution of cysteine by tyrosine at amino acid residue 1156 (C1156Y). Her tumor did not respond to a second-generation ALK inhibitor, but it did respond to lorlatinib (PF-06463922), a third-generation inhibitor. When her tumor relapsed, sequencing of the resistant tumor revealed an ALK L1198F mutation in addition to the C1156Y mutation. The L1198F substitution confers resistance to lorlatinib through steric interference with drug binding. However, L1198F paradoxically enhances binding to crizotinib, negating the effect of C1156Y and resensitizing resistant cancers to crizotinib. The patient received crizotinib again, and her cancer-related symptoms and liver failure resolved. (Funded by Pfizer and others; ClinicalTrials.gov number, NCT01970865.).
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              Comprehensive T cell repertoire characterization of non-small cell lung cancer

              Immunotherapy targeting T cells is increasingly utilized to treat solid tumors including non-small cell lung cancer (NSCLC). This requires a better understanding of the T cells in the lungs of patients with NSCLC. Here, we report T cell repertoire analysis in a cohort of 236 early-stage NSCLC patients. T cell repertoire attributes are associated with clinicopathologic features, mutational and immune landscape. A considerable proportion of the most prevalent T cells in tumors are also prevalent in the uninvolved tumor-adjacent lungs and appear specific to shared background mutations or viral infections. Patients with higher T cell repertoire homology between the tumor and uninvolved tumor-adjacent lung, suggesting a less tumor-focused T cell response, exhibit inferior survival. These findings indicate that a concise understanding of antigens and T cells in NSCLC is needed to improve therapeutic efficacy and reduce toxicity with immunotherapy, particularly adoptive T cell therapy.
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                Author and article information

                Journal
                Cancers (Basel)
                Cancers (Basel)
                cancers
                Cancers
                MDPI
                2072-6694
                14 July 2020
                July 2020
                : 12
                : 7
                : 1903
                Affiliations
                Departments of Hematopathology, Pathology and Thoracic/Head and Neck Medical Oncology, School of Health Professions, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030, USA; HChen7@ 123456mdanderson.org (H.C.); LHong@ 123456mdanderson.org (L.H.); GTang@ 123456mdanderson.org (G.T.); GAToruner@ 123456mdanderson.org (G.A.T.); WWang13@ 123456mdanderson.org (W.W.); SRoy2@ 123456mdanderson.org (S.R.C.); WYin1@ 123456mdanderson.org (W.Y.); HJung2@ 123456mdanderson.org (H.S.J.); jungu@ 123456mdanderson.org (J.G.); mark.routbort@ 123456mdanderson.org (M.J.R.); JZhang20@ 123456mdanderson.org (J.Z.); JKhoury@ 123456mdanderson.org (J.D.K.); ljmedeiros@ 123456mdanderson.org (L.J.M.)
                Author notes
                [* ]Correspondence: ztang@ 123456mdanderson.org ; Tel.: +1-713-563-4369
                Author information
                https://orcid.org/0000-0002-8079-9945
                https://orcid.org/0000-0001-6553-3279
                https://orcid.org/0000-0002-5305-6337
                https://orcid.org/0000-0003-2621-3584
                https://orcid.org/0000-0001-6577-8006
                Article
                cancers-12-01903
                10.3390/cancers12071903
                7409019
                32674491
                c6cc30f2-4895-433f-961c-454ad4a7bcf1
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 22 May 2020
                : 10 July 2020
                Categories
                Article

                lung cancer,alk,fluorescence in situ hybridization (fish),next-generation sequencing (ngs),rna sequencing (rna-seq),tyrosine kinase inhibitor (tki)

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