» Articles » PMID: 29890761

Current and Future Molecular Testing in NSCLC, What Can We Expect from New Sequencing Technologies?

Overview
Journal J Clin Med
Specialty General Medicine
Date 2018 Jun 13
PMID 29890761
Citations 37
Authors
Affiliations
Soon will be listed here.
Abstract

Recent changes in lung cancer care, including new approvals in first line and the introduction of high-throughput molecular technologies in routine testing led us to question ourselves on how deeper molecular testing may be helpful for the optimal use of targeted drugs. In this article, we review recent results in the scope of personalized medicine in lung cancer. We discuss biomarkers that have a therapeutic predictive value in lung cancer with a focus on recent changes and on the clinical value of large scale sequencing strategies. We review the use of second- and third-generation EGFR and ALK inhibitors with a focus on secondary resistance alterations. We discuss anti-BRAF and anti-MEK combo, emerging biomarkers as NRG1 and NTRKs fusions and immunotherapy. Finally, we discuss the different technical issues of comprehensive molecular profiling and show how large screenings might refine the prediction value of individual markers. Based on a review of recent publications (2012⁻2018), we address promising approaches for the treatment of patients with lung cancers and the technical challenges associated with the identification of new predictive markers.

Citing Articles

Biomarker testing in lung cancer: from bench to bedside.

Batra U, Nathany S Oncol Rev. 2025; 18():1445826.

PMID: 39834530 PMC: 11743711. DOI: 10.3389/or.2024.1445826.


Evaluating circulating cell-free DNA and DNA integrity index as biomarkers in non-small cell lung cancer.

Ezzeldin N, El-Lebedy D, Hassan M, Shalaby A, Hussein S, Gharib A J Egypt Natl Canc Inst. 2024; 36(1):21.

PMID: 38880832 DOI: 10.1186/s43046-024-00219-1.


Droplet Digital PCR as a Molecular Tool for the Detection of the T790M Mutation in NSCLC Patients with the Activating Mutations.

Durgut S, Salihefendic L, Pecar D, ceko I, Mulahuseinovic N, Izmirlija M Balkan J Med Genet. 2024; 26(2):21-26.

PMID: 38482255 PMC: 10932593. DOI: 10.2478/bjmg-2023-0020.


Serum cytokine levels and other associated factors as possible immunotherapeutic targets and prognostic indicators for lung cancer.

Zhao Y, Jia S, Zhang K, Zhang L Front Oncol. 2023; 13:1064616.

PMID: 36874133 PMC: 9977806. DOI: 10.3389/fonc.2023.1064616.


Clinical Response to Seribantumab, an Anti-Human Epidermal Growth Factor Receptor-3 Immunoglobulin 2 Monoclonal Antibody, in a Patient With Metastatic Pancreatic Ductal Adenocarcinoma Harboring an Fusion.

Thavaneswaran S, Chan W, Asghari R, Grady J, Deegan M, Jansen V JCO Precis Oncol. 2022; 6:e2200263.

PMID: 36455193 PMC: 9812631. DOI: 10.1200/PO.22.00263.


References
1.
Dong Z, Zhong W, Zhang X, Su J, Xie Z, Liu S . Potential Predictive Value of and Mutation Status for Response to PD-1 Blockade Immunotherapy in Lung Adenocarcinoma. Clin Cancer Res. 2017; 23(12):3012-3024. DOI: 10.1158/1078-0432.CCR-16-2554. View

2.
Kobayashi Y, Mitsudomi T . Not all epidermal growth factor receptor mutations in lung cancer are created equal: Perspectives for individualized treatment strategy. Cancer Sci. 2016; 107(9):1179-86. PMC: 5021039. DOI: 10.1111/cas.12996. View

3.
Peters S, Camidge D, Shaw A, Gadgeel S, Ahn J, Kim D . Alectinib versus Crizotinib in Untreated ALK-Positive Non-Small-Cell Lung Cancer. N Engl J Med. 2017; 377(9):829-838. DOI: 10.1056/NEJMoa1704795. View

4.
Mambetsariev I, Vora L, Yu K, Salgia R . Effective osimertinib treatment in a patient with discordant T790 M mutation detection between liquid biopsy and tissue biopsy. BMC Cancer. 2018; 18(1):314. PMC: 5863467. DOI: 10.1186/s12885-018-4222-z. View

5.
Imielinski M, Berger A, Hammerman P, Hernandez B, Pugh T, Hodis E . Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing. Cell. 2012; 150(6):1107-20. PMC: 3557932. DOI: 10.1016/j.cell.2012.08.029. View