Publications by authors named "Hongquan Xing"

Nearly half of lung large cell neuroendocrine carcinoma (LCNEC) patients are diagnosed at an advanced stage and face a high early death risk. Our objective was to develop models for assessing early death risk in stage IV LCNEC patients. We used surveillance, epidemiology, and end results (SEER) databases to gather data on patients with stage IV LCNEC to construct models and conduct internal validation.

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Article Synopsis
  • Crizotinib (CRZ) is a medication used to treat ALK-positive lung adenocarcinoma, but its effectiveness is often hindered by the overexpression of P-glycoprotein, which leads to multidrug resistance (MDR).
  • To combat this MDR, researchers developed a targeted nanosystem called ZIF-90@ICG that disrupts mitochondrial function, reduces ATP levels, and decreases P-gp expression, helping to enhance the drug's effectiveness.
  • Additionally, the nanosystem was modified with hyaluronic acid to specifically target cancer cells, resulting in increased accumulation of CRZ in these cells and improving the treatment outcomes for patients resistant to ALK inhibitors.
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Objectives: Our purpose is to evaluate the patterns of organ metastasis and the prognosis in lung adenosquamous carcinoma patients with organ metastasis.

Methods: We collected the data from the surveillance epidemiology and end results database, covering the period of 2000-2018. Cox regression, Kaplan-Meier and log-rank analyses were performed.

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Cardiovascular mortality (CVM) is a growing concern for cancer survivors. This study aimed to investigate the mortality patterns of individuals with typical carcinoid (TC) tumors, identify independent predictors of CVM, and compare these risk variables with those associated with TC deaths. The Surveillance, Epidemiology, and End Results (SEER) database from 2000 to 2019 was utilized for obtaining data on patients with TC.

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Lung cancer (LC) is one of the most incident malignancies and a leading cause of cancer mortality worldwide. Common tumorigenic drivers of LC mainly include genetic alterations of EGFR, ALK, KRAS, BRAF, ROS1, and MET. Small inhibitory molecules and antibodies selectively targeting these alterations or/and their downstream signaling pathways have been approved for treatment of LC.

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