Literature DB >> 31335390

Clinical Applications of Next-Generation Sequencing in Precision Oncology.

Chris A Karlovich1, P Mickey Williams.   

Abstract

The ability of next-generation sequencing (NGS) to comprehensively assess the molecular profile of a tumor specimen has transformed the clinical testing landscape in oncology. Accordingly, recent years have seen broad uptake of clinical NGS to inform cancer patient management. However, significant challenges remain. The annotation and clinical interpretation of variants identified by NGS tests often require rigorous review and may vary between laboratories. While a clearer regulatory path has emerged, reimbursement for NGS tests remains a subject of continuing debate. Basket clinical studies such as the National Cancer Institute Molecular Analysis of Therapy Choice are evaluating the degree to which matching of a targeted therapy to tumor molecular profile by NGS can be applied independently of tissue histology. Newer applications of NGS such as for circulating tumor DNA testing and to identify novel RNA fusion driver events continue to expand its clinical utility.

Entities:  

Year:  2019        PMID: 31335390      PMCID: PMC6658137          DOI: 10.1097/PPO.0000000000000385

Source DB:  PubMed          Journal:  Cancer J        ISSN: 1528-9117            Impact factor:   3.360


  34 in total

1.  Using SIFT and PolyPhen to predict loss-of-function and gain-of-function mutations.

Authors:  Sarah E Flanagan; Ann-Marie Patch; Sian Ellard
Journal:  Genet Test Mol Biomarkers       Date:  2010-08

Review 2.  The emerging complexity of gene fusions in cancer.

Authors:  Fredrik Mertens; Bertil Johansson; Thoas Fioretos; Felix Mitelman
Journal:  Nat Rev Cancer       Date:  2015-06       Impact factor: 60.716

3.  CTLA4 blockade broadens the peripheral T-cell receptor repertoire.

Authors:  Lidia Robert; Jennifer Tsoi; Xiaoyan Wang; Ryan Emerson; Blanca Homet; Thinle Chodon; Stephen Mok; Rong Rong Huang; Alistair J Cochran; Begoña Comin-Anduix; Richard C Koya; Thomas G Graeber; Harlan Robins; Antoni Ribas
Journal:  Clin Cancer Res       Date:  2014-02-28       Impact factor: 12.531

4.  Identification of Factors Affecting the Success of Next-Generation Sequencing Testing in Solid Tumors.

Authors:  Rashmi S Goswami; Rajyalakshmi Luthra; Rajesh R Singh; Keyur P Patel; Mark J Routbort; Kenneth D Aldape; Hui Yao; Hyvan D Dang; Bedia A Barkoh; Jawad Manekia; L Jeffrey Medeiros; Sinchita Roy-Chowdhuri; John Stewart; Russell R Broaddus; Hui Chen
Journal:  Am J Clin Pathol       Date:  2016-02-12       Impact factor: 2.493

5.  Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing.

Authors:  Garrett M Frampton; Alex Fichtenholtz; Geoff A Otto; Kai Wang; Sean R Downing; Jie He; Michael Schnall-Levin; Jared White; Eric M Sanford; Peter An; James Sun; Frank Juhn; Kristina Brennan; Kiel Iwanik; Ashley Maillet; Jamie Buell; Emily White; Mandy Zhao; Sohail Balasubramanian; Selmira Terzic; Tina Richards; Vera Banning; Lazaro Garcia; Kristen Mahoney; Zac Zwirko; Amy Donahue; Himisha Beltran; Juan Miguel Mosquera; Mark A Rubin; Snjezana Dogan; Cyrus V Hedvat; Michael F Berger; Lajos Pusztai; Matthias Lechner; Chris Boshoff; Mirna Jarosz; Christine Vietz; Alex Parker; Vincent A Miller; Jeffrey S Ross; John Curran; Maureen T Cronin; Philip J Stephens; Doron Lipson; Roman Yelensky
Journal:  Nat Biotechnol       Date:  2013-10-20       Impact factor: 54.908

6.  Analytical Validation and Application of a Targeted Next-Generation Sequencing Mutation-Detection Assay for Use in Treatment Assignment in the NCI-MPACT Trial.

