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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.
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页数:15
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