Primary resistance to ALK inhibitors in KLC1/ALK-rearranged pleural metastatic lung adenocarcinoma: a case report

被引:4
作者
Siblini, Laura [1 ,3 ]
Schott, Roland [1 ]
Trensz, Philippe [1 ]
Pencreach, Erwan [2 ]
Bender, Laura [1 ]
机构
[1] Inst Cancerol Strasbourg Europe, Med Oncol Dept, Strasbourg, France
[2] Univ Hosp Strasbourg, Mol Biol Dept, Strasbourg, France
[3] Inst Cancerol Strasbourg Europe, Med Oncol Dept, 17 Rue Albert Calmette, F-67200 Strasbourg, France
关键词
Kinesin light chain 1/anaplastic lymphoma kinase rearrangement (KLC1/ALK rearrangement); non-small-lung carcinoma; primary resistance; case report; TYROSINE KINASE INHIBITOR; CRIZOTINIB; CANCER; FUSION; BRIGATINIB; GENE;
D O I
10.21037/tlcr-23-482
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Anaplastic lymphoma kinase (ALK) rearrangement confers sensitivity to second-and third generation ALK inhibitors, which have become the standard of care for ALK-positive non-small cell lung carcinoma (NSCLC). However, primary resistance to these inhibitors remains a rare and poorly understood phenomenon, especially in cases involving kinesin light chain 1 (KLC1)/ALK-rearranged metastatic NSCLC.Case Description: In this report, we present a unique and challenging case of primary resistance to second-and third-generation ALK tyrosine kinase inhibitors (TKIs) attributed to KLC1/ALK gene fusion partners in a patient with ALK-positive pleural metastatic NSCLC. The patient's disease progression was rapid and unresponsive to multiple lines of ALK-targeted therapies, including alectinib, brigatinib, and lorlatinib, underscoring the need for a deeper understanding of primary resistance mechanisms in such cases.Conclusions: The occurrence of primary resistance to ALK inhibitors in metastatic NSCLC with ALK rearrangement is an infrequent occurrence, and its underlying mechanisms remain elusive. This case emphasizes the importance of further research to elucidate the specific mechanisms of primary resistance to ALK TKIs in non-canonical ALK fusion partners like KLC1. Developing targeted therapies for such rare cases is a clinical challenge that warrants continued investigation and innovation in the field of precision oncology.
引用
收藏
页码:2342 / 2346
页数:5
相关论文
共 22 条
[1]   Brigatinib Versus Crizotinib in ALK Inhibitor-Naive Advanced ALK-Positive NSCLC: Final Results of Phase 3 ALTA-1L Trial [J].
Camidge, D. Ross ;
Kim, Hye Ryun ;
Ahn, Myung-Ju ;
Yang, James C. H. ;
Han, Ji-Youn ;
Hochmair, Maximilian J. ;
Lee, Ki Hyeong ;
Delmonte, Angelo ;
Campelo, Maria Rosario Garcia ;
Kim, Dong-Wan ;
Griesinger, Frank ;
Felip, Enriqueta ;
Califano, Raffaele ;
Spira, Alexander I. ;
Gettinger, Scott N. ;
Tiseo, Marcello ;
Lin, Huamao M. ;
Liu, Yuyin ;
Vranceanu, Florin ;
Niu, Huifeng ;
Zhang, Pingkuan ;
Popat, Sanjay .
JOURNAL OF THORACIC ONCOLOGY, 2021, 16 (12) :2091-2108
[2]   Genomic alterations in lung adenocarcinoma [J].
Devarakonda, Siddhartha ;
Morgensztern, Daniel ;
Govindan, Ramaswamy .
LANCET ONCOLOGY, 2015, 16 (07) :E342-E351
[3]   Serial liquid biopsies for detection of treatment failure and profiling of resistance mechanisms in KLC1-ALK-rearranged lung cancer [J].
Dietz, Steffen ;
Christopoulos, Petros ;
Gu, Lisa ;
Volckmar, Anna-Lena ;
Endris, Volker ;
Yuan, Zhao ;
Ogrodnik, Simon J. ;
Zemojtel, Tomasz ;
Heussel, Claus-Peter ;
Schneider, Marc A. ;
Meister, Michael ;
Muley, Thomas ;
Reck, Martin ;
Schlesner, Matthias ;
Thomas, Michael ;
Stenzinger, Albrecht ;
Sueltmann, Holger .
