| Title: |
Discovery of a putative blood-based protein signature associated with response to ALK tyrosine kinase inhibition |
| Authors: |
Couëtoux du Tertre, Mathilde; Marques, Maud; McNamara, Suzan; Gambaro, Karen; Hoffert, Cyrla; Tremblay, Lise; Bouchard, Nicole; Diaconescu, Razvan; Blais, Normand; Couture, Christian; Pelsser, Vincent; Wang, Hangjun; McIntosh, Laura; Hindie, Valérie; Parent, Stephane; Cortes, Laetitia; Breton, Yannick-André; Pottiez, Gwenael; Croteau, Pascal; Higenell, Valerie; Izzi, Luisa; Spatz, Alan; Cohen, Victor; Batist, Gerald; Agulnik, Jason |
| Contributors: |
Personalized Medicine Partnership for Cancer; Pfizer Canada; Fonds de Recherche du Québec - Santé |
| Source: |
Clinical Proteomics ; volume 17, issue 1 ; ISSN 1542-6416 1559-0275 |
| Publisher Information: |
Springer Science and Business Media LLC |
| Publication Year: |
2020 |
| Description: |
Background ALK tyrosine kinase inhibition has become a mainstay in the clinical management of ALK fusion positive NSCLC patients. Although ALK mutations can reliably predict the likelihood of response to ALK tyrosine kinase inhibitors (TKIs) such as crizotinib, they cannot reliably predict response duration or intrinsic/extrinsic therapeutic resistance. To further refine the application of personalized medicine in this indication, this study aimed to identify prognostic proteomic biomarkers in ALK fusion positive NSCLC patients to crizotinib. Methods Twenty-four patients with advanced NSCLC harboring ALK fusion were administered crizotinib in a phase IV trial which included blood sampling prior to treatment. Targeted proteomics of 327 proteins using MRM-MS was used to measure plasma levels at baseline (including pre-treatment and early treatment blood samples) and assess potential clinical association. Results Patients were categorized by duration of response: long-term responders [PFS ≥ 24 months (n = 7)], normal responders [3 < PFS < 24 months (n = 10)] and poor responders [PFS ≤ 3 months (n = 5)]. Several proteins were identified as differentially expressed between long-term responders and poor responders, including DPP4, KIT and LUM. Next, using machine learning algorithms, we evaluated the classification potential of 40 proteins. Finally, by integrating the different analytic methods, we selected 22 proteins as potential candidates for a blood-based prognostic signature of response to crizotinib in NSCLC patients harboring ALK fusion. Conclusion In conjunction with ALK mutation, the expression of this proteomic signature may represent a liquid biopsy-based marker of long-term response to crizotinib in NSCLC. Expanding the utility of prognostic biomarkers of response duration could influence choice of therapy, therapeutic sequencing, and potentially the need for alternative or combination therapy. Trial registration ClinicalTrials.gov, NCT02041468. Registered 22 January 2014, ... |
| Document Type: |
article in journal/newspaper |
| Language: |
English |
| DOI: |
10.1186/s12014-020-9269-6 |
| DOI: |
10.1186/s12014-020-9269-6.pdf |
| DOI: |
10.1186/s12014-020-9269-6/fulltext.html |
| Availability: |
http://dx.doi.org/10.1186/s12014-020-9269-6; https://link.springer.com/content/pdf/10.1186/s12014-020-9269-6.pdf; https://link.springer.com/article/10.1186/s12014-020-9269-6/fulltext.html |
| Rights: |
https://creativecommons.org/licenses/by/4.0 ; https://creativecommons.org/licenses/by/4.0 |
| Accession Number: |
edsbas.F0A47ECF |
| Database: |
BASE |