Treatment of Thoracic SMARCA4-Deficient Undifferentiated Tumors: Where We Are and Where We Will Go

被引:9
|
作者
Longo, Vito [1 ]
Catino, Annamaria [1 ]
Montrone, Michele [1 ]
Montagna, Elisabetta Sara [1 ]
Pesola, Francesco [1 ]
Marech, Ilaria [1 ]
Pizzutilo, Pamela [1 ]
Nardone, Annalisa [2 ]
Perrone, Antonella [1 ]
Gesualdo, Monica [1 ]
Galetta, Domenico [1 ]
机构
[1] IRCCS Ist Tumori Giovanni Paolo II, Med Thorac Oncol Unit, I-70124 Bari, Italy
[2] IRCCS Ist Tumori Giovanni Paolo II, Unita Operat Complessa Radioterapia, I-70124 Bari, Italy
关键词
SMARCA4-UT; immunotherapy; clinicopathological features; SMALL-CELL CARCINOMA; CHROMATIN-REMODELING COMPLEX; SWI/SNF COMPLEX; SMARCA4; DIFFERENTIATION; SARCOMA; CDK4/6; REPRESSION; INHIBITORS; MORPHOLOGY;
D O I
10.3390/ijms25063237
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recently, the fifth edition of the WHO classification recognized the thoracic SMARCA4-deficient undifferentiated tumor (SMARCA4-UT) as a separate entity from conventional non-small cell lung cancer with SMARCA4 deficiency because of the different clinicopathological characteristics of these two diseases. SMARCA4-UT mainly occurs in young to middle-aged adults and involves a large mass compressing the tissues surrounding the mediastinum and lung parenchyma. Unfortunately, SMARCA4-UT shows a high probability of recurrence after upfront surgery as well as radiotherapy resistance; moreover, chemotherapy has low efficacy. Moreover, given the recent classification of SMARCA4-UT, no data concerning specific clinical trials are currently available. However, several case reports show immunotherapy efficacy in patients with this disease not only in a metastatic setting but also in a neoadjuvant manner, supporting the development of clinical trials. In addition, preclinical data and initial clinical experiences suggest that inhibiting pathways such as CDK4/6, AURKA, ATR, and EZH2 may be a promising therapeutic approach to SMARCA4-UT.
引用
收藏
页数:15
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