Publications by authors named "Noriaki Sunaga"

Histologic transformation from non-small cell to small cell lung cancer (SCLC) is a resistance mechanism to immune checkpoint inhibitors. We report herein a case of lung adenocarcinoma who developed liver and brain metastases during adjuvant atezolizumab therapy. The patient underwent a craniotomy to resect a brain metastasis, which was pathologically diagnosed as SCLC.

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BACKGROUND Most Fusobacterium necrophorum infections originate in the head and neck region. Infections originating from sites other than the head and neck are rare but are more common in older than in younger adults and have a higher mortality rate than that of infections originating from the head and neck region. CASE REPORT We present the case of a previously healthy 16-year-old female patient who developed bacteremia and pleural effusions with a burn ulcer on the lower leg but had no abnormality in the head and neck region.

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Background: Autoimmune pulmonary alveolar proteinosis (APAP) is a diffuse lung disease that causes abnormal accumulation of lipoproteins in the alveoli; however, its pathogenesis remains unclear. Recently, APAP cases have been reported during the course of dermatomyositis. The combination of these two diseases may be coincidental; however, it may have been overlooked because differentiating APAP from a flare-up of interstitial pneumonia associated with dermatomyositis is challenging.

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Background: The antifibrotic agents pirfenidone and nintedanib have been shown to be effective in patients with idiopathic pulmonary fibrosis (IPF). However, discontinuation of antifibrotic drugs is a major clinical concern because of the lack of alternative treatment options. Therefore, we identified factors that may be useful for predicting the termination of antifibrotic agents.

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Background: Regional lymph node recurrence after radical surgery for non-small cell lung cancer (NSCLC) is an oligo-recurrent disease; however, no treatment strategy has been established. In the present study we aimed to determine the clinical outcomes of postoperative regional lymph node recurrence and identify prognostic predictors in the era of molecular-targeted therapy.

Methods: We retrospectively analyzed data on clinical characteristics and outcomes of patients with regional lymph node recurrence after surgery who underwent treatment for NSCLC between 2002 and 2022.

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Epidermal growth factor (EGF) signaling regulates multiple cellular processes and plays an essential role in tumorigenesis. Epiregulin (EREG), a member of the EGF family, binds to the epidermal growth factor receptor (EGFR) and ErbB4, and it stimulates EGFR-related downstream pathways. Increasing evidence indicates that both the aberrant expression and oncogenic function of EREG play pivotal roles in tumor development in many human cancers, including non-small cell lung cancer (NSCLC).

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Background: Molecular abnormalities in the Wnt/β-catenin pathway confer malignant phenotypes in lung cancer. Previously, we identified the association of leucine-rich repeat-containing G protein-coupled receptor 6 (LGR6) with oncogenic Wnt signaling, and its downregulation upon β-catenin knockdown in non-small cell lung cancer (NSCLC) cells carrying CTNNB1 mutations. The aim of this study was to explore the mechanisms underlying this association and the accompanying phenotypes.

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Circulating tumor DNA (ctDNA) provides molecular information on tumor heterogeneity. The prognostic usefulness of ctDNA after first-line epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) are limited. Therefore, the present study evaluated ctDNA during osimertinib administration as a second-line or more setting to identify the relationship between EGFR mutation levels and outcomes in patients with advanced non-small cell lung cancer (NSCLC).

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  • GRHL2 is a transcription factor that plays a complex role in cancer, acting as both an oncogene and tumor suppressor, but its function in lung cancer was previously unclear.
  • Recent meta-analysis indicates that GRHL2 expression is elevated in lung cancer tissues compared to normal tissues, likely due to gene amplification, but does not correlate with overall survival outcomes.
  • Knockdown experiments demonstrate that GRHL2 influences epithelial-to-mesenchymal transition (EMT) in lung cancer cells in a cell type-dependent manner, affecting signaling pathways and proliferation differently across various lung cancer cell lines.
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  • A study was conducted to develop a multigene mutation test called MINtS that uses easily obtained cytological specimens instead of tissue samples, which are more difficult to source.* -
  • The research involved 500 specimens from 19 institutions, successfully detecting druggable mutations in 63% of adenocarcinomas, highlighting the test's effectiveness.* -
  • Some discrepancies were found between MINtS results and traditional methods for certain genes, but further validation confirmed the accuracy of MINtS, paving the way for future multigene testing using cytological samples.*
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  • Eosinophilic granulomatosis with polyangiitis (EGPA) is a type of systemic vasculitis that damages small to medium-sized blood vessels and can harm various organs due to high eosinophil levels.
  • Recent treatment guidelines for active non-severe EGPA have included the use of the anti-interleukin-5 antibody mepolizumab, but its effectiveness for severe cases isn't clearly established.
  • In a case study, a patient with EGPA and a serious complication (small intestine perforation) was treated successfully with steroids, immunoglobulin therapy, and mepolizumab, leading to remission, suggesting mepolizumab could be beneficial for severe EGPA cases.
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  • * It has recently been approved in Japan for treating unresectable thymic carcinoma, although there's limited real-world evidence of its effectiveness.
  • * A case study showed that a patient with chemotherapy-resistant thymic carcinoma had a strong, 17-month response to a modified dosing schedule of lenvatinib, indicating that strategic dosing can improve outcomes.
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Epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors are standard therapeutic agents for non-small cell lung cancer (NSCLC) patients with major EGFR mutations such as exon 19 deletions and a L858R mutation, whereas treatment strategies for cases with uncommon EGFR mutations remain to be fully established. Here, we report a long-term (≥20 years from initial diagnosis) NSCLC survivor carrying EGFR L858R and L747V mutations. The patient received gefitinib monotherapy, systemic chemotherapy/chemoimmunotherapy, and local consolidative therapies for oligometastatic lesions, and responded to afatinib rechallenge with a progression-free survival of 12 months.

