Publications by authors named "Ryohiko Ozaki"

Immune checkpoint inhibitors (ICIs) targeting programmed death ligand-1 (PD-L1) provide clinical benefits for various advanced malignancies. However, the predictive factors that determine sensitivity to ICIs have not been fully elucidated. We focused on tumor-derived CXCL10/11 as a pivotal factor that determines the response to PD-L1 blockade by regulating T cell accumulation and tumor angiogenesis.

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Article Synopsis
  • - Histological transformation from lung adenocarcinoma to small-cell lung cancer (SCLC) can occur as a resistance mechanism to EGFR-TKIs, typically seen during treatment, but can also happen long after stopping the drugs.
  • - The study reports three cases where patients experienced this transformation with rapid tumor progression and increased levels of SCLC markers.
  • - Emphasizing continuous monitoring of tumor behavior and SCLC markers is crucial to prevent delays in diagnosis and ensure timely treatment adjustments.
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Background: Granulocyte colony-stimulating factor (G-CSF) has the potential to attenuate the anti-tumor immune responses of T-cells by increasing immune suppressive neutrophils and myeloid-derived suppressor cells. However, the clinical impact of G-CSF on the efficacy of immunotherapy remains unknown. This multi-center retrospective analysis evaluated the impact of G-CSF in patients with extensive-stage small-cell lung cancer (ES-SCLC) treated with chemo-immunotherapy.

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Article Synopsis
  • Immune checkpoint inhibitors (ICIs) and chemoimmunotherapy are key treatments for thoracic cancers, but it's unclear which chemotherapy agents are best to combine with ICIs for effectiveness in non-small cell lung cancer (NSCLC).
  • Researchers tested various chemotherapeutics (including 5-fluorouracil, pemetrexed, and platinum) to see which best induced immunogenic cell death (ICD), a desirable immune response, and found that 5-FU was the most effective.
  • The study concluded that 5-FU, especially when combined with platinum, not only triggers ICD but also enhances immune response, making it a potentially optimal partner for ICIs in treating thoracic cancers.
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A non-smoker woman with advanced lung adenocarcinoma was referred to us. The Oncomine Dx target test (ODxTT), a next-generation sequencing (NGS)-based hot spots panel test, did not detect any driver mutations, so we treated her with chemo-immunotherapy. After second-line chemotherapy, we performed FoundationOne CDx, a NGS-based comprehensive genomic profiling (CGP) test, and identified a rare variant of exon 19 deletion that had not been covered by ODxTT.

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Article Synopsis
  • A man with non-small-cell lung cancer experienced dyspnea after receiving an immune checkpoint inhibitor (ICI), leading to a CT scan that revealed complex lung issues.
  • Despite being treated with high-dose steroids for suspected ICI-related pneumonitis, his condition worsened with increased fibrosis and lung volume loss.
  • A re-assessment found a pre-existing autoimmune disorder indicated by the presence of anti-aminoacyl-tRNA synthetase antibody, stressing the need for careful evaluation of autoimmune conditions in patients with unusual ICI-related lung complications.
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Fibrocytes, which are bone marrow-derived collagen-producing cells, have been reported to be involved in pathogenesis of pulmonary fibrosis. Our previous study reported that tumor-infiltrating fibrocytes play a role in tumor progression and drug resistance in lung cancer. The present study therefore examined chemotactic factors for fibrocytes in tissues of non-small cell lung cancer (NSCLC) and their prognostic significance.

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Background: Treatment of non-small cell lung cancer (NSCLC) patients with interstitial lung disease (ILD) is limited because of the risk of its acute exacerbation (AE). Furthermore, the efficacy and safety of second-line chemotherapy for these patients is unclear.

Methods: To investigate the efficacy and safety of second-line chemotherapy for NSCLC patients with ILD, we retrospectively reviewed patients who were treated at our institute between April 2010 and December 2018.

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Background: Osimertinib is a standard first-line treatment for advanced non-small-cell lung cancer (NSCLC) harboring epidermal growth factor receptor (EGFR) mutations. Although malignant pleural effusion (PE) is a common clinical problem in NSCLC, information about the efficacy of osimertinib in patients with PE is limited, especially regarding its efficacy in EGFR T790M-negative patients with PE remains unclear.

Methods: We retrospectively reviewed the medical records of patients with NSCLC harboring EGFR mutations who were treated with osimertinib in our institution between May 2016 and December 2020.

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Pulmonary pleomorphic carcinoma is often refractory to chemotherapy and follows an aggressive clinical course. Immune checkpoint inhibitors (ICIs) have revolutionized the treatment of advanced lung cancer, and a few cases with pleomorphic carcinoma have been reported to show tumor shrinkage after therapy with ICIs. When treating patients with ICIs, patient selection is essential, and monitoring and management of immune-related adverse events, including pneumonitis, are needed.

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Background: Nivolumab is used for the treatment of malignant pleural mesothelioma (MPM). However, immune-related adverse events (irAEs) occur in patients treated with nivolumab. Several studies have reported the correlation between irAEs and therapeutic effects of immune checkpoint inhibitor, but none have reported the correlation in MPM.

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A 61-year-old man had hypertension with stenosis in the left renal artery. When his fever, abdominal pain, and renal dysfunction progressed, he was admitted to our hospital. He was diagnosed with polyarthritis nodosa.

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