ALK-rearranged squamous cell carcinoma of the lung

被引:9
作者
Meng, Qiyi [1 ]
Dong, Yujie [2 ]
Tao, Hong [1 ]
Shi, Liang [1 ]
Tong, Li [1 ]
Tang, Junfang [1 ]
Zhang, Shucai [1 ]
Liu, Zhe [1 ]
机构
[1] Capital Med Univ, Beijing TB & Thorac Tumor Res Inst, Beijing Chest Hosp, Dept Med Oncol, Beijing, Peoples R China
[2] Capital Med Univ, Beijing Chest Hosp, Beijing TB & Thorac Tumor Res, Dept Pathol, Beijing, Peoples R China
关键词
ALK inhibitor drug; ALK rearrangement; immunotherapy; PDL1; squamous cell carcinoma; CANCER PATIENTS; FUSION GENE; CRIZOTINIB; IMMUNOHISTOCHEMISTRY; CHEMOTHERAPY; GUIDELINE; FISH;
D O I
10.1111/1759-7714.13818
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background ALK rearrangement is a very rare subset of squamous cell carcinoma (SCC) and one of the clinical features in patients is lack of data. Here, we report eight patients diagnosed with SCC of the lung harboring ALK rearrangement. Methods We collected primary NSCLC samples at the Beijing Chest Hospital between January 2012 and December 2018 for Ventana (D5F3) immunohistochemical detection. Among the 148 patients was diagnosed ALK-rearranged non small cell lung cancer (NSCLC), only eight cases was SCC. We collected patients information from electronic patent records (EPRs). Results The eight cases of SCC were diagnosed by immunohistochemistry (IHC). Two were given crizotinib as second-line therapy. One patient had stable disease (SD) and progression-free survival (PFS) of six months. The other patient had progressive disease (PD) but PFS was only one month. The side effects were tolerable. This report identified 31 cases of ALK rearrangement in SCC patients from a literature search (including the eight patients in this study). These fusion genes are often seen in a younger age group (mean age: 55.6 years) and non-smokers (18/31, 58.1%). A total of 20 cases received an ALK inhibitor as first- or second-line treatment which included 11 with a partial response (PR), four with SD, and five with PD. The DCR and ORR was 75.0% (15/20) and 55.0% (11/20), respectively. The median duration time of therapy was 6.4 +/- 4.4 months. Conclusions Patients with ALK-rearranged SCC obtained clinical benefit from ALK-inhibitor therapy, especially those who were non-smokers and whose tumors had been identified by IHC+/FISH+.
引用
收藏
页码:1106 / 1114
页数:9
相关论文
共 39 条
[1]   A rare case of squamous cell carcinoma of the lung harbouring ALK and BRAF activating mutations [J].
Alrifai, Doraid ;
Popat, Sanjay ;
Ahmed, Merina ;
Gonzalez, David ;
Nicholson, Andrew G. ;
du Parcq, John ;
Benepal, Tim .
LUNG CANCER, 2013, 80 (03) :339-340
[2]  
Bolzacchini Elena, 2017, J Thorac Oncol, V12, pe55, DOI 10.1016/j.jtho.2017.01.013
[3]   ALK/EML4 Fusion Gene May Be Found in Pure Squamous Carcinoma of the Lung [J].
Calio, Anna ;
Nottegar, Alessia ;
Gilioli, Eliana ;
Bria, Emilio ;
Pilotto, Sara ;
Peretti, Umberto ;
Kinspergher, Stefania ;
Simionato, Francesca ;
Pedron, Serena ;
Knuutila, Sakari ;
Tortora, Giampaolo ;
Eccher, Albino ;
Santo, Antonio ;
Tondulli, Luca ;
Inghirami, Giorgio ;
Tabbo, Fabrizio ;
Martignoni, Guido ;
Chilosi, Marco ;
Scarpa, Aldo ;
Brunelli, Matteo .
JOURNAL OF THORACIC ONCOLOGY, 2014, 9 (05) :729-732
[4]  
Chinese Association of Oncologists Chinese Society for Clinical Cancer Chemotherapy, 2013, Zhonghua Zhong Liu Za Zhi, V35, P478
[5]   Lung cancer epidemiology: contemporary and future challenges worldwide [J].
Didkowska, Joanna ;
Wojciechowska, Urszula ;
Manczuk, Marta ;
Lobaszewski, Jakub .
ANNALS OF TRANSLATIONAL MEDICINE, 2016, 4 (08)
[6]   New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1) [J].
Eisenhauer, E. A. ;
Therasse, P. ;
Bogaerts, J. ;
Schwartz, L. H. ;
Sargent, D. ;
Ford, R. ;
Dancey, J. ;
Arbuck, S. ;
Gwyther, S. ;
Mooney, M. ;
Rubinstein, L. ;
Shankar, L. ;
Dodd, L. ;
Kaplan, R. ;
Lacombe, D. ;
Verweij, J. .
EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) :228-247
[7]   ALK inhibitors for non-small cell lung cancer: A systematic review and network meta-analysis [J].
Elliott, Jesse ;
Bai, Zemin ;
Hsieh, Shu-Ching ;
Kelly, Shannon E. ;
Chen, Li ;
Skidmore, Becky ;
Yousef, Said ;
Zheng, Carine ;
Stewart, David J. ;
Wells, George A. .
PLOS ONE, 2020, 15 (02)
[8]   Lung cancer: current therapies and new targeted treatments [J].
Hirsch, Fred R. ;
Scagliotti, Giorgio V. ;
Mulshine, James L. ;
Kwon, Regina ;
Curran, Walter J. ;
Wu, Yi-Long ;
Paz-Ares, Luis .
LANCET, 2017, 389 (10066) :299-311
[9]   EML4-ALK rearrangement in squamous cell carcinoma shows significant response to anti-ALK inhibitor drugs crizotinib and alectinib [J].
Huang, Thomas ;
Engelmann, Brigitte J. ;
Morgan, Rachael M. ;
Absher, Kimberly J. ;
Kolesar, Jill M. ;
Villano, John L. .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2018, 81 (05) :965-968
[10]   Discrepancies between FISH and immunohistochemistry for assessment of the ALK status are associated with ALK 'borderline'-positive rearrangements or a high copy number: a potential major issue for anti-ALK therapeutic strategies [J].
Ilie, M. I. ;
Bence, C. ;
Hofman, V. ;
Long-Mira, E. ;
Butori, C. ;
Bouhlel, L. ;
Lalvee, S. ;
Mouroux, J. ;
Poudenx, M. ;
Otto, J. ;
Marquette, C. H. ;
Hofman, P. .
ANNALS OF ONCOLOGY, 2015, 26 (01) :238-244