Literature DB >> 31032071

Multiple primary lung cancer: a rising challenge.

Chen Chen1, Xiaojie Huang2, Muyun Peng1, Wenliang Liu1, Fenglei Yu1, Xiang Wang1.   

Abstract

With the use of high-resolution chest imaging system and lung cancer screening program, patients with multiple primary lung cancers (MPLCs) are becoming a growing population in clinical practice worldwide. The diagnostic criteria for MPLCs has been established and modified by three major lung cancer research institutes. However, due to the fact that the differential diagnosis between MPLCs and a recurrence, metastatic, or satellite lesion arising from the original lesion remains ambiguous and confusing, there is still insufficient evidence to support a uniform guideline. Newly developed molecular and genomic methods have the potential to better define the relationship among multiple lesions and bring the possibility of targeted therapy. Surgical resection remains the first choice for the treatment of MPLCs and detailed strategy should be carefully planned taking characteristics of the tumor and status of patients into consideration. For those who are intolerant to surgery, a new technology called stereotactic body radiation therapy (SBRT) is now an optional therapeutic strategy. Furthermore, multiple GGOs are unique MPLCs that need special attentions in the clinical practice.

Entities:  

Keywords:  Multiple primary lung cancers (MPLCs); diagnosis; ground-glass opacity (GGO); stereotactic body radiation therapy (SBRT); surgery

Year:  2019        PMID: 31032071      PMCID: PMC6465434          DOI: 10.21037/jtd.2019.01.56

Source DB:  PubMed          Journal:  J Thorac Dis        ISSN: 2072-1439            Impact factor:   2.895


  14 in total

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7.  Next-generation sequencing facilitates differentiating between multiple primary lung cancer and intrapulmonary metastasis: a case series.

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Authors:  Baodong Liu; Xin Ye
Journal:  Thorac Cancer       Date:  2020-08-03       Impact factor: 3.500

10.  Lung cancer A549 cells suppressed with overexpressed HNF1B or PCDHA13 inhibited PI3K/AKT phosphorylation.

Authors:  Chunyan Kang; Lingxiao Wang; Dandan Wang; Xiuzhi Zhang; Jie Chen
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