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Diseases caused by Mycobacterium avium complex (MAC) infection in the lungs are increasing worldwide. The recurrence rate of MAC-pulmonary disease (PD) has been reported to be as high as 25-45%. A significant percentage of recurrences occurs because of reinfection with a new genotype from the environment.

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  • - The study investigates the relationship between sarcoidosis and tumor development, analyzing data from 312 cases of sarcoidosis and noting 25 patients who were diagnosed with malignant tumors after their sarcoidosis diagnosis.
  • - Analysts found that some markers related to sarcoidosis activity, such as serum angiotensin I-converting enzyme levels and mediastinal lymph node size, decreased at the time of malignant tumor diagnosis, suggesting a potential link between decreasing sarcoidosis activity and tumor development.
  • - Patients with a history of malignant tumors tended to be older and exhibited less severe cases of sarcoidosis, indicating that prior tumors may impact the progression and treatment of the disease, particularly regarding the use of corticosteroid therapy.
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  • - Sarcoidosis, a disease causing granuloma formation in various organs like the lungs, is diagnosed mainly through clinicopathologic findings with traditional markers being ACE and sIL-2R, though new specific markers are needed.
  • - This study found that serum neuron-specific enolase (NSE) levels are elevated in sarcoidosis patients and correlate positively with ACE and sIL-2R levels, with the best diagnostic sensitivity achieved when combining NSE with these traditional markers.
  • - Elevated serum NSE not only differentiates sarcoidosis from small cell lung cancer (SCLC) and other benign conditions but also reflects disease activity and treatment response, showing potential as a marker for diagnosis and monitoring of sarcoidosis.
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  • Obesity is linked to worse outcomes in patients with anti-ARS antibody-related interstitial lung disease (ILD), as it affects lung function and increases disease relapse rates.
  • A study involving 58 patients found that obese individuals had lower lung diffusing capacity and higher fat deposits compared to nonobese patients.
  • The research highlights the importance of measuring chest fat using CT scans to predict ILD relapses, particularly noting that higher levels of certain fat types correlate with increased disease severity.
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  • * A study compared the treatment continuity of two antifibrotic drugs, pirfenidone and nintedanib, in 261 IPF patients, concluding that although both groups had similar overall treatment discontinuation rates, nintedanib was linked to a higher discontinuation rate due to adverse events within the first year (76% vs. 37%).
  • * The findings suggest that while both drugs have their challenges, better management of side effects in nintedanib can lead to longer treatment durations, helping to prevent disease worsening
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Recent advances in molecular biology and the resultant identification of driver oncogenes have achieved major progress in precision medicine for non-small-cell lung cancer (NSCLC). v-Ki-ras2 Kirsten rat sarcoma viral oncogene () is the most common driver in NSCLC, and targeting KRAS is considerably important. The recent discovery of covalent KRAS G12C inhibitors offers hope for improving the prognosis of NSCLC patients, but the development of combination therapies corresponding to tumor characteristics is still required given the vast heterogeneity of -mutated NSCLC.

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Coronavirus disease 2019 (COVID-19) has become a global pandemic since its discovery in December 2019, and as the disease continues to evolve, varying complications associated with it continue to arise. In this regard, computed tomography has played an extremely important role in the diagnosis and evaluation of COVID-19 pneumonia and its complications. We encountered a case of a male patient with neurofibromatosis (type I) who developed concurrent pneumothorax and pleural effusion during his recovery period from severe COVID-19 pneumonia.

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  • The FAM83G protein family, specifically the S356 site, interacts with PKD1/PKCμ and affects the phosphorylation of heat shock protein 27 (HSP27), which is involved in cell survival and apoptosis.
  • Overexpression of wild-type FAM83G decreased cell viability and altered HSP27 phosphorylation, while a phosphorylation-resistant mutant did not affect cell number or apoptosis induction.
  • In lung cancer cells, FAM83G mRNA levels varied, suggesting a complex role in cancer biology where its phosphorylation might influence HSP27 and apoptosis pathways.
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  • Recent studies suggest afatinib is effective for non-small cell lung cancer (NSCLC) patients with rare EGFR mutations, but its long-term effectiveness through rechallenge is still under investigation.
  • This report features a case where a patient with dual EGFR mutations (G719C and S768I) had a significant survival outcome after receiving afatinib again followed by chemotherapy.
  • The findings highlight the potential benefit of combining treatments and the importance of timing rebiopsies for optimizing therapy in NSCLC cases with uncommon mutations.
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Background: Lung cancer is the leading cause of cancer-related deaths. Although epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) are effective for advanced non-small cell lung cancer (NSCLC) harboring EGFR mutations, some patients experience little or no response. The Glasgow prognostic score (GPS) is an inflammation-related score based on C-reactive protein (CRP) and albumin concentrations, and has prognostic value in various cancer settings.

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Background/aim: The efficacy of the combination of amrubicin and bevacizumab against advanced non small-cell lung cancer (NSCLC), as a second or third-line treatment, was evaluated.

Patients And Methods: Amrubicin was administered for 3 days to patients with previously treated advanced NSCLC, whereas bevacizumab was administered on day 1 of each cycle; this regimen was repeated every 3 weeks.

Results: Among the 16 patients, an overall response rate of 12.

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