Authors:  Chih-Jian Lih; David J Sims; Robin D Harrington; Eric C Polley; Yingdong Zhao; Michele G Mehaffey; Thomas D Forbes; Biswajit Das; William D Walsh; Vivekananda Datta; Kneshay N Harper; Courtney H Bouk; Lawrence V Rubinstein; Richard M Simon; Barbara A Conley; Alice P Chen; Shivaani Kummar; James H Doroshow; Paul M Williams
Journal:  J Mol Diagn       Date:  2015-11-18       Impact factor: 5.568

7.  PD-1 blockade induces responses by inhibiting adaptive immune resistance.

Authors:  Paul C Tumeh; Christina L Harview; Jennifer H Yearley; I Peter Shintaku; Emma J M Taylor; Lidia Robert; Bartosz Chmielowski; Marko Spasic; Gina Henry; Voicu Ciobanu; Alisha N West; Manuel Carmona; Christine Kivork; Elizabeth Seja; Grace Cherry; Antonio J Gutierrez; Tristan R Grogan; Christine Mateus; Gorana Tomasic; John A Glaspy; Ryan O Emerson; Harlan Robins; Robert H Pierce; David A Elashoff; Caroline Robert; Antoni Ribas
Journal:  Nature       Date:  2014-11-27       Impact factor: 49.962

8.  Evaluation of Hybridization Capture Versus Amplicon-Based Methods for Whole-Exome Sequencing.

Authors:  Eric Samorodnitsky; Benjamin M Jewell; Raffi Hagopian; Jharna Miya; Michele R Wing; Ezra Lyon; Senthilkumar Damodaran; Darshna Bhatt; Julie W Reeser; Jharna Datta; Sameek Roychowdhury
Journal:  Hum Mutat       Date:  2015-07-15       Impact factor: 4.878

9.  The Path(way) Less Traveled: A Pathway-Oriented Approach to Providing Information about Precision Cancer Medicine on My Cancer Genome.

Authors:  Alexandria D Taylor; Christine M Micheel; Ingrid A Anderson; Mia A Levy; Christine M Lovly
Journal:  Transl Oncol       Date:  2016-04       Impact factor: 4.243

10.  Analytical and Clinical Validation of a Digital Sequencing Panel for Quantitative, Highly Accurate Evaluation of Cell-Free Circulating Tumor DNA.

Authors:  Richard B Lanman; Stefanie A Mortimer; Oliver A Zill; Dragan Sebisanovic; Rene Lopez; Sibel Blau; Eric A Collisson; Stephen G Divers; Dave S B Hoon; E Scott Kopetz; Jeeyun Lee; Petros G Nikolinakos; Arthur M Baca; Bahram G Kermani; Helmy Eltoukhy; AmirAli Talasaz
Journal:  PLoS One       Date:  2015-10-16       Impact factor: 3.240

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  3 in total

1.  Private Payer and Medicare Coverage for Circulating Tumor DNA Testing: A Historical Analysis of Coverage Policies From 2015 to 2019.

Authors:  Michael P Douglas; Stacy W Gray; Kathryn A Phillips
Journal:  J Natl Compr Canc Netw       Date:  2020-07       Impact factor: 11.908

2.  Germline Testing Data Validate Inferences of Mutational Status for Variants Detected From Tumor-Only Sequencing.

Authors:  Nahed Jalloul; Israel Gomy; Samantha Stokes; Alexander Gusev; Bruce E Johnson; Neal I Lindeman; Laura Macconaill; Shridar Ganesan; Judy E Garber; Hossein Khiabanian
Journal:  JCO Precis Oncol       Date:  2021-11-17

3.  SmMIP-tools: a computational toolset for processing and analysis of single-molecule molecular inversion probes derived data.

Authors:  Jessie J F Medeiros; Jose-Mario Capo-Chichi; Liran I Shlush; John E Dick; Andrea Arruda; Mark D Minden; Sagi Abelson
Journal:  Bioinformatics       Date:  2022-02-12       Impact factor: 6.937

  3 in total

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