Landscape and Treatment Options of Shapeshifting Small Cell Lung Cancer

被引:1
|
作者
Gu, Yijun [1 ]
Benavente, Claudia A. [1 ,2 ,3 ]
机构
[1] Univ Calif Irvine, Dept Pharmaceut Sci, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Dev & Cell Biol, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Chao Family Comprehens Canc Ctr, Irvine, CA 92697 USA
关键词
small cell lung cancer; tumor plasticity; immunotherapy; targeted therapy; ANTIBODY-DRUG CONJUGATE; CIRCULATING TUMOR DNA; ROVALPITUZUMAB TESIRINE; MOUSE MODEL; C-KIT; NEUROENDOCRINE; EXPRESSION; P53; HETEROGENEITY; INHIBITION;
D O I
10.3390/jcm13113120
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Small cell lung cancer (SCLC) is a deadly neuroendocrine malignancy, notorious for its rapid tumor growth, early metastasis, and relatively "cold" immune environment. Only standard chemotherapies and a few immune checkpoint inhibitors have been approved for SCLC treatment, revealing an urgent need for novel therapeutic approaches. Moreover, SCLC has been recently recognized as a malignancy with high intratumoral and intertumoral heterogeneity, which explains the modest response rate in some patients and the early relapse. Molecular subtypes defined by the expression of lineage-specific transcription factors (ASCL1, NEUROD1, POU2F3, and, in some studies, YAP1) or immune-related genes display different degrees of neuroendocrine differentiation, immune cell infiltration, and response to treatment. Despite the complexity of this malignancy, a few biomarkers and targets have been identified and many promising drugs are currently undergoing clinical trials. In this review, we integrate the current progress on the genomic landscape of this shapeshifting malignancy, the characteristics and treatment vulnerabilities of each subtype, and promising drugs in clinical phases.
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页数:21
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