Squamous-cell carcinomas of the lung: emerging biology, controversies, and the promise of targeted therapy

被引:159
作者
Drilon, Alexander [1 ]
Rekhtman, Natasha [2 ]
Ladanyi, Marc [2 ,3 ]
Paik, Paul [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Thorac Oncol Serv, Dept Med, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Human Oncol & Pathogenesis Program, New York, NY 10021 USA
关键词
FIBROBLAST-GROWTH-FACTOR; CISPLATIN PLUS GEMCITABINE; PHASE-III TRIAL; FACTOR RECEPTOR; COPY NUMBER; CLINICOPATHOLOGICAL FEATURES; 1ST-LINE CHEMOTHERAPY; PROMOTER METHYLATION; ONCOGENE MUTATIONS; CANCER INCIDENCE;
D O I
10.1016/S1470-2045(12)70291-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Squamous-cell carcinomas of the lung (SQCLCs) are defined by unique clinicopathological and molecular characteristics that have evolved substantially over time. Historically, these neoplasms were the most common subtype of non-small-cell lung cancers and were regarded as central tumours with high molecular complexity without targetable genetic abnormalities. Today, the incidence of SQCLCs is surpassed by adenocarcinomas of the lung with a shift towards peripheral squamous tumours. Differential responses to cytotoxic and biological treatments have reshaped our approach to standard therapies. Additionally, evidence of unique biology has emerged with the discovery of SOX2 amplification, NFE2L2 and KEAP1 mutations, PI3K pathway changes, FGFR1 amplification, and DDR2 mutations. These discoveries have ushered in a new era of targeted therapeutic agents for patients with this disease. This Review draws attention to the distinct clinical and pathological characteristics of SQCLCs, summarises present experience with existing cytotoxic and targeted therapies, and discusses emerging treatments based on new insights into the biology of this disease.
引用
收藏
页码:E418 / E426
页数:9
相关论文
共 78 条
  • [1] [Anonymous], 2004, Pathology and Genetics of Tumours of the Urinary System and Male Genital Organs
  • [2] SOX2 is an amplified lineage-survival oncogene in lung and esophageal squamous cell carcinomas
    Bass, Adam J.
    Watanabe, Hideo
    Mermel, Craig H.
    Yu, Soyoung
    Perner, Sven
    Verhaak, Roel G.
    Kim, So Young
    Wardwell, Leslie
    Tamayo, Pablo
    Gat-Viks, Irit
    Ramos, Alex H.
    Woo, Michele S.
    Weir, Barbara A.
    Getz, Gad
    Beroukhim, Rameen
    O'Kelly, Michael
    Dutt, Amit
    Rozenblatt-Rosen, Orit
    Dziunycz, Piotr
    Komisarof, Justin
    Chirieac, Lucian R.
    LaFargue, Christopher J.
    Scheble, Veit
    Wilbertz, Theresia
    Ma, Changqing
    Rao, Shilpa
    Nakagawa, Hiroshi
    Stairs, Douglas B.
    Lin, Lin
    Giordano, Thomas J.
    Wagner, Patrick
    Minna, John D.
    Gazdar, Adi F.
    Zhu, Chang Qi
    Brose, Marcia S.
    Cecconello, Ivan
    Ribeiro, Ulysses, Jr.
    Marie, Suely K.
    Dahl, Olav
    Shivdasani, Ramesh A.
    Tsao, Ming-Sound
    Rubin, Mark A.
    Wong, Kwok K.
    Regev, Aviv
    Hahn, William C.
    Beer, David G.
    Rustgi, Anil K.
    Meyerson, Matthew
    [J]. NATURE GENETICS, 2009, 41 (11) : 1238 - U105
  • [3] p40 (ΔNp63) is superior to p63 for the diagnosis of pulmonary squamous cell carcinoma
    Bishop, Justin A.
    Teruya-Feldstein, Julie
    Westra, William H.
    Pelosi, Giuseppe
    Travis, William D.
    Rekhtman, Natasha
    [J]. MODERN PATHOLOGY, 2012, 25 (03) : 405 - 415
  • [4] HPV Analysis in Distinguishing Second Primary Tumors From Lung Metastases in Patients With Head and Neck Squamous Cell Carcinoma
    Bishop, Justin A.
    Ogawa, Takenori
    Chang, Xiaofei
    Illei, Peter B.
    Gabrielson, Edward
    Pai, Sara I.
    Westra, William H.
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2012, 36 (01) : 142 - 148
  • [5] Braakhuis BJM, 2003, CANCER RES, V63, P1727
  • [6] ALK-Rearranged Lung Cancer Adenosquamous Lung Cancer Masquerading as Pure Squamous Carcinoma
    Chaft, Jamie E.
    Rekhtman, Natasha
    Ladanyi, Marc
    Riely, Gregory J.
    [J]. JOURNAL OF THORACIC ONCOLOGY, 2012, 7 (04) : 768 - 769
  • [7] Coexistence of PIK3CA and Other Oncogene Mutations in Lung Adenocarcinoma-Rationale for Comprehensive Mutation Profiling
    Chaft, Jamie E.
    Arcila, Maria E.
    Paik, Paul K.
    Lau, Christopher
    Riely, Gregory J.
    Pietanza, M. Catherine
    Zakowski, Maureen F.
    Rusch, Valerie
    Sima, Camelia S.
    Ladanyi, Marc
    Kris, Mark G.
    [J]. MOLECULAR CANCER THERAPEUTICS, 2012, 11 (02) : 485 - 491
  • [8] Somatic mutations of the protein kinase gene family in human lung cancer
    Davies, H
    Hunter, C
    Smith, R
    Stephens, P
    Greenman, C
    Bignell, G
    Teague, B
    Butler, A
    Edkins, S
    Stevens, C
    Parker, A
    O'Meara, S
    Avis, T
    Barthorpe, S
    Brackenbury, L
    Buck, G
    Clements, B
    Cole, J
    Dicks, E
    Edwards, K
    Forbes, S
    Gorton, M
    Gray, K
    Halliday, K
    Harrison, R
    Hills, K
    Hinton, J
    Jones, D
    Kosmidou, V
    Laman, R
    Lugg, R
    Menzies, A
    Perry, J
    Petty, R
    Raine, K
    Shepherd, R
    Small, A
    Solomon, H
    Stephens, Y
    Tofts, C
    Varian, J
    Webb, A
    West, S
    Widaa, S
    Yates, A
    Brasseur, F
    Cooper, CS
    Flanagan, AM
    Green, A
    Knowles, M
    [J]. CANCER RESEARCH, 2005, 65 (17) : 7591 - 7595
  • [9] Inhibition of collagen-induced discoidin domain receptor 1 and 2 activation by imatinib, nilotinib and dasatinib
    Day, Elizabeth
    Waters, Beatrice
    Spiegel, Katrin
    Alnadaf, Tanja
    Manley, Paul W.
    Buchdunger, Elisabeth
    Walker, Christoph
    Jarai, Gabor
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 2008, 599 (1-3) : 44 - 53
  • [10] Rarity of AKT1 and AKT3 E17K mutations in squamous cell carcinoma of lung
    Do, Hongdo
    Salemi, Renato
    Murone, Carmel
    Mitchell, Paul L.
    Dobrovic, Alexander
    [J]. CELL CYCLE, 2010, 9 (21) : 4411 - 4412