Best practices in epidermal growth factor receptor T790M testing for advanced non-small-cell lung cancer in Hong Kong

被引:0
作者
Nyaw, Jonathan S. F. [1 ]
Cheung, K. M. [2 ]
Hioe, F. [3 ]
Kam, Michael T. Y. [4 ]
Lau, Johnny K. S. [5 ]
Lau, Y. M. [6 ]
Leung, Dennis K. C. [5 ]
Lim, Fiona M. Y. [7 ]
机构
[1] Tuen Mun Hosp, Dept Clin Oncol, Hong Kong, Peoples R China
[2] Queen Elizabeth Hosp, Dept Clin Oncol, Hong Kong, Peoples R China
[3] Pamela Youde Nethersole Eastern Hosp, Dept Pathol, Hong Kong, Peoples R China
[4] Pamela Youde Nethersole Eastern Hosp, Dept Clin Oncol, Hong Kong, Peoples R China
[5] Queen Mary Hosp, Dept Clin Oncol, Hong Kong, Peoples R China
[6] Prince Wales Hosp, Dept Clin Oncol, Hong Kong, Peoples R China
[7] Princess Margaret Hosp, Dept Oncol, Hong Kong, Peoples R China
关键词
TYROSINE KINASE INHIBITORS; ACQUIRED-RESISTANCE; THERAPY; PROGRESSION; MANAGEMENT; BIOPSY; CTDNA;
D O I
10.12809/hkmj219632
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The T790M mutation in the epidermal growth factor receptor gene causes most acquired resistance to firstor second-line epidermal growth factor receptor- tyrosine kinase inhibitors in advanced non-smallcell lung cancer. The results of T790M testing can guide subsequent treatment. Despite the availability of guidelines from international organisations, T790M testing practices in Hong Kong must be streamlined and adapted to the Hospital Authority setting. To address this issue, a panel of experts in oncology and pathology met for discussion of key topics regarding T790M testing practices in Hong Kong, including the appropriate timing of testing and re-testing, as well as optimal testing methods. All panel members voted on the results of the discussion to achieve consensus. Items supported by a majority vote were adopted as consensus statements regarding current best practices for T790M testing in Hong Kong. Among the topics discussed, the panel agreed that T790M testing should be initiated upon radiological progression, including symptomatic disease progression or central nervous system-only progression. The experts also preferred initial testing with liquid biopsy, using the widely available digital polymerase chain reaction platform. This document provides the final consensus statements, as well asa testing and treatment workflow, for clinicians in Hong Kong to use as guidance in T790M testing.
引用
收藏
页码:240 / 246
页数:7
相关论文
共 35 条
  • [1] Osimertinib for Patients With Leptomeningeal Metastases Associated With EGFR T790M-Positive Advanced NSCLC: The AURA Leptomeningeal Metastases Analysis
    Ahn, Myung-Ju
    Chiu, Chao-Hua
    Cheng, Ying
    Han, Ji-Youn
    Goldberg, Sarah B.
    Greystoke, Alastair
    Crawford, Jeffrey
    Zhao, Yanqiu
    Huang, Xiangning
    Johnson, Martin
    Vishwanathan, Karthick
    Yates, James W. T.
    Brown, Andrew P.
    Mendoza-Naranjo, Ariadna
    Mok, Tony
    [J]. JOURNAL OF THORACIC ONCOLOGY, 2020, 15 (04) : 637 - 648
  • [2] Tumour heterogeneity in the clinic
    Bedard, Philippe L.
    Hansen, Aaron R.
    Ratain, Mark J.
    Siu, Lillian L.
    [J]. NATURE, 2013, 501 (7467) : 355 - 364
  • [3] EGFR Mutations in Cell-free Plasma DNA from Patients with Advanced Lung Adenocarcinoma: Improved Detection by Droplet Digital PCR
    Buder, Anna
    Setinek, Ulrike
    Hochmair, Maximilian J.
    Schwab, Sophia
    Kirchbacher, Klaus
    Keck, Andrea
    Burghuber, Otto C.
    Pirker, Robert
    Filipits, Martin
    [J]. TARGETED ONCOLOGY, 2019, 14 (02) : 197 - 203
  • [4] Acquired Resistance to First-Line Afatinib and the Challenges of Prearranged Progression Biopsies
    Campo, Meghan
    Gerber, David
    Gainor, Justin F.
    Heist, Rebecca S.
    Temel, Jennifer S.
    Shaw, Alice T.
    Fidias, Panos
    Muzikansky, Alona
    Engelman, Jeffrey A.
    Sequist, Lecia V.
    [J]. JOURNAL OF THORACIC ONCOLOGY, 2016, 11 (11) : 2022 - 2026
  • [5] Feasibility and clinical impact of re-biopsy in advanced non small-cell lung cancer: A prospective multicenter study in a real-world setting (GFPC study 12-01)
    Chouaid, Christos
    Dujon, Cecile
    Do, Pascal
    Monnet, Isabelle
    Madroszyk, Anne
    Le Caer, Herve
    Auliac, Jean Bernard
    Berard, Henri
    Thomas, Pascal
    Lena, Herve
    Robinet, Gilles
    Baize, Nathalie
    Bizieux-Thaminy, Acya
    Fraboulet, Gislaine
    Locher, Chrystele
    Le Treut, Jacques
    Hominal, Stephane
    Vergnenegre, Alain
    [J]. LUNG CANCER, 2014, 86 (02) : 170 - 173
  • [6] Acquired Resistance to Targeted Therapies Against Oncogene-Driven Non-Small-Cell Lung Cancer: Approach to Subtyping Progressive Disease and Clinical Implications
    Gandara, David R.
    Li, Tianhong
    Lara, Primo N.
    Kelly, Karen
    Riess, Jonathan W.
    Redman, Mary W.
    Mack, Philip C.
    [J]. CLINICAL LUNG CANCER, 2014, 15 (01) : 1 - 6
  • [7] Digital PCR-Based Detection of EGFR Mutations in Paired Plasma and CSF Samples of Lung Adenocarcinoma Patients with Central Nervous System Metastases
    Huang, Ruofan
    Xu, Xiao
    Li, Dong
    Chen, Kun
    Zhan, Qiong
    Ge, Mengxi
    Zhou, Xinli
    Liang, Xiaohua
    Guan, Ming
    [J]. TARGETED ONCOLOGY, 2019, 14 (03) : 343 - 350
  • [8] Clinical Definition of Acquired Resistance to Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Non-Small-Cell Lung Cancer
    Jackman, David
    Pao, William
    Riely, Gregory J.
    Engelman, Jeffrey A.
    Kris, Mark G.
    Jaenne, Pasi A.
    Lynch, Thomas
    Johnson, Bruce E.
    Miller, Vincent A.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (02) : 357 - 360
  • [9] Australian recommendations for EGFR T790M testing in advanced non-small cell lung cancer
    John, Thomas
    Bowden, Jeffrey J.
    Clarke, Stephen
    Fox, Stephen B.
    Garrett, Kerryn
    Horwood, Keith
    Karapetis, Christos S.
    [J]. ASIA-PACIFIC JOURNAL OF CLINICAL ONCOLOGY, 2017, 13 (04) : 296 - 303
  • [10] EGFR mutation status in tumour-derived DNA from pleural effusion fluid is a practical basis for predicting the response to gefitinib
    Kimura, H.
    Fujiwara, Y.
    Sone, T.
    Kunitoh, H.
    Tamura, T.
    Kasahara, K.
    Nishio, K.
    [J]. BRITISH JOURNAL OF CANCER, 2006, 95 (10) : 1390 - 1395