COLD SPRING HARBOR MOLECULAR CASE STUDIES, 2019, 5 (06)
[4]   ALK-rearrangement in non-small-cell lung cancer (NSCLC) [J].
Du, Xue ;
Shao, Yun ;
Qin, Hai-Feng ;
Tai, Yan-Hong ;
Gao, Hong-Jun .
THORACIC CANCER, 2018, 9 (04) :423-430
[5]   Oncogene-addicted metastatic non-small-cell lung cancer: ESMO Clinical Practice Guideline for diagnosis, treatment and follow-up [J].
Hendriks, L. E. ;
Kerr, K. M. ;
Menis, J. ;
Mok, T. S. ;
Nestle, U. ;
Passaro, A. ;
Peters, S. ;
Planchard, D. ;
Smit, E. F. ;
Solomon, B. J. ;
Veronesi, G. ;
Reck, M. .
ANNALS OF ONCOLOGY, 2023, 34 (04) :339-357
[6]   Coexistence of p16/CDKN2A homozygous deletions and activating EGFR mutations in lung adenocarcinoma patients signifies a poor response to EGFR-TKIs [J].
Jiang, Juhong ;
Gu, Yingying ;
Liu, Jing ;
Wu, Ruibin ;
Fu, Lin ;
Zhao, Jin ;
Guan, Yubao .
LUNG CANCER, 2016, 102 :101-107
[7]  
Kang J, 2018, J Clin Oncol, V36
[8]   Impact of TP53 mutation status on systemic treatment outcome in ALK-rearranged non-small-cell lung cancer [J].
Kron, A. ;
Alidousty, C. ;
Scheffler, M. ;
Merkelbach-Bruse, S. ;
Seidel, D. ;
Riedel, R. ;
Ihle, M. A. ;
Michels, S. ;
Nogova, L. ;
Fassunke, J. ;
Heydt, C. ;
Kron, F. ;
Ueckeroth, F. ;
Serke, M. ;
Krueger, S. ;
Grohe, C. ;
Koschel, D. ;
Benedikter, J. ;
Kaminsky, B. ;
Schaaf, B. ;
Braess, J. ;
Sebastian, M. ;
Kambartel, K. -O. ;
Thomas, R. ;
Zander, T. ;
Schultheis, A. M. ;
Buettner, R. ;
Wolf, J. .
ANNALS OF ONCOLOGY, 2018, 29 (10) :2068-2075
[9]   Anaplastic Lymphoma Kinase Inhibition in Non-Small-Cell Lung Cancer [J].
Kwak, Eunice L. ;
Bang, Yung-Jue ;
Camidge, D. Ross ;
Shaw, Alice T. ;
Solomon, Benjamin ;
Maki, Robert G. ;
Ou, Sai-Hong I. ;
Dezube, Bruce J. ;
Jaenne, Pasi A. ;
Costa, Daniel B. ;
Varella-Garcia, Marileila ;
Kim, Woo-Ho ;
Lynch, Thomas J. ;
Fidias, Panos ;
Stubbs, Hannah ;
Engelman, Jeffrey A. ;
Sequist, Lecia V. ;
Tan, WeiWei ;
Gandhi, Leena ;
Mino-Kenudson, Mari ;
Wei, Greg C. ;
Shreeve, S. Martin ;
Ratain, Mark J. ;
Settleman, Jeffrey ;
Christensen, James G. ;
Haber, Daniel A. ;
Wilner, Keith ;
Salgia, Ravi ;
Shapiro, Geoffrey I. ;
Clark, Jeffrey W. ;
Iafrate, A. John .
NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (18) :1693-1703
[10]   Potential Unreliability of Uncommon ALK, ROS1, and RET Genomic Breakpoints in Predicting the Efficacy of Targeted Therapy in NSCLC [J].
Li, Weihua ;
Guo, Lei ;
Liu, Yutao ;
Dong, Lin ;
Yang, Lin ;
Chen, Li ;
Liu, Kaihua ;
Shao, Yang ;
Ying, Jianming .
JOURNAL OF THORACIC ONCOLOGY, 2021, 16 (03) :404-418