Publications by authors named "T Shukuya"

Background: MET gene exon 14 skipping was identified as a potential driver mutation that occurs in approximately 3%-4% of patients with nonsmall cell lung cancer (NSCLC), typically in the absence of other driver mutations. Capmatinib and tepotinib were the first MET- tyrosine kinase inhibitors (MET-TKIs) approved by the FDA and PMDA, specifically for patients with metastatic NSCLC. Several studies have reported acquired resistance after MET-TKI treatment for MET mutation-positive NSCLC.

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Objectives: This study aimed to investigate the characteristics of patients with recurrent or advanced non-small cell lung cancer (NSCLC) treated with tyrosine kinase inhibitors (TKIs) or immune-checkpoint inhibitors (ICIs) who developed secondary malignancies, as well as evaluate the impact of these secondary malignancies on the course of lung cancer.

Materials And Methods: This study included 112 patients with postoperative recurrent or advanced NSCLC, who received TKIs, ICIs, or immune combination therapy as the primary treatment modality between April 1, 2013, and March 31, 2020, and achieved long-term survival (≥2 years). Secondary malignancies were defined as newly diagnosed cancers in other organs occurring after NSCLC treatment initiation.

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Article Synopsis
  • Cancer cachexia frequently occurs in advanced non-small cell lung cancer (NSCLC) and its impact on chemotherapy is not fully understood.
  • A study involving 887 NSCLC patients identified that 31.7% experienced weight loss indicative of cachexia, with variations in quality of life (QOL) observed across different treatment groups.
  • Results showed that quality of life declined more significantly in chemotherapy patients compared to those receiving targeted therapies or immune checkpoint inhibitors, especially within the first week of treatment.
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Article Synopsis
  • - The study examined genomic alterations in non-small cell lung cancer (NSCLC) across a large sample of over 75,000 patients in the US and compared findings with a Japanese cohort to identify differences based on race, sex, and age.
  • - Significant variations in genetic alterations were observed: for example, EGFR mutations were more common in East Asian patients, while ALK mutations were prevalent in Admixed American, East Asian, and South Asian groups compared to others.
  • - Additionally, the analysis showed clear distinctions in mutation prevalence linked to sex and age, with certain mutations like EGFR and ALK being more frequent in females, while mutations such as TP53 and KEAP1 were more common in males; older patients
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Article Synopsis
  • Small cell lung cancer (SCLC) is a very aggressive and hard-to-treat cancer that hasn't seen much improvement in treatments for over 15 years.
  • Researchers looked at a database to find weak points in SCLC that could help develop new therapies.
  • They discovered that two important genes, SKP2 and CKS1B, are crucial for SCLC and blocking SKP2 could be a promising way to treat patients, no matter what specific type of cancer they have.
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